Coloring components, films, color filters, solid-state imaging elements and image display devices

Abstract

This invention provides a coloring composition comprising a coloring agent A containing dye a and a resin B. Dye a contains dye a1, which comprises a cationic AX+ and anionic AZ- having a pigment structure. The content of dye a1 in dye a is 50% by mass or more. Resin B contains resin b1, which has an acid value and an amine value, with the amine value being higher than the acid value. This invention also provides a film, a color filter, a solid-state imaging element, and an image display device using the coloring composition.

Description

Coloring composition, film, color filter, solid-state imaging element and image display device The present invention relates to a coloring composition containing the Guchiyamaguchi star dye. Furthermore, the present invention relates to a film, a color filter, a solid-state imaging element and an image display device using a colored composition. In recent years, with the popularity of digital cameras, mobile phones with cameras, etc., the demand for solid-state imaging components such as charge-coupled element (CCD) image sensors has increased greatly. As the core device of a display or optical element, a color filter is used. The coloring pixels of each color of the color filter are made of a coloring composition containing a coloring agent such as a dye. For example, Patent Document 1 describes a coloring composition containing the Guchiyamaguchi star dye. [Patent Document 1] Japanese Patent Laid-Open No. 2016-133604 The present inventors conducted in-depth research on the coloring composition containing the Guchiyamaguchi star dye, and found that there is room for further improvement in the pattern linearity of the pixels obtained using the coloring composition. Therefore, the object of the present invention is to provide a color composition capable of forming pixels with excellent pattern linearity. Furthermore, an object of the present invention is to provide a film, a color filter, a solid-state imaging element and an image display device using a colored composition. The present invention provides the following. <1> A coloring composition, which comprises a coloring composition containing a coloring agent A and a resin B, in which the dye a contains a cation AX containing a pigment structure of the guchiyamaguchi + and anion AZ - The content of the above-mentioned dye a is 50% by mass or more. The above-mentioned resin B contains the resin b1 having an acid value and an amine value and an amine value higher than the acid value. <2> The coloring composition as described in <1>, wherein the content of the above-mentioned coloring agent A in the total solid component of the coloring composition is 30 to 70 mass %. <3> The coloring composition as described in <1> or <2>, wherein the above-mentioned cation AX is the above-mentioned cation AX + and the above anion AZ - Bonding via covalent bonds. <4> The coloring composition as described in any one of <1> to <3>, wherein the anion AZ is - Iimide anion. <5> The coloring composition as claimed in any one of <1> to <4>, wherein the above-mentioned Guchiyamaguchi star dye a1 has an acid group. <6> The coloring composition as described in any one of <1> to <5>, wherein the above-mentioned Koichiaki star dye a1 is a dye polymer having more than two Koichiaki star pigment structures in one molecule. <7> The coloring composition as claimed in any one of <1> to <6>, wherein the above-mentioned coloring agent A further contains a pigment. <8> The coloring composition as described in <7>, wherein the above pigment contains at least one selected from the group consisting of quinacridone pigment, di- urethral phenol azo pigment, and diketopyrrolopyrrole pigment. <9> The coloring composition as described in <7>, wherein the above-mentioned pigment contains at least one selected from the group consisting of colorimetric index pigment red 122, colorimetric index pigment red 202, colorimetric index pigment red 209, colorimetric index pigment red 254, colorimetric index pigment red 269, colorimetric index pigment red 272, colorimetric index pigment purple 19 and colorimetric index pigment purple 23. <10> The coloring composition as claimed in any one of <1> to <9>, wherein the resin b1 comprises a resin having a repeating unit of a graft chain. <11> The coloring composition as claimed in any one of <1> to <10> further contains an ionic compound C, which is a cationic CX + and anionic CZ - The following formula (A) is the maximum absorption wavelength in the range of 400 to 700 nm. λ ) indicates that the absorbance of the ratio is less than 5, E=A 1 / (c×l) ···(A λ ) Formula (A λ ), E represents the specific absorbance of the ionic compound C at the maximum absorption wavelength in the range of 400 to 700 nm, A 1 The absorbance of the ionic compound C at the maximum absorption wavelength in the range of 400 to 700 nm is indicated, l represents the groove length in unit of cm, and c represents the concentration of the ionic compound C in the solution represented by mg / ml. <12> The coloring composition as claimed in any one of <1> to <11>, which is used to form a purple-red pixel. <13> A film obtained by using the coloring composition of any one of <1> to <12>. <14> A color filter comprising the film as described in <13>. <15> A solid-state imaging element, which includes the film described in <13>. <16> An image display device comprising the film described in <13>. [Invention effect] According to the present invention, it is possible to provide a color composition capable of forming pixels with excellent pattern linearity. Furthermore, a film, a color filter, a solid-state imaging element and an image display device using a colored composition can be provided. The contents of the present invention will be described in detail below. In this specification, "~" means the meaning of using the values ​​described before and after it as the lower limit value and the upper limit value. In the labels of groups (atomic groups) in this specification, the unlabeled and unsubstituted labels include groups (atomic groups) without substituents and also include groups (atomic groups) with substituents. For example, "alkyl" includes not only an alkyl group (unsubstituted alkyl group) without a substituent, but also an alkyl group (substituted alkyl group) with a substituent. In this specification, as long as "exposure" is not specifically specified, it includes not only exposure using light, but also drawing using particle beams such as electron beams, ion beams, etc. Also, as the light used in exposure, there are examples of photoreflective rays or radiation such as bright rays of mercury lamps, far ultraviolet rays, extreme ultraviolet rays (EUV light), X-rays, electron beams, etc. In this specification, "(meth)acrylate" means both or either of acrylate and methacrylate, "(meth)acrylic acid" means both or either of acrylic acid and methacrylic acid, and "(meth)acryl" means both or of acrylic and methacryl. In this specification, marks marked before and after the name (for example, A, B, C, etc.) are terms used to distinguish the constituent elements and do not limit the types of constituent elements, the number of constituent elements, and the advantages and disadvantages of constituent elements. In this specification, Me in the structural formula represents methyl, Et represents ethyl, Bu represents butyl, and Ph represents phenyl. In this specification, the weight average molecular weight and the quantity average molecular weight are the polystyrene conversion values ​​measured by GPC (gel permeation chromatography) method. In this specification, the total solid component refers to the total mass of the component that removes the solvent from all components of the composition. In this specification, the term "step" includes not only independent steps, but also included in this term, even if it cannot be clearly distinguished from other steps. <Coloring Composition> The coloring composition of the present invention includes a coloring composition containing a coloring agent A and resin B, characterized in that dye a contains a cation AX containing a pigment structure of Guchiyamaguchi. + and anion AZ - The content of the above-mentioned guchi Yamaguchi star dye a1 in the dye a is 50% by mass or more, and the above-mentioned resin B contains the resin b1 having an acid value and an amine value and an amine value higher than the acid value. According to the coloring composition of the present invention, by containing the above-mentioned resin b1, the aggregation of the guchi Yamaguchi star dye a1 with each other in the film or the aggregation of the coloring agent other than the guchi Yamaguchi star dye a1 and the guchi Yamaguchi star dye a1 and the guchi Yamaguchi star dye a1 can be suppressed. Therefore, by using the coloring composition of the present invention, pixels with excellent pattern linearity can be formed. It is preferred that the coloring composition of the present invention be a coloring composition for forming a purple-red pixel. Regarding the coloring composition of the present invention, when the absorbance of light with a wavelength of 540 nm is set to 1, it is preferable that the maximum absorbance of light in the wavelength range of 400 to 450 nm is 0.5 or less and the maximum absorbance of light in the wavelength range of 600 to 700 nm is 0.5 or less. It is more preferable to have a maximum absorbance of light in the wavelength range of 400 to 450 nm or less, and it is even more preferable to have a maximum absorbance of 0.2 or less. It is more preferable that the maximum absorbance of light in the wavelength range of 600 to 700 nm is 0.3 or less, and it is even more preferable. The coloring composition having such spectral characteristics can be preferably used as a coloring composition for forming purple-red pixels. Regarding the coloring composition of the present invention, when the absorbance of light with a wavelength of 540 nm is set to 1, it is preferred that there are wavelength ranges of 450 to 520 nm and wavelength ranges of 550 to 600 nm respectively, respectively. From the reason why the color separation from the colored pixels of other colors such as blue and yellow can be sufficiently separated, and the color reproducibility of the image sensor can be improved, it is more preferable that the wavelength at the short wavelength side of 0.3 (hereinafter also referred to as λ1) exists in the wavelength range of 460 to 510 nm, and it is even more preferable that the wavelength range of 470 to 500 nm. Furthermore, for the same reason as above, it is more preferable that the wavelength at which the absorbance is a wavelength side of 0.3 (hereinafter also referred to as λ2) exists in the wavelength range of 560 to 595 nm, and it is more preferable that the wavelength range of 570 to 590 nm is present. Furthermore, from the reason that the color separation performance of the colored pixels of other colors can be fully ensured and the amount of light incident on the photodiode can be fully ensured, it is preferable that the difference between λ2 and λ1 (λ2-λ1) is 60-120 nm, and 70-110 nm is more preferable. The absorbance Aλ at a certain wavelength λ can be defined by the following formula (Ab1). Aλ=-log(Tλ / 100) ····(Ab1) Aλ is the absorbance at wavelength λ, and Tλ is the transmittance at wavelength λ (%). In the present invention, the absorbance value may be a value measured in a solution state, and may be a value of a film made of a colored composition. When the absorbance is measured in a film state, the colored composition is coated on a glass substrate by spin coating or the like, and dried at 100°C for 2 minutes using a heating plate or the like, and then the light illuminance is 20 mW / cm 2 , exposure amount 1J / cm 2 The i-ray exposure was performed under conditions, and then heated on a heating plate at 100°C for 20 minutes, and the measurement was preferably performed using a film (film) obtained by cooling to normal temperature. The absorbance can be measured using a previously known spectrophotometer. When a film having a thickness of 0.6 μm is formed using the coloring composition of the present invention, it is preferable that the maximum transmittance of light in the wavelength range of 400 to 500 nm in the thickness direction of the film is 70% or more, the minimum transmittance of light in the wavelength range of 450 to 600 nm is 30% or less, and the maximum transmittance of light in the wavelength range of 550 to 700 nm is 70% or more, and the wavelength range of light in the thickness direction of the film is 50% or more, respectively. In this condition, it is more preferable that the maximum transmittance of light in the wavelength range of 400 to 500 nm is 75% or more, and it is even more preferable that 80% or more. It is more preferable that the minimum transmittance of light in the wavelength range of 450 to 600 nm is 20% or less, and it is even more preferable that the minimum transmittance of light in the wavelength range of 450 to 600 nm is 20%, and it is even more preferable. It is more preferable that the maximum transmittance of light at a wavelength range of 550 to 700 nm is 80% or more, and it is even more preferable that 90% or more. The transmittance of light in the thickness direction of the film shows that it is more preferable that the wavelength on the short-wave side of 50% exists in the wavelength range of 460 to 495 nm, and it is even more preferable that the wavelength exists in the wavelength range of 470 to 490 nm. The transmittance of light in the thickness direction of the film shows that it is more preferable that the wavelength on the wavelength side of the 50% wavelength exists in the wavelength range of 560 to 595 nm, and it is even more preferable that the wavelength exists in the wavelength range of 570 to 590 nm. The coloring composition of the present invention can be preferably used as a solid-state imaging element. Furthermore, the coloring composition of the present invention can be preferably used as a color filter. Specifically, the purple-red pixels that can be preferably used to form the color filter. Hereinafter, each component used in the coloring composition of the present invention will be described. <<Color A>> The coloring composition of the present invention contains a coloring agent A (hereinafter referred to as a coloring agent). The colorant is used with dye a (hereinafter referred to as dye). The colorant may be a dye only, but it is preferred to contain dyes and pigments from the reason that it can further improve the pattern linearity of the pixels. Furthermore, when pigments and dyes are used in combination, it is preferable that the content of the pigment is 10 to 900 parts by mass relative to 100 parts by mass of the dye. It is preferable that the lower limit is 65 parts by mass or more, and it is preferable that the lower limit is 130 parts by mass or more. The upper limit is preferably 400 parts by mass or less, and it is more preferably 200 parts by mass or less. In addition, in this specification, pigments refer to pigment compounds that are difficult to dissolve in a solvent. Regarding pigments, it is preferable that the solubility of 100 g of water at 23°C and 100 g of cyclohexanone at 23°C is not reaching 1 g. Furthermore, in this specification, dye refers to a pigment compound dissolved in water or an organic solvent. Regarding the dye, it is preferable that the solubility of 100 g of cyclohexanone at 23°C is 1 g or more, and it is preferable that 5 g or more. <<<Dyes>> - Keiyamaguchi Snake Dye- In the coloring composition of the present invention, the dye contains cation AX containing a pigment structure of Keiyamaguchi Snake Dye. + and anion AZ - The Noguchi Yamaguchi star dye a1 (hereinafter also known as the Koji Yamaguchi star dye). The content of the dye contained in the coloring composition of the present invention is 50% by mass or more, preferably 60% by mass or more, and more than 80% by mass or more, and actually only the content of the dye is 50% by mass or more. In addition, the dye in this specification is only the dye that is Keiyamaguchi Star dye, which means that the content of Keiyamaguchi Star dye in the dye is 99% by mass or more, and it is preferred that the dye is only Keiyamaguchi Star dye. Anion AZ in Guchiyamaguchi star dye - Can be present in cationic AX + outside the molecule. "Anion AZ" - Available in cationic AX + "extramolecular" refers to anion AZ - No covalent bonding to cation AX + bond, but with cation AX + The state of existence of independent structural units. Examples of the form of the Guchiyamaguchi star dye mentioned above include salt. Hereinafter, anion outside the molecule that exists in cations is also called relative anion. From the reason that it is possible to form pixels with better linearity, the Hirayaguchi star dye is through covalent bonds and cation AX + and anion AZ - Compounds with bonded structures are preferred. That is, it is preferred that the Guchiyamaguchi star dye is an internal salt (also known as zwitterionic) type compound. As anion AZ - Examples of the types of fluorine anions, chlorine anions, bromine anions, iodine anions, cyanide ions, perchloric acid anions, carboxylic acid anions, sulfonic acid anions, phosphorus-containing atom anions, anions containing boron atoms (borate anions, etc.), imide anions, methylated anions, SbF 6 - et al., the isoimide anion, the methylated anion and the anion containing boron atoms are preferred, the isoimide anion and the methylated anion are better, and the isoimide anion is further preferred, the isoimide anion is further preferred from the reason that the pixels with better pattern linearity can be formed. As the iside anion, it is preferred that anion having a bis(sulfonyl)imide anion structure is anion. As the methylated anion, it is preferred that anion having a tri(sulfonyl)methylated anion structure is anion. Examples of anion having a bis(sulfonyl)imide anion structure include anion having a partial structure represented by formula (AZ-1). Examples of anion having a tri(sulfonyl)methylated anion structure include anion having a partial structure represented by formula (AZ-2). [Chemical Formula 1] The wave lines in the above formula represent bonding bonds with other atoms or atomic groups. It is also preferred that Guchiyamaguchi star dye is a compound with an acid group. According to this aspect, by the interaction with resin b1 and the like, the condensation of the Guchiyamaguchi star dye in the film can be more effectively suppressed, and pixels with better pattern linearity can be formed. Examples of the acid group include carboxyl, sulfo group, phosphate group, etc., and the carboxyl group and sulfo group are preferred, and the carboxyl group is more preferred. It is also preferred that the guchiyamaguchi star dye a1 is a compound having a polymerizable group. According to this aspect, the condensation of the Guchiyamaguchi star dye in the film can be more effectively suppressed, and pixels with better linear patterns can be formed. Examples of the polymerizable group include groups containing ethylene unsaturated bonds, such as vinyl, (meth)allyl, and (meth)acryl. As a preferred aspect of the Guchiyamaguchi star dye, a compound represented by the formula (XT) can be mentioned. [Chemical Formula 2] In formula (XT), Rxt 1 , Rxt 2 , Rxt 3 and Rxt 4 Independently representing hydrogen atoms or substituents, Rxt 5 It represents a substituent, and m represents an integer from 0 to 5. X represents a relative anion. When X does not exist, Rxt 1 ~Rxt 5 At least one of the anions is contained. Rxt in formula (XT) 1 ~Rxt 5 Examples of the acceptable substituents include groups, acid groups, polymerizable groups and groups represented by the following formula (xt-1). Examples of the acid group include carboxyl, sulfo group, phosphate group, etc., and the carboxyl group and sulfo group are preferred, and the carboxyl group is more preferred. Examples of the polymerizable group include groups containing ethylene unsaturated bonds, such as vinyl, (meth)allyl, and (meth)acryl. Rxt 1 and Rxt 3 It is preferred that it is independently aryl or alkyl. Also, Rxt 2 and Rxt 4 It is preferred that it is independently a hydrogen atom or an alkyl group. Furthermore, the above-mentioned alkyl and aryl groups may further have a substituent. As further substituents, groups, acid groups, polymerizable groups mentioned in the substituents T described later, and groups represented by the following formula (xt-1). [Chemical Formula 3] In formula (xt-1), Rxt 100 Alkanediyl group having 1 to 10 carbon atoms, and a -CH that constitutes alkanediyl group 2 - Can be -O-, -CO-, -NRs 10 -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-, Rs 10 Represents a hydrogen atom or an alkyl group with a carbon number of 1 to 20, Rs 1 ~Rs 3 The hydrogen atom, the hydroxyl group, the alkyl group having 1 to 4 carbon atoms, or the alkoxy group having 1 to 4 carbon atoms, respectively, and * represents a bonding bond with the nitrogen atom of the formula (XT). For details of the groups represented by formula (xt-1), please refer to the records in paragraphs 0010 to 0065 of Japanese Patent Laid-Open No. 2016-027075, which are included in this specification. m of formula (xt-1) represents an integer from 0 to 5, an integer from 0 to 3 is preferred, and an integer from 0 to 2 is more preferred. Rxt in formula (XT) 1 and Rxt 2 , Rxt 3 and Rxt 4 , and Rxt when m is more than 2 5 The two may be independently bonded to each other to form a saturated ring of 5, 6 or 7 members, or an unsaturated ring of 5, 6 or 7 members. Examples of the ring formed include pyrrole ring, furan ring, thiophene ring, pyrazole ring, imidazole ring, triazole ring, thiazole ring, pyrrole ring, piperidine ring, cyclopentene ring, cyclohexene ring, benzene ring, pyridine ring, pyridine ring, pyridine ring, pyridine ring, pyridine ring, pyridine ring, pyridine ring, pyridine ring, pyridine ring, pyridine ring, and pyridine ring are preferred. The formed ring may further include a group, an acid group, a polymerizable group, and a group represented by formula (xt-1) mentioned later. X of formula (XT) represents a relative anion. When X does not exist, Rxt 1 ~Rxt 5 At least one of the anions is contained. As a relative anion, there are no particular limitations. It can be an organic anion or an inorganic anion. It is preferred that the relative anion is an organic anion. Examples of the relative anions include fluorine anions, chlorine anions, bromine anions, iodine anions, cyanide ions, perchloric acid anions, non-nucleophilic anions, and the like. From the viewpoint of heat resistance, non-nucleophilic anions are preferred. As an example of relative anions, known non-nucleophilic anions described in paragraph 0075 of Japanese Patent Laid-Open No. 2007-310315 include, and these contents are included in this specification. Here, non-nucleophilicity refers to the properties of pigments not being attacked by heating. Compared with the anion, it is better to have an anion with a bis(sulfonyl)imide anion, etc., anion with a bis(sulfonyl)imide anion, a methylated anion, etc., anion with a tris(sulfonyl)methylated anion, anion with a tris(sulfonyl)methylated anion, anion with a boron atom (for example, tetrafluoroborate anion, tetraphenyl borate anion, tetrafluorophenyl borate anion, etc.), anion with a boron atom (for example, tetrafluoroborate anion, tetraphenyl borate anion, tetrafluorophenyl borate anion, etc.), anion with anion and methylated anion are more preferred, and anion with anion is even more preferred. It is preferred that the isine anion which is a relative anion represented by the formula (AZ1-1). Furthermore, it is preferable that the methylated anion as the relative anion is an anion represented by the formula (AZ1-2). [Chemical Formula 4] In formula (AZ1-1), Rz 1 and Rz 2 Individually represent halogen atoms or alkyl groups when Rz 1 and Rz 2 When the alkyl group is independently represented, Rz 1 and Rz 2 The ring can be formed by bonding, in formula (AZ1-2), Rz 3 ~Rz 5 Individually represent halogen atoms or alkyl groups when Rz 3 and Rz 4 When the alkyl group is independently represented, Rz 3 and Rz 4 Can bond to form a ring when Rz 4 and Rz 5 When the alkyl group is independently represented, Rz 4 and Rz 5 Can bond to form a ring when Rz 3 and Rz 5 When the alkyl group is independently represented, Rz 3 and Rz 5 It can be bonded to form a ring. In formula (AZ1-1), Rz 1 and Rz 2 The halogen atom or alkyl group is independently represented, respectively. Examples of the halogen atom include fluorine atom, chlorine atom, bromine atom, and iodine atom, and halogen atom is preferred. It is preferable that the carbon number of the alkyl group is from 1 to 10, 1 to 6 is more preferable, and 1 to 3 is more preferable. Examples of alkyl groups include linear, branched, and cyclic, and linear or branched are preferred, and linear is more preferred. The alkyl group may have a substituent or may be unsubstituted. It is preferable that the alkyl group is an alkyl group having a halogen atom as a substituent, and it is preferable that the alkyl group (fluoroalkyl group) having a fluorine atom as a substituent. Furthermore, it is preferred that the fluoroalkyl group is a perfluoroalkyl group. In formula (AZ1-2), Rz 3 ~Rz 5 The halogen atom or alkyl group is independently represented, respectively. The ranges of halogen atoms and alkyl groups are the same as those described in formula (AZ1-1), and the preferred ranges are also the same. It is preferable that the molecular weight of the relative anion represented by X of formula (XT) is 100 to 1000, and it is more preferable that 200 to 500. Rxt of the formula (XT) 1 ~Rxt 5 When at least one of the anions contains anion, examples include carboxylic acid anion, sulfonic acid anion, phosphorus-containing anion, anion containing boron atoms, anion containing anion, anion containing boron atoms, anion containing anion, anion containing a boron atom, anion containing anion, anion containing anion, anion containing anion, anion and a methylated anion are preferred, anion containing a boron atom, anion and a methylated anion are preferred, and anion is particularly preferred. As the iside anion, it is preferred that anion having a bis(sulfonyl)imide anion structure is anion. As the methylated anion, it is preferred that anion having a tri(sulfonyl)methylated anion structure is anion. Rxt of the formula (XT) 1 ~Rxt 5 When at least one of the anions is contained, Rxt 1 ~Rxt 5 It is preferred that at least one of the groups represented by formula (P-1), groups represented by formula (P-2), or groups containing at least one of the above, and it is preferred that the groups represented by formula (P-2) or groups represented by formula (P-2). [Chemical Formula 5] Lp of formula (P-1) 1 A single bond or a divalent linking group. Lp 1 Examples of the divalent linking groups are 1 to 6 carbon alkyl groups, 6 to 12 carbon alkyl groups, and -NR Lp1 -, -O-, -S-, -CO-, -SO 2 -or groups formed from combinations of these. It is preferable that at least a portion of the hydrogen atom of the above-mentioned alkyl-extended alkyl group is replaced by a fluorine atom, and it is preferable that the perfluoro-extended alkyl group is preferable. Specific examples of such alkyl groups include difluoromethylene, tetrafluoroethyl, hexafluoropropyl, etc. It is preferable that at least a portion of the hydrogen atom of the aryl group is replaced by a fluorine atom. Specific examples of such aryl groups include tetrafluorophenyl, hexafluoro-1-naphthalene, hexafluoro-2-naphthalene, etc. Lp of formula (P-1) 1 is a single bond, from -NR Lp1 -, -SO 2 A group formed by a combination of a fluorine atom-containing alkyl group, a group formed by a combination of -O- and a fluorine atom-containing aryl group, or a -NR Lp1 -, -SO 2 A group formed by combining a alkyl group containing a fluorine atom is preferred. Xp of formula (P-1) 1 Indicates-SO 3 - , -COO - , -PO 4 H - Or anion containing boron atoms, -SO 3 - or -COO - It is preferred. Lp of formula (P-2) 2 It represents a single bond or a divalent linking group, and a single bond is preferred. As LP 2 Examples of the divalent linking groups are 1 to 6 carbon alkyl groups, 6 to 12 carbon alkyl groups, -O-, -S-, or groups formed from combinations of the like. Lp of formula (P-2) 3 Indicates-SO 2 -or-CO-,-SO 2 -For better. G of formula (P-2) represents a carbon atom or a nitrogen atom, and the nitrogen atom is preferred. Regarding n of formula (P-2), when G is a carbon atom, it means 2, and when G is a nitrogen atom, it means 1. Rp of formula (P-2) 1 It represents an alkyl group containing a fluorine atom or an aryl group containing a fluorine atom. When n is 2, 2 Rp 1 It can be the same or different. Rp 1 It is preferable that the carbon number of the alkyl group containing fluorine atoms is 1 to 10, 1 to 6 are more preferable, and 1 to 3 are more preferable. Rp 1 It is preferable that the carbon number of the aryl group containing fluorine atoms is 6 to 20, 6 to 14 is more preferable, and 6 to 10 is more preferable. The alkyl group containing a fluorine atom and the aryl group containing a fluorine atom may further have a substituent. Examples of the substituent include groups, acid groups, polymerizable groups, etc. mentioned below in the substituent T. Examples of the substituent T include the following groups. Halogen atom (for example, fluorine atom, chlorine atom, bromine atom, iodine atom), alkyl group (the alkyl group with 1 to 30 carbon atoms are preferred), alkenyl group (the alkenyl group with 2 to 30 carbon atoms are preferred), alkynyl group (the aryl group with 6 to 30 carbon atoms are preferred), amine group (the amine group with 0 to 30 carbon atoms are preferred), alkoxy group (the alkyl group with 1 to 30 carbon atoms are preferred), aryloxy group (the aryloxy group with 6 to 30 carbon atoms are preferred), heteroaryloxy group, acyl group ( Alkyl groups with 2 to 30 carbon atoms are preferred), alkoxycarbonyl groups (analkoxycarbonyl groups with 2 to 30 carbon atoms are preferred), aryloxycarbonyl groups (analkoxycarbonyl groups with 7 to 30 carbon atoms are preferred), heteroaryloxycarbonyl groups, acyloxy groups (analkoxycarbonyl groups with 2 to 30 carbon atoms are preferred), acylamine groups (analkoxycarbonyl groups with 2 to 30 carbon atoms are preferred), alkoxycarbonylamine groups (analkoxycarbonylamine groups with 7 to 30 carbon atoms are preferred), Aminosulfonyl (aminosulfonyl group with 0 to 30 carbon atoms is preferred), amineformyl (aminoformyl group with 1 to 30 carbon atoms is preferred), alkylthio (aminosulfonyl group with 1 to 30 carbon atoms is preferred), arylthio (aminosulfonyl group with 6 to 30 carbon atoms is preferred), heteroarylthio (aminosulfonyl group with 1 to 30 carbon atoms is preferred), alkylsulfonyl group (aminosulfonyl group with 1 to 30 carbon atoms is preferred), arylsulfonyl group (aminosulfonyl group with 6 to 30 carbon atoms is preferred), heteroarylsulfonyl group (aminosulfonyl group with 1 to 30 carbon atoms is preferred), alkylsulfonyl group Acyl group (preferably from 1 to 30 carbon atoms), arylsulfinyl group (preferably from 6 to 30 carbon atoms), heteroarylsulfinyl group (preferably from 1 to 30 carbon atoms), urea group (preferably from 1 to 30 carbon atoms), hydroxyl group, carboxyl group, carboxyl group, sulfonyl group, sulfonyl group, sulfonyl group, phosphate group, phosphate group, salt of phosphate group, carboxylic acid amido group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group, sulfonyl group Among the carboxyl group salts, sulfo group salts and phosphate group salts, alkali metal ions (Li) are mentioned as the atoms or atom groups that constitute the salt. + , Na + , K + ), alkaline earth metal ions (Ca 2+ , Mg 2+ ), ammonium ions, imidazolium ions, pyridinium ions, phosphonium ions, etc. When such groups are groups that can be further substituted, they may further have a substituent. Examples of the substituent include groups described in the above-mentioned substituent T. It is also preferred that the dye polymer with more than 2 guchiyaguchi star dyes in one molecule are dyed polymers. According to this aspect, the condensation of the Guchiyamaguchi star dye in the film can be more effectively suppressed, and pixels with better linear patterns can be formed. It is preferred that the dye polymer is a compound having more than three guchiyamaguchi astrin pigment structure in one molecule. The upper limit of the number of pigment structures of the Guchiyamaguchi star is not particularly limited, but it can also be set to 100 or less. It is preferable that the weight average molecular weight (Mw) of the dye polymer is 2000 to 50,000. It is preferable that the lower limit is 3000 or more, and it is preferable that the lower limit is 6000 or more. It is preferable that the upper limit is 30,000 or less, and it is preferable that the upper limit is 20,000 or less. It is preferable that the acid value of the dye polymer is 10 to 120 mgKOH / g. It is preferable that the lower limit is 15 mgKOH / g or more, and it is preferable that the lower limit is 15 mgKOH / g or more. It is preferable that the upper limit is 90 mgKOH / g or less, and it is preferable that the upper limit is 80 mgKOH / g or less. As the dye Yamaguchi star dye used as the dye polymer, a dye polymer having a repeating unit represented by formula (A) (hereinafter also referred to as a dye polymer (A)), a dye polymer having a repeating unit represented by formula (B) (hereinafter also referred to as a dye polymer (B)), a dye polymer having a repeating unit represented by formula (C) (hereinafter also referred to as a dye polymer (C)), and a dye polymer represented by formula (D) (hereinafter also referred to as a dye polymer (D)), a dye polymer (A) or a dye polymer (D) are preferred. (Dye Polymer (A)) The dye Polymer (A) contains repeating units represented by formula (A). The proportion of the repeating units represented by formula (A) is preferably 10 mass % or more of all the repeating units constituting the dye polymer (A), more preferably 20 mass % or more, more preferably 30 mass % or more, and more than 50 mass % or more. The upper limit can be set to 100 mass% or less, or 95 mass% or less. [Chemical Formula 6] In formula (A), A 1 Represents a 3-valent linking group, L 1 It represents a single bond or a divalent linking group, and DyeI represents a pigment structure of Guchiyamaguchi. A as formula (A) 1 Examples of the three-valent linking groups represented by the trivalent linking group include poly(meth)acrylic linking group, polythylene alkylimine linking group, polyester linking group, polyurethane linking group, polyurea linking group, polyamide linking group, polyether linking group, polystyrene linking group, bisphenol linking group, and novolac linking group, and the poly(meth)acrylic linking group is preferred. L of formula (A) 1 A single bond or a divalent linking group. Examples of the divalent linking group include alkyl, aryl, heterocyclic group, -CH=CH-, -O-, -S-, -CO-, -COO-, -NR-, -CONR-, -OCO-, -SO-, -SO-, -SO-, -SO-, 2 - and a connecting group formed by connecting two or more of these. Here, R represents a hydrogen atom, an alkyl group, an aryl group or a heterocyclic group. It is preferable that the carbon number of the alkyl group is 1 to 30. It is more preferable to have an upper limit of 25 or less, and it is even more preferable to have an upper limit of 20 or less. It is more preferable that the lower limit is 2 or more, and it is even more preferable that the lower limit is 2 or more. The alkyl group may be any of linear, branched, or cyclic. The alkyl group may have a substituent or may be unsubstituted. It is preferable that the carbon number of the aryl group is 6 to 20, and it is preferable that 6 to 12 is more preferable. The aryl group may have a substituent or may be unsubstituted. It is preferred that the heterocyclic group is a 5-membered ring or a 6-membered ring. It is preferred that the heteroatoms of the heterocyclic group are oxygen atoms, nitrogen atoms and sulfur atoms. It is preferable that the number of heteroatoms of the heterocyclic group has 1 to 3. The heterocyclic group may have a substituent or may be unsubstituted. It is preferable that the pigment structure of the guchi Yamaguchi star represented by DyeI of Formula (A) is that it is a residue after removing one hydrogen atom from the compound represented by Formula (XT). The dye polymer (A) may contain other repeating units in addition to the repeating units represented by formula (A). Other repeating units include repeating units having polymerizable groups, repeating units having acid groups, and the like. Examples of the polymerizable group include groups containing ethylene unsaturated bonds, such as vinyl, (meth)allyl, and (meth)acryl. Examples of the acid group include carboxyl, sulfo, and phosphate groups. It is preferred that the proportion of repeating units having polymerizable groups is 50 mass% or less of all repeating units constituting the dye polymer (A). For example, it is preferable that the lower limit is 1 mass% or more, and it is preferable that the lower limit is 3 mass% or more. It is preferable that the upper limit is 35% by mass or less, and it is preferable that the upper limit is 30% by mass or less. It is preferred that the proportion of the repeating units having an acid group is 50 mass% or less of all the repeating units constituting the dye polymer (A). For example, it is preferable that the lower limit is 1 mass% or more, and it is preferable that the lower limit is 3 mass% or more. It is preferable that the upper limit is 35% by mass or less, and it is preferable that the upper limit is 30% by mass or less. (Dye Polymer (B)) The dye Polymer (B) contains repeating units represented by formula (B). The proportion of the repeating units represented by formula (B) is preferably 10 mass % or more of all the repeating units constituting the dye polymer (B), more preferably 20 mass % or more, more preferably 30 mass % or more, and more preferably 50 mass % or more. The upper limit can be set to 100 mass% or less, or 95 mass% or less. [Chemical Formula 7] In formula (B), A 2 Represents a 3-valent linking group, L 2 Represents single bond or divalent linking group, DyeII means having the ability to be with Y 2 The ionic bonded or bonded group of the ionic bonded group, Y 2 Represents a group capable of ion bonding or coordination bonding to DyeII. A of formula (B) 2 Meaning and formula (A) 1 The meanings of the same, and the preferred range is the same. L of formula (B) 2 A single bond or a divalent linking group. Examples of the divalent linking group include alkyl, aryl, heterocyclic group, -CH=CH-, -O-, -S-, -CO-, -COO-, -NR-, -CONR-, -OCO-, -SO-, -SO-, -SO-, -SO-, 2 - and a connecting group formed by connecting two or more of these. Here, R represents a hydrogen atom, an alkyl group, an aryl group or a heterocyclic group, respectively. Details of the divalent linking group, with L of formula (A) 1 same. L 2 It is preferable to be a single bond or a single bond, a aryl group, -NH-, -CO-, -O-, -COO-, -OCO- and a divalent linking group formed by combining two or more of these. As Y that can be with formula (B) 2 The group represented by DyeII ion bonding or coordination bonding includes anionic group and cationic group. Examples of the anionic group include -SO 3 - , -COO - , -PO 4 H - , a group having an anionic structure containing a boron atom, a group having a bis(sulfonyl)imide anionic structure, and a group having a tri(sulfonyl)methylated anionic structure, etc. Specifically, a group represented by formula (AN-1) and a group represented by formula (AN-2) can be mentioned. [Chemical Formula 8] In formula (AN-1), L AN1 Represents a single bond or divalent linker, R AN1 Indicates-SO 3 - , -COO - , -PO 4 H - , a group having an anionic structure containing boron atoms. As L AN1 The divalent linking group represented by -NR AN10 -, -O-, -SO 2 -, it is preferable that the alkyl group containing fluorine atoms, the aryl group containing fluorine atoms, or the group formed from the combination of these. In particular, by -NR AN10 -, -SO 2 A group formed by a combination of a fluorine atom-containing alkyl group, a group formed by a combination of -O- and a fluorine atom-containing aryl group, or a -NR AN10 -, -SO 2 A group formed by combining a alkyl group containing a fluorine atom is preferred. -NR AN10 -Medium,R AN10 It represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, and the hydrogen atom is preferred. It is preferable that the carbon number of the alkyl group containing fluorine atoms is 1 to 10, 1 to 6 are more preferable, and 1 to 3 are more preferable. It is more preferable that the alkyl group is perfluorochromatoyl group. Specific examples of the fluorine-substituted alkyl group include difluoromethylene, tetrafluoroethyl, hexafluoropropyl, etc. It is preferable that the carbon number of the aryl group containing fluorine atoms is 6 to 20, 6 to 14 is more preferable, and 6 to 10 is more preferable. Specific examples of the aryl group containing fluorine atoms include tetrafluorophenyl, hexafluoro-1-naphthalene, hexafluoro-2-naphthalene, etc. In formula (AN-2), L AN2 It represents a single bond or a divalent linking group, and a single bond is preferred. As L AN2 Examples of the divalent linking groups are 1 to 6 carbon alkyl groups, 6 to 12 carbon alkyl groups, -O-, -S-, or groups formed from combinations of the like. L AN3 Indicates-SO 2 -or-CO-,-SO 2 -For better. G represents a carbon atom or a nitrogen atom, and nitrogen atom is preferred. When G is a carbon atom, n represents 2, and when G is a nitrogen atom, n represents 1. R AN2 It represents an alkyl group containing a fluorine atom or an aryl group containing a fluorine atom. R AN2 It is preferable that the carbon number of the alkyl group containing fluorine atoms is 1 to 10, 1 to 6 are more preferable, and 1 to 3 are more preferable. R AN2 It is preferable that the carbon number of the aryl group containing fluorine atoms is 6 to 20, 6 to 14 is more preferable, and 6 to 10 is more preferable. Examples of the cationic group include substituted or unsubstituted onium cations (for example, ammonium, pyridinium, imidazolium, phosphonium, etc.), and ammonium cations are particularly preferred. Examples of the ammonium cation include -N(R) 3 + . R independently represents a hydrogen atom or an alkyl group, and at least one of R represents an alkyl group. It is preferable that the carbon number of the alkyl group is from 1 to 10, and it is preferable that 1 to 5 is more preferable. The alkyl group may be any of linear, branched, or cyclic, but the linear chain is preferred. DyeII of formula (B) has the ability to be with Y 2 The pigment structure of the ionic bonded or bonded group. As a can with Y 2 Examples of the ionic bonding or bonding groups include anionic groups and cationic groups. Specific examples of anionic group and cationic group include the above-mentioned groups. The pigment structure of the guchi Yamaguchi star represented by DyeII of formula (B) is the structure represented by formula (XT) above, and is Rxt of formula (XT) 1 ~Rxt 5 At least one of the 2 The structure of the ionic bonded or coordination bonded group is preferred as a substituent. The dye polymer (B) may contain other repeating units represented by the formula (B). Furthermore, the repeating unit represented by formula (A) above and the repeating unit represented by formula (C) later may be further included. (Dye Polymer (C)) The dye Polymer (C) contains repeating units represented by formula (C). The proportion of the repeating units represented by formula (C) is preferably 10 mass % or more of all the repeating units constituting the dye polymer (C), more preferably 20 mass % or more, more preferably 30 mass % or more, and more preferably 50 mass % or more. The upper limit can be set to 100 mass% or less, or 95 mass% or less. [Chemical Formula 9] In formula (C), L 3 Represents a single bond or divalent linker, DyeIII represents a guchiyamaguchi astral pigment structure, m represents 0 or 1. L of formula (C) 3 A single bond or a divalent linking group. Examples of the divalent linking group include alkyl, aryl, heterocyclic group, -CH=CH-, -O-, -S-, -CO-, -COO-, -NR-, -CONR-, -OCO-, -SO-, -SO-, -SO-, -SO-, 2 - and a connecting group formed by connecting two or more of these. Here, R represents a hydrogen atom, an alkyl group, an aryl group or a heterocyclic group, respectively. It is preferable that the carbon number of the alkyl group and the alkyl group is 1 to 30. It is more preferable to have an upper limit of 25 or less, and it is even more preferable to have an upper limit of 20 or less. It is more preferable that the lower limit is 2 or more, and it is even more preferable that the lower limit is 2 or more. The alkyl group and the alkyl group may be any of a linear, branched or cyclic. It is preferable that the carbon number of the aryl and the aryl group is 6 to 20, and it is preferable that 6 to 12 are more preferable. It is preferred that the heterocyclic group is a 5-membered ring or a 6-membered ring. It is preferred that the heteroatoms of the heterocyclic group are oxygen atoms, nitrogen atoms and sulfur atoms. It is preferable that the number of heteroatoms of the heterocyclic group has 1 to 3. The alkyl group, the aryl group, the heterocyclyl group, the alkyl group and the aryl group may not be substituted, and may also have a substituent. Examples of the substituent include groups, polymerizable groups, and acid groups mentioned in the above-mentioned substituent T. L of formula (C) 3 It is a alkyl group, a aryl group, -NH-, -CO-, -O-, -COO-, -OCO-, -S-, -SO 2 It is preferable to combine two or more of these linking groups. It is preferable that the pigment structure of the guchi Yamaguchi star represented by DyeIII of formula (C) is that the residue after removing two hydrogen atoms from the compound represented by formula (XT) mentioned above. m of formula (C) represents 0 or 1, and 1 is preferred. Dye polymer (C) may contain other repeat units as described in dye polymer (A) in addition to the repeat units represented by general formula (C). (Dye Polymer (D)) The dye Polymer (D) is a compound represented by formula (D). [Chemical Formula 10] In formula (D), L 4 Connection groups representing (n+k) valence, n represents an integer of 2 to 20, k represents an integer of 0 to 20, DyeIV represents a pigment structure of guchiyamaguchi, P 4 Represents substituents, n DyeIVs can be different respectively. When k is more than 2, multiple Ps 4 It can be different, n+k represents an integer of 2 to 20. It is preferred that n of formula (D) is 2 to 14, more preferably 2 to 8, especially preferably 2 to 7, and more preferably 2 to 6. It is preferred that k is 1 to 13, 1 to 10 is more preferred, 1 to 8 is more preferred, 1 to 7 is particularly preferred, and 1 to 6 is further preferred. L as formula (D) 4 The (n+k) valence linking group represented by the (n+k) valence include a group consisting of 1 to 100 carbon atoms, 0 to 10 nitrogen atoms, 0 to 50 oxygen atoms, 1 to 200 hydrogen atoms, and 0 to 20 sulfur atoms. As a linking group with a valence of (n+k), it is preferable that a group formed by combining two or more structural units or less structural units (a ring structure can be formed). * in the following formula represents the bonding bond. [Chemical Formula 11] L 4 It is preferable that the (n+k)-valent linking group represented is a linking group derived from a multifunctional thiol, a linking group derived from a multifunctional alcohol or a linking group derived from an acid anhydride, and it is preferable that the linking group derived from a multifunctional thiol. L 4 It is preferable that the linking group of the (n+k) valence represented by the group represented by any one of the formulas (Za-1) to (Za-4). [Chemical Formula 12] In formula (Za-1), La 3 A group that represents a trivalent one, Ta 3 A single bond or a divalent linking group, there are 3 Ta 3 They can be the same or different from each other. In formula (Za-2), La 4 A 4-valent group, Ta 4 A single bond or a divalent linking group, there are 4 Ta 4 They can be the same or different from each other. In formula (Za-3), La 5 A group that represents a valent valentine, Ta 5 A single bond or a divalent linking group, there are 5 Ta 5 They can be the same or different from each other. In formula (Za-4), La 6 A group representing a 6-valent one, Ta 6 A single bond or a divalent linking group, 6 Ta exists 6 They can be the same or different from each other. In the above formula, * represents a bond. As Ta 3 ~Ta 6 The divalent linking group represented by divalent include alkyl, aryl, heterocyclic group, -CH=CH-, -O-, -S-, -CO-, -COO-, -NR-, -CONR-, -OCO-, -SO-, -SO- 2 - and a connecting group formed by connecting two or more of these. Here, R represents a hydrogen atom, an alkyl group, an aryl group or a heterocyclic group, respectively. Ta 3 ~Ta 6 It is preferred that the divalent linking group represented is a group containing -S-, and it is more preferred that -S- is more preferred. It is preferable that the carbon number of the alkyl group and the alkyl group is 1 to 30. It is more preferable to have an upper limit of 25 or less, and it is even more preferable to have an upper limit of 20 or less. It is more preferable that the lower limit is 2 or more, and it is even more preferable that the lower limit is 2 or more. The alkyl group and the alkyl group may be any of a linear, branched or cyclic. It is preferable that the carbon number of the aryl and the aryl group is 6 to 20, and it is preferable that 6 to 12 are more preferable. It is preferred that the heterocyclic group is a 5-membered ring or a 6-membered ring. It is preferred that the heteroatoms of the heterocyclic group are oxygen atoms, nitrogen atoms and sulfur atoms. It is preferable that the number of heteroatoms of the heterocyclic group has 1 to 3. The alkyl group, the aryl group, the heterocyclyl group, the alkyl group and the aryl group may not be substituted, and may also have a substituent. Examples of the substituent include groups, polymerizable groups, and acid groups mentioned in the above-mentioned substituent T. As La 3 Examples of the trivalent group represented include a group obtained by removing one hydrogen atom from the above-mentioned divalent linking group. As La 4 Examples of the tetravalent group represented by the divalent linking group are groups obtained by removing two hydrogen atoms from the above-mentioned divalent linking group. As La 5 Examples of the devalential group are groups obtained by removing three hydrogen atoms from the above-mentioned divalent linking group. As La 6 The expressed hexavalent group includes a group obtained by removing 4 hydrogen atoms from the above-mentioned divalent linking group. La 3 ~La 6 The 3-6-valent group represented may have the above-mentioned substituents. Specific examples of the (n+k) value linking groups include linking groups described in paragraphs 0071 to 0072 of Japanese Patent Publication No. 2008-222950, ​​linking groups described in paragraphs 0176 of Japanese Patent Publication No. 2013-029760, and linking groups described in paragraphs 0022 to 0024 of International Publication No. 2016 / 031442, etc. It is preferable that the pigment structure of the guchi Yamaguchi star represented by DyeIV of formula (D) is a residue after removing one hydrogen atom from the compound represented by formula (XT). P as formula (D) 4 Examples of the substituents represented include groups, acid groups, polymerizable groups, etc. mentioned in the above-mentioned substituents T. Also, P 4 The represented substituent may be a polymer chain having a monovalent repetitive unit. As the polymer chain having a monovalent polymer chain with repeating units, it is preferred that the polymer chain having a monovalent polymer chain derived from the vinyl compound is monovalent. When k is more than 2, k P 4 It can be the same or different. When P 4 When a polymer chain with a valent valence of repeating units and k is 1, P 4 It is preferred to have a polymer chain with 2 to 20 (2 to 15 are preferred, and 2 to 10 are further preferred) derived from the monovalent unit of the vinyl compound. Also, when P 4When a polymer chain with a 1-valent repeating unit and k is more than 2, k P 4 The average number of repeating units derived from vinyl compounds in the vinyl compound is preferably 2 to 20 (2 to 15 are preferred, and 2 to 10 are further preferred). When P 4 When a polymer chain with a monovalent repetitive unit is used, the average value of the number of repetitive units and the number of repetitive units can be obtained by nuclear magnetic resonance (NMR). When P 4 When it is a polymer chain with a monovalent repetitive unit, it is a component P 4 The repeating unit may include other repeating units described in the description of the above-mentioned pigment polymer (A). It is preferred that the other repeating units have one or more selected from the above-mentioned repeating units having an acid group and a repeating unit having a polymerizable group. When P 4 When a repeating unit containing an acid group is included, the proportion of the repeating unit containing an acid group is relative to P 4 It is preferred that all repeating units are 10 to 80 mol%, and it is more preferred that 10 to 65 mol%. When P 4 When the repeating unit with a polymerizable group is included, the proportion of the repeating unit with a polymerizable group is relative to P. 4 It is preferred that all repeating units are 10 to 80 mol%, and it is more preferred that 10 to 65 mol%. It is preferred that the pigment polymer (D) is a compound represented by formula (D-1). (DyeIV-L 43 ) n -L 41 -(L 42 -P 4 ) k ···(D-1) In formula (D-1), L 41 Connection groups representing (n+k) valence, n represents an integer of 2 to 20, k represents an integer of 0 to 20, DyeIV represents a pigment structure of guchiyamaguchi, P 4 Indicates substituent, L 42 and L 43 Independently representing single bond or divalent linking groups, n DyeIV and L 43 Can be different, when k is more than 2, multiple Ps 4 and L 42 It can be different, n+k represents an integer of 2 to 20. DyeIV, P of formula (D-1) 4 , n and k meaning and formula (D) DyeIV, P 4 , n and k have the same meanings, and the preferred range is also the same. L of formula (D-1) 41 The (n+k) valence linking group represented by the (n+k) valence include a group consisting of 1 to 100 carbon atoms, 0 to 10 nitrogen atoms, 0 to 50 oxygen atoms, 1 to 200 hydrogen atoms, and 0 to 20 sulfur atoms. As a linking group with a valence of (n+k), it is preferable that a group formed by combining two or more structural units or less structural units (a ring structure can be formed). * in the following formula represents the bonding bond. [Chemical Formula 13] L of formula (D-1) 42 and L 43 The divalent linking group represented by divalent include alkyl, aryl, heterocyclic group, -CH=CH-, -O-, -S-, -CO-, -COO-, -NR-, -CONR-, -OCO-, -SO-, -SO- 2 - and a connecting group formed by connecting two or more of these. Here, R represents a hydrogen atom, an alkyl group, an aryl group or a heterocyclic group, respectively. L 42 and L 43 It is preferred that the group containing -S- is more preferred. It is preferable that the carbon number of the alkyl group and the alkyl group is 1 to 30. It is more preferable to have an upper limit of 25 or less, and it is even more preferable to have an upper limit of 20 or less. It is more preferable that the lower limit is 2 or more, and it is even more preferable that the lower limit is 2 or more. The alkyl group and the alkyl group may be any of a linear, branched or cyclic. It is preferable that the carbon number of the aryl and the aryl group is 6 to 20, and it is preferable that 6 to 12 are more preferable. It is preferred that the heterocyclic group is a 5-membered ring or a 6-membered ring. It is preferred that the heteroatoms of the heterocyclic group are oxygen atoms, nitrogen atoms and sulfur atoms. It is preferable that the number of heteroatoms of the heterocyclic group has 1 to 3. The alkyl group, the aryl group, the heterocyclyl group, the alkyl group and the aryl group may not be substituted, and may also have a substituent. Examples of the substituent include groups, polymerizable groups, and acid groups mentioned in the above-mentioned substituent T. As the Guchiyamaguchi star dye, the colorimetric index (C.I.) acidic red 51, C.I. acidic red 52, C.I. acidic red 87, C.I. acidic red 92, C.I. acidic red 94, C.I. acidic red 289, C.I. acidic red 388, rose red B (edible red No. 5), acidic rhodamine G, C.I. acidic purple 9, C.I. acidic purple 9, C.I. acidic purple 30, compounds described in Japanese Patent Publication No. 2016-027075, compounds described in Japanese Patent Publication No. 2016-102191, and compounds described in paragraphs 0091-0109 of International Publication No. 2020 / 195962. -Other Dyes - The colorant used in the coloring composition of the present invention may further contain dyes other than Guchiyamaguchi Sakayashi dye (hereinafter also referred to as other dyes). Examples of other dyes include pyrrolemethylene dyes, triarylmethane dyes, quinacridone dyes, cyanine dyes, and anthraquinone dyes. <<<Pigment>>> It is preferred that the colorant used in the coloring composition of the present invention contains a pigment. Examples of pigments include quinacridone pigments, di- tetra-pigments, azo pigments, naphthol azo pigments, diketopyrrolopyrrole pigments, etc. It is preferred to be at least one type selected from quinacridone pigments, di- tetra-pigments, naphthol azo pigments, and diketopyrrolopyrrole pigments, and it is better to be selected from quinacridone pigments, di- tetra-pigments, and diketopyrrolopyrrole pigments. It is better to be selected from quinacridone pigments, di- tetra-pigments and diketopyrrolopyrrole pigments. From the reason that the effects of the present invention can be more obvious, quinacridone pigments are particularly preferred. Furthermore, it is preferable that at least one pigment selected from the group consisting of quinacridone pigment, di- cal pigment, naphthol azo pigment and diketopyrrolopyrrole pigment (at least one pigment selected from the group consisting of quinacridone pigment, di- cal pigment and diketopyrrolopyrrole pigment) in the pigment contained in the coloring composition of the present invention is preferably 10 mass % or more, more preferably 12 mass % or more, and more than 15 mass % or more. It is preferable that the average primary particle diameter of the pigment is 50 nm or less, it is more preferable that the pigment is less than 47 nm or less, and it is even more preferable that the pigment is less than 45 nm or less. The lower limit is not particularly limited, but it is preferred to be 10 nm or more, and it is more preferred to be 20 nm or more. As long as the average primary particle diameter of the pigment is 50 nm or less, fine pixels with excellent pattern linearity can be formed. In addition, in this specification, the average primary particle size of the pigment means that the pigment is observed using a transmission electron microscope (for example, a device that follows the JEM-2100F type electric field emission transmission electron microscope manufactured by JEOL Ltd.) and the quantity average particle size is determined from the obtained photos. Specifically, the projected area of ​​the pigment is calculated by the above-mentioned device, and the equivalent circle diameter of each pigment is calculated from it. More specifically, after measuring the equivalent circle diameters of 100 pigments, the average primary particle diameter of the pigments was calculated by arithmetic average of the equivalent circle diameters of 80 pigments except the 10 largest side and the 10 smallest side. It is preferred that the pigment used in the coloring composition of the present invention is a purple-red pigment. Examples of the purple-red pigment include pigments with high absorbance of light of green wavelengths and low absorbance of light of red and blue wavelengths. It is preferable that the extremely absorbing wavelength of the purple-red pigment exists in the wavelength range of 500 to 600 nm, it is preferable that the wavelength range of 500 to 590 nm, it is further preferable that the wavelength range of 500 to 585 nm, and it is particularly preferable that the wavelength range of 500 to 580 nm. Furthermore, regarding the purple-red pigment, when the absorbance of the extremely absorbing wavelength in the range of 500 to 600 nm is set to 1, it is preferable that the wavelength of the absorbance becomes 0.5 exists at a wavelength shorter than the extremely absorbing wavelength, and it is preferable that the wavelength exists at a range of 450 nm or more, and it is more preferable that the wavelength exists at a range of 460 nm or more, and it is more preferable that the wavelength exists at a range of 470 nm or more. Furthermore, regarding the purple-red pigment, when the absorbance of the extremely absorbing wavelength in the range of 500 to 600 nm is set to 1, it is preferable that the wavelength of the absorbance becomes 0.5 exists at a wavelength side longer than the extremely absorbing wavelength, it is preferable that the range of the existence of the extremely absorbing wavelength is more preferable, the range of the existence of the extremely absorbing wavelength is more preferable, and the range of the existence of the less than 630 nm is more preferable, and the range of the existence of the less than 620 nm is particularly preferable. Furthermore, with regard to the purple-red pigment, it is preferable that the difference between the extremely absorption wavelength and the wavelength λ1 (when the absorbance of the extremely absorption wavelength is set to 1, the wavelength shorter than the absorbance is 0.5) is preferably 110 nm or less, more preferably 100 nm or less, and more preferably 90 nm or less. Furthermore, it is preferable that the difference between the wavelength λ2 (when the absorbance of the extremely absorbing wavelength is set to 1, the wavelength that is longer than the absorbance of the extremely absorbing wavelength is 0.5) and the extremely absorbing wavelength is 110 nm or less, it is more preferable, and it is even better to be less than 100 nm or less, and it is even better to be less than 90 nm or less. Furthermore, with regard to the purple-red pigment, it is preferable that the difference between wavelength λ2 and wavelength λ1 (λ2-λ1) is 130 nm or less, it is more preferable that the difference between 120 nm or less, it is more preferable that the difference between 115 nm or less, and it is particularly preferable that the difference between 110 nm or less. The pigments used in the coloring composition of the present invention are preferably those selected from the group consisting of at least one type selected from C.I. pigment red 122, C.I. pigment red 202, C.I. pigment red 209, C.I. pigment red 242, C.I. pigment red 254, C.I. pigment red 269, C.I. pigment red 272, C.I. pigment purple 19 and C.I. pigment purple 23, and include at least one selected from C.I. pigment red 122, C.I. pigment red 202, C.I. pigment red 23. It is better to include at least one type of red 209, C.I. pigment red 254, C.I. pigment red 269, C.I. pigment red 272, C.I. pigment purple 19 and C.I. pigment purple 23. It is better to include at least one type of red selected from C.I. pigment red 122, C.I. pigment red 254 and C.I. pigment purple 23. Hereinafter, C.I. Pigment Red 122, C.I. Pigment Red 202, C.I. Pigment Red 209, C.I. Pigment Red 242, C.I. Pigment Red 254, C.I. Pigment Red 269, C.I. Pigment Red 272, C.I. Pigment Purple 19, and C.I. Pigment Purple 23 are also called specific pigments. This particular pigment is also a purple-red pigment. It is preferred that the above-mentioned specific pigments are at least one selected from C.I. pigment red 122, C.I. pigment red 202, C.I. pigment red 209, C.I. pigment red 254, C.I. pigment red 269, C.I. pigment red 272, C.I. pigment purple 19 and C.I. pigment purple 23, and it is more preferred that at least one selected from C.I. pigment red 122, C.I. pigment red 254 and C.I. pigment purple 23. Furthermore, it is preferable that the content of the specific pigment in the pigment contained in the coloring composition of the present invention is 5 mass % or more, more preferably 10 mass % or more, and more preferably 15 mass % or more. It is preferable that the content of the colorant in the total solid component of the coloring composition is 30 to 70 mass %. It is preferable that the lower limit is 35% by mass or more, and it is preferable that the lower limit is 40% by mass or more. It is preferable that the upper limit is 65% by mass or less, and it is preferable that the upper limit is 60% by mass or less. It is preferable that the content of dye in the total solid component of the coloring composition is 5 to 70% by mass. It is preferable that the lower limit is 10% by mass or more, and it is preferable that the lower limit is 15% by mass or more. It is preferable that the upper limit is 65% by mass or less, and it is preferable that the upper limit is 60% by mass or less. It is preferable that the content of the Yamaguchi star dye in the total solid component of the coloring composition is 5 to 70 mass %. It is preferable that the lower limit is 10% by mass or more, and it is preferable that the lower limit is 15% by mass or more. It is preferable that the upper limit is 65% by mass or less, and it is preferable that the upper limit is 60% by mass or less. It is preferable that the content of pigment in the total solid component of the coloring composition is 5 to 70 mass %. It is preferable that the lower limit is 10% by mass or more, and it is preferable that the lower limit is 15% by mass or more. It is preferable that the upper limit is 65% by mass or less, and it is preferable that the upper limit is 60% by mass or less. Furthermore, the content of the pigment is preferably 10 to 900 parts by mass of the 100 parts by mass of the guchiyamaguchi star dye. It is preferable that the lower limit is 65 parts by mass or more, and it is preferable that the lower limit is 130 parts by mass or more. The upper limit is preferably 400 parts by mass or less, and it is more preferably 200 parts by mass or less. Furthermore, the total content of the colorant contained in the coloring composition is preferably 50 to 100 mass % and 80 to 100 mass % is preferably 80 to 100 mass % is better, 90 to 100 mass % is better, 90 to 100 mass % is more preferred, 90 to 100 mass % is more preferred, and 99 to 100 mass % is even more preferred. Furthermore, the total content of the above-mentioned specific pigment and the Guchiyamaguchi star dye in the coloring composition is preferably 50 to 100 mass %, 80 to 100 mass %, 90 to 100 mass %, and 99 to 100 mass % are more preferred. <<Resin B>> The coloring composition of the present invention contains resin B (hereinafter also referred to as resin). For example, resin is blended for the use of particles such as pigments and the like in the composition and the use of binders. In addition, resins mainly used to disperse pigments and other particles are also called dispersants. However, such use of resin is an example, and it can also be used for purposes other than such use. <<<Resin b1>>> The resin used in the coloring composition of the present invention contains resin b1 having an acid value and an amine value and an amine value higher than an acid value. Resin b1 can be used as a binder. Furthermore, when the colorant used in the colorant composition of the present invention is a pigment containing, resin b1 can also be used as a dispersant. It is preferred that resin b1 has an acid group and an amine group. Examples of the acid group include carboxyl groups, sulfo groups, phosphate groups, etc., and carboxyl groups and sulfo groups are preferred. The amine group may be any one of a primary amine group, a secondary amine group, a tertiary amine group and a quadratic amine group. Furthermore, the amine group may be a cyclic amine group. It is preferable that the acid value of resin b1 is 10 mgKOH / g or more, it is preferable that 15 mgKOH / g or more, and it is even better that 20 mgKOH / g or more. It is preferable that the upper limit of the acid value is 130 mgKOH / g or less, it is preferable that the upper limit of 120 mgKOH / g or less, and it is further preferable that the upper limit of 110 mgKOH / g or less. It is preferable that the amine value of resin b1 is 10 mgKOH / g or more, it is preferable that 15 mgKOH / g or more, and it is even better that 20 mgKOH / g or more. It is preferable that the upper limit of the amine value is 130 mgKOH / g or less, it is preferable that the upper limit of amine value is 120 mgKOH / g or less, and it is further preferable that the upper limit of amine value is 110 mgKOH / g or less. It is preferable that the difference between the amine value and the acid value of resin b1 (amine value-acid value) is 100 mgKOH / g or less, it is preferable that 70 mgKOH / g or less, and it is further preferable that 50 mgKOH / g or less. It is preferable that the weight average molecular weight of resin b1 is 5000 to 50000. It is preferable that the upper limit is 45,000 or less, and it is preferable that the upper limit is 40,000 or less. It is preferable that the lower limit is 6000 or more, and it is preferable that the lower limit is 8000 or more. The resin b1 may have a polymerizable group. Examples of the polymerizable group include groups containing ethylene unsaturated bonds, such as vinyl, (meth)allyl, and (meth)acryl. It is also preferred that resin b1 is a resin containing repeating units having graft chains. According to this state, pixels with better pattern linearity can be formed. In addition, in this specification, the graft chain refers to a polymer chain extending from the main chain branch of the repeating unit. As the graft chain, it is preferable that the number of atoms other than hydrogen atoms is 40 to 10,000, it is preferable that the number of atoms other than hydrogen atoms is 50 to 2,000, and it is even better that the number of atoms other than hydrogen atoms is 60 to 500. It is preferred that the graft chain is a repeating unit including at least one structure selected from the group consisting of polyether structure, polyester structure, poly(meth)acrylic acid structure, polystyrene structure, polyurethane structure, polyurea structure and polyamide structure, it is preferred that the repeating unit including at least one structure selected from the group consisting of polyether structure, polyester structure, poly(meth)acrylic acid structure and polystyrene structure, it is further preferred that the repeating unit including polyether structure or polyester structure is particularly preferred, and the repeating unit including polyester structure is particularly preferred. As the repeating unit of the polyester structure, the repeating unit of the structure represented by formula (G-1), formula (G-4), or formula (G-5). As the repeating unit of the polyether structure, the repeating unit of the structure represented by formula (G-2) can be mentioned. As the repeating unit of the poly(meth)acrylic structure, the repeating unit of the structure represented by formula (G-3) can be mentioned. As the repeating unit of the polystyrene structure, the repeating unit of the structure represented by formula (G-6) can be mentioned. [Chemical Formula 14] In the above formula, R G1 and R G2 The radial alkyl group is independently represented. As R G1 and R G2 The alkyl group represented is not particularly limited. It is preferable to have a linear or branched alkyl group having 1 to 20 carbon atoms, a linear or branched alkyl group having 2 to 16 carbon atoms, and a linear or branched alkyl group having 3 to 12 carbon atoms, a linear or branched alkyl group having 3 to 12 carbon atoms. In the above formula, R G3 Represents a hydrogen atom or methyl group, Q G1 Indicates -O- or -NH-,L G1 Represents a single bond or divalent linker, R G4 Represents a hydrogen atom or a substituent. As L G1 Examples of the divalent linking groups are alkyl groups (the alkyl group with 1 to 12 carbons are preferred), alkoxy group (the alkyl group with 1 to 12 carbons are preferred), an oxyalkylcarbonyl group (the alkylcarbonyl group with 1 to 12 carbons are preferred), an aryl group (the aryl group with 6 to 20 carbons are preferred), -NH-, -SO-, and -SO 2 -, -CO-, -O-, -COO-, OCO-, -S- and a group formed by combining two or more of these. As R G4 Examples of the substituents represented include hydroxy, carboxyl, alkyl, aryl, heterocyclic, alkoxy, aryloxy, heteroepoxy, alkyl sulfide group, aryl sulfide group, heterocyclic sulfide group, group containing ethylene unsaturated bonds, epoxy group, oxetanyl, and blocked isocyanate group. R G5 Represents a hydrogen atom or methyl group, R G6 Represents aryl. R G6 It is preferable that the carbon number of the aryl group represented is 6 to 30, 6 to 20 is more preferable, and 6 to 12 is more preferable. R G6 The represented aryl group may have a substituent. Examples of the substituent include hydroxy, carboxyl, alkyl, aryl, heterocyclyl, alkoxy, aryloxy, heteroepoxy, alkyl sulfide group, aryl sulfide group, heterocyclic sulfide group, group containing ethylene unsaturated bonds, epoxy group, oxetanyl, and blocked isocyanate group. As the terminal structure of the graft chain, there is no particular limitation. It can be a hydrogen atom or a substituent. Examples of the substituent include alkyl, aryl, heteroaryl, alkoxy, aryloxy, heteroaryloxy, alkyl sulfide group, aryl sulfide group, heteroaryl sulfide group, and the like. Among them, from the viewpoint of inhibiting the aggregation of the Guchiyamaguchi star dye and dispersibility of the pigment, groups with spatial repulsion effects are preferred, and alkyl groups or alkoxy groups with 5 to 24 carbon atoms are preferred. The alkyl group and the alkoxy group may be any of a linear, branched and cyclic, and it is preferable to be a linear or branched. As the graft chain, the structure represented by formula (G-1a), formula (G-2a), formula (G-3a), formula (G-4a), formula (G-5a) or formula (G-6a) is preferred, and the structure represented by formula (G-1a), formula (G-4a) or formula (G-5a) is better. [Chemical Formula 15] In the above formula, R G1 and R G2 Represents the alkyl group, R G3 Represents a hydrogen atom or methyl group, Q G1 Indicates -O- or -NH-,L G1 Represents a single bond or divalent linker, R G4 Represents a hydrogen atom or substituent, R G5 Represents a hydrogen atom or methyl group, R G6 Represents aryl, W 100 It represents a hydrogen atom or a substituent, and n1 to n6 independently represent two or more integers. R G1 ~R G6 , Q G1 , L G1 The meaning and R explained in formula (G-1) to (G-6) G1 ~R G6 , Q G1 , L G1 The meanings of the same, and the preferred range is the same. In formulas (G-1a) to (G-6a), W 100 It is preferred to be a substituent. Examples of the substituent include alkyl, aryl, heteroaryl, alkoxy, aryloxy, heteroaryloxy, alkyl sulfide group, aryl sulfide group, heteroaryl sulfide group, and the like. Among them, from the viewpoint of inhibiting the aggregation of the Guchiyamaguchi star dye and dispersibility of the pigment, groups with spatial repulsion are preferred, and alkyl groups or alkoxy groups with 5 to 24 carbon atoms are preferred. The alkyl group and the alkoxy group may be any of a linear, branched and cyclic, and it is preferable to be a linear or branched. In formulas (G-1a) to (G-6a), it is preferable that integers with n1 to n6 are 2 to 100, integers with 2 to 80 are more preferable, and integers with 8 to 60 are more preferable. In formula (G-1a), when n1 is two or more R in each repeating unit G1 They can be the same or different. Also, if there are more than 2 types of R G1When there are different repeating units, there is no particular limitation on the arrangement of each repeating unit, and it may be any one of irregular, alternating, or blocks. The same is true in formulas (G-2a) to formulas (G-6a). Furthermore, the graft chain is a structure represented by formula (G-1a), formula (G-4a) or formula (G-5a) and contains two or more R types. G1 Different repeating units have better structures. As the repeating unit having the graft chain, the repeating unit represented by formula (G-100) can be mentioned. [Chemical Formula 16] Where, X G100 Represents a 3-valent linking group, L G100 Represents a single bond or a divalent linkage, W 100 Indicates graft chain. As X G100 Examples of the three-valent linking groups represented by the trivalent linking group include poly(meth)acrylic linking group, polythylene alkylimine linking group, polyester linking group, polyurethane linking group, polyurea linking group, polyamide linking group, polyether linking group, and polystyrene linking group, and the poly(meth)acrylic linking group or polythylene alkylimine linking group is preferred. As L G100 Examples of the divalent linking groups are alkyl groups (preferably 1 to 12 carbon atoms), aryl groups (preferably 6 to 20 carbon atoms), -NH-, -SO-, and -SO 2 -, -CO-, -O-, -COO-, OCO-, -S- and groups obtained by combining two or more of these. As W 100 The graft chain represented by the above-mentioned graft chain can be mentioned. It is preferable that the repeating unit with the graft chain is a repeating unit represented by formula (G-101) or a repeating unit represented by formula (G-102). [Chemical Formula 17] In formula (G-101), R G100 Represents a hydrogen atom or alkyl group, L G101 Represents a single bond or a divalent linkage, W 101 Indicates graft chain. In formula (G-102), R G101 and R G102 Independently representing hydrogen atoms or alkyl groups, L G102 Represents a single bond or a divalent linkage, W 102 Indicates graft chain. L of formula (G-101) G101 and W 101 Meaning and formula (G-100) G100 and W 100 The meaning of the same. L of formula (G-102) G102 and W 102 Meaning and formula (G-100) G100 and W 100 The meaning of the same. R of formula (G-101) G100 The represented alkyl group, R of formula (G-102) G101 and R G102 It is preferable that the carbon number of the expressed alkyl group is 1 to 10, 1 to 5 is more preferable, and 1 to 3 is more preferable. The alkyl group may be any one of a straight chain, a branched chain, or a cyclic shape, and the linear chain is preferably. R G100 It is preferred to be a hydrogen atom or a methyl group, and it is more preferred to be a methyl group. R G101 and R G102 It is preferred that it is a hydrogen atom or a methyl group independently, and it is preferred that it is a hydrogen atom. It is preferable that the weight average molecular weight of the repeating unit having the graft chain is 1000 or more, it is more preferable that 1000 to 10000, and it is even more preferable that 1000 to 7500 is more preferable. In addition, in this specification, the weight average molecular weight of the repeating unit having the graft chain is a value calculated from the weight average molecular weight of the raw material monomer used in the polymerization of the same repeating unit. For example, repeating units with graft chains can be formed by polymerizing megamonomers. Here, a megamonium system refers to a polymeric compound in which polymeric groups are introduced at the end of the polymer. When a repeating unit with a grafted chain is formed using a megamonomer, the weight average molecular weight of the megamonomer corresponds to the repeating unit with a grafted chain. When the resin b is a resin containing repeating units having graft chains, it is preferable that the content of repeating units having graft chains in the total mass of the resin b is 5 to 95 mass%. It is preferable that the upper limit is 70% by mass or less, and it is preferable that the upper limit is 60% by mass or less. It is preferable that the lower limit is 30% by mass or more, and it is preferable that the lower limit is 40% by mass or more. <<<Other Resin>>> The coloring composition of the present invention can further contain a resin other than the above-mentioned resin b1 (hereinafter also referred to as other resins). Examples of other resins include resins that do not have acid values, resins that do not have amine values, and resins that have acid values ​​and amine values ​​and have higher acid values ​​than amine values. Examples of other resins include (meth)acrylic resin, epoxy resin, olefin resin, polycarbonate resin, polyether resin, polyaryl resin, polyester resin, polyether resin, polyether resin, polyphenylene resin, polyethylene ether phosphine oxide resin, polyimide resin, polyamide resin, polyamide resin, polyamide resin, polyolefin resin, cyclic olefin resin, polyester resin, styrene resin, vinyl acetate resin, polyvinyl alcohol resin, polyethylene acetal resin, polyurethane resin, polyurea resin, etc. Among these resins, one type may be used alone, or two or more types may be used in combination. As the cyclic olefin resin, the norcapnylene resin is preferred from the viewpoint of improving heat resistance. Examples of commercially available products of the norcapnine resin include ARTON series (for example, ARTON F4520) manufactured by JSR Corporation. In addition, as other resins, resins described in Examples of International Publication No. 2016 / 088645, resins described in Japanese Patent Application No. 2017-057265, resins described in Japanese Patent Application No. 2017-032685, resins described in Japanese Patent Application No. 8, resins described in Japanese Patent Application No. 2017-066240, resins described in Japanese Patent Application No. 2017-167513, resins described in Japanese Patent Application No. 2017-173787, and 00 of Japanese Patent Application No. 2017-206689 Resin described in paragraphs 41 to 0060, resins described in paragraphs 0022 to 0071 of Japanese Patent Application Publication No. 2018-010856, block polyisocyanate resin described in JPY 2016-222891, resins described in JPY 2020-122052, resins described in JPY 2020-111656, resins described in JPY 2020-139021, resins described in JPY 2017-138503, resins containing structural units having ring structures in the main chain and structural units having biphenyl groups in the side chain. Furthermore, as other resins, resins with skeletons can also be used preferably. Regarding resins with skeletons, reference can be made to the description of US Patent Application Publication No. 2017 / 0102610, which is incorporated into this specification. In addition, as other resins, resins described in paragraphs 0199 to 0233 of Japanese Patent Laid-Open No. 2020-186373, alkali-soluble resins described in JP-Open No. 2020-186325, and resins represented by Formula 10-2020-0078339 can also be used. It is preferable that the weight average molecular weight (Mw) of other resins is 3000 to 2000000. It is preferable that the upper limit is 1000000 or less, and it is preferable that the upper limit is 500000 or less. It is preferable that the lower limit is 4000 or more, and it is preferable that the lower limit is 5000 or more. As other resins, it is preferable to use a resin having an acid group. Examples of the acid group include carboxyl, phosphate group, sulfo group, phenolic hydroxyl group, and the like. A resin having an acid group can be used as an alkali-soluble resin. It is preferable that the acid value of the resin having an acid group is 30 to 500 mgKOH / g. It is more preferable to have a lower limit of 40 mgKOH / g or above, and it is particularly preferable to have a lower limit of 50 mgKOH / g or above. It is more preferable to have an upper limit of 400 mgKOH / g or less, it is even better to have an upper limit of 300 mgKOH / g or less, and it is particularly preferable to have an upper limit of 200 mgKOH / g or less. It is preferable that the weight average molecular weight (Mw) of the resin having an acid group is 5000 to 100,000, and it is preferable that 5000 to 50,000 is preferable. Furthermore, it is preferable that the number average molecular weight (Mn) of the resin having an acid group is 1000 to 20000. It is preferable that the resin having an acid group contains a repeating unit having an acid group in the side chain, and it is preferable that all the repeating units of the resin contain 5 to 70 mol% of the repeating units having an acid group in the side chain. The upper limit of the content of the repeating unit having an acid group in the side chain is preferably 50 mol% or less, and it is more preferably 30 mol% or less. It is preferable that the content of the repeating unit having an acid group in the side chain is 10 mol% or more, and it is preferable that the content of the repeating unit having an acid group in the side chain is 10 mol% or more, and it is preferable that the content of the repeating unit having an acid group in the side chain is 20 mol% or more. Regarding resins having acid groups, reference can be made to paragraphs 0558-0571 of Japanese Patent Application Publication No. 2012-208494 (corresponding to paragraphs 0685-0700 of US Patent Application Publication No. 2012 / 0235099) and to paragraphs 0076-0099 of Japanese Patent Application Publication No. 2012-198408, these contents are included in this specification. Furthermore, commercially available products can be used as resins having acid groups. Furthermore, there is no particular limitation on the method of introducing an acid group into the resin, but for example, the method described in Japanese Patent Laid-Open No. 6349629 can be mentioned. Further, as a method of introducing an acid group into the resin, a method of introducing an acid group into the hydroxyl group produced in the ring-opening reaction of an epoxy group and anhydride to introduce an acid group. Other resins can also be used with base resins. It is preferable that the resin having a base is a resin containing a repeating unit having a base in the side chain, it is preferable that the copolymer having a repeating unit having a base in the side chain and a repeating unit without a base, it is preferable that the block copolymer having a repeating unit having a base in the side chain and a repeating unit without a base is preferable. Resin with bases can be used as a dispersant. It is preferable that the amine value of the resin having a base is 5 to 300 mgKOH / g. It is preferable that the lower limit is 10 mgKOH / g or more, and it is preferable that the lower limit is 10 mgKOH / g or more. It is preferable that the upper limit is 200 mgKOH / g or less, and it is preferable that the upper limit is 100 mgKOH / g or less. As other resins, resins containing repeating units including compounds represented by the source free formula (ED1) and / or compounds represented by the formula (ED2) (hereinafter, these compounds are sometimes referred to as "ether dimers".) can also be used. [Chemical Formula 18] In formula (ED1), R 1 and R 2 Each independently represents a hydrogen atom or a hydrocarbon group having a carbon number of 1 to 25 which may have a substituent. [Chemical Formula 19] In formula (ED2), R represents a hydrogen atom or an organic group having 1 to 30 carbon atoms. As a specific example of formula (ED2), you can refer to the records of Japanese Patent Laid-Open No. 2010-168539. For specific examples of ether dimers, please refer to paragraph 0317 of Japanese Patent Laid-Open No. 2013-029760, which is included in this specification. As other resins, resins having polymerizable groups can also be used. Examples of the polymerizable group include groups containing ethylene unsaturated bonds, such as vinyl, (meth)allyl, and (meth)acryl. As other resins, resins containing repeating units of compounds represented by the free formula (X) can also be used. [Chemical Formula 20] Where, R 1 Represents a hydrogen atom or methyl group, R 21 and R 22 The alkyl group is independently represented, and n represents an integer of 0 to 15, respectively. R 21 and R 22 It is preferable that the carbon number of the alkyl group represented is 1 to 10, 1 to 5 is more preferable, 1 to 3 is more preferable, and 2 or 3 is more preferable. n means that integers from 0 to 5 are preferred, integers from 0 to 4 are more preferred, and integers from 0 to 3 are further preferred. Examples of the compound represented by formula (X) include ethylene oxide or propylene oxide modified (meth)acrylate of para-cumyl phenol. Examples of commercially available products include ARONIX M-110 (manufactured by TOAGOSEI CO., LTD.). As other resins, resins having aromatic carboxyl groups (hereinafter also referred to as resin Ac) can be used. In the resin Ac, the aromatic carboxyl group may be contained in the main chain of the repeating unit or the side chain of the repeating unit. It is preferred that the aromatic carboxyl group contains the main chain of the repeating unit. In the present specification, an aromatic carboxyl group refers to a group in which one or more carboxyl groups are bonded to the structure of an aromatic ring. Among the aromatic carboxyl groups, it is preferable that the number of carboxyl groups bonded to the aromatic ring is 1 to 4, and 1 to 2 are preferable. As other resins, resins as dispersants can be used. Examples of the dispersant include acidic dispersants (acid resins) and alkaline dispersants (alkaline resins). It is preferred that the acid group of the acid dispersant (acid resin) has a carboxy group. Furthermore, it is preferable that the bases of the alkali dispersant (alkaline resin) have an amine group. It is also preferred that the resin used as the dispersant be a graft resin. For details about graft resin, please refer to the records in paragraphs 0025 to 0094 of Japanese Patent Laid-Open No. 2012-255128, which are included in this specification. It is also preferred that the resin used as the dispersant is a polyimine-based dispersant containing nitrogen atoms at least one of the main chain and the side chain. As a polyimine dispersant, it is preferred that resins have a main chain and a side chain and have alkaline nitrogen atoms at least one of the main chain and a side chain. The main chain contains a partial structure with a functional group of pKa14 or less, and the number of atoms of the side chain is 40 to 10,000. As long as the alkaline nitrogen atom is a alkaline nitrogen atom, there is no particular limitation. Regarding the polyimine-based dispersant, reference can be made to the records of paragraphs 0102-0166 of Japanese Patent Laid-Open No. 2012-255128, and this content is included in this specification. It is also preferred that the resin used as the dispersant is a resin with a structure bonded to a plurality of polymer chains in the core. Examples of such resins include dendritic polymers (including star polymers). Furthermore, as specific examples of dendritic polymers, polymer compounds C-1 to C-31, etc. described in paragraphs 0196 to 0209 of Japanese Patent Laid-Open No. 2013-043962 can be mentioned. It is also preferred that the resin used as the dispersant is a resin containing the following repeating unit, which has a group containing an ethylene unsaturated bond in the side chain. The content of repeating units having groups containing ethylene unsaturated bonds in the side chain is preferably 10 mol% or more among all repeating units of the resin, more preferably 10 to 80 mol% and more preferably 20 to 70 mol%. Furthermore, as the dispersant, the resin described in Japanese Patent Publication No. 2018-087939, the block copolymer (EB-1) to (EB-9) described in paragraphs 0219 to 0221 of Japanese Patent Publication No. 6432077, the polyethyleneimine having a polyester side chain described in International Publication No. 2016 / 104803, the block copolymer described in International Publication No. 2019 / 125940, the block polymer having acrylamide structural unit described in Japanese Patent Publication No. 2020-066687, the block polymer having acrylamide structural unit described in Japanese Patent Publication No. 2020-066688, the block polymer having acrylamide structural unit described in International Publication No. 2016 / 104803, etc. can be used. Dispersants can also be obtained as commercial products. Specific examples include the Disperbyk series manufactured by BYK-Chemie GmbH, the SOLSPERSE series manufactured by Japan Lubrizol Corporation, and the Ajisper series manufactured by Ajinomoto Fine-Techno Co., Inc., etc. Furthermore, the product described in paragraph 0129 of Japanese Patent Application Publication No. 2012-137564 and the product described in paragraph 0235 of Japanese Patent Application Publication No. 2017-194662 can also be used as the dispersant. It is preferable that the resin content in the total solid component of the coloring composition is 5 to 40 mass %. It is preferable that the lower limit is 8 mass% or more, and it is preferable that the lower limit is 8 mass% or more. It is preferable that the upper limit is 30% by mass or less, and it is preferable that the upper limit is 20% by mass or less. It is preferable that the content of resin b1 in the total solid component of the coloring composition is 5 to 40 mass %. It is preferable that the lower limit is 8 mass% or more, and it is preferable that the lower limit is 8 mass% or more. It is preferable that the upper limit is 30% by mass or less, and it is preferable that the upper limit is 20% by mass or less. Furthermore, the content of resin b1 is preferably 10 to 160 parts by mass relative to 100 parts by mass of the Koichi-saka dye. It is preferable that the lower limit is 20 parts by mass or more, and it is preferable that the lower limit is 25 parts by mass or more. The upper limit is preferably 120 parts by mass or less, and it is more preferably 80 parts by mass or less. Furthermore, it is preferable that the content of resin b1 in the resin contained in the coloring composition is 5 to 100 mass %. It is preferable that the lower limit is 7% by mass or more, and it is preferable that the lower limit is 7% by mass or more. It is preferable that the upper limit is 90% by mass or less, and it is preferable that the upper limit is 80% by mass or less. As a preferred aspect of the coloring composition, a form containing the above-mentioned resin b1 and a resin having an acid group as other resins (hereinafter also referred to as resin b2). According to this aspect, since the acid group of resin b2 becomes hydrophilic, the permeability of the developer is improved, and the development of the unexposed portion between the patterns can be further improved, and the pattern linearity of the obtained pixel can be further improved. It is possible to further suppress the occurrence of developing residue, or to further suppress the occurrence of pixel defects. The acid value of resin b1 may be higher, lower or the same as that of resin b2. From the reason that the occurrence of developing residue caused by high concentration of colorants can be further suppressed, it is preferable that the acid value of resin b1 is higher than that of resin b2. Furthermore, it is preferable that the difference between the acid value of resin b1 and the acid value of resin b2 is 0 to 200 mgKOH / g. It is preferable that the lower limit of the above-mentioned difference is 10 mgKOH / g or more, and it is preferable that the lower limit of the above-mentioned difference is 10 mgKOH / g or more. It is preferable that the upper limit of the above-mentioned difference is 190 mgKOH / g or less, and it is preferable that the upper limit of the above-mentioned difference is 180 mgKOH / g or less. It is preferable that the content of resin b2 is 25 to 400 parts by mass relative to 100 parts by mass of resin b1 . It is preferable that the lower limit is 30 parts by mass or more, and it is preferable that the lower limit is 40 parts by mass or more. The upper limit is preferably 300 parts by mass or less, and it is more preferably 200 parts by mass or less. <<Pigment Derivatives>> The coloring composition of the present invention can contain pigment derivatives. When the colorant used in the coloring composition of the present invention is a pigment containing a pigment, it is preferred that the coloring composition of the present invention contains a pigment derivative. Pigment derivatives can be used as dispersion aids, for example. Examples of the pigment derivative include compounds having a structure in which an acid group or a base is bonded to the pigment backbone. Examples of the pigment skeleton constituting the pigment derivative include quinoline pigment skeleton, benzimidazolone pigment skeleton, benzothiazole pigment skeleton, iminium pigment skeleton, crotonium pigment skeleton, oxacin pigment skeleton, pyrrolopyrrol pigment skeleton, dikepyrrolopyrrol pigment skeleton, azo pigment skeleton, methinine pigment skeleton, Phthalocyanine pigment skeleton, naphthalocyanine pigment skeleton, anthraquinone pigment skeleton, quinacridone pigment skeleton, dithiol pigment skeleton, perylene pigment skeleton, thioindigo pigment skeleton, isoindoline pigment skeleton, isoindoline pigment skeleton, quinoline yellow pigment skeleton, iminium pigment skeleton, dithiol pigment skeleton, triarylmethane pigment skeleton, pyrrole methylene pigment skeleton, etc. Examples of the acid group include carboxyl, sulfo, phosphoric acid group, boric acid group, carboxylic acid amido group, sulfonic acid amido group, aimide group, and the like. Examples of the atom or atomic group that constitutes a salt include alkali metal ions (Li) + , Na + , K + ), alkaline earth metal ions (Ca 2+ , Mg 2+ ), ammonium ions, imidazolium ions, pyridinium ions, phosphonium ions, etc. As carboxylic acid amide group, it is from -NHCOR X1 The group represented is preferred. As sulfonate amide group, from -NHSO 2 R X2 The group represented is preferred. As an imidine group, from -SO 2 NHSO 2 R X3 , -CONHSO 2 R X4 , -CONHCOR X5 or -SO 2 NHCOR X6 The group represented is preferably -SO 2 NHSO 2 R X3 For better. R X1 ~R X6 Alkane or aryl are independently represented, respectively. R X1 ~R X6 The alkyl and aryl groups represented may have substituents. As the substituent, a halogen atom is preferred and a fluorine atom is more preferred. Examples of the base include an amine group, a pyridyl group and a salt thereof, an ammonium group and a phthalimide methyl group. Examples of the atoms or atomic groups that constitute the salt include hydroxide ions, halide ions, carboxylic acid ions, sulfonic acid ions, and phenoxide ions. Pigment derivatives can also be used with pigment derivatives with excellent visible transparency (hereinafter also referred to as transparent pigment derivatives). The maximum value (εmax) of the moor absorbance coefficient of transparent pigment derivatives in the wavelength region of 400 to 700 nm is 3000L·mol -1 ·cm -1 The following is preferred, 1000L·mol -1 ·cm -1 The following is better, 100L·mol -1 ·cm -1 The following is further preferred. The lower limit of εmax is, for example, 1L·mol -1 ·cm -1 The above can be 10L·mol -1 ·cm -1 above. Specific examples of pigment derivatives include compounds described in Japanese Patent Application No. 56-118462, compounds described in Japanese Patent Application No. 63-264674, compounds described in Japanese Patent Application No. 01-217077, and Japanese Patent Application No. 03-0099 The compound described in JPK No. 61, the compound described in JPK No. 03-026767, the compound described in JPK No. 03-153780, the compound described in JPK No. 03-045662, the compound described in JPK No. 04-285669, the compound described in JPK No. 06-145546, the compound described in JPK No. 06-212088, the compound described in JPK No. 06-240158 The compounds described in the publication, the compounds described in Japanese Patent Laid-Open No. 10-030063, the compounds described in Japanese Patent Laid-Open No. 10-195326, the compounds described in paragraphs 0086-0098 of International Publication No. 2011 / 024896, the compounds described in paragraphs 0063-0094 of International Publication No. 2012 / 102399, the compounds described in paragraphs 0082 of International Publication No. 2017 / 038252, and the compounds described in Japanese Patent Laid-Open No. 2015-151530 The compound described in paragraph 0171 of the publication, the compound described in paragraph 0162 to 0183 of Japanese Patent Publication No. 2011-252065, the compound described in JP-2003-081972, the compound described in JP-2003-081972, the compound described in JP-2015-172732, the compound described in JP-2014-199308, the compound described in JP-2014-085562 , the compound described in Japanese Patent Application No. 2014-035351, the compound described in Japanese Patent Application No. 2008-081565, the compound described in Japanese Patent Application No. 2019-109512, the compound described in Japanese Patent Application No. 2019-133154, the diketopyrrolopyrrol compound having a thiol linker described in International Publication No. 2020 / 002106, the benzimidazolone compound or its salt described in Japanese Patent Application No. 2018-168244. The content of the pigment derivative is preferably 1 to 30 parts by mass relative to 100 parts by mass of the pigment, and 3 to 20 parts by mass is more preferably . Furthermore, it is preferable that the total content of the pigment derivative and the colorant in the total solid component of the coloring composition is 35 mass % or more, it is more preferable that 40 mass % or more, it is even better, and it is even better that 45 mass % or more, and it is particularly preferable that 50 mass % or more. It is preferable that the upper limit is 80% by mass or less, it is more preferable that the upper limit is 70% by mass or less, and it is even more preferable that the upper limit is 65% by mass or less. The coloring composition of the present invention may contain only one type of pigment derivative, or may contain two or more types. When two or more pigment derivatives are contained, the total amount of these is preferably within the above range. By containing two or more pigment derivatives, the dispersion stability of the colored composition can be further improved. Furthermore, by using pigment derivatives with excellent visible transparency, the color change of the film after the heat resistance test or the light resistance test can be suppressed, so that the heat resistance and light resistance can be improved. Furthermore, by combining colored pigment derivatives and transparent pigment derivatives, dispersion stability, heat resistance and light resistance can be taken into account at a higher level. <<Ionic Compound C>> The coloring composition of the present invention can contain cation CX + and anionic CZ - salt (hereinafter also referred to as ionic compounds). By containing such a compound, the effect of making the pattern linear is better able to be better at the reason for interacting with the dyes to ease the interaction between the dyes. Regarding ionic compounds, the following formula (A) is at the maximum absorption wavelength in the range of 400 to 700 nm. λ ) It is preferred that the absorbance of the ratio is 5 or less, it is better that the absorbance of 3 or less, and it is further preferred that the absorbance of 1 or less is better. E=A / (c×l) ···(A λ ) Formula (A λ ) In ), E represents the specific absorbance of the ionic compound at the maximum absorption wavelength range of 400 to 700 nm, A represents the absorbance of the ionic compound at the maximum absorption wavelength range of 400 to 700 nm, l represents the groove length in unit cm, and c represents the concentration of the ionic compound in the solution represented by mg / ml. Examples of the method of measuring the specific absorbance of the ionic compound include a method of measuring the absorbance of the solution at 25°C using a tank with a light diameter length of 1 cm. The solvent in the determination of the specific absorbance can be used appropriately if it has sufficient solubility to the ionic compound. Examples of the preferred solvent include water, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, dimethyl molylithium, cyclohexanone, acetone, methanol, and the like. When the ionic compound has sufficient solubility in water, the solvent uses water. It is preferable that the molecular weight of the ionic compound is 80 to 5000. It is preferred that the upper limit is 3000 or less, it is more preferred that the upper limit is 2000 or less, it is further preferred that the upper limit is 1500 or less, and it is particularly preferred that the upper limit is 1210 or less. It is preferable that the lower limit is 100 or more, and it is preferable that the lower limit is 200 or more. Anion CZ as ionic compounds - Examples include imide anions, methylated anions, borate anions, phosphorus-containing atom anions, sulfonic acid anions, etc., and are preferred to be imide anions, methylated anions and borate anions, and are more preferred to be imide anions and methylated anions, and are even more preferred to be imide anions. Also, anionic CZ - It is preferred that anion containing at least one type selected from the group consisting of fluorine atoms and sulfur atoms. From the viewpoint of storage stability of the coloring composition, anion CZ of an ionic compound - It is preferable that the pKa of the conjugated acid is 0 or less, it is more preferable that the pKa of -5 or less, it is more preferable that the pKa of -8 or less, it is even better, it is even better than that the pKa of the conjugated acid is even better, it is especially preferable that the pKa of the conjugated acid is 0 or less, it is more preferable that the pKa of -10 or less, it is particularly preferable. The lower limit is not particularly limited, and can be set to -20 or above, or can be set to -18 or above. The pKa of the conjugated acid can be measured by, for example, the method described in J. Org. Chem. 2011, 76, 391-395. Anion CZ - It is preferred to be at least one type selected from the group consisting of anion having a partial structure represented by formula (CZ-1), anion having a partial structure represented by formula (CZ-2), anion having a partial structure represented by formula (CZ-3), anion having a partial structure represented by formula (CZ-4), and anion having a partial structure represented by formula (CZ-5), and at least one type selected from the group consisting of anion having a partial structure represented by formula (CZ-1), anion having a partial structure represented by formula (CZ-2), and anion having a partial structure represented by formula (CZ-3), and it is further preferred to be the group consisting of anion having a partial structure represented by formula (CZ-1) or anion having a partial structure represented by formula (CZ-2). The anion with a partial structure represented by formula (CZ-1) is an imide anion, the anion with a partial structure represented by formula (CZ-2) is a methylated anion, the anion represented by formula (CZ-3) is a borate anion, the anion represented by formula (CZ-4) is a sulfonic acid anion, and the anion represented by formula (CZ-5) is a phosphorus-containing atom anion. [Chemical Formula 21] In formula (CZ-1), R 111 and R 112 Independently expressed -SO 2 -or-CO-, in formula (CZ-2), R 113 Indicates-SO 2 -or-CO-,R 114 and R 115 Independently expressed -SO 2 -, -CO- or cyano group, in formula (CZ-3), R 116 ~R 119 The halogen atom, an alkyl group, an aryl group, an alkoxy group, an aryl group, an aryl group, or a cyano group, are respectively independently represented. In formula (CZ-4), R 120 It means a halogenated hydrocarbon that can be linked by a linking group having a nitrogen atom or an oxygen atom. In formula (CZ-5), R 121 ~R 126 The halogen atom or halogenated hydrocarbons are independently represented, respectively. In formula (CZ-1), R 111 and R 112 at least one of the representation -SO 2 -For better, R 111 and R 112 Both of the representations-SO 2 -For better. Anion having a partial structure represented by (CZ-1) in R 111 and R 112 It is preferable that at least one of the terminals has a halogen atom or an alkyl group (haloalkyl group) having a halogen atom as a substituent, and it is preferable that an alkyl group (fluoroalkyl group) having a fluorine atom or a fluorine atom as a substituent. It is preferable that the carbon number of fluoroalkyl groups is 1 to 10, 1 to 6 are more preferable, and 1 to 3 are more preferable. It is more preferable that the fluoroalkyl group is a perfluoroalkyl group. (CZ-2), R 113 ~R 115 at least one representation of -SO 2 -For better, R 113 ~R 115 At least 2 representations of -SO 2 -For better, R 113 ~R 115 All representations in -SO 2 -, or R 113 and R 115 Indicates-SO 2 -and R 114 Indicates -CO-, or R 114 and R 115 Indicates-SO 2 -and R 113 Indicates that -CO- is further preferred, R 113 ~R 115 All representations in -SO 2 - It is very good. Anion having a partial structure represented by (CZ-2) in R 113 ~R 115 It is preferable that at least one of the terminals has a halogen atom or an alkyl group (haloalkyl group) having a halogen atom as a substituent, and it is preferable that an alkyl group (fluoroalkyl group) having a fluorine atom or a fluorine atom as a substituent. Especially in R 113 ~R 115 It is preferable to have a halogen atom or a haloalkyl group at at least two terminals, and it is preferable to have a fluorine atom or a fluorine alkyl group. It is preferable that the carbon number of fluoroalkyl groups is 1 to 10, 1 to 6 are more preferable, and 1 to 3 are more preferable. It is more preferable that the fluoroalkyl group is a perfluoroalkyl group. In formula (CZ-3), R 116 ~R 119 The halogen atom, an alkyl group, an aryl group, an alkoxy group, an aryl group, an aryl group, or a cyano group, are respectively independently represented. The alkyl group, aryl group, alkoxy group and aryl group may have substituents or may be unsubstituted. When there is a substituent, it is preferable that the halogen atom or the alkyl group substituted with a halogen atom is preferable, and the fluorine atom or the alkyl group substituted with a fluorine atom is preferable. In formula (CZ-3), R 116 ~R 119 At least one of the cyano groups, halogen atoms, alkyl groups having halogen atoms as a substituent, aryl groups having halogen atoms as a substituent, and aryl groups having alkyl groups having halogen atoms as a substituent, R 116 ~R 119 All of the indices represent cyano groups, or aryl groups having a halogen atom (a fluorine atom is preferred) as a substituent. In formula (CZ-4), R 120 It means a halogenated hydrocarbon that can be linked by a linking group having a nitrogen atom or an oxygen atom. Halogenated hydrocarbons refer to monovalent hydrocarbon groups replaced by halogen atoms, and preferably monovalent hydrocarbon groups replaced by fluorine atoms. Examples of the hydrocarbon group include alkyl groups, aryl groups, etc. The monovalent hydrocarbon group substituted with a halogen atom may further have a substituent. Examples of the linking group having a nitrogen atom or an oxygen atom include -O-, -CO-, -COO-, -CO-NH- and the like. In formula (CZ-5), R 121 ~R 126 Each independently represents a halogen atom or a halogenated hydrocarbon. R 121 ~R 126 It is preferable that the halogenated hydrocarbon represented by the halogen hydrocarbon has an alkyl group that does not have a halogen atom as a substituent, and it is preferable that the alkyl group that has a fluorine atom as a substituent. It is preferable that anion having a partial structure represented by (CZ-1) is an anion represented by formula (CZ1-1). Furthermore, it is preferable that the anion having a partial structure represented by (CZ-2) is an anion represented by formula (CZ2-1). [Chemical Formula 22] In formula (CZ1-1), R 211 and R 212 Individually represent halogen atoms or alkyl groups when R 211 and R 212 When the alkyl group is independently represented, R 211 and R 212 The ring can be formed by bonding, in formula (CZ2-1), R 213 ~R 215 Individually represent halogen atoms or alkyl groups when R 213 and R 214 When the alkyl group is independently represented, R 213 and R 214 Can be bonded to form a ring when R 214 and R 215 When the alkyl group is independently represented, R 214 and R 215 Can be bonded to form a ring when R 213 and R 215 When the alkyl group is independently represented, R 213 and R 215 It can be bonded to form a ring. In formula (CZ1-1), R 211 and R 212 The halogen atom or alkyl group is independently represented, respectively. Examples of the halogen atom include fluorine atom, chlorine atom, bromine atom, and iodine atom, and halogen atom is preferred. It is preferable that the carbon number of the alkyl group is from 1 to 10, 1 to 6 is more preferable, and 1 to 3 is more preferable. Examples of alkyl groups include linear, branched, and cyclic, and linear or branched are preferred, and linear is more preferred. The alkyl group may have a substituent or may be unsubstituted. It is preferable that the alkyl group is an alkyl group having a halogen atom as a substituent, and it is preferable that the alkyl group (fluoroalkyl group) having a fluorine atom as a substituent. Furthermore, it is preferred that the fluoroalkyl group is a perfluoroalkyl group. In formula (CZ1-1), when R 211 and R 212 When the alkyl group is independently represented, R 211 and R 212 It can be bonded to form a ring. In formula (CZ2-1), R 213 ~R 215 The halogen atom or alkyl group is independently represented, respectively. The ranges of halogen atoms and alkyl groups are the same as those described in Formula (CZ1-1), and the preferred ranges are also the same. In formula (CZ2-1), when R 213 and R 214 When the alkyl group is independently represented, R 213 and R 214 It can be bonded to form a ring. Also, when R 214 and R 215 When the alkyl group is independently represented, R 214 and R 215 It can be bonded to form a ring. Also, when R 213 and R 215 When the alkyl group is independently represented, R 213 and R 215 It can be bonded to form a ring. As anion CZ - Specific examples include anion of the structure represented by formulas (MD-1) to (MD-18). [Chemical Formula 23] Also, as anion CZ - Specific examples can also be mentioned (CF 3 ) 3 PF 3 - , (C 2 F 5 ) 2 PF 4 - , (C 2 F 5 ) 3 PF 3 - ,[(CF 3 ) 2 CF] 2 PF 4 - ,[(CF 3 ) 2 CF] 3 PF 3 , (n-C 3 F 7 ) 2 PF 4 - , (n-C 3 F 7 ) 3 PF 3 - , (n-C 4 F 9 ) 3 PF 3 - , (C 2 F 5 ) (CF 3 ) 2 PF 3 - ,[(CF 3 ) 2 CFCF 2 ] 2 PF 4 - ,[(CF 3 ) 2 CFCF 2 ] 3 PF 3 , (n-C 4 F 9 ) 2 PF 4 - , (n-C 4 F 9 ) 3 PF 3 - , (C 2 F 4 H) (CF 3 ) 2 PF 3 - , (C 2 F 3 H 2 ) 3 PF 3 - , (C 2 F 5 ) (CF 3 ) 2 PF 3 - , (CF 3 ) 4 B - , CF 3 ) 3 BF - , (CF 3 ) 2 BF 2 - , (CF 3 )BF 3 - , (C 2 F 5 ) 4 B - , (C 2 F 5 ) 3 BF - , (C 2 F 5 )BF 3 - , (C 2 F 5 ) 2 BF 2 - , (CF 3 )(C 2 F 5 ) 2 BF - , (C 6 F 5 ) 4 B - ,[(CF 3 ) 2 C 6 H 3 ] 4 B - , (CF 3 C 6 H 4 ) 4 B - , (C 6 F 5 ) 2 BF 2 - , (C 6 F 5 )BF 3 - , (C 6 H 3 F 2 ) 4 B - , B (CN) 4 - , B (CN) F 3 - , B (CN) 2 F 2 - , B (CN) 3 F - , (CF 3 ) 3 B (CN) - , (CF 3 ) 2 B (CN) 2 - , (C 2 F 5 ) 3 B (CN) - , (C 2 F 5 ) 2 B (CN) 2 - , (n-C 3 F 7 ) 3 B (CN) - , (n-C 4 F 9 ) 3 B (CN) - , (n-C 4 F 9 ) 2 B (CN) 2 - , (n-C 6 F 13 ) 3 B (CN) - , (CHF 2 ) 3 B (CN) - , (CHF 2 ) 2 B (CN) 2 - , (CH 2 CF 3 ) 3 B (CN) - , (CH 2 CF 3 ) 2 B (CN) 2 - , (CH 2 C 2 F 5 ) 3 B (CN) - , (CH 2 C 2 F 5 ) 2 B (CN) 2 - , (CH 2 CH 2 C 3 F 7 ) 2 B (CN) 2 - , (n-C 3 F 7 CH 2 ) 2 B (CN) 2 - , (C 6 H 5 ) 3 B (CN) - and anions of the following structures. [Chemical Formula 24] [Chemical Formula 25] [Chemical Formula 26] Among ionic compounds, CX + , as long as it can cancel anion CZ - The charge structure is enough. From easily reduced with anion CZ - cationic CX + It is preferable that the molecular weight is 2 to 500, 2 to 200, and 6 to 90 are further preferable. As cation CX + , the monomer metal atom is preferably cation, carbocation, ammonium cation, phosphonium cation or vitro cation, and the monomer metal atom is more preferably cation or ammonium cation. Also, cationic CX + It is also preferred that cations with a divalent or above are cations. According to this condition, a stronger film can be formed, and defects of the developed film can be more effectively suppressed. Examples of the cations of the monomeric metal atom include lithium (Li) cations, beryllium (Be) cations, sodium (Na) cations, magnesium (Mg) cations, aluminum (Al) cations, potassium (K) cations, calcium (Ca) cations, scandium (Sc ) Cation, Ti (Ti) cation, Vanadium (V) cation, Chromium (Cr) cation, Manganese (Mn) cation, Iron (Fe) cation, Cobalt (Co) cation, Nickel (Ni) cation, Copper (Cu) cation, Zinc (Zn) cation, Ga (Ga) cation, Germanium (Ge) cation, Rubidium (Rb) cation, Strontium (Sr) cation, Cadmium (C d) cations, indium (In) cations, tin (Sn) cations, cesium (Cs) cations, barium (Ba) cations, mercury (Hg) cations, thallium (Tl) cations, lead (Pb) cations, bismuth (Bi) cations, oxotinium (Fr) cations, radium (Ra) cations, lanthanum (La) cations, cerium (Ce) cations, neodymium (Nd) cations, etc. Among them, lithium (Li) cation, sodium (Na) cation, magnesium (Mg) cation, aluminum (Al) cation, potassium (K) cation, calcium (Ca) cation, copper (Cu) cation, zinc (Zn) cation, gallium (Ga) cation, rubidium (Rb) cation, strontium (Sr) cation, indium (In) cation, cesium (Cs) cation, barium (Ba) cation, lanthanum (La) cation, cerium (Ce) cation, neodymium (Nd ) cations are preferred, lithium (Li) cation, sodium (Na) cation, magnesium (Mg) cation, aluminum (Al) cation, potassium (K) cation, calcium (Ca) cation, strontium (Sr) cation, copper (Cu) cation, zinc (Zn) cation, lanthanum (La) cation, cerium (Ce) cation, neodymium (Nd) cation, and lithium (Li) cation, sodium (Na) cation, and potassium (K) cation are further preferred. Examples of the ammonium cation include cations represented by the following formula (CX-1). [Chemical Formula 27] In formula (CX-1), R AN1 ~R AN4 The hydrogen atoms contained in these can be independently represented by 1 to 20 carbon atoms, and -CH=CH 2 or -CH=CHR b replace. Furthermore, -O-, -S-, -CO-, -NH- or -NR may be inserted between the carbon-carbon bonds of the alkyl group and the alkenyl group. b -. Also, R AN1 ~R AN4 It can be bonded to each other to form a heterocyclic ring containing nitrogen atoms with 3 to 10 members. At this time, the hydrogen atoms contained in the heterocycle can be passed through -R b , -OH substitutes. R b A monovalent saturated hydrocarbon group with 1 to 10 carbon atoms. Specific examples of ammonium cations include tetramethylammonium cation, tetraethylammonium cation, tetrapropylammonium cation, tetrabutylammonium cation, monoethyltrimethylammonium cation, monopropyltrimethylammonium cation, monobutyltrimethylammonium cation, monostearyltriphenylammonium cation, distearyldimethylammonium cation, tristearyl monomethylammonium cation, stearyl trimethylammonium cation, trioctyldimethylammonium cation, dioctyldimethylammonium cation, stearyl trimethylammonium cation, trioctyldimethylammonium cation, trioctyldimethylammonium cation, dioctyldimethylammonium cation, trioctyldimethylammonium cation, and dioctyldimethylammonium cation, stearyltrimethylammonium cation, trioctyldimethylammonium cation, and dioctyldimethylammonium cation, A yl ammonium cation, monolauryl trimethylammonium cation, dilauryl dimethylammonium cation, trilauryl methylammonium cation, tripentyl benzyl ammonium cation, trihexyl benzyl ammonium cation, trioctyl benzyl ammonium cation, trilactyl benzyl ammonium cation, trilactyl benzyl ammonium chlorine cation, benzyl dimethyl stearyl ammonium cation, benzyl dimethyloctyl ammonium cation, dialkyl (alkyl is C14-C18) dimethylammonium cation and the cation of the structure shown below. [Chemical Formula 28] It is preferable that the content of the ionic compound in the total solid component of the coloring composition is 0.1 to 15 mass %. It is preferable that the upper limit is 12 mass % or less, and it is preferable that the upper limit is 10 mass % or less. It is preferable that the lower limit is 0.5% by mass or more, and it is preferable that 1% by mass or more. The content of the ionic compound is preferably 0.05 to 4.00 mol with respect to 1 mol of Koichia dye, more preferably 0.05 to 3.00 mol, and more preferably 0.05 to 2.00 mol. <<Polymerizable Compound>> It is preferred that the coloring composition of the present invention contains a polymerizable compound. As the polymerizable compound, a well-known compound that can be crosslinked by free radicals, acids or heat can be used. It is preferred that the polymerizable compound is a compound having a group containing an ethylene unsaturated bond. Examples of the group containing the ethylene unsaturated bond include vinyl, (meth)allyl, (meth)acryl, etc. It is preferred that the polymerizable compound used in the present invention is a free radical polymerizable compound. The polymerizable compound may be any of the chemical forms such as monomers, prepolymers, and oligos, but the monomers are preferred. It is preferable that the molecular weight of the polymerizable compound is 100 to 3000. It is more preferable to have an upper limit of 2000 or less, and it is even more preferable to have an upper limit of 1500 or less. It is more preferable to have a lower limit of 150 or more, and it is even more preferable to have a lower limit of 250 or more. It is preferable that the polymerizable compound is a compound containing three or more groups containing ethylene unsaturated bonds, it is preferable that the compound containing 3 to 15 groups containing ethylene unsaturated bonds, and it is preferable that the compound containing 3 to 6 groups containing ethylene unsaturated bonds. Furthermore, it is preferable that the (meth)acrylate compound with a polymerizable compound having a 3-15-functional function, and it is preferable that the (meth)acrylate compound having a 3-6-functional function is preferable. Specific examples of polymerizable compounds include the compounds described in Japanese Patent Application No. 2009-288705, the paragraphs 0095-0108 of Japanese Patent Application No. 2013-029760, the paragraphs 0254-0257 of Japanese Patent Application No. 2008-292970, the paragraphs 0034-0038 of Japanese Patent Application No. 2013-253 224, the paragraphs 0477 of Japanese Patent Application No. 2012-208494, the compounds described in Japanese Patent Application No. 2017-048367, the Japanese Patent Application No. 6057891, and the Japanese Patent Application No. 6031807, and the contents are included in this specification. As polymerizable compounds, dipentantetyl tris(meth)acrylate (as commercially available, KAYARAD D-330; manufactured by Nippon Kayaku Co., Ltd.), dipentantetyl tet(meth)acrylate (as commercially available, KAYARAD D-320; manufactured by Nippon Kayaku Co., Ltd.), dipentantetyl penta(meth)acrylate (as commercially available, KAYARAD D-310; manufactured by Nippon Kayaku Co., Ltd.), dipentantetyl hexa(meth)acrylate (as commercially available, KAYARAD DPHA; manufactured by Nippon Kayaku Co., Ltd., NK ESTER A-DPH-12E; manufactured by SHIN-NAKAMURA CHEMICAL Co., Ltd.) and compounds of such (meth)acryl groups bonded through ethylene glycol and / or propylene glycol residues (eg, SR454, SR499 commercially available from SARTOMER Company, Inc.) are preferred. Furthermore, as the polymerizable compound, diglycerol EO (ethylene oxide) modified (meth)acrylate (manufactured as a commercial product, M-460; TOAGOSEI CO., LTD.), neopentylene tetraacrylate (manufactured by SHIN-NAKAMURA CHEMICAL Co., Ltd., NK ESTER A-TMMT), 1,6-hexanediol diacrylate (manufactured by Nippon Kayaku Co., Ltd., KAYARAD HDDA), RP-1040 (manufactured by Nippon Kayaku Co., Ltd.), ARONIX TO-2349 (manufactured by TOAGOSEI CO., LTD.), NK Oligo UA-7200 (manufactured by SHIN-NAKAMURA CHEMICAL Co., Ltd.), DPHA-40H (manufactured by Nippon Kayaku Co., Ltd.), UA-306H, UA-306T, UA-306I, AH-600, T-600, AI-600, LINC-202UA (manufactured by KYOEISHA CHEMICAL Co.,LTD.), 8UH-1006, 8UH-1012 (the above is manufactured by Taisei Fine Chemical Co., Ltd.), LIGHT ACRYLATE POB-A0 (KYOEISHA CHEMICAL Manufactured by Co., LTD.) etc. In addition, trifunctional (meth)acrylate compounds such as trimethylolpropane tri(meth)acrylate, trimethylolpropane propylene oxide modified tri(meth)acrylate, trimethylolpropane ethylene oxide modified tri(meth)acrylate, trimethylolpropane ethylene oxide modified tri(meth)acrylate, isomerocyanate ethylene oxide modified tri(meth)acrylate, neopentyl tri(meth)acrylate, etc. can be used as the polymerizable compound. Examples of commercially available products of the three-functional (meth)acrylate compounds include ARONIX M-309, M-310, M-321, M-350, M-360, M-313, M-315, M-306, M-305, M-303, M-452, M-450 (manufactured by TOAGOSEI CO., LTD.), NK ESTER A9300, A-GLY-9E, A-GLY-20E, A-TMM-3, A-TMM-3LM-N, A-TMPT, TMPT (manufactured by SHIN-NAKAMURA CHEMICAL Co., Ltd.), and KAYARAD GPO-303, TMPTA, THE-330, TPA-330, PET-30 (manufactured by Nippon Kayaku Co., Ltd.), etc. Furthermore, a compound having an acid group can be used for the polymerizable compound. By using a polymerizable compound having an acid group, the polymerizable compound in the unexposed portion can be easily removed during development, and the generation of the developing residue can be suppressed. Examples of the acid group include carboxyl groups, sulfo groups, phosphate groups, etc., and the carboxyl group is preferred. Examples of commercially available products of polymerizable compounds having acid groups include ARONIX M-510, M-520, ARONIX TO-2349 (manufactured by TOAGOSEI CO., LTD.). As the preferred acid value of the polymerizable compound having an acid group, 0.1 to 40 mgKOH / g is preferred, and 5 to 30 mgKOH / g is preferred. As long as the acid value of the polymerizable compound is 0.1 mgKOH / g or more, the solubility of the developer is good, and as long as it is 40 mgKOH / g or less, it is advantageous in terms of production or operation. Furthermore, a polymerizable compound can also be used with a caprolactone structure. Examples of commercially available products of polymerizable compounds having a caprolactone structure include KAYARAD DPCA-20, DPCA-30, DPCA-60, DPCA-120 (above, manufactured by Nippon Kayaku Co., Ltd.) and the like. Furthermore, a polymerizable compound having a stretch alkoxy group can also be used as a polymerizable compound. It is preferable that the polymerizable compound having a ethyleneoxy group is a polymerizable compound having an ethyleneoxy group and / or a ethylene propyloxy group is preferable, and the 3-6-functional (meth)acrylate compound having 4 to 20 ethyleneoxy groups is preferable. Examples of the polymerizable compound having a stretch alkoxy group include compounds with the following structures. Examples of commercially available products of polymerizable compounds having a stretch alkoxy group include SR-494, a 4-functional (meth)acrylate having 4 ethyleneoxy groups produced by SARTOMER Company, Inc., and a 3-functional (meth)acrylate having 3 isobutyleneoxy groups produced by Nippon Kayaku Co., Ltd., and the like. [Chemical Formula 29] Furthermore, polymerizable compounds having a backbone can be used as polymerizable compounds. Examples of commercially available products that have a polymerizable compound having a skeleton include OGSOL EA-0200, EA-0300 (a (meth)acrylate monomer having a skeleton) and the like. As the polymerizable compound, it is also preferable to use a compound that does not contain an environmentally controlled substance such as toluene. Examples of commercially available products of such compounds include KAYARAD DPHA LT, KAYARAD DPEA-12 LT (manufactured by Nippon Kayaku Co., Ltd.). It is preferable that the content of the polymerizable compound in the total solid component of the coloring composition is 0.1 to 50 mass %. It is preferable that the lower limit is 0.5 mass % or more, it is more preferable that 1 mass % or more, and it is even more preferable that 5 mass % or more. It is preferable that the upper limit of the total content is 45% by mass or less, it is more preferable that the upper limit of 40% by mass or less, and it is even better that the upper limit of 30% by mass or less is even better. Only one type of polymerizable compounds may be used, or two or more types may be used. When two or more types are used, the total amount of these is preferably within the above range. <Photopolymerization Initiator> It is also preferable that the coloring composition of the present invention contains a photopolymerization initiator. As the photopolymerization initiator, there are no particular limitations, and it can be appropriately selected from the well-known photopolymerization initiator. For example, it is preferred that compounds have photosensitive properties for light from the ultraviolet region to the visible region. It is preferred that the photopolymerization initiator is a photoradical polymerization initiator. Examples of the photopolymerization initiator include halogenated hydrocarbon derivatives (for example, compounds having a tri-branch, compounds having a diazole backbone, etc.), acylphosphine compounds, hexaaryl bisimidazole compounds, oxime compounds, organic peroxides, sulfur compounds, ketone compounds, aromatic onium salts, α-hydroxyketone compounds, α-amine ketone compounds, and the like. From the viewpoint of exposure sensitivity, the photopolymerization initiator is a trihalomethyl tris(R) compound, benzyldimethylketal compound, α-hydroxyketal compound, α-amine ketone compound, acylphosphine compound, phosphine oxide compound, metallocene compound, oxime compound, hexaarylbisimidazole compound, onium compound, benzothiazole compound, benzophenone compound, acetophenone compound, cyclopentadiene-benzene-ferrome compound, halomethyldiazole compound and 3-aryl substituted coumarin compound, compound selected from oxime compound, α-hydroxyketone compound, α-amine ketone compound and acylphosphine compound, and the oxime compound is further preferred. Also, as the photopolymerization initiator, there are compounds described in paragraphs 0065 to 0111 of Japanese Patent Publication No. 2014-130173, compounds described in Japanese Patent Publication No. 6301489, MATERIAL STAGE 37 to 60p, vol.19, No. 3, 2019, light polymerization initiator described in International Publication No. 2018 / 221177, light polymerization initiator described in International Publication No. 2018 / 110179, light polymerization initiator described in Japanese Publication No. 2019-043864, light polymerization initiator described in Japanese Publication No. 2019-044030, and Japanese Publication No. 2019- The peroxide-based initiator described in JPY No. 167313, the amine-acetophenone-based initiator having a 㗁zolidyl group described in JPY No. 2020-055992, the oxime-based photopolymerization initiator described in JPY No. 2013-190459, the polymer described in JPY No. 2020-172619, and the compounds represented by Formula 1 described in JPY No. 2020 / 152120, etc., are included in this specification. Specific examples of the hexaaryl bisimidazole compound include 2,2’,4-tris(2-chlorophenyl)-5-(3,4-dimethoxyphenyl)-4,5-diphenyl-1,1’-biimidazole and the like. Examples of commercially available products of α-hydroxyketone compounds include Omnirad 184, Omnirad 1173, Omnirad 2959, Omnirad 127 (above been manufactured by IGM Resins B.V.), Irgacure 184, Irgacure 1173, Irgacure 2959, Irgacure 127 (above was manufactured by BASF) and the like. Examples of commercially available products of α-amine ketone compounds include Omnirad 907, Omnirad 369, Omnirad 369E, Omnirad 379EG (above been manufactured by IGM Resins B.V.), Irgacure 907, Irgacure 369, Irgacure 369E, Irgacure 379EG (above was manufactured by BASF) and the like. Examples of commercially available products of acylphosphine compounds include Omnirad 819, Omnirad TPO (above been manufactured by IGM Resins B.V.), Irgacure 819, Irgacure TPO (above was manufactured by BASF) and the like. Examples of the oxime compounds include compounds described in JPY 2001-233842, compounds described in JPY 2000-080068, compounds described in JPY 2006-342166, compounds described in J.C.S. Perkin II (1979, pp. 1653-1660), compounds described in J.C.S. Perkin II (1979, pp. 156-162), Journal of Photopolymer Science and The compounds described in Technology (1995, pages 202-232), the compounds described in Japanese Patent Publication No. 2000-066385, the compounds described in Japanese Patent Publication No. 2004-534797, the compounds described in Japanese Patent Publication No. 2006-342166, the compounds described in Japanese Patent Publication No. 2017-019766, the compounds described in Japanese Patent Publication No. 6065596, and the International Publication No. 2015 The compounds described in / 152153, the compounds described in International Publication No. 2017 / 051680, the compounds described in Japanese Patent Publication No. 2017-198865, the compounds described in paragraphs 0025 to 0038 of International Publication No. 2017 / 164127, the compounds described in International Publication No. 2013 / 167515, the compounds described in Japanese Patent No. 5430746, the compounds described in Japanese Patent No. 5647738, and the compounds described in Japanese Patent No. 5647738, etc. Specific examples of the oxime compound include 3-benzoyloxyimidobutane-2-one, 3-acetyloxyimidobutane-2-one, 3-propyloxyimidobutane-2-one, 2-acetyloxyimidopentan-3-one, 2-acetyloxyimido-1-phenylpropan-1-one, 2-benzoyloxyimido-1-phenylpropan-1-one, 3-(4-toluenesulfonyloxy)imidobutane-2-one, 2-ethoxycarbonyloxyimido-1-phenylpropan-1-one, 1-[4-(phenylthio)phenyl]-3-cyclohexanyl-propan-1,2-dione-2-(O-acetyl oxime). Examples of commercially available products include Irgacure OXE01, Irgacure OXE02, Irgacure OXE03, Irgacure OXE04 (the above is manufactured by BASF Company), TR-PBG-304, TR-PBG-327 (manufactured by Tronly), and Adeka Optomer N-1919 (manufactured by ADEKA CORPORATION, and light polymerization initiator 2 described in Japanese Patent Laid-Open No. 2012-014052). Furthermore, as the oxime compound, it is also preferable to use a compound that has no color properties or a compound that has high transparency and is not prone to discoloration. Examples of commercially available products include ADEKA ARKLS NCI-730, NCI-831, NCI-930 (the above is manufactured by ADEKA CORPORATION). As the photopolymerization initiator, an oxime compound having a cylindrical ring can also be used. Specific examples of the oxime compound having a radius include compounds described in Japanese Patent Laid-Open No. 2014-137466, compounds described in Japanese Patent No. 6636081, and compounds described in Korean Publication No. 10-2016-0109444. As the photopolymerization initiator, an oxime compound that has at least one benzene ring having a carbazole ring can be used to form the skeleton of the naphthalene ring. Specific examples of such oxime compounds include compounds described in International Publication No. 2013 / 083505. As the photopolymerization initiator, an oxime compound having a fluorine atom can also be used. Specific examples of the oxime compound having a fluorine atom include compounds described in Japanese Patent Application Publication No. 2010-262028, compounds 24, 36-40 described in Japanese Patent Application Publication No. 2014-500852, and compounds (C-3) described in Japanese Patent Application Publication No. 2013-164471, etc. As the photopolymerization initiator, an oxime compound having a nitro group can be used. It is also preferable that the oxime compound having a nitro group be a dimer. Specific examples of oxime compounds having nitro include paragraphs 0031 to 0047 of Japanese Patent Publication No. 2013-114249, compounds described in paragraphs 0008 to 0012, and compounds described in paragraphs 007 to 0079 of Japanese Patent No. 4223071, compounds described in paragraphs 0007 to 0025 of Japanese Patent No. 4223071, and ADEKA ARKLS NCI-831 (manufactured by ADEKA CORPORATION). As the photopolymerization initiator, an oxime compound having a benzofuran skeleton can also be used. As a specific example, OE-01 to OE-75 described in International Publication No. 2015 / 036910 can be mentioned. As the photopolymerization initiator, an oxime compound formed by bonding a substituent with a hydroxyl group to a carbazole backbone can also be used. Examples of such photopolymerization initiators include compounds described in International Publication No. 2019 / 088055 and the like. Specific examples of oxime compounds which can be used in the present invention are shown below, but the present invention is not limited to these. [Chemical Formula 30] [Chemical Formula 31] [Chemical Formula 32] It is preferable that the oxime compound has a very large absorption wavelength in the range of wavelength 350 to 500 nm, and it is preferable that the oxime compound has a very large absorption wavelength in the range of wavelength 360 to 480 nm. Furthermore, from the viewpoint of sensitivity, the high moor absorbance coefficient of the oxime compound at a wavelength of 365 nm or a wavelength of 405 nm is preferred, 1000 to 300,000 is more preferred, 2000 to 300,000 is more preferred, and 5000 to 200,000 is more preferred. The moor absorbance coefficient of the compound can be measured using a well-known method. For example, it is preferable to use a spectrophotometer (a spectrophotometer manufactured by Varian) to measure at a concentration of 0.01 g / L using an ethyl acetate solvent. As the photopolymerization initiator, it is also preferable to use Irgacure OXE01 (manufactured by BASF) and / or Irgacure OXE02 (manufactured by BASF) and Omnirad 2959 (manufactured by IGM Resins B.V.) in combination. As the photopolymerization initiator, a photoradical polymerization initiator with a 2-functional or 3-functional or above can be used. By using such a photoradical polymerization initiator, more than two radicals are generated from one molecule of the photoradical polymerization initiator, so good sensitivity can be obtained. Furthermore, when a compound with an asymmetric structure is used, the crystallinity decreases, and the solubility in a solvent or the like is improved, and it becomes difficult to precipitate over time, thereby improving the time stability of the colored composition. Specific examples of photoradical polymerization initiators with 2-functional or 3-functional or above include Japanese Special Table No. 2010-527339, Japanese Special Table No. 2011-524436, International Publication No. 2015 / 004565, Japanese Special Table No. 0407-0412, Japanese Special Table No. 2016-532675, dimers of oxime compounds described in paragraphs 0039-0055 of International Publication No. 2017 / 033680, and compounds described in Japanese Special Table No. 2013-522445 of Japanese Special Table No. 2013-522445 of Japanese Special Table No. 2013-522445 (E) and compound (G), Cmpd1-7 described in International Publication No. 2016 / 034963, oxime ester light initiator described in paragraph 0007 of Japanese Patent Publication No. 2017-523465, light initiator described in paragraph 0020-0033 of Japanese Patent Publication No. 2017-167399, light polymerization initiator described in paragraph 0017-0026 of Japanese Patent Publication No. 2017-151342, oxime ester light initiator described in paragraph 6469669, etc. It is preferable that the content of the photopolymerization initiator in the total solid component of the coloring composition is 0.1 to 30 mass %. For example, the lower limit is preferably 0.5 mass % or more, and more preferably 1 mass % or more. It is preferable that the upper limit is 20% by mass or less, and it is preferable that the upper limit is 15% by mass or less. Only one type of photopolymerization initiator can be used, or two or more types can be used. When two or more types are used, the total amount of these is preferably within the above range. <<Solvent>> It is preferred that the coloring composition of the present invention contains a solvent. Examples of the solvent include organic solvents. There is basically no particular limitation on the type of solvent as long as the solubility of each component or the coating property of the composition. Examples of the organic solvent include an ester-based solvent, a ketone-based solvent, an alcohol-based solvent, an amide-based solvent, an ether-based solvent, and a hydrocarbon-based solvent. For details of these, please refer to paragraph 0223 of International Publication No. 2015 / 166779, which is incorporated into this specification. Furthermore, it is also possible to preferably use an ester-based solvent with a cyclic alkyl group substituted with a ketone-based solvent with a cyclic alkyl group substituted with a ketone-based solvent. Specific examples of organic solvents include polyethylene glycol monomethyl ether, dichloromethane, methyl 3-ethoxypropionate, ethyl 3-ethoxypropionate, ethyl saluthacetate, ethyl lactate, diethylene glycol dimethyl ether, butyl acetate, methyl 3-methoxypropionate, 2-heptanone, 3-pentanone, 4-heptanone, cyclohexanone, 2-methyl cyclohexanone, 3-methyl cyclohexanone, 4-methyl cyclohexanone, 4-methyl cyclohexanone, cyclohexanone, cyclohexanone, cyclohexanone, cyclohexanone, cyclohexanone, cyclohexanone, cyclohexanone, cyclopentanone, ethyl carbitol acetate, butyl carbitol acetate, propylene glycol monomethyl ether, propylene glycol monomethyl ether, propylene glycol monomethyl ether, propylene glycol monomethyl ether, propylene glycol monomethyl ether, propylene glycol monomethyl ether, propylene glycol monomethyl ether Ether acetate, 3-methoxy-N,N-dimethylpropionylamine, 3-butoxy-N,N-dimethylpropionylamine, propylene glycol diacetate, 3-methoxybutanol, methyl ethyl ketone, γ-butyrolactone, cyclobutanol, anisole, 1,4-diacetyloxybutane, diethylene glycol monoethyl ether acetate, 1,3-butylene glycol diacetate, dipropylene glycol methyl ether acetate, diacetol (as alias, diacetol, 4-hydroxy-4-methyl-2-pentanone), propyl 2-methoxy-1-propanol, isopropanol, etc. However, it is preferred to reduce aromatic hydrocarbons (benzene, toluene, xylene, ethylbenzene, etc.) as organic solvents for environmental reasons (for example, the total amount of organic solvent can be set to 50 mass ppm (parts per million ratio), 10 mass ppm or less, or 1 mass ppm or less) relative to the total amount of organic solvent). In the present invention, it is preferable to use an organic solvent with a small metal content, and it is preferable to use a metal content of the organic solvent at 10 mass ppb (parts per billion: parts per billion) or less. Organic solvents at the mass ppt (parts per trillion: mega fraction) grade can be used as required, such organic solvents provided by Toyo Gosei Co., Ltd. (Chemical Industry Daily, November 13, 2015). Examples of methods for removing impurities such as metals from organic solvents include distillation (molecular distillation, thin film distillation, etc.) or filtration using a filter. As the filter pore diameter of the filter used for filtering, it is preferred to be 10 μm or less, it is more preferred to be 5 μm or less, and it is even more preferred to be 3 μm or less. It is better to have the material of the filter as polytetrafluoroethylene, polyethylene or nylon. Organic solvents may contain isomers (compounds with the same number of atoms but different structures). Furthermore, only one isomer may be contained, or a plurality of isomer may be contained. It is preferable that the content of peroxide in the organic solvent is 0.8 mmol / L or less, and it is preferable that the content of peroxide is essentially free of peroxide. The solvent content in the coloring composition is preferably 10 to 95 mass %, 20 to 90 mass % is more preferably 30 to 90 mass % and 30 to 90 mass % is even more preferably . Furthermore, from the viewpoint of environmental control, it is preferable that the colored composition of the present invention does not contain environmental control substances in essence. In addition, in the present invention, the content of the environmentally controlled substance in the colored composition is preferably 50 mass ppm or less, 30 mass ppm or less, 10 mass ppm or less, and 1 mass ppm or less is particularly preferred. Examples of environmentally controlled substances include benzene; alkyl benzene such as toluene and xylene; halogenated benzene such as chlorobenzene. These are registered as environmentally controlled substances under the REACH (Registration Evaluation Authorization and Restriction of Chemicals), PRTR (Pollutant Release and Transfer Register), VOC (Volatile Organic Compounds), etc., and the amount of use or operation method is strictly limited. Sometimes these compounds are used as solvents when each component or the like used in the production of the coloring composition, and are mixed into the coloring composition as a residual solvent. From the perspective of safety and environmental friendliness for the human body, it is better to minimize these substances. As a method of reducing environmentally controlled substances, a method of heating or reducing pressure within the system to reach above the boiling point of the environmentally controlled substance, thereby reducing the environmentally controlled substance by distilling and removing the environmentally controlled substance from the system. Furthermore, when a small amount of environmentally controlled substance is removed by distillation, in order to improve efficiency, azeotropy is also useful as a solvent having the same boiling point as the solvent. Furthermore, when a compound having radical polymerization is contained, in order to prevent the radical polymerization reaction from undergoing in the process of decompression distillation and removing crosslinking, a polymerization inhibitor or the like may be added to perform decompression distillation and removal. Such distillation removal methods can be performed in any one of the stages of the raw material, the stages of the product obtained by reacting the raw material (for example, a polymerized resin solution or a multifunctional monomer solution), or the stages of mixing the colored compositions produced by mixing the compounds. <<Compound with a cyclic ether group>> The coloring composition of the present invention can contain a compound with a cyclic ether group. According to this aspect, the moisture resistance of the obtained film can be further improved. Examples of the cyclic ether group include epoxy group, oxetanyl group, etc. It is preferred that the compound having a cyclic ether group is a compound having an epoxy group (hereinafter also referred to as an epoxy compound). The compound having a cyclic ether group may be a low molecular weight (for example, the molecular weight is less than 1000), or a macromolecular compound (for example, if the molecular weight is 1000 or more, and the weight average molecular weight is 1000 or more). It is preferable that the weight average molecular weight of the cyclic ether group is 200 to 100,000, and it is preferable that 500 to 50,000 is preferable. It is preferable that the upper limit of the weight average molecular weight is 10,000 or less, it is more preferable that the upper limit of 5,000 or less, and it is even more preferable that the upper limit of 3,000 or less. As the compound having a cyclic ether group, it is also possible to use a compound described in paragraphs 0034-0036 of Japanese Patent Application Publication No. 2013-011869, a compound described in paragraphs 0147-0156 of Japanese Patent Application Publication No. 2014-043556, a compound described in paragraphs 0085-0092 of Japanese Patent Application Publication No. 2014-089408, and a compound described in JPY 2017-179172. Examples of commercially available products of compounds having cyclic ether groups include DENACOL EX-212L, EX-212, EX-214L, EX-214, EX-216L, EX-216, EX-321L, EX-321, EX-850L, EX-850 (above, manufactured by Nagase ChemteX Corporation), ADEKA RESIN EP-4000S, EP-4003S, EP-4010S, EP-4011S (above, ADEKA Manufactured by CORPORATION), NC-2000, NC-3000, NC-7300, XD-1000, EPPN-501, EPPN-502 (above, manufactured by ADEKA CORPORATION), CELLOXIDE 2021P, CELLOXIDE 2081, CELLOXIDE 2083, CELLOXIDE 2085, EHPE3150, EPOLEAD PB 3600, PB 4700 (above, manufactured by Daicel Corporation), CYCLOMER P ACA 200M, ACA 230AA, ACA Z250, ACA Z251, ACA Z300, ACA Z320 (above, manufactured by Daicel Corporation), jER1031S, jER157S65, jER152, jER154, jER157S70 (above, manufactured by Mitsubishi Chemical Corporation.), Aron Oxetane OXT-121, OXT-221, OX-SQ, PNOX (above, manufactured by TOAGOSEI CO., LTD.), Adekaglycylol ED-505 (manufactured by ADEKA CORPORATION, containing epoxy monomer), Marproof G-0150M, G-0105SA, G-0130SP, G-0250SP, G-1005S, G-1005SA, G-1010S, G-2050M, G-01100, G-01758 (manufactured by NOF CORPORATION., containing epoxy polymer), OXT-101, OXT-121, OXT-212, OXT-221 (above, manufactured by TOAGOSEI CO., LTD., containing oxetane monomer), OXE-10, OXE-30 (above, OSAKA ORGANIC CHEMICAL INDUSTRY Manufactured by LTD, oxetanyl monomer), BATG (manufactured by SHOWA DENKO K.K.), etc. It is preferable that the content of the compound having a cyclic ether group in the total solid component of the coloring composition is 0.1 to 20 mass %. It is preferable that the lower limit is 0.5% by mass or more, and it is preferable that 1% by mass or more. It is preferable that the upper limit is 15% by mass or less, and it is preferable that the upper limit is 10% by mass or less. Only one type of compound having a cyclic ether group may be used, or two or more types may be used. When two or more types are used, the total amount of these is preferably within the above range. <<Hardening Accelerator>> The coloring composition of the present invention may contain a hardening accelerator. Examples of the hardening accelerator include thiol compounds, hydroxymethyl compounds, amine compounds, phosphonium salt compounds, amidine salt compounds, amide compounds, base generators, isocyanate compounds, alkoxysilane compounds, onium salt compounds, and the like. Specific examples of hardening accelerators include compounds described in paragraphs 0094-0097 of International Publication No. 2018 / 056189, compounds described in paragraphs 0246-0253 of Japanese Patent Publication No. 2015-034963, compounds described in paragraphs 0186-0251 of Japanese Patent Publication No. 2013-041165, and compounds described in JPY 2014-055114 of Japanese Patent Publication No. 2014-055114 of Japanese Patent Publication No. 2014-055114 Sub-compounds, compounds described in paragraphs 0071 to 0080 of Japanese Patent Publication No. 2012-150180, alkoxysilane compound having epoxy groups described in JP-2011-253054, compounds described in JP-20085 to 0092 of JP-5765059, epoxy hardener containing carboxyl groups described in JP-2017-036379, etc. When the hardening accelerator is contained, it is preferable that the hardening accelerator content in the total solid component of the coloring composition is 0.3 to 8.9 mass %, and it is more preferable that the hardening accelerator content is 0.8 to 6.4 mass %. <<Ultraviolet absorber>> The coloring composition of the present invention can contain an ultraviolet absorber. Examples of the ultraviolet absorber include conjugated diene compounds, amine diene compounds, salicylate compounds, benzophenone compounds, benzotriazole compounds, acrylonitrile compounds, hydroxyphenyl trismuth compounds, indole compounds, trismuth compounds, dibenzoyl compounds, and the like. Specific examples of such compounds include paragraphs 0038-0052 of Japanese Patent Publication No. 2009-217221, paragraphs 0052-0072 of Japanese Patent Publication No. 2012-208374, paragraphs 0317-0334 of Japanese Patent Publication No. 2013-068814, paragraphs 0061-0080 of Japanese Patent Publication No. 2016-162946, paragraphs 0052 of International Publication No. 2021 / 131355, paragraphs 0074, and paragraphs 0022-0024 of International Publication No. 2021 / 132247, and paragraphs 0022-0024 of International Publication No. 2021 / 132247. These contents are included in this specification. Examples of commercially available products of ultraviolet absorbers include UV-503 (manufactured by DAITO CHEMICAL CO., LTD.), Tinuvin series manufactured by BASF, Uvinul series, Sumika Chemtex Company, and Sumisorb series manufactured by Sumika Chemtex Company, and Limited. Also, as the benzotriazole compound, the MYUA series produced by MIYOSHI OIL & FAT CO., LTD. (Chemical Industry Daily, February 1, 2016). Furthermore, the ultraviolet absorber can also be used as a compound described in paragraphs 0049-0059 of Japanese Patent No. 6268967, a compound described in paragraphs 0059-0076 of International Publication No. 2016 / 181987, and a sulfhydryl substituted benzotriazole type ultraviolet absorber described in International Publication No. 2020 / 137819. It is preferable that the content of the ultraviolet absorber in the total solid component of the coloring composition is 0.01 to 10 mass %, and it is preferable that 0.01 to 5 mass %. Only one type of ultraviolet absorber can be used, or two or more types can be used. When two or more types are used, the total amount of these is preferably within the above range. <<Polymerization Inhibitor>> The coloring composition of the present invention can contain a polymerization inhibitor. Examples of the polymerization inhibitor include hydroquinone, p-methoxyphenol, di-tri-butyl-p-cresol, pentylphenol, tertiary butylcatechol, benzenequinone, 4,4’-thiobis(3-methyl-6-tri-butylphenol), 2,2’-methylene bis(4-methyl-6-tri-butylphenol), and N-nitrosophenylhydroxylamine salt (ammonium salt, first cerium salt, etc.). Among them, p-methoxyphenol is preferred. When the polymerization inhibitor is contained, it is preferable that the polymerization inhibitor content in the total solid component of the coloring composition is 0.0001 to 5 mass %. The polymerization inhibitor may be only one type, or two or more types may be. When two or more types are contained, the total amount is preferably within the above range. <<Silane Coupling Agent>> The coloring composition of the present invention can contain a silane coupling agent. In this specification, a silane coupling agent refers to a silane compound having a hydrolyzable group and a functional group other than it. Furthermore, a hydrolyzable group refers to a substituent that is directly bonded to a silicon atom and can generate a siloxane bond through at least one of the hydrolysis and condensation reactions. Examples of the hydrolyzable group include halogen atom, alkoxy group, acyloxy group, and the like, and the alkoxy group is preferred. That is, it is preferred that the silane coupling agent is a compound having an alkoxy silicon group. Furthermore, as functional groups other than hydrolyzable groups, for example, vinyl, (meth)allyl, (meth)acryl, thiol, epoxy, oxetanyl, amine, urea, sulfhydryl, thioether, isocyanate, phenyl, etc., the amine, (meth)acryl and epoxy group are preferred. Specific examples of silane coupling agents include N-β-amine ethyl-γ-amine propylmethyldimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., product name KBM-602), N-β-amine ethyl-γ-amine propyl trimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., product name KBM-603), N-β-amine ethyl-γ-amine propyl trimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., product name KBE-602), and γ-amine propyl trimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., product name KBE-602), and Shin-Etsu Chemical Co., Ltd., product name KBE-Etsu Chemical Co., Ltd., product name KBE-602, and Shin-Etsu Chemical Co., Ltd., product name KBM-903), γ-amine-propyltriethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., product name KBE-903), 3-methacryloxypropylmethyldimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., product name KBM-502), 3-methacryloxypropyltriethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., product name KBM-503), etc. Furthermore, specific examples of silane coupling agents include compounds described in paragraphs 0018-0036 of Japanese Patent Publication No. 2009-288703 and compounds described in paragraphs 0056-0066 of Japanese Patent Publication No. 2009-242604, and these contents are included in this specification. The content of the silane coupling agent in the total solid component of the coloring composition is preferably 0.01 to 15.0 mass %, and more preferably 0.05 to 10.0 mass %. The silane coupling agent may be only one type, or two or more types may be. When two or more types are contained, the total amount is preferably within the above range. <<Surface Active Agent>> The coloring composition of the present invention can contain an surfactant. As the surfactant, various surfactants such as fluorine-based surfactants, nonionic surfactants, cationic surfactants, anionic surfactants, polysilicon oxygen-based surfactants can be used. It is preferred that the surfactant is a polysilicon oxygen-based surfactant or a fluorine-based surfactant. As for the surfactant, the surfactant described in paragraphs 0238 to 0245 of International Publication No. 2015 / 166779 and the surfactant described in JP-Open No. 2020-008634 are mentioned, and the contents are included in this specification. The fluorine content in the fluorine-based surfactant is preferably 3 to 40 mass %, 5 to 30 mass % is more preferably 7 to 25 mass % is particularly preferably . From the viewpoint of uniformity of thickness or liquid saving of coating film, fluorine-based surfactant whose fluorine content is within this range is effective, and the solubility in the colored composition is also good. Examples of fluorine-based surfactants include surfactants described in paragraphs 0060 to 0064 of Japanese Patent Publication No. 2014-041318 (corresponding to paragraphs 0060 to 0064 of International Publication No. 2014 / 017669), and surfactants described in paragraphs 0117 to 0132 of Japanese Patent Publication No. 2011-132503, and are included in this specification. As commercially available products of fluorine-based surfactants, for example, MEGAFACE F-171, F-172, F-173, F-176, F-177, F-141, F-142, F-143, F-144, F-437, F-475, F-477, F-479, F-482, F-554, F-555-A, F-556, F-557, F-558, F-559, F-56 0. F-561, F-565, F-563, F-568, F-575, F-780, EXP, MFS-330, R-01, R-40, R-40-LM, R-41, R-41-LM, RS-43, TF-1956, RS-90, R-94, RS-72-K, DS-21 (above DIC Corporation), FLUORAD FC430, FC431, FC171 (above Sumitomo 3M Limited), SURFLON S-382, SC-101, SC-103, SC-104, SC-105, SC-1068, SC-381, SC-383, S-393, KH-40 (above is made by AGC INC.), PolyFox PF636, PF656, PF6320, PF6520, PF7002 (above is made by OMNOVA SOLUTIONS INC.), Futurgent 208G, 215M, 245F, 601AD, 601ADH2, 602A, 610FM, 710FL, 710FM, 710FS, FTX-218 (above is made by NEOS COMPANY LIMITED manufacturing) etc. Furthermore, an acrylic compound can also be used as a fluorine-based surfactant, which has a molecular structure containing a functional group containing a fluorine atom, and upon heating, the portion containing a functional group containing a fluorine atom is cut off and the fluorine atom volatilizes. Examples of such fluorine-based surfactants include the MEGAFACE DS series manufactured by DIC Corporation (Chemical Industry Daily (February 22, 2016) and Nikkei Industry News (February 23, 2016)), and MEGAFACE DS-21 can be mentioned, for example. Furthermore, it is also preferable to use a polymer with a fluorine-containing atomic vinyl ether compound having a fluorinated alkyl group or a fluorinated alkyl ether group and a hydrophilic vinyl ether compound. Examples of such fluorine-based surfactants include fluorine-based surfactants described in Japanese Patent Laid-Open No. 2016-216602, and this content is included in this specification. Fluorine-based surfactants can also use block polymers. The fluorine-based surfactant can also preferably use a fluorine-containing polymer compound, which contains: a repeating unit derived from a (meth)acrylate compound having a fluorine atom; and a repeating unit derived from a (meth)acrylate compound having two or more (preferably five or more) alkoxy groups (preferably ethyleneoxy groups and propoxy groups). Furthermore, the fluorine-containing surfactant and the following compounds described in paragraphs 0016 to 0037 of Japanese Patent Laid-Open No. 2010-032698 are also exemplified as fluorine-based surfactant used in the present invention. [Chemical Formula 33] The weight average molecular weight of the above-mentioned compound is preferably 3000 to 50000, for example 14000. Among the above compounds, % of the proportion of repeating units is mol%. Furthermore, fluorine-based surfactants can also be used as fluorine-containing polymers having groups containing ethylene unsaturated bonds in the side chain. Specific examples include compounds described in paragraphs 0050-0090 and paragraphs 0289-0295 of Japanese Patent Laid-Open No. 2010-164965, MEGAFACE RS-101, RS-102, RS-718K, RS-72-K, etc. manufactured by DIC Corporation. Furthermore, the fluorine-based surfactant can also be used as a compound described in paragraphs 0015-0158 of Japanese Patent Laid-Open No. 2015-117327. Furthermore, from the viewpoint of environmental regulation, it is also preferable to use the surfactant described in International Publication No. 2020 / 084854 as a substitute for the surfactant having a perfluoroalkyl group having a carbon number of 6 or more. Furthermore, it is also preferable to use the fluorimide salt compound represented by the formula (fi-1) as the surfactant. [Chemical Formula 34] In formula (fi-1), m represents 1 or 2, n represents integers from 1 to 4, a represents 1 or 2, X a+ Represents a valent metal ion, primary ammonium ion, secondary ammonium ion, tertiary ammonium ion, quadrilateral ammonium ion or NH 4 + . Examples of nonionic surfactants include glycerol, trimethylolpropane, trimethylolethane and the ethoxylates and propoxylates (for example, glycerol propoxylate, glycerol ethoxylate, etc.), polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene oil-based ether, polyoxyethylene octyl phenyl ether, polyoxyethylene nonyl phenyl ether, polyethylene glycol dilaurate, polyethylene glycol distearate, sorbitol fatty acid esters, Pluronic L10, L31, L61, L62, 10R5, 17R2, 25R2 (manufactured by BASF Company), Tetronic 304, 701, 704, 901, 904, 150R1 (manufactured by BASF Company), SOLSPERSE 20000 (manufactured by Japan Lubrizol Corporation), NCW-101, NCW-1001, NCW-1002 (manufactured by FUJIFILM Wako Pure Chemical Corporation), PIONIN D-6112, D-6112-W, D-6315 (manufactured by Takemoto Oil & Fat Co., Ltd.), OLFIN E1010, Surfynol 104, 400, 440 (manufactured by Nissin Chemical Industry Co., Ltd.), etc. Examples of polysilicon oxygen-based surfactants include DC3PA, SH7PA, DC11PA, SH21PA, SH28PA, SH29PA, SH30PA, SH8400, SH 8400 FLUID, FZ-2122, 67 Additive, 74 Additive, M Additive, SF 8419 OIL (above been manufactured by Dow Corning Toray Co., Ltd.), TSF-4300, TSF-4445, TSF-4460, and TSF-4452 (above are Momentive Performance Materials). Manufactured by Inc.), KP-341, KF-6000, KF-6001, KF-6002, KF-6003 (above is manufactured by Shin-Etsu Chemical Co., Ltd.), BYK-307, BYK-322, BYK-323, BYK-330, BYK-333, BYK-3760, BYK-UV3510 (above is manufactured by BYK-Chemie GmbH), etc. Furthermore, the polysilicon oxygen-based surfactant can also be used as a compound of the following structure. [Chemical Formula 35] It is preferable that the content of the surfactant in the total solid component of the coloring composition is 0.001% to 5.0% by mass, and it is more preferable that 0.005% to 3.0% by mass. The surfactant may be only one type, or two or more types may be. When two or more types are contained, the total amount is preferably within the above range. <<Antioxidant>> The coloring composition of the present invention can contain an antioxidant. Examples of the antioxidant include phenol compounds, phosphite compounds, sulfide compounds, and the like. As the phenol compound, any phenol compound known as a phenol-based antioxidant can be used. Examples of the preferred phenol compound include hindered phenol compounds. It is preferred that compounds have substituents at sites adjacent to phenolic hydroxyl groups. As the aforementioned substituent, a substituted or unsubstituted alkyl group having 1 to 22 carbon atoms is preferred. Furthermore, it is also preferred that an antioxidant is a compound having a phenol group and a phosphite group in the same molecule. Furthermore, phosphorus-based antioxidants can also be used as an antioxidant. It is preferable that the content of the antioxidant in the total solid component of the coloring composition is 0.01 to 20 mass %, and it is preferable that 0.3 to 15 mass %. When an antioxidant is contained, only one type of antioxidant can be used, or two or more types of antioxidant can be used. When two or more types are used, the total amount is preferably within the above range. <<Other Components>> The coloring composition of the present invention may contain sensitizers, hardening accelerators, fillers, heat hardening accelerators, plasticizers and other additives as needed (for example, conductive particles, fillers, defoamers, flame retardants, leveling agents, peeling accelerators, perfumes, surface tension regulators, chain transfer agents, etc.). By appropriately containing these components, properties such as physical properties of the film can be adjusted. Regarding these components, for example, the description of paragraph 0183 of Japanese Patent Application Publication No. 2012-003225 (corresponding to paragraph 0237 of US Patent Application Publication No. 2013 / 0034812), and the description of paragraphs 0101-0104, paragraphs 0107-0109 of Japanese Patent Application Publication No. 2008-250074, are included in this specification. Furthermore, the coloring composition of the present invention may contain potential antioxidants as needed. As the potential antioxidant, the following compounds are mentioned: the site where the antioxidant works is protected by a protective group and the protective group is detached and acts as an antioxidant by heating at 100 to 250°C or heating at 80 to 200°C in the presence of an acid / base catalyst. Examples of potential antioxidants include compounds described in International Publication No. 2014 / 021023, International Publication No. 2017 / 030005, and Japanese Patent Laid-Open No. 2017-008219. Examples of commercially available products of potential antioxidants include ADEKA ARKLS GPA-5001 (manufactured by ADEKA CORPORATION). Furthermore, the coloring composition of the present invention may contain a phosphonium containing an aromatic group as described in Japanese Patent Laid-Open No. 2020-079833. In order to adjust the refractive index of the obtained film, the coloring composition of the present invention may contain metal oxides. Examples of the metal oxide include TiO 2 , ZrO 2 , Al 2 O 3 , SiO 2 wait. It is preferable that the primary particle size of the metal oxide is 1 to 100 nm, it is more preferable that 3 to 70 nm, and it is even more preferable that 5 to 50 nm. The metal oxide may have a core-shell structure. Also, at this time, the core part may be hollow. The coloring composition of the present invention may contain a light resistance improver. Examples of light resistance improvement agents include compounds described in paragraphs 0036-0037 of Japanese Patent Publication No. 2017-198787, compounds described in paragraphs 0029-0034 of Japanese Patent Publication No. 2017-146350, compounds described in paragraphs 0036-0037 of Japanese Patent Publication No. 2017-129774, compounds described in paragraphs 0049-0052 of Japanese Patent Publication No. 20 Compounds described in paragraphs 0031 to 0034 of JP-17-129674, compounds described in paragraphs 0058 to 0059 of JP-17-122803, compounds described in paragraphs 0036 to 0037 of JP-122803, compounds described in paragraphs 0051 to 0054 of JP-2017 / 164127, compounds described in paragraphs 0025 to 0039 of JP-2017 / 164127, and compounds described in paragraphs 2017-186546 The compounds described in paragraphs 0034 to 0047 of Japanese Patent Publication No. 2015-025116, the compounds described in paragraphs 0019 to 0041 of Japanese Patent Publication No. 2012-145604, the compounds described in paragraphs 0018 to 0021 of Japanese Patent Publication No. 2012-103475, the compounds described in paragraphs 0018 to 0021 of Japanese Patent Publication No. 2011 The compounds described in paragraphs 0015 to 0018 of JP-257591, the compounds described in paragraphs 0017 to 0021 of JP-2011-191483, the compounds described in paragraphs 0108 to 0116 of JP-2011-145668, the compounds described in paragraphs 0103 to 0153 of JP-2011-253174, and the compounds described in paragraphs 0103 to 0153 of JP-2011-253174, etc. From the viewpoint of environmental regulation, sometimes the use of perfluoroalkyl sulfonic acid and its salts, as well as perfluoroalkyl carboxylic acid and its salts are restricted. In the colored composition of the present invention, when the content of the above-mentioned compound is reduced, the content of perfluoroalkylsulfonic acid (especially perfluoroalkylsulfonic acid with a carbon number of 6 to 8 perfluoroalkyl) and its salts, and perfluoroalkylcarboxylic acid (especially perfluoroalkylcarboxylic acid with a carbon number of 6 to 8 perfluoroalkyl) and its salts are preferably in the range of 0.01 ppb to 1,000 ppb, more preferably in the range of 0.05 ppb to 500 ppb, and even more preferably in the range of 0.1 ppb to 300 ppb. The coloring composition of the present invention may contain substantially no perfluoroalkyl sulfonic acid and its salts, as well as perfluoroalkyl carboxylic acid and its salts. For example, by using compounds that can replace perfluoroalkyl sulfonic acids and salts, and compounds that can replace perfluoroalkyl carboxylic acids and salts, compositions that do not contain perfluoroalkyl sulfonic acids and salts, and perfluoroalkyl carboxylic acids and salts, can be selected. Examples of the compounds that can replace the controlled compound include compounds that are excluded from the controlled object due to differences in the carbon number of perfluoroalkyl groups. Among them, the above content does not hinder the use of perfluoroalkyl sulfonic acid and its salt, as well as perfluoroalkyl carboxylic acid and its salt. The coloring composition of the present invention may contain perfluoroalkyl sulfonic acid and its salts, as well as perfluoroalkyl carboxylic acid and its salts within the maximum allowable range. The moisture content of the colored composition of the present invention is usually 3 mass % or less, preferably 0.01 to 1.5 mass % and more preferably 0.1 to 1.0 mass % range. The moisture content can be determined by the Karl Fischer method. The coloring composition of the present invention can be used to adjust the viscosity for the purpose of adjusting the film surface shape (flatness, etc.), the film thickness, etc. The viscosity value may be appropriately selected as needed, but for example, 0.3 mPa·s to 50 mPa·s at 25°C is preferred, and 0.5 mPa·s to 20 mPa·s is preferred. As the method of measuring viscosity, for example, a cone plate type viscometer can be used and the measurement can be performed while adjusting the temperature to 25°C. <Container Container> As the storage container of the colored composition of the present invention, there are no particular limitations, and a known storage container can be used. Furthermore, as the storage container, it is preferable to use a multi-layer bottle that forms the inner wall of the container consists of six kinds of resins of six layers, and a bottle that has a seven-layer structure with six kinds of resins is set as a container. Such containers include, for example, containers described in Japanese Patent Laid-Open No. 2015-123351. <Processing method for coloring composition> The coloring composition of the present invention can be prepared by mixing the aforementioned components. When preparing the colored composition, all the components can be dissolved and / or dispersed in a solvent at the same time to prepare the colored composition, or each component can be appropriately made into two or more solutions or dispersions as needed, and mixed them during use (on application) to prepare a colored composition. Furthermore, when preparing the colored composition, the process including dispersing the pigment is preferred. In the pigment dispersion process, as the mechanical force used to disperse the pigment, compression, extrusion, impact, shearing, and pore etching can be mentioned. Specific examples of such processes include bead milling, sand milling, roller milling, ball milling, coating stirring, microjets, high-speed impeller, sand mixing, jet mixing, high-pressure wet microparticulation, ultrasonic dispersion, etc. Furthermore, when pulverizing pigments in a sand mill (bead mill), it is preferable to perform treatment under conditions whereby microbeads with small diameter are used, filling rate of microbeads, etc., and the crushing efficiency is increased. Furthermore, after the pulverization treatment, it is preferable to remove coarse particles by filtration, centrifugation, etc. In addition, regarding the process and dispersing machine for dispersing pigments, the process and dispersing machine described in paragraph 0022 of Japanese Patent Publication No. 2015-157893, Japan Patent Publication No. 2015-157893. Furthermore, in the process of dispersing pigments, the fine-refining of particles can be performed by the salt grinding step. For example, the materials, machines, processing conditions, etc. used in the salt grinding step can be found in Japanese Patent Application Publication No. 2015-194521 and Japanese Patent Application Publication No. 2012-046629. When preparing the colored composition, it is preferable to filter the colored composition with a filter for the purpose of removing impurities and reducing defects. As the filter, it can be used without particular limitation as long as it is a filter used for filtering purposes or the like. For example, filters using fluororesins such as polytetrafluoroethylene (PTFE), polyvinylidene difluoroethylene (PVDF), polyamide resins such as nylon (for example, nylon-6, nylon-6, 6), polyolefin resins such as polyethylene and polypropylene (PP) (including high-density and ultra-high molecular weight polyolefin resins) are mentioned. Among these materials, polypropylene (including high-density polypropylene) and nylon are preferred. It is preferable that the pore diameter of the filter is 0.01 to 7.0 μm, it is more preferable that 0.01 to 3.0 μm, and it is even more preferable that 0.05 to 0.5 μm. As long as the aperture of the filter is within the above range, fine foreign matter can be removed more accurately. Regarding the aperture value of the filter, the nominal value of the filter manufacturer can be referenced. Regarding filters, various filters provided by Nihon Pall Ltd. (DFA4201NXEY, DFA4201NAEY, DFA4201J006P, etc.), Advantec Toyo Kaisha, Ltd., Nihon Entegris K.K. (Formerly Nippon Mykrolis Corporation) and KITZ MICROFILTER Corporation can be used. Furthermore, it is also preferable to use a fibrous filter material as a filter. Examples of the fibrous filter material include polypropylene fiber, nylon fiber, glass fiber, etc. Examples of commercially available products include SBP type series (SBP008, etc.), TPR type series (TPR002, TPR005, etc.), and SHPX type series (SHPX003, etc.) manufactured by ROKI TECHNO CO., LTD. When using filters, different filters (for example, the first filter and the second filter, etc.) can be combined. In this case, the filtering using each filter can be performed only once or twice or more. Furthermore, filters of different pore sizes can be combined within the above range. Furthermore, the dispersion may be filtered only by using a first filter, and after mixing other components, the dispersion may be filtered using a second filter. <Moisture> The film of the present invention is a film obtained by using the above-mentioned coloring composition of the present invention. The film of the present invention can be used in a color filter. More specifically, purple-red pixels of color filters can be used. The film thickness of the film of the present invention can be adjusted appropriately according to the purpose. For example, it is preferred that the film thickness is 20 μm or less, it is more preferred that the film thickness is 10 μm or less, and it is even more preferred that the film thickness is 5 μm or less. It is preferable that the lower limit of the film thickness is 0.1 μm or more, it is more preferable that the film thickness is 0.2 μm or more, and it is even more preferable that the film thickness is 0.3 μm or more. The maximum transmittance of light in the wavelength range of 400 to 500 nm of the film of the present invention is preferably 70% or more, more preferably 75% or more, and more preferably 80% or more. Furthermore, it is preferable that the minimum transmittance of light in the wavelength range of 450 to 600 nm of the film of the present invention is 30% or less, more preferable that 20% or less, and more preferable that 15% or less. Furthermore, it is preferable that the maximum transmittance of light at a wavelength range of 550 to 700 nm of the film of the present invention is 70% or more, more preferably 80% or more, and more preferably 90% or more. In addition, with regard to the film of the present invention, it is preferable that the transmittance of light of 50% exists in the wavelength range of 450 to 500 nm and the wavelength range of 550 to 600 nm, respectively. The transmittance of light shows that the wavelength on the short-wave side of 50% is preferably present in the range of wavelengths 460 to 495 nm, and it is more preferably present in the range of wavelengths 470 to 490 nm. The transmittance of light shows that the wavelength on the wavelength side of 50% is preferably present in the range of wavelengths of 560 to 595 nm, and it is more preferably present in the range of wavelengths of 570 to 590 nm. The film having such spectral characteristics can be preferably used as a purple-red pixel. <Color Filter> The color filter of the present invention has the above-mentioned film of the present invention. Specifically, it is preferred that the color filter of the present invention has a purple-red pixel of the film of the present invention as the color filter. It is preferable that the color filter of the present invention further contains a colored pixel selected from the group consisting of red pixels, green pixels, blue pixels, cyan pixels and yellow pixels. As a form of the color filter of the present invention, a color filter consisting of the film of the present invention includes a purple-red pixel, a cyan pixel and a yellow pixel. The color filter of the present invention can be used in solid-state imaging devices such as CCD (charge coupled element), CMOS (complementary metal oxide film semiconductor), and image display devices. In the color filter of the present invention, the film thickness of the film can be adjusted appropriately according to the purpose. It is preferred that the film thickness is 5 μm or less, it is more preferred that the film thickness is 1 μm or less, and it is even more preferred that the film thickness is 0.6 μm or less. It is preferable that the lower limit of the film thickness is 0.1 μm or more, it is more preferable that the film thickness is 0.2 μm or more, and it is even more preferable that the film thickness is 0.3 μm or more. It is preferable that the width of the pixels contained in the color filter is 0.2 to 10.0 μm. It is preferred that the lower limit is 0.4 μm or more, it is more preferred that the lower limit is 0.5 μm or more, and it is even more preferred that the lower limit is 0.6 μm or more. It is preferred that the upper limit is 5.0 μm or less, it is more preferred that the upper limit is 2.0 μm or less, it is further preferred that the upper limit is 1.0 μm or less, and it is even more preferred that the upper limit is 0.8 μm or less. Furthermore, it is preferable that the Young's coefficient of the pixel is 0.5 to 20 GPa, and it is preferable that the Young's coefficient of the pixel is 2.5 to 15 GPa. It is preferable that each pixel contained in the color filter has high flatness. Specifically, it is preferable that the surface roughness Ra of the pixel is 100 nm or less, it is more preferable that the surface roughness of 40 nm or less, and it is even more preferable that the surface roughness of 15 nm or less. The lower limit is not limited, but it is preferred, for example, to be 0.1 nm or more. The surface roughness of the pixel can be measured, for example, using an AFM (Atomic Force Microscope) Dimension3100 manufactured by Veeco Instruments Inc. Furthermore, the contact angle of water on the pixel can be appropriately set to a preferred value, but is typically in the range of 50 to 110°. The contact angle can be measured, for example, using a contact angle meter CV-DT·A type (manufactured by Kyowa Interface Science Co., Ltd.). Furthermore, it is preferable that the volume resistance value of the pixel is high. Specifically, the volume resistance value of the pixel is 10 9 Ω·cm or above is preferred, 10 11 It is better to have Ω·cm or above. The upper limit is not limited, but for example, 10 14 It is preferred that Ω·cm or less. The volume resistance value of the pixel can be measured using, for example, an ultra-high resistance meter 5410 (manufactured by Advantest Corporation). In the color filter, a protective layer may be provided on the surface of the pixel. By providing a protective layer, various effects such as oxidation resistance, low reflectance, hydrophilization, and shielding of light of specific wavelengths (ultraviolet rays, near infrared rays, etc.) can be imparted. As the thickness of the protective layer, 0.01 to 10 μm is preferred, and 0.1 to 5 μm is preferred. Examples of the method of forming the protective layer include a method of coating a resin composition dissolved in an organic solvent and forming a chemical vapor deposition method, a method of attaching the formed resin by a follower. Examples of the components that constitute the protective layer include (meth)acrylic resin, olefin resin, polycarbonate resin, polyether resin, polyaryl resin, polyolefin resin, polyether resin, polyether resin, polyphenylene resin, polyethyl ether phosphine oxide resin, polyimide resin, polyamide imide resin, polyolefin resin, cyclic olefin resin, polyester resin, styrene resin, polyol resin, polyvinylidene chloride resin, melamine resin, amine ester resin, amide resin, polyamide resin, alkyd resin, epoxy resin, modified polysilicon resin, fluorine resin, polyacrylonitrile resin, cellulose resin, Si, C, W, Al 2 O 3 , Mo, SiO 2 , Si 2 N 4 The like may also contain two or more of these ingredients. For example, when the protective layer is for the purpose of oxidation resistance, the protective layer contains polyol resin and SiO 2 and Si 2 N 4 It is preferred. Furthermore, when the protective layer is intended for low reflectivity, it is preferable that the protective layer contains (meth)acrylic resin and fluororesin. When a protective layer is formed by coating the resin composition, a known method such as a spin coating method, a casting method, a screen printing method, and an inkjet method can be used as a coating method of the resin composition. The organic solvent contained in the resin composition can be used as a well-known organic solvent (for example, propylene glycol 1-monomethyl ether 2-acetate, cyclopentanone, ethyl lactate, etc.). When the protective layer is formed by the chemical vapor deposition method, a well-known chemical vapor deposition method (thermochemical vapor deposition method, a plasma chemical vapor deposition method, and a photochemical vapor deposition method) can be used as the chemical vapor deposition method. The protective layer may contain organic and inorganic particles, absorbers of light of specific wavelengths (for example, ultraviolet rays, near infrared rays, etc.), refractive index regulators, antioxidants, adhesives, surfactants and other additives as needed. Examples of organic and inorganic fine particles include polymer fine particles (for example, silicone resin fine particles, polystyrene fine particles, melamine resin fine particles), titanium oxide, zinc oxide, zirconium oxide, indium oxide, aluminum oxide, titanium nitride, titanium nitride, magnesium fluoride, hollow silicon dioxide, silicon dioxide, calcium carbonate, barium sulfate, and the like. A well-known absorber for light of a specific wavelength can be used. The content of such additives can be adjusted appropriately, but it is preferable to be 0.1 to 70 mass % with respect to the total mass of the protective layer, and 1 to 60 mass % is further preferable. Furthermore, as the protective layer, the protective layer described in paragraphs 0073 to 0092 of Japanese Patent Laid-Open No. 2017-151176 can also be used. The color filter may also have the following structure in which pixels are embedded in spaces separated by partitions, for example, in the shape of squares. <Method for Manufacturing Color Filter> Next, a method for manufacturing a color filter using the color composition of the present invention will be described. The manufacturing method of a color filter includes the step of forming a colored composition layer on the support using the colored composition of the present invention, the step of exposing the colored composition layer in a pattern, and the step of developing and removing the unexposed portion of the colored composition layer to form a pattern (pixel). The steps of baking the coloring composition layer (pre-baking step) and the steps of baking and developing patterns (pixels) (post-baking step) can be set according to needs. In the step of forming the color composition layer, a color composition layer is formed on the support using the color composition of the present invention. As the support body, there are no particular limitations and can be appropriately selected according to the purpose. For example, a glass substrate, a silicon substrate, etc. are mentioned, and a silicon substrate is preferred. Furthermore, a charge-coupled element (CCD), a complementary metal oxide film semiconductor (CMOS), a transparent conductive film, and the like may be formed on the silicon substrate. Furthermore, a black matrix is ​​formed on the silicon substrate to isolate each pixel. In addition, in order to improve adhesion with the upper layer, prevent diffusion of substances, or planarize the substrate surface, a base layer may also be provided on the silicon substrate. As the coating method of the coloring composition, a well-known method can be used. For example, various printing methods such as drop addition method (drip casting); slit coating method; spraying method; roller coating method; spin coating method (spin coating); cast coating method; slit spin coating method; pre-wetting method (for example, as described in Japanese Patent Laid-Open No. 2009-145395); inkjet (for example, on-demand method, piezoelectric method, thermal method), nozzle jetting and other spray-based printing, flexographic printing, screen printing, gravure printing, reverse offset printing, metal mask printing, etc.; transfer methods using molds, etc.; nano-imprinting methods, etc. The application method in inkjet is not particularly limited. For example, the method described in "Expansion and Use of Inkjet - Unlimited Possibilities Appeared in Patents - is issued in February 2005, Sumitbe Techon Research Co., Ltd." (especially pages 115 to 133) or Japanese Patent Publication No. 2003-262716, Japanese Patent Publication No. 2003-185831, Japanese Patent Publication No. 2003-261827, Japanese Patent Publication No. 2012-126830, Japanese Patent Publication No. 2006-169325, etc. Furthermore, regarding the coating method of the colored composition, reference can be made to the description of International Publication No. 2017 / 030174 and International Publication No. 2017 / 018419, which are included in this specification. The colored composition layer formed on the support can be dried (pre-baked). When the film is manufactured by a low-temperature process, pre-baking may also be avoided. When pre-baking is performed, it is preferred that the pre-baking temperature is 150°C or less, it is more preferred that the pre-baking temperature is 120°C or less, and it is even more preferred that the pre-baking temperature is 110°C or less. The lower limit can be set to 50°C or above, for example, or 80°C or above. The pre-baking time is preferably 10 to 300 seconds, 40 to 250 seconds is more preferably 80 to 220 seconds, and further preferably 80 to 220 seconds. Pre-baking can be performed using heating plates, ovens, etc. Next, the colored composition layer is exposed in a pattern form (exposure step). For example, a step exposure machine, a scanning exposure machine, or the like is used to expose the colored composition layer through a mask having a predetermined mask pattern, thereby allowing exposure to the pattern. In this way, the exposed part can be hardened. Examples of radiation (light) that can be used during exposure include g-rays, i-rays, etc. Also, light with a wavelength of 300 nm or less (preferably light with a wavelength of 180 to 300 nm) can be used. Examples of light at a wavelength of 300 nm or less include KrF rays (wavelength 248 nm), ArF rays (wavelength 193 nm), etc., and KrF rays (wavelength 248 nm) are preferred. Furthermore, a long wavelength light source of 300 nm or more can be used. Furthermore, during exposure, light can be continuously irradiated to expose, or pulse irradiation can be performed to expose (pulse exposure). In addition, pulse exposure refers to an exposure method in which light is repeatedly irradiated and paused to be exposed in a short period of time (for example, below milliseconds) as a period. For example, the irradiation amount (exposure amount) is 0.03 to 2.5J / cm 2 It is preferred, 0.05 to 1.0J / cm 2 For better. The oxygen concentration during exposure can be appropriately selected. In addition to being performed under the atmosphere, it can also be exposed in a low oxygen environment (for example, 15 volume%, 5 volume%, or substantially anaerobic) environment (for example, high oxygen environment with an oxygen concentration exceeding 21 volume%, (for example, 22 volume%, 30 volume%, or 50 volume%). Furthermore, the exposure illuminance can be appropriately set, and can usually be selected from 1000W / m. 2 ~100000W / m 2 (For example, 5000W / m 2 , 15000W / m 2 Or 35000W / m 2 ) range. The conditions of the oxygen concentration and exposure illuminance can be appropriately combined, for example, the oxygen concentration can be set to be 10 volume % and the illuminance is 10000 W / m. 2 , oxygen concentration is 35% by volume and illuminance is 20000W / m 2 wait. Next, the unexposed portion of the colored composition layer is removed to form a pattern (pixel). It is possible to use a developing solution to remove the unexposed portion of the colored composition layer. Thus, the colored composition layer of the unexposed portion in the exposure step is dissolved in the developer, leaving only the photohardened part remaining. For example, it is preferable that the temperature of the developer is 20 to 30°C. It is preferable that the development time is 20 to 180 seconds. In addition, in order to improve the removal of residue, the step of removing the developer every 60 seconds can be repeated to further supply a new developer. Examples of the developer include organic solvents, alkaline developer, etc., and alkaline developer can be preferably used. As the alkali developer, it is preferable to obtain an alkaline aqueous solution (alkaline developer) obtained by diluting the alkali agent with pure water. Examples of the alkaline agent include, for example, organic alkali compounds such as ammonia, ethylamine, diethylamine, dimethylethanolamine, diethylene glycolamine, diethanolamine, hydroxyamine, ethylenediamine, tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetrabutylammonium hydroxide, ethyltrimethylammonium hydroxide, benzyltrimethylammonium hydroxide, dimethylbis(2-hydroxyethyl)ammonium hydroxide, choline, pyrrole, piperidine, 1,8-diazabicyclo[5.4.0]-7-undecene, or inorganic alkaline compounds such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium bicarbonate, sodium silicate, and sodium metasilicate. From the environmental and safety aspects, it is preferred that the alkali agent is a compound with a large molecular weight. The alkaline agent concentration in the alkaline aqueous solution is preferably 0.001 to 10 mass % and more preferably 0.01 to 1 mass % %. Furthermore, the developer may further contain a surfactant. Examples of the surfactant include the above-mentioned surfactant, and nonionic surfactant is preferred. From the viewpoint of ease of transportation, storage, etc., the developer can be made into a concentrate first and diluted to a desired concentration when used. The dilution ratio is not particularly limited, and it can be set in a range of 1.5 to 100 times, for example. Furthermore, it is also preferable to clean (rinse) with pure water after development. Furthermore, it is preferable to perform flushing by rotating the support body formed with the developed color composition layer while supplying the rinsing liquid to the developed color composition layer. Furthermore, it is also preferable to move the nozzle that emits the flushing liquid from the center portion of the support body to the peripheral portion of the support body. At this time, when the nozzle is moved from the center part of the support body to the peripheral part, the nozzle can be moved gradually while gradually reducing the movement speed. By rinsing in this way, intra-surface unevenness of rinsing can be suppressed. Furthermore, the same effect can be obtained by gradually reducing the rotation speed of the support while moving the nozzle from the center part of the support body to the peripheral part. After the development, it is preferable to perform additional exposure treatment and heating treatment (post-baking) after drying. Additional exposure treatment and post-baking are hardened after development for completely hardening. For example, it is preferable to have a heating temperature of 100 to 240°C and 200 to 240°C in post-baking. In order to achieve the above conditions, heating mechanisms such as heating plates, convection ovens (hot air circulation dryers), high-frequency heating machines, etc. can be used to post-bake the developed film in a continuous or intermittent manner. When performing additional exposure processing, it is preferable that the light used for exposure is light of light of 400 nm or less. Furthermore, the additional exposure process can be performed by the method described in Korean Publication No. 10-2017-0122130. <Solid-State Image Capture Element> The solid-state image capturing element of the present invention has the above-mentioned film of the present invention. As the structure of the solid-state imaging element, there is no particular limitation as long as the film of the present invention is provided and the solid-state imaging element is provided, and the following structures can be mentioned, for example. On the substrate are provided with a plurality of photodiodes in the light receiving area that constitutes a solid-state imaging element (CCD (charge coupled element) image sensor, a CMOS (complementary metal oxide film semiconductor) image sensor, etc.), and a transmission electrode including polycrystalline silicon, etc., on the photodiode and the transmission electrode, there is a shielding film with an opening of the light receiving portion of the light-diode body, and an element protection film formed of silicon nitride, etc., which covers the entire shielding film and light receiving portion of the light-diode body, and a color filter structure is provided on the element protection film. Furthermore, a structure having a light-concentrating mechanism (such as a microlens, etc.) on the element protective film and under the color filter (near the substrate side) or a structure having a light-concentrating mechanism on the color filter, etc. may be provided. Furthermore, the color filter may also have the following structure in which each colored pixel is embedded in a space separated by a partition wall into a square shape, for example. At this time, the refractive index of the partition wall is lower than that of each colored pixel. Examples of the imaging device having such a structure include devices described in Japanese Patent Laid-Open No. 2012-227478, Japanese Patent Laid-Open No. 2014-179577, and International Publication No. 2018 / 043654. Furthermore, as shown in Japanese Patent Laid-Open No. 2019-211559, an ultraviolet absorbing layer can be provided in the structure of the solid-state imaging element to improve light resistance. The imaging device equipped with the solid-state imaging element of the present invention can also be used as a vehicle-mounted camera or a surveillance camera in addition to a digital camera or an electronic machine (mobile phone, etc.) having an imaging function. <Image Display Device> The image display device of the present invention includes the film of the present invention described above. Examples of the image display device include liquid crystal display devices, organic electroluminescent display devices, etc. Definition of image display devices or details of each image display device are described in, for example, "electronic display device (Issue in 1990 by Akio Sasaki, Kogyo Chosakai Publishing Co., Ltd., 1990)" and "display device (Issue in 1989 by Shunjo Ibuki, Sangyo Tosho Publishing Co., Ltd., 1989 by)". Also, regarding the liquid crystal display device, for example, it is described in "Next Generation Liquid Crystal Display Technology (editored by Uchida Ryuo, Kogyo Chosakai Publishing Co., Ltd., 1994)". There is no particular limitation to the application of the liquid crystal display device of the present invention, for example, it can be applied to various methods described in the above-mentioned "Next Generation Liquid Crystal Display Technology". [Example] Hereinafter, the present invention will be described in detail with reference to examples. The materials, usage amount, proportion, processing content, processing order, etc. shown in the following examples can be appropriately changed as long as they do not deviate from the spirit of the present invention. Therefore, the scope of the present invention is not limited to the specific examples shown below. In the structural formula shown below, Me represents methyl and Pr represents propyl. <Method of Determination of Acid Value> The acid value represents the weight of potassium hydroxide required for neutralizing the acidic component per 1 g of solid components. Specifically, the measured sample was dissolved in a mixed solvent of tetrahydrofuran / water=9 / 1, and the resulting solution was neutralized and titrated in a 0.1M aqueous sodium hydroxide solution using a potential difference titration device (product name: AT-510, manufactured by KYOTO ELECTRONICS MANUFACTURING CO., LTD.) at 25°C. The inflection point of the titration pH curve is used as the end point of the titration, and the acid value is calculated using the following formula. A=56.11×Vs×0.1×f / w A: Acid value (mgKOH / g) Vs: The amount of 0.1mol / l sodium hydroxide aqueous solution required for titration (mL) f: The titration amount of 0.1mol / l sodium hydroxide aqueous solution w: The mass of the sample is measured (g) (solid composition conversion) <Method for measuring amine value of resin> The amine value represents the weight of potassium hydroxide required for neutralizing the alkaline component per 1 g of solid component. Specifically, the measured sample was dissolved in a mixed solvent of tetrahydrofuran / water=9 / 1, and the resulting solution was neutralized and titrated in a 0.1M aqueous sodium hydroxide solution using a potential difference titration device (product name: AT-510, manufactured by KYOTO ELECTRONICS MANUFACTURING CO., LTD.) at 25°C. The inflection point of the titration pH curve is used as the end point of the titration, and the acid value is calculated using the following formula. A=56.11×Vs×0.1×f / w A: Acid value (mgKOH / g) Vs: The amount of 0.1mol / l sodium hydroxide aqueous solution required for titration (mL) f: The titration amount of 0.1mol / l sodium hydroxide aqueous solution w: The mass of the sample is measured (g) (solid composition conversion) <Production of Dispersion> The raw materials described in the following table were mixed, and 230 parts by mass of zirconium dioxide microbeads having a diameter of 0.3 mm were added, and the dispersion was performed using a coating stirrer for 5 hours, and the microbeads were filtered and separated to produce 1 to 14, 101 to 104. [Table 1] The detailed contents of the materials represented by abbreviations in the above table are as follows. (Pigment) Pg-1: C.I. Pigment Red 122 (Qicarone Pigment) Pg-2: C.I. Pigment Red 254 (Diketopyrrolol Pigment) Pg-3: C.I. Pigment Purple 23 (Dimen㗁𠯤 Pigment) Pg-4: C.I. Pigment Red 242 (Azo Pigment) (Dispersant) P-1: Resin with the following structure (weight average molecular weight 11000, amine value 105.3 mgKOH / g, acid value 105.0 mgKOH / g, Molby marked on the main chain as repeating units, and the value marked on the side chain as repeating units.) [Chemical Formula 36] P-2: Resin with the following structure (weight average molecular weight 21000, amine value 47.0 mgKOH / g, acid value 36.0 mgKOH / g, value marked on the main chain is Moerby, and value marked on the side chain is the number of repeating units.) [Chemical Formula 37] P-3: Resin with the following structure (weight average molecular weight 23000, amine value 45.0 mgKOH / g, acid value 32.3 mgKOH / g, Molby marked on the main chain as repeating units, and the value marked on the side chain as repeating units.) [Chemical Formula 38] CP-1: Resin with the following structure (weight average molecular weight 11000, amine value 0 mgKOH / g, acid value 69.2 mgKOH / g, and the value marked on the main chain is the repeating unit.) [Chemical Formula 39] CP-2: Resin with the following structure (weight average molecular weight 11000, amine value 0 mgKOH / g, acid value 195.4 mgKOH / g, and the value marked on the main chain is the repeating unit.) [Chemical Formula 40] CP-3: Resin with the following structure (weight average molecular weight 26000, amine value 0 mgKOH / g, acid value 80 mgKOH / g, a, b, and c marked on the main chain represent the moorbi of the repeating unit, a:b:c=1:1:1.) [Chemical Formula 41] CP-4: AjisperPB821 (manufactured by Ajinomoto Fine-Techno Co., Inc., amine value 10 mgKOH / g, acid value 17 mgKOH / g) (Solvent) S-1: Cyclohexanone <Production of Colored Composition> The raw materials described in the following table were mixed and stirred, and then a nylon filter (manufactured by Nihon Pall Ltd.) with a pore size of 0.45 μm was used to produce the colored composition. The unit of the value recorded in the content column is parts mass. [Table 2] [Table 3] [Table 4] [Table 5] [Table 6] [Table 7] [Table 8] [Table 9] In the above table, the details of the raw materials recorded in the abbreviation are as follows. (Dye solution) A-1: ​​12.3 mass % cyclohexanone solution of solid component of dye with the following structure (Guiyamaguchi Sei dye, weight average molecular weight 10000) [Chemical formula 42] A-2: A solid component 12.3 mass % cyclohexanone solution of dye with the following structure (Guiyamaguchi Shin- dye, weight average molecular weight 9000) [Chemical formula 43] A-3: 12.3 mass % cyclohexanone solution of solid composition of dye (Guiyamaguchi Sei dye) with the following structure [Chemical Formula 44] A-4: 12.3 mass % cyclohexanone solution of solid composition of dye (Guiyamaguchi Sei dye) with the following structure [Chemical Formula 45] A-5: 12.3 mass % cyclohexanone solution of solid composition of dye (Guiyamaguchi Sei dye) with the following structure [Chemical Formula 46] A-6: C.I. Solid component 12.3 mass % cyclohexanone solution of C.I. Solid component 12.3 mass % cyclohexanone solution of C.I. Solid component 12.3 mass % cyclohexanone solution of dye with the following structure [Chemical Formula 47] A-8: C.I. Solid component 12.3 mass % cyclohexanone solution of C.I. Acid Red 289 (Guiyamaguchi Sina dye) (Dispersible liquid) Dispersion liquids 1-14, 101-104: The above-mentioned dispersion liquids 1-14, 101-104 (Resin) P-1, P-2, CP-1, CP-4: Resin represented by the above-mentioned dispersants P-1, P-2, CP-1, CP-4 (Polymerizing compound) M-1: Compound with the following structure [Chemical Formula 48] M-2: Compounds with the following structure [Chemical Formula 49] (Photopolymerization initiator) I1: Irgacure OXE01 (manufactured by BASF Company) I2: Compounds with the following structure [Chemical Formula 50] (epoxy compound) Ep-1: epoxy compound (1,2-epoxy-4-(2-ethylene oxide) cyclohexane adduct of 2,2’-bis(hydroxymethyl)-1-butanol) Ep-2: Compounds with the following structure [Chemical Formula 51] (Addant) C-1: Compounds with the following structure (silane coupling agent) [Chemical formula 52] (Ionic Compound) B-1: Compound with the following structure [Chemical Formula 53] B-2: Compounds with the following structure [Chemical Formula 54] B-3: Lithium tetrafluoroborate (BF 4 - Li + ) Regarding the ionic compounds B-1 to B-3, each compound is dissolved in methanol to prepare a measurement solution, and the absorbance of the solution at 25°C was measured using a tank with a light diameter length of 1 cm. The above formula (A) at the maximum absorption wavelength range of 400 to 700 nm. λ ) The ratio absorbances indicated are all below 5. (surfactant) W-1: KF-6001 (silicon-based surfactant, made by Shin-Etsu Chemical Co., Ltd.. Methanol modified polydimethylsiloxane at both ends.) W-2: Compounds with the following structure (the value marked on the main chain is the moor ratio, indicating that the proportion of the repeating unit is moor%. Weight average molecular weight: 14000) [Chemical Formula 55] (Solvent) S-1: Cyclohexanone S-2: Propylene glycol monomethyl ether acetate The content of the colorant in the total solid component of each coloring composition, the content of the dye in the coloring agent, and the content of the Yamaguchi-seki dye in the dye are as follows. The content of the colorant in the total solid components of each coloring composition is recorded in the "Colorant Content" column, the content of dye in the coloring agent is recorded in the "Dye Content" column, and the content of the Guchiyashi Yasukashi dye in the dye is recorded in the "Guchiyashi Yasukashi Dye Content" column. [Table 10] [Table 11] [Table 12] [Table 13] <Evaluation of Pattern Linear, Development Residue, and Defects> The base layer formation composition (made by CT-4000L, FUJIFILM Electronic Materials Co., Ltd.) was coated on a silicon wafer with a diameter of 8 inches (20.32 cm) using a spin coating machine, and a base layer was formed by heating the base layer at 220°C for 300 seconds. The film thickness of each colored composition after baking is 0.5 μm was applied to the silicon wafer with the base layer by spin coating method, and then heated at 100°C for 2 minutes using a heating plate to obtain the composition layer. Next, light with a wavelength of 365 nm was 1000 mJ / cm using an i-line stepper exposure device (FPA-3000i5+, manufactured by Canon Co., Ltd.) 2 The exposure amount was exposed to the composition layer through a mask of a dot pattern of 1.0 μm square. Next, the silicon wafer formed with the exposed composition layer was placed on a horizontal rotating table of a rotary / spray developer (DW-30 type, Chemitronics Co., Ltd.), and the rotary immersion development was performed at 23°C for 60 seconds using a developer (60% dilution solution of FUJIFILM Electronic Materials Co., Ltd.). Then, the silicon wafer was fixed to the horizontal rotating table in a vacuum suction cup, and the silicon wafer was rotated at a rotation number of 50 rpm by a rotating device, and pure water was supplied from the spray nozzle in a spray shape above its rotation center, and the spray drying was performed. Further, a heating plate at 200°C was used for 300 seconds to heat treatment (post-baking) to form a pixel (coloring pattern). A silicon wafer with pixels formed was observed by scanning electron microscope (SEM, magnification: 10,000), and pattern linearity, development residue and defect were evaluated according to the following evaluation criteria. ~ Evaluation reference for pattern linearity~ A: Pixels with a line width of 1.0 μm are formed with good linearity B: There is a very small gap for pixels with a line width of 1.0 μm, but there is no problem in practice C: There is a little gap for pixels with a line width of 1.0 μm, but there is an undeveloped part between the pixels. ~Evaluation reference for developing residue ~ A: No residue is confirmed at all outside the pixel formation area (unexposed part) B: Very few residues are confirmed outside the pixel formation area (unexposed part) but there is no problem in practice C: A little residue is confirmed outside the pixel formation area (unexposed part) but there is no problem in practice D: The residue is clearly confirmed outside the pixel formation area (unexposed part) ~Base evaluation criteria for defects~ A: No defect is confirmed at the edge of the pixel B: Very few defects are confirmed at the edge of the pixel, but there is no problem in practice C: A little defect is confirmed at the edge of the pixel, but there is no problem in practice D: There is obviously defect at the edge of the pixel <Evaluation of Wet Resistance> A high temperature and high humidity test was performed for 1,000 hours of exposure to the film produced above at a temperature of 85°C and a relative humidity of 85%. The transmittance in the range of 400 to 1100 nm of the film before and after the high-temperature and high-humidity test was measured, and the rate of change in the transmittance was calculated based on the measured wavelength, and the maximum value of the change in the transmittance was calculated, and the humidity resistance was evaluated according to the following reference. Regarding the measurement of transmittance, each sample was subjected to five times, and an average value of three results except the maximum value and the minimum value were used. Furthermore, the maximum value of the transmittance change amount refers to the change amount at a wavelength with the largest change amount of transmittance in the range of 400 to 1100 nm in the film before and after the high-temperature and high-humidity test. A: The maximum value of the change in transmittance is less than 2% B: The maximum value of the change in transmittance is greater than 2% and less than 3% C: The maximum value of the change in transmittance is greater than 3% and less than 5% D: The maximum value of the change in transmittance is greater than 5% [Table 14] [Table 15] [Table 16] [Table 17] As shown in the above table, the evaluation ratio of pattern linearity in the Example is good. Furthermore, the evaluation of the developing residue, defects and moisture resistance of the Example was also good. none.

Claims

1. A coloring composition comprising a coloring agent A containing a dye a, a resin B, and an ionic compound C, wherein the dye a contains a dye a1 comprising a cationic AX+ and an anionic AZ- having a pigment structure, the content of the dye a1 in the dye a is 50% by mass or more, the resin B contains a resin b1 having an acid value and an amine value, with the amine value being higher than the acid value, the ionic compound C is a salt of a cationic CX+ and an anionic CZ-, and the specific absorbance at the maximum absorption wavelength in the wavelength range of 400 nm to 700 nm, expressed by the following formula (Aλ), is 5 or less: E = A1 / (c × l) ··· (Aλ) In formula (Aλ), E represents the specific absorbance of the ionic compound C at the maximum absorption wavelength in the wavelength range of 400 nm to 700 nm, A1 represents the absorbance of the ionic compound C at the maximum absorption wavelength in the wavelength range of 400 nm to 700 nm, and l represents the groove length in cm. c represents the concentration of ionic compound C in the solution, expressed in mg / ml.

2. The coloring composition as described in claim 1, wherein the content of the aforementioned colorant A in the total solids component of the coloring composition is 30% to 70% by mass.

3. The coloring composition as described in claim 1 or claim 2, wherein the aforementioned dye a1 is formed by the aforementioned cation AX+ and the aforementioned anion AZ- through covalent bonds.

4. The coloring composition as described in claim 1 or claim 2, wherein the aforementioned anion AZ-series aceimine anion.

5. The coloring composition as described in claim 1 or claim 2, wherein the aforementioned dye a1 has an acid group.

6. The coloring composition as described in claim 1 or claim 2, wherein the aforementioned dye a1 is a dye polymer having two or more pigment structures in one molecule.

7. The coloring composition as described in claim 1 or claim 2, wherein the aforementioned colorant A further contains a pigment.

8. The coloring composition as claimed in claim 7, wherein the aforementioned pigment contains at least one selected from quinacrine pigments, dipigment pigments, naphthol azo pigments, and diketopyrrolopyrrole pigments.

9. The coloring composition as claimed in claim 7, wherein the aforementioned pigment contains at least one selected from the colorimetric index pigment red 122, colorimetric index pigment red 202, colorimetric index pigment red 209, colorimetric index pigment red 254, colorimetric index pigment red 269, colorimetric index pigment red 272, colorimetric index pigment purple 19 and colorimetric index pigment purple 23.

10. The coloring composition as described in claim 1 or claim 2, wherein the aforementioned resin b1 is a resin comprising repeating units having grafted chains.

11. The coloring composition as described in claim 1 or claim 2, used to form magenta pixels.

12. A membrane obtained using a coloring composition as described in claim 1 or claim 2.

13. A color filter comprising a membrane as described in claim 12.

14. A solid-state imaging element comprising a film as described in claim 12.

15. An image display device comprising a film as described in claim 12.