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

Abstract

This invention provides a coloring composition, a membrane, a color filter, a solid-state imaging element, and an image display device capable of suppressing the formation of developing residues and forming a film with excellent heat shrinkage resistance and moisture resistance. The coloring composition contains a colorant, a resin, a polymerizable compound, a photopolymerization initiator, and a solvent. The photopolymerization initiator contains an oxime compound having hydroxyl groups, and the resin includes a resin having alicyclic epoxy groups.

Description

Coloring components, films, filters, solid-state imaging elements and image display devices This invention relates to a coloring composition comprising a colorant, a resin, a polymerizable compound, a photopolymerization initiator, and a solvent. Furthermore, this invention relates to a film, a filter, a solid-state imaging element, and an image display device made using the coloring composition. In recent years, the widespread use of digital cameras and camera-equipped mobile phones has led to a significant increase in demand for solid-state imaging components such as charge-coupled device (CCD) image sensors. Color filters, as core devices in displays or optical components, are used. Color filters typically have pixels containing the three primary colors of red, green, and blue, and function to decompose transmitted light into these three primary colors. The pixels of a color filter are manufactured using a coloring composition containing a colorant and patterns formed by methods such as photolithography. Patent Document 1 describes a technique for manufacturing a color filter using a coloring composition containing a colorant, an epoxy resin, a photopolymerization initiator, a polymerizable compound, and a solvent. [Patent Document 1] International Publication No. 2021 / 039491 When using coloring components and creating pixels by forming patterns using photolithography, it is better to have less developing residue. Furthermore, regarding films formed using coloring compositions, it is desirable for them to have low thermal shrinkage and to be less prone to voids even when pixels are exposed to high humidity environments. In recent years, even higher standards have been required for these properties. Based on the inventors' research, it was found that the coloring composition disclosed in Patent Document 1 is insufficient to achieve the coexistence of these properties, and there is still room for further improvement. Therefore, the object of the present invention is to provide a coloring composition capable of suppressing the generation of developing residue and forming a film with excellent heat shrinkage resistance and moisture resistance. Furthermore, the object of the present invention is to provide a film, a color filter, a solid-state imaging element, and an image display device. Based on the inventors' research, it was discovered that the above-mentioned objectives can be achieved by the coloring composition described later, thus completing the present invention. Therefore, the present invention provides the following. <1> A coloring composition comprising a colorant, a resin, a polymerizable compound, a photopolymerization initiator, and a solvent, wherein the photopolymerization initiator comprises a hydroxyl-containing oxime compound, and the resin comprises a resin having an alicyclic epoxy group. <2> A coloring composition as described in <1>, wherein the alicyclic epoxy group is a group having a polycyclic aliphatic hydrocarbon ring. <3> A coloring composition as described in <1> or <2>, wherein the polymerizable compound comprises an epoxy-modified (meth)acrylate compound. <4> A coloring composition as described in any one of <1> to <3>, wherein the hydroxyl-containing oxime compound is an oxime compound containing a hydroxyl group and a thioether group. <5> A coloring composition as described in any one of <1> to <4>, wherein the photopolymerization initiator further comprises a photopolymerization initiator other than the aforementioned hydroxyl-containing oxime compound. <6> A coloring composition as described in any one of <1> to <5>, further comprising a cyclic silicate compound. <7> A membrane obtained using any one of the coloring compositions described in <1> to <6>. <8> A filter having the membrane described in <7>. <9> A solid-state imaging element having the membrane described in <7>. <10> An image display device having the membrane described in <7>. [Effects of the Invention] According to the present invention, a coloring composition capable of suppressing the generation of developing residue and forming a film with excellent heat shrinkage resistance and moisture resistance can be provided. Furthermore, the present invention can provide a film, a color filter, a solid-state imaging element, and an image display device. The present invention will now be described in detail. In this specification, “~” is used to mean that the values ​​listed before and after it are included as lower and upper limits. In the designation of groups (atomic groups) in this specification, the designations without substituted and unsubstituted include both groups (atomic groups) without substituents and groups (atomic groups) with substituents. For example, “alkyl” includes not only alkyl groups without substituents (unsubstituted alkyl groups) but also alkyl groups with substituents (substituted alkyl groups). In this specification, “exposure”, unless otherwise specified, includes not only exposure using light but also depiction using particle beams such as electron beams and ion beams. Furthermore, examples of light used in exposure include the bright-line spectrum of mercury lamps, far-ultraviolet light (represented by excimer lasers), extreme ultraviolet light (EUV light), X-rays, electron beams, and other photochemical rays or radiation. In this specification, "(meth)acrylate" means either or both of acrylate and methacrylate; "(meth)acrylic acid" means either or both of acrylic acid and methacrylic acid; and "(meth)acrylyl" means either or both of acrylyl and methacrylyl. In this specification, the weight-average molecular weight and number-average molecular weight are converted values ​​of polystyrene determined using GPC (gel permeation chromatography). In this specification, total solids content refers to the total mass of the components after removing the solvent from all components of the composition. In this specification, pigment refers to a compound that is not readily soluble in a solvent. In this specification, the term "step" includes not only independent steps, but also steps that cannot be clearly distinguished from other steps, as long as the desired effect of the step is achieved. <Coloring Composition> The coloring composition of the present invention is characterized by containing a colorant, a resin, a polymerizable compound, a photopolymerization initiator, and a solvent, wherein the photopolymerization initiator contains an oxime compound having hydroxyl groups, and the resin includes a resin having alicyclic epoxy groups. The coloring composition according to the present invention can suppress the formation of developing residue and form a film with excellent heat shrinkage resistance and moisture resistance. The coloring composition of the present invention contains a resin having alicyclic epoxy groups and an oxime compound having hydroxyl groups. Therefore, during film formation, the hydroxyl groups derived from the oxime compound can promote the curing of the resin having alicyclic epoxy groups, resulting in a film with high crosslinking density. Thus, a film with excellent heat shrinkage resistance and moisture resistance can be formed. Furthermore, by using the oxime compound having hydroxyl groups as a photopolymerization initiator, the hydrophilicity of the film can be improved, and the unexposed component layer can be effectively removed by the developing solution. Therefore, the formation of developing residue can also be suppressed. The coloring composition of the present invention can be preferably used as a coloring composition for forming filters. Examples of filters include color filters and infrared cut-off filters, with color filters being preferred. As a color filter, an example is a filter that has colored pixels that allow light of a specific wavelength to pass through, and it is preferable to have a filter that has at least one colored pixel selected from red pixels, blue pixels, green pixels, yellow pixels, cyan pixels and magenta pixels. An infrared transmission filter is a filter that allows at least a portion of infrared light to be transmitted. Preferably, an infrared transmission filter is a filter that blocks at least a portion of visible light while allowing at least a portion of infrared light to be transmitted. As an infrared transmission filter, a filter that satisfies the following spectral characteristics: a maximum transmittance of 20% or less (preferably 15% or less, more preferably 10% or less) in the wavelength range of 400–640 nm and a minimum transmittance of 70% or more (preferably 75% or more, more preferably 80% or more) in the wavelength range of 1100–1300 nm. Preferably, an infrared transmission filter satisfies any one of the following spectral characteristics (1) to (5). (1): A filter having a maximum transmittance of 20% or less (preferably 15% or less, more preferably 10% or less) in the wavelength range of 400 to 640 nm and a minimum transmittance of 70% or more (preferably 75% or more, more preferably 80% or more) in the wavelength range of 800 to 1500 nm. (2): A filter having a maximum transmittance of 20% or less (preferably 15% or less, more preferably 10% or less) in the wavelength range of 400 to 750 nm and a minimum transmittance of 70% or more (preferably 75% or more, more preferably 80% or more) in the wavelength range of 900 to 1500 nm. (3): A filter with a maximum transmittance of 20% or less (preferably 15% or less, more preferably 10%) in the wavelength range of 400 to 830 nm and a minimum transmittance of 70% or more (preferably 75% or more, more preferably 80% or more) in the wavelength range of 1000 to 1500 nm. (4): A filter with a maximum transmittance of 20% or less (preferably 15% or less, more preferably 10%) in the wavelength range of 400 to 950 nm and a minimum transmittance of 70% or more (preferably 75% or more, more preferably 80% or more) in the wavelength range of 1100 to 1500 nm. (5): A filter with a maximum transmittance of 20% or less (preferably 15% or less, more preferably 10%) in the wavelength range of 400 to 1050 nm and a minimum transmittance of 70% or more (preferably 75% or more, more preferably 80% or more) in the wavelength range of 1200 to 1500 nm. The concentration of the solid component in the coloring composition of the present invention is preferably 5 to 30% by mass. The lower limit is preferably 7.5% by mass or more, and more preferably 10% by mass or more. The upper limit is preferably 25% by mass or less, and more preferably 20% by mass or less. The components used in the coloring composition of the present invention will be described below. <<Coloring Agent>> The coloring composition of the present invention contains a coloring agent. Examples of coloring agents include yellow, orange, red, green, purple, and blue coloring agents. The coloring agent can be a pigment or a dye. The pigment can be either an inorganic pigment or an organic pigment, but organic pigments are preferred from the viewpoints of the amount of color variation, ease of dispersion, and safety. The average primary particle size of the pigment is preferably 1–200 nm. A lower limit of 5 nm or more is preferred, and 10 nm or more is even more preferred. An upper limit of 180 nm or less is preferred, 150 nm or less is even more preferred, and 100 nm or less is even more preferred. If the average primary particle size of the pigment is within the above range, the dispersion stability of the pigment in the coloring composition is good. Furthermore, in this invention, the primary particle size of the pigment can be determined by observing the primary particles of the pigment using a transmission electron microscope and based on the obtained photographs. Specifically, the projected area of ​​the primary particles of the pigment is calculated, and the corresponding equivalent circle diameter is determined as the primary particle size of the pigment. Also, the average primary particle size in this invention is set as the arithmetic mean of the primary particle sizes of 400 pigment particles. Furthermore, the primary particles of the pigment refer to unaggregated independent particles. The crystallite size of organic pigments is preferably 0.1–50 nm, more preferably 0.5–30 nm, and further preferably 1–15 nm. The crystallite size can be determined using an X-ray diffraction apparatus from the half-width at half-maximum (WHM) of the diffraction peaks and calculated using the Scherrer formula. The crystallite size of organic pigments can be adjusted using known methods such as adjusting manufacturing conditions and post-manufacturing pulverization. Phthalocyanine compounds and squaric acid cyanine compounds can be cited as green colorants, with phthalocyanine compounds being preferred. Specific examples of green colorants include CI pigments green 7, 10, 36, 37, 58, 59, 62, 63, 64, 65, and 66. Furthermore, zinc halide phthalocyanine pigments with an average of 10 to 14 halogen atoms, 8 to 12 bromine atoms, and 2 to 5 chlorine atoms per molecule can also be used as green colorants. Specific examples include compounds described in International Publication No. 2015 / 118720. Furthermore, as a green colorant, compounds described in Chinese Patent Application No. 106909027, phthalocyanine compounds with phosphate esters as ligands described in International Publication No. 2012 / 102395, phthalocyanine compounds described in Japanese Patent Application Publication No. 2019-008014, phthalocyanine compounds described in Japanese Patent Application Publication No. 2018-180023, compounds described in Japanese Patent Application Publication No. 2019-038958, aluminum phthalocyanine compounds described in Japanese Patent Application Publication No. 2020-070426, core-shell pigments described in Japanese Patent Application Publication No. 2020-076995, and diarylmethane compounds described in Japanese Patent Application Publication No. 2020-504758, etc., can also be used. As green colorants, CI pigment green 7, 36, 58, 59, 62, and 63 are preferred, with CI pigment green 7, 36, 58, and 59 being even better. Examples of red colorants include diketopyrrolopyrrole compounds, anthraquinone compounds, azo compounds, naphthol compounds, methylimine compounds, styracin compounds, quinacrine compounds, perylene compounds, and indigo compounds. Specific examples of red colorants include CI (colorimetric index) pigment reds 1, 2, 3, 4, 5, 6, 7, 9, 10, 14, 17, 22, 23, 31, 38, 41, 48:1, 48:2, 48:3, 48:4, 49, 49:1, 49:2, 52:1, 52:2, 53:1, 57:1, 60:1, 63:1, 66, 67, 81:1, 81:2, 81:3, 83, 88, 90, 105, 112, 119, 122, 123, 144, and 1. Red pigments in the following colors: 46, 149, 150, 155, 166, 168, 169, 170, 171, 172, 175, 176, 177, 178, 179, 184, 185, 187, 188, 190, 200, 202, 206, 207, 208, 209, 210, 216, 220, 224, 226, 242, 246, 254, 255, 264, 269, 270, 272, 279, 291, 294, 295, 296, 297, etc. Furthermore, as a red colorant, it is also possible to use the following: diketopyrrolopyrrole compounds in which at least one bromine atom is substituted in the structure described in Japanese Patent Application Publication No. 2017-201384; diketopyrrolopyrrole compounds described in paragraphs 0016-0022 of Japanese Patent No. 6248838; diketopyrrolopyrrole compounds described in International Publication No. 2012 / 102399; diketopyrrolopyrrole compounds described in International Publication No. 2012 / 117965; brominated diketopyrrolopyrrole compounds described in Japanese Patent Application Publication No. 2020-085947; naphthol azo compounds described in Japanese Patent Application Publication No. 2012-229344; red colorants described in Japanese Patent No. 6516119; and Japanese Patent No. The red colorant described in Japanese Patent Application Publication No. 6525101, the brominated diketone pyrrolopyrrole compound described in paragraph 0229 of Japanese Patent Application Publication No. 2020-090632, the anthraquinone compound described in Korean Patent Application Publication No. 10-2019-0140741, the anthraquinone compound described in Korean Patent Application Publication No. 10-2019-0140744, the perylene compound described in Japanese Patent Application Publication No. 2020-079396, the perylene compound described in Japanese Patent Application Publication No. 2020-083982, the guchi-guchi-sei compound described in Japanese Patent Application Publication No. 2018-035345, and the diketone pyrrolopyrrole compound described in paragraphs 0025 to 0041 of Japanese Patent Application Publication No. 2020-066702, etc.Furthermore, as a red colorant, compounds having the following structure can also be used: an aromatic ring group formed by introducing a group with a bonded oxygen atom, sulfur atom, or nitrogen atom into the aromatic ring is bonded to a diketopyrrole skeleton. Lumogen F Orange 240 (manufactured by BASF, a red pigment, perylene pigment) can also be used as a red colorant. For red colorants, CI Pigment Red 122, 177, 179, 254, 255, 264, 269, 272, and 291 are preferred, with CI Pigment Red 254, 264, and 272 being even better. Examples of yellow coloring agents include azo compounds, methylimine compounds, isoindoline compounds, pteridine compounds, quinoline yellow compounds, and perylene compounds. Specific examples of yellow colorants include CI Pigment Yellow 1, 2, 3, 4, 5, 6, 10, 11, 12, 13, 14, 15, 16, 17, 18, 20, 24, 31, 32, 34, 35, 35:1, 36, 36:1, 37, 37:1, 40, 42, 43, 53, 55, 60, 61, 62, 63, 65, 73, 74, 77, 81, 83, 86, 93, 94, 95, 97, 98, 100, 101, 104, 106, 108, 109, 110, 113, 114, 115, 116, 117, 118, 119, 12 Yellow pigments in the following digits: 0, 123, 125, 126, 127, 128, 129, 137, 138, 139, 147, 148, 150, 151, 152, 153, 154, 155, 156, 161, 162, 164, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 179, 180, 181, 182, 185, 187, 188, 193, 194, 199, 213, 214, 215, 228, 231, 232, 233, 234, 235, 236, etc. As a yellow coloring agent, azobarbiturate nickel complexes with the following structure can be used. [Chemical Formula 1] Furthermore, as a yellow coloring agent, compounds described in Japanese Patent Application Publication No. 2017-201003, Japanese Patent Application Publication No. 2017-197719, Japanese Patent Application Publication No. 2017-171912 (paragraphs 0011-0062, 0137-0276), Japanese Patent Application Publication No. 2017-171913 (paragraphs 0010-0062, 0138-0295), Japanese Patent Application Publication No. 2017-171914 (paragraphs 0011-0062, 0139-0190), and Japanese Patent Application Publication No. 2017-171915 (paragraphs 0010-0065, 0142-0222) can also be used. The compounds described in Japanese Patent Application Publication No. 2013-054339, Japanese Patent Application Publication No. 2014-026228, Japanese Patent Application Publication No. 2018-062644, Japanese Patent Application Publication No. 2018-203798, Japanese Patent Application Publication No. 2018-062578, Japanese Patent No. 6432076, Japanese Patent Application Publication No. 2018-155881, and Japanese Patent Application Publication No. 2018-111757. Quinoline yellow compounds, quinoline yellow compounds described in Japanese Patent Application Publication No. 2018-040835, quinoline yellow compounds described in Japanese Patent Application Publication No. 2017-197640, quinoline yellow compounds described in Japanese Patent Application Publication No. 2016-145282, quinoline yellow compounds described in Japanese Patent Application Publication No. 2014-085565, quinoline yellow compounds described in Japanese Patent Application Publication No. 2014-021139, quinoline yellow compounds described in Japanese Patent Application Publication No. 2013-209614, quinoline yellow compounds described in Japanese Patent Application Publication No. 2013-209435, quinoline yellow compounds described in Japanese Patent Application Publication No. 2013-181015, quinoline yellow compounds described in Japanese Patent Application Publication No. 2013-06 The quinoline yellow compounds described in Japanese Patent Application Publication No. 1622, Japanese Patent Application Publication No. 2013-032486, Japanese Patent Application Publication No. 2012-226110, Japanese Patent Application Publication No. 2008-074987, Japanese Patent Application Publication No. 2008-081565, Japanese Patent Application Publication No. 2008-074986, Japanese Patent Application Publication No. 2008-074985, Japanese Patent Application Publication No. 2008-050420, and Japanese Patent Application Publication No. 2008-031281.The following compounds are described in Japanese Patent Publication No. 48-032765, Japanese Patent Application Publication No. 2019-008014, Japanese Patent No. 6607427, Korean Patent Publication No. 10-2014-0034963, Japanese Patent Application Publication No. 2017-095706, Taiwan Patent Application Publication No. 201920495, Japanese Patent No. 6607427, Japanese Patent Application Publication No. 2020-033525, Japanese Patent Application Publication No. 2020-033524, and Japanese Patent Application Publication No. 2020-03 The compounds described in Japanese Patent Application Publication No. 3523, Japanese Patent Application Publication No. 2020-033522, Japanese Patent Application Publication No. 2020-033521, International Patent Application Publication No. 2020 / 045200, International Patent Application Publication No. 2020 / 045199, International Patent Application Publication No. 2020 / 045197, azo compounds described in Japanese Patent Application Publication No. 2020-093994, perylene compounds described in International Patent Application Publication No. 2020 / 105346, quinoline yellow compounds described in Japanese Patent Application Publication No. 2020-517791, compounds represented by the following formula (QP1), and compounds represented by the following formula (QP2). Furthermore, from the viewpoint of improving color value, polymerizing these compounds is also preferable. [Chemical Formula 2] In formula (QP1), X 1 ~X 16 Each can independently represent a hydrogen atom or a halogen atom, Z 1 This refers to an alkyl group having 1 to 3 carbon atoms. A specific example of a compound represented by formula (QP1) is the compound described in paragraph 0016 of Japanese Patent No. 6443711. [Chemical Formula 3] In formula (QP2), Y 1 ~Y 3 Each halogen atom is represented independently. n and m represent integers from 0 to 6, and p represents integers from 0 to 5. (n+m) is 1 or more. As a specific example of a compound represented by formula (QP2), the compound described in paragraphs 0047 to 0048 of Japanese Patent No. 6432077 can be cited. For yellow colorants, CI Pigment Yellow 117, 129, 138, 139, 150, and 185 are preferred. Examples of orange colorants include CI Pigment Orange 2, 5, 13, 16, 17:1, 31, 34, 36, 38, 43, 46, 48, 49, 51, 52, 55, 59, 60, 61, 62, 64, 71, and 73. Examples of purple pigments include CI pigments purple 1, 19, 23, 27, 32, 37, 42, 60, and 61. Examples of blue colorants include CI Pigment Blue 1, 2, 15, 15:1, 15:2, 15:3, 15:4, 15:6, 16, 22, 29, 60, 64, 66, 79, 80, 87, and 88. Furthermore, aluminum phthalocyanine compounds containing phosphorus atoms can also be used as blue colorants. Specific examples include compounds described in paragraphs 0022 to 0030 of Japanese Patent Application Publication No. 2012-247591 and paragraph 0047 of Japanese Patent Application Publication No. 2011-157478. Regarding the optimal diffraction angles of various pigments, please refer to Japanese Patent Nos. 6561862, 6413872, 6281345, 2020-026503, and 2020-033526, the contents of which are incorporated herein by reference. Furthermore, as pyrrolopyrrole pigments, it is preferable that the crystallite size in the direction corresponding to the maximum peak in the X-ray diffraction pattern on one of the eight planes (±1±1±1) of the crystal lattice is 140 Å or less. Moreover, regarding the physical properties of pyrrolopyrrole pigments, it is preferable to set them as described in paragraphs 0028 to 0073 of Japanese Patent No. 2020-097744. Furthermore, from the viewpoint of improving spectroscopic properties, zinc halide phthalocyanine pigments with Raman spectra as described in Japanese Patent No. 6744002 are also preferable as pigments. Also, from the viewpoint of viscosity adjustment, pigments with controlled contact angles as described in International Publication No. 2019 / 107166 are also preferable. Coloring agents can also be dyes. There are no particular restrictions on the dyes used, and well-known dyes can be used. Examples include pyrazole azo, aniline azo, triarylmethane, anthraquinone, anthraquinone, benzylene, oxacyanine, pyrazolotriazole azo, pyridone azo, anthocyanin, phenanthrene, pyrrolopyrazole azomethine, phthalocyanine, benzo[a]piperan, indigo, and pyrrole methylene dyes. Pigment polymers can also be used as colorants. Pigment polymers are preferably dyes that are dissolved in a solvent. Furthermore, pigment polymers can form particles. When pigment polymers are in particle form, they are usually used in a dispersed state in a solvent. Pigment polymers in particle state can be obtained, for example, by emulsion polymerization; specific examples include the compound and manufacturing method described in Japanese Patent Application Publication No. 2015-214682. Pigment polymers having two or more pigment structures per molecule are preferred, with three or more pigment structures being preferable. There is no particular upper limit, but it can also be set to 100 or less. The plurality of pigment structures in one molecule can be the same pigment structure or different pigment structures. The weight-average molecular weight (Mw) of the pigment polymer is preferably 2000 to 50000. A lower limit of 3000 or more is preferred, and 6000 or more is even more preferred. An upper limit of 30000 or less is preferred, and 20000 or less is even more preferred. The pigment polymers may also include compounds described in Japanese Patent Application Publication No. 2011-213925, Japanese Patent Application Publication No. 2013-041097, Japanese Patent Application Publication No. 2015-028144, Japanese Patent Application Publication No. 2015-030742, and International Publication No. 2016 / 031442. The colorant can be a triarylmethane dye polymer as described in Korean Patent Publication No. 10-2020-0028160, a guji guji compound as described in Japanese Patent Application Publication No. 2020-117638, a phthalocyanine compound as described in International Patent Publication No. 2020 / 174991, an isoindoline compound or a salt thereof as described in Japanese Patent Application Publication No. 2020-160279, a compound represented by formula 1 as described in Korean Patent Publication No. 10-2020-0069442, or a compound represented by formula 1 as described in Korean Patent Publication No. 10-2020-0028160. The compounds represented by Formula 1 described in Publication No. 069730, Korean Patent Publication No. 10-2020-0069070, Korean Patent Publication No. 10-2020-0069067, Korean Patent Publication No. 10-2020-0069062, zinc halide phthalocyanine pigments described in Japanese Patent No. 6809649, and isoindoline compounds described in Japanese Unexamined Patent Application Publication No. 2020-180176. The colorant can be rotaxane, and the pigment skeleton can be used for cyclic structures of rotaxane, rod-shaped structures, or both. Two or more colorants can be used in combination. Furthermore, when two or more colorants are used in combination, black can be formed by the combination of the two or more colorants. Examples of such combinations include the following (1) to (7): (1) A combination containing red and blue colorants. (2) A combination containing red, blue, and yellow colorants. (3) A combination containing red, blue, yellow, and purple colorants. (4) A combination containing red, blue, yellow, purple, and green colorants. (5) A combination containing red, blue, yellow, and green colorants. (6) A combination containing red, blue, and green colorants. (7) A combination containing yellow and purple colorants. When a coloring composition contains two or more colorants and presents black in combination with two or more colorants, such a coloring composition can be better used as a coloring composition for forming infrared transmission filters. The content of colorant in the total solids of the coloring composition is preferably 25% by mass or more, more preferably 30% by mass or more, and further preferably 40% by mass or more. The upper limit is preferably 80% by mass or less, more preferably 75% by mass or less, and further preferably 70% by mass or less. <<Resin>> The coloring composition of the present invention contains resin. For example, resin is incorporated for purposes such as dispersing pigments in coloring compositions or as an adhesive. Additionally, resin primarily used for dispersing pigments in coloring compositions is also referred to as a dispersant. However, this use of resin is only one example; resin can also be used for purposes other than this. (Resins with alicyclic epoxy groups) The resins contained in the coloring composition of the present invention include resins with alicyclic epoxy groups (hereinafter also referred to as alicyclic epoxy resins). Furthermore, an alicyclic epoxy group refers to a single-valent functional group having a cyclic structure formed by the condensation of an epoxy ring and an aliphatic hydrocarbon ring. For the purpose of easily forming films with superior heat shrinkage resistance, it is preferable that the alicyclic epoxy group is a group having a polycyclic aliphatic hydrocarbon ring. That is, it is preferable that the alicyclic epoxy group is a group formed by the condensation of a polycyclic aliphatic hydrocarbon ring and an epoxy ring. Here, a polycyclic aliphatic hydrocarbon ring refers to an aliphatic hydrocarbon ring with a structure in which two or more monocyclic aliphatic hydrocarbon rings share one or more carbon atoms. Specific examples of polycyclic aliphatic hydrocarbon rings include isocamphene rings, adamantane rings, dicyclopentene rings, dicyclopentane rings, tricyclodecane rings, norcamphene rings, and norcamphene rings. Examples of alicyclic epoxy groups include those represented by formula (e-1). [Chemical Formula 4] In equation (e-1), ring A E1* indicates an aliphatic hydrocarbon ring, and * indicates a bond. Ring A of equation (e-1) E1 The aliphatic hydrocarbon ring represented can be a monocyclic aliphatic hydrocarbon ring or a polycyclic aliphatic hydrocarbon ring, but polycyclic aliphatic hydrocarbon rings are preferred because they are easier to form films with better heat resistance and shrinkage. Specific examples of alicyclic epoxy groups include the groups shown below, with those represented by formula (e-1-3) and formula (e-1-4) being preferred. In the following formulas, * indicates a bond. [Chemical Formula 5] Alicyclic epoxy resins are preferably resins containing repeating units having alicyclic epoxy groups. Examples of repeating units having alicyclic epoxy groups include those represented by formula (E1). [Chemical Formula 6] In equation (E1), X a1 L represents a trivalent linkage base. a1 Z represents a single-bond or divalent linkage base. a1 It represents an alicyclic epoxy group. X as in equation (E1) a1 Examples of trivalent linkages include poly(meth)acrylic acid linkages, polyalkylimide linkages, polyester linkages, polyurethane linkages, polyurea linkages, polyamide linkages, polyether linkages, polystyrene linkages, bisphenol linkages, and phenolic varnish linkages. Poly(meth)acrylic acid linkages, polyether linkages, polyester linkages, bisphenol linkages, and phenolic varnish linkages are preferred, polyether linkages, phenolic varnish linkages, and poly(meth)acrylic acid linkages are even more preferred, and poly(meth)acrylic acid linkages are even more preferred. L as in equation (E1) a1 Examples of divalent linkages include alkyl groups (preferably alkyl groups with 1 to 12 carbon atoms), aryl groups (preferably aryl groups with 6 to 20 carbon atoms), -NH-, -SO-, and -SO-. 2-, -CO-, -O-, -COO-, -OCO-, -S-, and groups consisting of two or more of these. The alkyl group can be straight-chain, branched, or cyclic, with straight-chain or branched being preferred. Furthermore, the alkyl group can have substituents or may be unsubstituted. Examples of substituents include hydroxyl and alkoxy groups. Z in equation (E1) a1Examples of alicyclic epoxy groups include those represented by formula (e-1), with those represented by formula (e-1-3) and formula (e-1-4) being more preferred. Resins containing repeating units with alicyclic epoxy groups preferably contain at least one repeating unit selected from repeating units represented by formula (E1-1) and repeating units represented by formula (E1-2). The resin may contain only one repeating unit from repeating units represented by formula (E1-1) and repeating units represented by formula (E1-2), or it may contain repeating units represented by formula (E1-1) and repeating units represented by formula (E1-2) separately. When containing both repeating units, the ratio of repeating units represented by formula (E1-1) to repeating units represented by formula (E1-2), expressed in molar ratios, is preferably 5:95 to 95:5, more preferably 10:90 to 90:10, and further preferably 20:80 to 80:20. [Chemical Formula 7] In equations (E1-1) and (E1-2), L E1 R represents a single-bonded or divalent linkage base. E10 Represents a hydrogen atom or a substituent. As R E10 Examples of substituents include alkyl and aryl groups, with alkyl being preferred. Alkyl groups with 1 to 10 carbon atoms are preferred, 1 to 5 are more preferred, and 1 to 3 are even more preferred. R E10 Hydrogen atoms or methyl groups are preferred. As L E1 Examples of divalent linkages include alkyl groups (preferably alkyl groups with 1 to 12 carbon atoms), aryl groups (preferably aryl groups with 6 to 20 carbon atoms), -NH-, -SO-, and -SO-. 2-, -CO-, -O-, -COO-, -OCO-, -S-, and groups consisting of two or more of these. The alkyl group can be straight-chain, branched, or cyclic, with straight-chain or branched being preferred. Furthermore, the alkyl group can have substituents or may be unsubstituted. Examples of substituents include hydroxyl and alkoxy groups. The content of repeating units with alicyclic epoxy groups is preferably 1 to 100 mol% among all repeating units in a resin containing repeating units with alicyclic epoxy groups. The upper limit is preferably 90 mol% or less, and more preferably 80 mol% or less. The lower limit is preferably 2 mol% or more, and more preferably 3 mol% or more. Resins containing repeating units with alicyclic epoxy groups can have other repeating units besides those with alicyclic epoxy groups. Examples of other repeating units include repeating units with acid groups and repeating units with groups containing vinyl unsaturated bonds. Examples of acid groups include phenolic hydroxyl, carboxyl, sulfonyl, and phosphate groups, with phenolic hydroxyl or carboxyl being preferred, and carboxyl being even more preferred. Examples of groups containing vinyl unsaturated bonds include vinyl, styryl, (methyl)allyl, and (methyl)acrylyl. Examples of repeating units containing acid groups include those represented by formula (E2). Examples of repeating units containing vinyl unsaturated bonds include those represented by formula (E3). [Chemical Formula 8] In equation (E2), X b1 L represents a trivalent linkage base. b1 Z represents a single-bond or divalent linkage base. b1 This represents an acid group. In formula (E3), X c1 L represents a trivalent linkage base. c1 Z represents a single-bond or divalent linkage base. c1 This indicates a group containing an ethylene-like unsaturated bond. As X from equation (E2) b1 The trivalent linkage base represented and X from equation (E3) c1 Examples of trivalent linkages include poly(meth)acrylic acid linkages, polyalkylimide linkages, polyester linkages, polyurethane linkages, polyurea linkages, polyamide linkages, polyether linkages, polystyrene linkages, bisphenol linkages, and phenolic varnish linkages. Poly(meth)acrylic acid linkages, polyether linkages, polyester linkages, bisphenol linkages, and phenolic varnish linkages are preferred, polyether linkages, phenolic varnish linkages, and poly(meth)acrylic acid linkages are even more preferred, and poly(meth)acrylic acid linkages are even more preferred. L as in equation (E2) b1 The divalent linkage base represented and the L in formula (E3) c1Examples of divalent linkages include alkyl groups (preferably alkyl groups with 1 to 12 carbon atoms), aryl groups (preferably aryl groups with 6 to 20 carbon atoms), -NH-, -SO-, and -SO-. 2-, -CO-, -O-, -COO-, -OCO-, -S-, and groups consisting of two or more of these. The alkyl group can be straight-chain, branched, or cyclic, with straight-chain or branched being preferred. Furthermore, the alkyl group can have substituents or may be unsubstituted. Examples of substituents include hydroxyl and alkoxy groups. Z as in equation (E2) b1 Examples of acid groups that can be represented include phenolic hydroxyl, carboxyl, sulfonyl, and phosphate groups. Phenolic hydroxyl or carboxyl groups are preferred, with carboxyl groups being even more preferred. Z as in equation (E3) c2 Examples of groups containing vinyl unsaturated bonds include vinyl, styryl, (methyl)allyl, and (methyl)acrylyl. When a resin containing repeating units with alicyclic epoxy groups also contains repeating units with acid groups, the content of repeating units with acid groups is preferably 10 to 80 mol% among all repeating units in the resin containing repeating units with alicyclic epoxy groups. The upper limit is preferably 70 mol% or less, and more preferably 60 mol% or less. The lower limit is preferably 15 mol% or more, and more preferably 20 mol% or more. When a resin containing repeating units with alicyclic epoxy groups also contains repeating units with groups containing vinyl unsaturated bonds, the content of repeating units with groups containing vinyl unsaturated bonds is preferably 1 to 20 mol% among all repeating units in the resin containing repeating units with alicyclic epoxy groups. The upper limit is preferably 18 mol% or less, and more preferably 15 mol% or less. The lower limit is preferably 3 mol% or more, and more preferably 5 mol% or more. Resins containing repeating units with alicyclic epoxy groups are preferably further found to contain repeating units with aromatic hydrocarbon rings. Benzene rings or naphthalene rings are preferred as aromatic hydrocarbon rings, with benzene rings being more preferred. The aromatic hydrocarbon ring may have substituents. Examples of substituents include alkyl groups. When a resin with a cyclic ether group contains repeating units with aromatic hydrocarbon rings, the content of the repeating units with aromatic hydrocarbon rings is preferably 1 to 65 mol% among all repeating units in the resin with a cyclic ether group. An upper limit of 45 mol% or less is preferred, and 30 mol% or less is more preferred. A lower limit of 2 mol% or more is preferred, and 3 mol% or more is more preferred. Examples of repeating units with aromatic hydrocarbon rings include repeating units derived from monofunctional polymeric compounds having aromatic hydrocarbon rings such as vinyltoluene or benzyl (meth)acrylate. The weight average molecular weight of alicyclic epoxy resin is preferably 5,000 to 30,000. A lower limit of 7,000 or above is preferred, and 9,000 or above is even better. An upper limit of 25,000 or below is preferred, 20,000 or below is even better, and 15,000 or below is further preferred. The epoxy equivalent of alicyclic epoxy resins is preferably 50–500 g / eq. The lower limit is preferably above 100 g / eq, and above 150 g / eq is even better. The upper limit is preferably below 450 g / eq, and below 400 g / eq is even better. Furthermore, the epoxy equivalent of alicyclic epoxy resins is calculated by dividing the molecular weight of the alicyclic epoxy resin by the number of alicyclic epoxy groups contained in the alicyclic epoxy resin. The preferred acid value for alicyclic epoxy resins is 50–200 mg KOH / g. A lower limit of 75 mg KOH / g or higher is preferred, and 100 mg KOH / g or higher is even better. An upper limit of 175 mg KOH / g or lower is preferred, and 150 mg KOH / g or lower is even better. (Other resins) The coloring composition of the present invention may contain resins other than the alicyclic epoxy resins described above (hereinafter also referred to as other resins). Other resins include, for example, (meth)acrylic resin, epoxy resin, (meth)acrylamide resin, olefin-thiol resin, polycarbonate resin, polyether resin, polyaryl ester resin, polyurethane resin, polyetherurethane resin, polystyrene resin, polyaryl ether phosphine oxide resin, polyimide resin, polyamide-imide resin, polyolefin resin, cyclic olefin resin, polyester resin, styrene resin, and silicone resin. Furthermore, as the resin, the resin described in the examples of International Publication No. 2016 / 088645, the resin described in Japanese Patent Application Publication No. 2017-057265, the resin described in Japanese Patent Application Publication No. 2017-032685, the resin described in Japanese Patent Application Publication No. 2017-075248, the resin described in Japanese Patent Application Publication No. 2017-066240, the resin described in Japanese Patent Application Publication No. 2017-167513, the resin described in Japanese Patent Application Publication No. 2017-173787, the resin described in paragraphs 0041 to 0060 of Japanese Patent Application Publication No. 2017-206689, and the resin described in paragraphs 0022 to 0071 of Japanese Patent Application Publication No. 2018-010856, etc., can also be used. The block polyisocyanate resin described in Japanese Patent Application Publication No. 2016-222891, the resin described in Japanese Patent Application Publication No. 2020-122052, the resin described in Japanese Patent Application Publication No. 2020-111656, the resin described in Japanese Patent Application Publication No. 2020-139021, the resin described in Japanese Patent Application Publication No. 2017-138503 containing structural units having a ring structure in the main chain and a biphenyl structure in the side chain, the resin described in paragraphs 0199 to 0233 of Japanese Patent Application Publication No. 2020-186373, the alkali-soluble resin described in Japanese Patent Application Publication No. 2020-186325, and the resin represented by Formula 1 described in Korean Patent Publication No. 10-2020-0078339. For other resins, a weight-average molecular weight (Mw) of 3,000 to 2,000,000 is preferred. An upper limit of less than 1,000,000 is preferred, and less than 500,000 is even better. A lower limit of more than 4,000 is preferred, and more than 5,000 is even better. Among other resins, resins with acid groups are preferred. Examples of acid groups include carboxyl groups, phosphate groups, sulfonyl groups, and phenolic hydroxyl groups. The acid value of the resin containing acid groups is preferably 30–500 mg KOH / g. A lower limit of 40 mg KOH / g or higher is more preferred, and 50 mg KOH / g or higher is especially preferred. An upper limit of 400 mg KOH / g or lower is more preferred, 300 mg KOH / g or lower is further preferred, and 200 mg KOH / g or lower is especially preferred. The weight-average molecular weight (Mw) of the resin containing acid groups is preferably 5,000–100,000, and 5,000–50,000 is even more preferred. Furthermore, the number-average molecular weight (Mn) of the resin containing acid groups is preferably 1,000–20,000. Resins containing acid groups preferably contain repeating units with acid groups on their side chains, and more preferably, contain 5 to 70 mol% of repeating units with acid groups on their side chains in the total repeating units of the resin. The upper limit of the content of repeating units with acid groups on their side chains is preferably 50 mol% or less, and more preferably 30 mol% or less. The lower limit of the content of repeating units with acid groups on their side chains is preferably 10 mol% or more, and more preferably 20 mol% or more. Regarding resins containing acid groups, for example, please refer to paragraphs 0558 to 0571 of Japanese Patent Application Publication No. 2012-208494 (corresponding to paragraphs 0685 to 0700 of U.S. Patent Application Publication No. 2012 / 0235099) and paragraphs 0076 to 0099 of Japanese Patent Application Publication No. 2012-198408, the contents of which are incorporated herein by reference. Furthermore, commercially available resins containing acid groups can also be used. There are no particular limitations on the method for introducing acid groups into the resin, but for example, the method described in Japanese Patent Publication No. 6349629 can be cited. In addition, as a method for introducing acid groups into the resin, a method of introducing acid groups by reacting the hydroxyl group generated in the ring-opening reaction of the epoxy group with an acid anhydride can also be cited. Resins containing base groups can also be used as other resins. Resins containing base groups are preferably resins containing repeating units with base groups on their side chains, more preferably copolymers containing repeating units with and without base groups on their side chains, and even more preferably block copolymers containing repeating units with and without base groups on their side chains. Resins containing base groups can also be used as dispersants. The amine value of resins containing base groups is preferably 5–300 mg KOH / g. A lower limit of 10 mg KOH / g or more is preferred, and 20 mg KOH / g or more is preferred. An upper limit of 200 mg KOH / g or less is preferred, and 100 mg KOH / g or less is preferred. Commercially available resins containing basic groups include DISPERBYK-161, 162, 163, 164, 166, 167, 168, 174, 182, 183, 184, 185, 2000, 2001, 2050, 2150, 2163, 2164, BYK-LPN6919 (all manufactured by BYK-Chemie GmbH), and SOLSPERSE. Models 11200, 13240, 13650, 13940, 24000, 26000, 28000, 32000, 32500, 32550, 32600, 33000, 34750, 35100, 35200, 37500, 38500, 39000, 53095, 56000, 7100 (all manufactured by Japan Lubrizol Corporation), Efka PX 4300, 4330, 4046, 4060, 4080 (all manufactured by BASF Corporation), etc. Furthermore, the resin containing a base group can also use the block copolymer (B) described in paragraphs 0063 to 0112 of Japanese Patent Application Publication No. 2014-219665, the block copolymer A1 described in paragraphs 0046 to 0076 of Japanese Patent Application Publication No. 2018-156021, and the ethylene resin containing a base group described in paragraphs 0150 to 0153 of Japanese Patent Application Publication No. 2019-184763, and these contents are incorporated into this specification. Other resins, preferably resins with acid groups and resins with base groups, are also preferred. This approach can further improve the storage stability of the resin composition. When using both resins with acid groups and resins with base groups, the content of the resin with base groups is preferably 20 to 500 parts by weight relative to 100 parts by weight of the resin with acid groups, more preferably 30 to 300 parts by weight, and further preferably 50 to 200 parts by weight. As other resins, it is also preferable to use resins containing repeating units derived from monomeric components, which include compounds represented by formula (ED1) and / or compounds represented by formula (ED2) (hereinafter, these compounds are sometimes referred to as "ether dimers"). [Chemical Formula 9] In equation (ED1), R 1 and R 2 Each can independently represent a hydrogen atom or a hydrocarbon group having 1 to 25 carbon atoms and may have substituents. [Chemical Formula 10] In formula (ED2), R represents a hydrogen atom or an organic group having 1 to 30 carbon atoms. For details regarding formula (ED2), please refer to Japanese Patent Application Publication No. 2010-168539, which is incorporated herein by reference. For specific examples of ether dimers, please refer to paragraph 0317 of Japanese Patent Application Publication No. 2013-029760, which is incorporated herein by reference. As other resins, resins containing repeating units derived from compounds represented by the free formula (X) are also preferred. [Chemical Formula 11] In the formula, R 1 R represents a hydrogen atom or a methyl group. 21 and R 22 Each alkyl group is represented independently, and n represents an integer from 0 to 15. R 21 and R 22 The number of carbon atoms in the alkyl group is preferably 1 to 10, more preferably 1 to 5, further preferably 1 to 3, and especially preferably 2 or 3. n represents an integer from 0 to 15, with integers from 0 to 5 being preferred, integers from 0 to 4 being more preferred, and integers from 0 to 3 being further preferred. Examples of compounds represented by formula (X) include ethylene oxide or propylene oxide-modified (meth)acrylates of paracumyl phenol. Commercially available examples include ARONIX M-110 (manufactured by TOAGOSEI CO.,LTD.). As for other resins, resins with polymerizable groups are preferred. Examples of polymerizable groups include groups containing vinyl unsaturated bonds and cyclic ether groups. Examples of groups containing vinyl unsaturated bonds include vinyl, styrene, (methyl)allyl, and (meth)acrylyl. Examples of cyclic ether groups include epoxy and oxetyl groups. As other resins, it is preferable to use a resin having aromatic carboxyl groups (hereinafter also referred to as resin Ac). In resin Ac, the aromatic carboxyl groups may be contained in the main chain of the repeating unit or in the side chain of the repeating unit. It is preferable that the aromatic carboxyl groups are contained in the main chain of the repeating unit. Furthermore, in this specification, an aromatic carboxyl group refers to a group having a structure in which one or more carboxyl groups are bonded to an aromatic ring. In aromatic carboxyl groups, it is preferable that the number of carboxyl groups bonded to the aromatic ring is 1 to 4, and more preferably 1 to 2. Resin Ac is preferably a resin containing at least one repeating unit selected from repeating units represented by formula (Ac-1) and repeating units represented by formula (Ac-2). [Chemical Formula 12] In equation (Ac-1), Ar 1 Indicates a group containing an aromatic carboxyl group, L 1 Indicates -COO- or -CONH-, L 2 This represents a divalent linked base. In equation (Ac-2), Ar... 10 Indicates a group containing an aromatic carboxyl group, L 11 Indicates -COO- or -CONH-, L 12 P represents a trivalent linkage base. 10 This represents a polymer chain. In equation (Ac-1), Ar is... 1 Examples of aromatic carboxyl groups include those derived from aromatic tricarboxylic anhydrides and those derived from aromatic tetracarboxylic anhydrides. Examples of aromatic tricarboxylic anhydrides and aromatic tetracarboxylic anhydrides include compounds with the following structures: [Chemical Formula 13] In the above formula, Q 1 Indicates single bond, -O-, -CO-, -COOCH 2CH 2OCO-、-SO 2-、-C(CF 3) 2. A group represented by formula (Q-1) or formula (Q-2) below. [Chemical Formula 14] Ar 1 The aromatic carboxyl group represented can be a polymerizable group. Polymerizable groups containing vinyl unsaturated bonds and cyclic ether groups are preferred, with groups containing vinyl unsaturated bonds being even more preferred. As Ar 1 Specific examples of groups containing aromatic carboxyl groups include those represented by formula (Ar-11), formula (Ar-12), and formula (Ar-13). [Chemical Formula 15] In equation (Ar-11), n1 represents an integer from 1 to 4, with 1 or 2 being preferred, and 2 being even better. In equation (Ar-12), n2 represents an integer from 1 to 8, with 1 to 4 being preferred, 1 or 2 being even better, and 2 being further preferred. In equation (Ar-13), n3 and n4 independently represent integers from 0 to 4, with 0 to 2 being preferred, 1 or 2 being even better, and 1 being further preferred. At least one of n3 and n4 is an integer greater than or equal to 1. In equation (Ar-13), Q... 1 Indicates single bond, -O-, -CO-, -COOCH 2CH 2OCO-、-SO 2-、-C(CF 3) 2. A group represented by formula (Q-1) or formula (Q-2) above. In formulas (Ar-11) to (Ar-13), *1 indicates a group related to L. 1 The bond position. In equation (Ac-1) L 1 It can be represented as -COO- or -CONH-, with -COO- being preferred. In equation (Ac-1), L is... 2 Examples of divalent linkages include alkyl groups, aryl groups, -O-, -CO-, -COO-, -OCO-, -NH-, -S-, and groups formed by combinations of two or more of these. Preferably, the alkyl group has 1 to 30 carbon atoms, more preferably 1 to 20, and further preferably 1 to 15. The alkyl group can be straight-chain, branched, or cyclic. Preferably, the aryl group has 6 to 30 carbon atoms, more preferably 6 to 20, and further preferably 6 to 10. Both alkyl and aryl groups can have substituents. Examples of substituents include hydroxyl groups. 2 The divalent linkage base represented is composed of -L 2a The -O- group is preferred. L 2a Examples of suitable substituents include alkyl groups; aryl groups; groups formed by combining alkyl and aryl groups; and groups formed by combining at least one of alkyl and aryl groups and at least one of -O-, -CO-, -COO-, -OCO-, -NH-, and -S-, with alkyl groups being preferred. The number of carbon atoms in the alkyl group is preferably 1 to 30, more preferably 1 to 20, and further preferably 1 to 15. The alkyl group can be straight-chain, branched, or cyclic. alkyl and aryl groups can have substituents. Examples of substituents include hydroxyl groups. In equation (Ac-2), Ar is... 10 The meaning of the aromatic carboxyl group represented is the same as that of Ar in formula (Ac-1). 1 The meanings are the same, and the preferred range is also the same. In formula (Ac-2) L 11It can be represented as -COO- or -CONH-, with -COO- being preferred. In equation (Ac-2), L is... 12 The trivalent linked group represented may include hydrocarbon groups, -O-, -CO-, -COO-, -OCO-, -NH-, -S-, and groups formed by combining two or more of these. Hydrocarbon groups may include aliphatic hydrocarbon groups and aromatic hydrocarbon groups. It is preferred that the aliphatic hydrocarbon group has 1 to 30 carbon atoms, more preferably 1 to 20, and further preferably 1 to 15. The aliphatic hydrocarbon group can be straight-chain, branched, or cyclic. It is preferred that the aromatic hydrocarbon group has 6 to 30 carbon atoms, more preferably 6 to 20, and further preferably 6 to 10. The hydrocarbon group may have substituents. Examples of substituents include hydroxyl groups. 12 The trivalent linker represented by formula (L12-1) is preferred, and the group represented by formula (L12-2) is even more preferred. [Chemical Formula 16] In equation (L12-1), L 12b X represents a trivalent linkage base. 1 S represents S, and *1 represents L in equation (Ac-2). 11 The bond position, *2 indicates the P in equation (Ac-2) 10 The bond position. As L 12b The trivalent linkage represented can be a hydrocarbon group; a combination of hydrocarbon groups and a group formed by at least one of -O-, -CO-, -COO-, -OCO-, -NH- and -S-, etc., with hydrocarbon groups or groups formed by a combination of hydrocarbon groups and -O- being preferred. In equation (L12-2), L 12c X represents a trivalent linkage base. 1 S represents S, and *1 represents L in equation (Ac-2). 11 The bond position, *2 indicates the P in equation (Ac-2) 10 The bond position. As L 12c The trivalent linkage represented can be a hydrocarbon group; a combination of hydrocarbon groups and a group formed by selecting at least one of -O-, -CO-, -COO-, -OCO-, -NH- and -S-, etc., with hydrocarbon groups being preferred. In equation (Ac-2), P 10 P represents a polymer chain. 10 The polymer chain represented preferably has at least one structure selected from polyester, polyether, polystyrene, and poly(meth)acrylic acid structures. Polymer chain P 10 A weight-average molecular weight of 500–20,000 is preferred. A lower limit of 1,000 or higher is preferred. An upper limit of less than 10,000 is preferred, less than 5,000 is more preferred, and less than 3,000 is even more preferred. If P 10 If the weight average molecular weight is within the above range, the pigment in the composition will have good dispersibility. When the resin having aromatic carboxyl groups is a resin having repeating units represented by formula (Ac-2), the resin can preferably be used as a dispersant. P 10 The polymer chain represented may contain polymerizable groups. Examples of polymerizable groups include groups containing vinyl unsaturated bonds and cyclic ether groups. Other resins may also be used, including at least one selected from graft polymers, star polymers, block copolymers, and resins in which at least one end of a polymer chain is sealed with an acid group. Such resins are preferably used as dispersants. Examples of graft polymers include resins having repeating units containing graft chains and resins having repeating units represented by the above formula (Ac-2). Examples of graft chains include those containing at least one structure selected from polyester, polyether, polystyrene, and poly(meth)acrylic acid structures. The terminal structure of the graft chain is not particularly limited; it can be a hydrogen atom or a substituent. Examples of substituents include alkyl, alkoxy, and alkylthioether groups. From the viewpoint of improving pigment dispersibility, groups with steric repulsion effects are preferred, and alkyl or alkoxy groups with 5 to 30 carbon atoms are preferred. Alkyl and alkoxy groups can be linear, branched, or cyclic, with linear or branched forms being preferred. Specific examples of grafted polymers include the resins described in Japanese Patent Application Publication No. 2012-255128, paragraphs 0025-0094; Japanese Patent Application Publication No. 2009-203462, paragraphs 0022-0097; and Japanese Patent Application Publication No. 2012-255128, paragraphs 0102-0166. As a star polymer, resins with a structure in which a plurality of polymer chains are bonded to the core can be cited. Specific examples of star polymers include polymers C-1 to C-31 as described in paragraphs 0196 to 0209 of Japanese Patent Application Publication No. 2013-043962. As block copolymers, it is preferable to have block copolymers containing polymers with repeating units containing acid groups or bases (hereinafter also referred to as block A) and block copolymers containing polymers without repeating units containing acid groups and bases (hereinafter also referred to as block B). Block copolymers can also be the block copolymers described in paragraphs 0063 to 0112 of Japanese Patent Application Publication No. 2014-219665 and the block copolymers A1 described in paragraphs 0046 to 0076 of Japanese Patent Application Publication No. 2018-156021, the contents of which are incorporated herein by reference. Examples of resins in which at least one end of a polymer chain is sealed with an acid group include resins containing a polymer chain having at least one end sealed with an acid group, selected from polyester, polyether, and poly(meth)acrylic acid structures. Examples of acid groups that seal the end of the polymer chain include carboxyl, sulfonyl, and phosphate groups. Other resins can also be used as dispersants. Examples of dispersants include acidic dispersants (acidic resins) and basic dispersants (basic resins). Here, acidic dispersant (acidic resin) refers to a resin in which the amount of acid groups exceeds the amount of base groups. When the total amount of acid groups and base groups is set to 100 mol%, a resin with an acid group amount of 70 mol% or more is preferred. It is preferable that the acid group in the acidic dispersant (acidic resin) is a carboxyl group. It is preferable that the acid value of the acidic dispersant (acidic resin) is 10 to 105 mg KOH / g. Similarly, basic dispersant (basic resin) refers to a resin in which the amount of base groups exceeds the amount of acid groups. When the total amount of acid groups and base groups is set to 100 mol%, a resin with a base group amount exceeding 50 mol% is preferred. Alkaline dispersants are preferably those with amine groups as their base. Dispersants are also available as commercially available products. Specific examples include the Disperbyk series (e.g., Disperbyk-111, 161, 2001, etc.) manufactured by BYK-Chemie GmbH, the SOLSPERSE series (e.g., SOLSPERSE20000, 76500, etc.) manufactured by Lubrizol Japan Ltd., the Ajispar series manufactured by Ajinomoto Fine-Techno Co., Inc., A208F (manufactured by DKS Co., Ltd.), H-3606 (manufactured by DKS Co., Ltd.), and SANDET ET (manufactured by SANYO KASEI CO.,LTD.). Furthermore, products described in paragraph 0129 of Japanese Patent Application Publication No. 2012-137564 and paragraph 0235 of Japanese Patent Application Publication No. 2017-194662 can also be used as dispersants. The resin content in the total solids of the coloring composition is preferably 20-60% by mass. The upper limit is preferably below 55% by mass, and below 50% by mass is even more preferred. The lower limit is preferably above 25% by mass, and above 30% by mass is even more preferred. The content of alicyclic epoxy resin in the total solids composition of the coloring composition is preferably 10-55% by mass. The upper limit is preferably below 50% by mass, and more preferably below 45% by mass. The lower limit is preferably above 15% by mass, and more preferably above 20% by mass. The content of alicyclic epoxy resin in the coloring composition is preferably 50% by mass or more, more preferably 60% by mass or more, and even more preferably 70% by mass or more. The upper limit can be set to 100% by mass or less, or 90% by mass or less. The coloring composition of the present invention may contain only one type of resin, or it may contain two or more types of resin. When it contains two or more types of resin, it is preferable that the total amount of them is within the range described above. <<Polymerizable Compounds>> The coloring composition of the present invention contains polymerizable compounds. Examples of polymerizable compounds include compounds having groups containing vinyl unsaturated bonds. Examples of groups containing vinyl unsaturated bonds include vinyl, (methyl)allyl, and (meth)acrylyl. It is preferable that the polymerizable compound used in the present invention is a free radical polymerizable compound. As a polymerizable compound, it can be in any chemical form, such as a monomer, prepolymer, or oligomer, but a monomer is preferred. A molecular weight of 100–2500 is preferred. An upper limit of 2000 or less is preferred, and 1500 or less is even better. A lower limit of 150 or more is preferred, and 250 or more is even better. From the viewpoint of the storage stability of the coloring composition, it is preferable that the number of groups containing vinyl unsaturated bonds (hereinafter referred to as the C=C value) in the polymerizable compound is 2 to 14 mmol / g. The lower limit is preferably 3 mmol / g or higher, more preferably 4 mmol / g or higher, and further preferably 5 mmol / g or higher. The upper limit is preferably 12 mmol / g or lower, more preferably 10 mmol / g or lower, and further preferably 8 mmol / g or lower. The C=C value of the polymerizable compound is calculated by dividing the number of groups containing vinyl unsaturated bonds in one molecule of the polymerizable compound by the molecular weight of the polymerizable compound. The polymerizable compound is preferably a compound containing three or more groups with vinyl unsaturated bonds, and even more preferably a compound containing four or more groups with vinyl unsaturated bonds. From the viewpoint of the storage stability of the coloring composition, it is preferable that the number of groups with vinyl unsaturated bonds is 15 or less, more preferably 10 or less, and even more preferably 6 or less. Furthermore, the polymerizable compound is preferably a (meth)acrylate compound with three or more functional groups, more preferably a (meth)acrylate compound with three to 15 functional groups, even more preferably a (meth)acrylate compound with three to 10 functional groups, and especially preferably a (meth)acrylate compound with three to six functional groups. Specific examples of polymerizable compounds include those described in Japanese Patent Application Publication No. 2009-288705 (paragraphs 0095-0108), Japanese Patent Application Publication No. 2013-029760 (paragraph 0227), Japanese Patent Application Publication No. 2008-292970 (paragraphs 0254-0257), Japanese Patent Application Publication No. 2013-253224 (paragraphs 0034-0038), Japanese Patent Application Publication No. 2012-208494 (paragraph 0477), Japanese Patent Application Publication No. 2017-048367, Japanese Patent No. 6057891, and Japanese Patent No. 6031807, the contents of which are incorporated herein by reference. Polymerizing compounds are preferably alkylene oxide-modified (meth)acrylate compounds. Using such polymerizing compounds can further suppress the formation of developer residues. Examples of alkylene oxide-modified (meth)acrylate compounds include those in which the (meth)acrylate group is bonded via an alkoxy group. alkylene oxide-modified (meth)acrylate compounds are preferably alkylene oxide-modified (meth)acrylate compounds. The epoxide-modified (meth)acrylate compound is preferably a compound represented by formula (Z-4) or a compound represented by formula (Z-5). [Chemical Formula 17] In equations (Z-4) and (Z-5), E independently represents -((CH) 2) y CH 2O)- or -((CH) 2) y CH(CH) 3) O)-, y each independently represents an integer from 0 to 10, and X each independently represents a (meth)acrylic group, a hydrogen atom, or a carboxyl group. In formula (Z-4), the total number of (meth)acrylic groups is 3 or 4, m each independently represents an integer from 0 to 10, and the sum of all m groups is an integer from 0 to 40. In formula (Z-5), the total number of (meth)acrylic groups is 5 or 6, n each independently represents an integer from 0 to 10, and the sum of all n groups is an integer from 0 to 60. In equation (Z-4), it is preferable for m to be an integer from 0 to 6, and even better if it is an integer from 0 to 4. Furthermore, it is preferable for the sum of all m to be an integer from 2 to 40, even better if it is an integer from 2 to 16, and especially better if it is an integer from 4 to 8. In equation (Z-5), it is preferable for n to be an integer from 0 to 6, and even better if it is an integer from 0 to 4. Furthermore, it is preferable for the sum of all n to be an integer from 3 to 60, even better if it is an integer from 3 to 24, and especially better if it is an integer from 6 to 12. Also, E in equation (Z-4) or equation (Z-5) is also known as -((CH) 2) y CH 2O)- or -((CH) 2) y CH(CH) 3) The morphology of the O)-terminus bond with the X atom is preferred. Specific examples of alkylene oxide-modified (meth)acrylate compounds include alkylene oxide-modified dinepentylenetetrol tri(meth)acrylate, alkylene oxide-modified dinepentylenetetrol tetra(meth)acrylate, alkylene oxide-modified dinepentylenetetrol penta(meth)acrylate, and alkylene oxide-modified dinepentylenetetrol hexa(meth)acrylate. Commercially available products of epoxy-modified (meth)acrylate compounds include NK Ester M-DPH-6E, M-DPH-12E, A-DPH-6E, A-DPH-12E (manufactured by SHIN-NAKAMURA CHEMICAL Co., Ltd.), and KAYARAD DPEA-12 (manufactured by Nippon Kayaku Co., Ltd.). As a polymerizable compound, polyneoprene tetraol poly(meth)acrylate as shown in formula (Z-6) below can also be used. [Chemical Formula 18] In equation (Z-6), X 1 ~X 6 Each of these groups independently represents a hydrogen atom or a (meth)acrylic acid group, where n represents an integer from 1 to 10. Where X... 1 ~X 6 At least one of them is (meth)acrylic acid. As polymerizable compounds, dinepentylenetetroxide tri(meth)acrylate (commercially available as KAYARAD D-330; manufactured by Nippon Kayaku Co., Ltd.), dinepentylenetetroxide tetra(meth)acrylate (commercially available as KAYARAD D-320; manufactured by Nippon Kayaku Co., Ltd.), dinepentylenetetroxide penta(meth)acrylate (commercially available as KAYARAD D-310; manufactured by Nippon Kayaku Co., Ltd.), dinepentylenetetroxide hexa(meth)acrylate (commercially available as KAYARAD DPHA; manufactured by Nippon Kayaku Co., Ltd., NK EsterA-DPH-12E; manufactured by SHIN-NAKAMURA CHEMICAL Co., Ltd.), and diglycerol EO (ethylene oxide) modified (meth)acrylate (commercially available as M-460; manufactured by TOAGOSEI CO., Ltd.) can also be used. (Manufactured by LTD.), Neopentyl tetraacrylate (manufactured by SHIN-NAKAMURA CHEMICAL Co., Ltd., NK EsterA-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.), 8UH-1006, 8UH-1012 (manufactured by Taisei Fine Chemical Co., Ltd.), LIGHT ACRYLATE POB-A0 (manufactured by KYOEISHA CHEMICAL Co.,LTD.), etc. As polymerizable compounds, trifunctional (meth)acrylate compounds such as trimethylolpropane tri(meth)acrylate, trimethylolpropane-propylene oxide modified tri(meth)acrylate, trimethylolpropane-ethylene oxide modified tri(meth)acrylate, ethylene oxide isocyanate modified tri(meth)acrylate, and neopentyl tertrol tri(meth)acrylate are also preferred. Commercially available trifunctional (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-3L, A-TMM-3LM-N, A-TMPT, TMPT (manufactured by SHIN-NAKAMURA CHEMICAL Co.,Ltd.), KAYARAD GPO-303, TMPTA, THE-330, TPA-330, PET-30 (manufactured by Nippon Kayaku Co.,Ltd.), etc. As polymerizable compounds, compounds with acid groups such as carboxyl, sulfonyl, and phosphoric acid groups can also be used. Commercially available examples of such compounds include ARONIX M-305, M-510, M-520, and ARONIX TO-2349 (manufactured by TOAGOSEI CO.,LTD.). Compounds having a caprolactone structure can also be used as polymerizable compounds. For information on compounds having a caprolactone structure, please refer to paragraphs 0042 to 0045 of Japanese Patent Application Publication No. 2013-253224, which is incorporated herein by reference. Examples of compounds having a caprolactone structure include DPCA-20, DPCA-30, DPCA-60, and DPCA-120, commercially available from Nippon Kayaku Co., Ltd. under the KAYARAD DPCA series. As polymerizable compounds, polymerizable compounds with a fusiform backbone can also be used. Examples of commercially available products include OGSOL EA-0200 and EA-0300 (manufactured by Osaka Gas Chemicals Co., Ltd., (meth)acrylate monomers with a fusiform backbone). As polymeric compounds, it is preferable to use compounds that are substantially free of environmentally regulated substances such as toluene. Commercially available examples of such compounds include KAYARAD DPHA LT and KAYARAD DPEA-12 LT (manufactured by Nippon Kayaku Co., Ltd.). As polymerizable compounds, urethane acrylates as described in Japanese Patent Publication Nos. 48-041708, 51-037193, 02-032293, and 02-016765, or urethane ester compounds with an ethylene oxide backbone as described in Japanese Patent Publication Nos. 58-049860, 56-017654, 62-039417, and 62-039418, are also preferred. Furthermore, polymerizable compounds having an amino group structure or a sulfide structure within the molecule as described in Japanese Patent Publication Nos. 63-277653, 63-260909, and 01-105238 are also preferred. Furthermore, commercially available products such as 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, and LINC-202UA (manufactured by KYOEISHA CHEMICAL Co.,LTD.) can also be used for polymerizable compounds. The content of polymeric compounds in the total solids of the coloring composition is preferably 1 to 35% by mass. The upper limit is preferably 30% by mass or less, more preferably 25% by mass or less, further preferably 20% by mass or less, and especially preferably 10% by mass or less. The lower limit is preferably 2% by mass or more, and more preferably 5% by mass or more. The coloring composition of the present invention may contain only one polymeric compound, or it may contain two or more polymeric compounds. When it contains two or more polymeric compounds, the total amount of these compounds is preferably within the above-mentioned range. <<Photopolymerization Initiator>> The coloring composition of the present invention contains a photopolymerization initiator. Among the coloring compositions of the present invention, those containing oxime compounds having hydroxyl groups are used as photopolymerization initiators. Hereinafter, oxime compounds having hydroxyl groups used as photopolymerization initiators will also be referred to as specific oxime compounds. It is preferred that a particular oxime compound has 1 to 4 hydroxyl groups, more preferably 1 or 2, and even more preferably 1. The molecular weight of the specific oxime compound is preferably 200–800. A lower limit of 250 or higher is preferred, and 300 or higher is even better. An upper limit of 750 or lower is preferred, and 700 or lower is even better. For the purpose of achieving a high level of both promoting the hardening reaction and inhibiting development residue, the hydroxyl value of a specific oxime compound is preferably 0.5–10.0 mmol / g. A lower limit of 1.0 mmol / g or higher is preferred, and 1.5 mmol / g or higher is even better. An upper limit of 8.0 mmol / g or lower is preferred, and 6.0 mmol / g or lower is even better. The hydroxyl value of a specific oxime compound is calculated by dividing the number of hydroxyl groups contained in one molecule of the specific oxime compound by the molecular weight of the specific oxime compound. The oxime compound is preferably one containing a hydroxyl and a thioether group. Using such an oxime compound enhances the effects of the invention. Specific examples of particular oxime compounds include compounds with the following structure: [Chemical Formula 19] The photopolymerization initiator contained in the coloring composition of the present invention may be substantially only the specific oxime compound mentioned above, or may further contain photopolymerization initiators other than the specific oxime compound mentioned above (hereinafter also referred to as other photopolymerization initiators). When the photopolymerization initiator is substantially only a specific oxime compound, it is preferable from the viewpoint that the rectangularity of the pattern shape can be further improved. Furthermore, in this specification, "the photopolymerization initiator is substantially only a specific oxime compound" means that the specific oxime compound in the photopolymerization initiator is 99% by mass or more, 99.9% by mass or more is preferred, and only a specific oxime compound is even more preferred. When the photopolymerization initiator contains other photopolymerization initiators besides the specific oxime compound, it is preferable from the viewpoint of further improving the adhesion of the developed pattern. When the photopolymerization initiator contains other photopolymerization initiators besides the specific oxime compound, it is preferable that the content of the other photopolymerization initiators is 10 to 50 parts by mass relative to 100 parts by mass of the specific oxime compound. A lower limit of 20 parts by mass or more is preferable, and 25 parts by mass or more is more preferable. An upper limit of 45 parts by mass or less is preferable, and 40 parts by mass or less is more preferable. Other photopolymerization initiators include halogenated hydrocarbon derivatives (e.g., compounds with a trihalomethane skeleton, compounds with an acediazole skeleton, etc.), acetyphosphine compounds, hexaaryl diimidazole compounds, oxime compounds, organic peroxides, sulfur compounds, ketone compounds, aromatic onium salts, α-hydroxy ketone compounds, α-amino ketone compounds, etc., with trihalomethane trihalomethane compounds, benzyl dimethyl ketal compounds, α-hydroxy ketone compounds, α-amino ketone compounds, acetyphosphine compounds, phosphine oxide compounds, metallocene compounds, oxime compounds, hexaaryl diimidazole compounds, onium compounds, benzothiazole compounds, benzophenone compounds, acetophenone compounds, cyclopentadiene-benzene-iron complexes, halomethyl acediazole compounds, and 3-aryl substituted coumarin compounds being more preferred. Compounds selected from oxime compounds, α-hydroxy ketone compounds, α-amino ketone compounds, and acetyphosphine compounds are even more preferred, with oxime compounds being even more preferred. Furthermore, other photopolymerization initiators include compounds described in paragraphs 0065 to 0111 of Japanese Patent Application Publication No. 2014-130173, compounds described in Japanese Patent No. 6301489, peroxide-based photopolymerization initiators described in MATERIAL STAGE 37-60p, vol.19, No.3, 2019, photopolymerization initiators described in International Publication No. 2018 / 221177, photopolymerization initiators described in International Publication No. 2018 / 110179, photopolymerization initiators described in Japanese Patent Application Publication No. 2019-043864, photopolymerization initiators described in Japanese Patent Application Publication No. 2019-044030, and others. The peroxide-based initiators described in Japanese Patent Application Publication No. 167313, the aminoacetophenone-based initiators with an acezolidinyl group described in Japanese Patent Application Publication No. 2020-055992, the oxime-based photopolymerization initiators described in Japanese Patent Application Publication No. 2013-190459, the polymers described in Japanese Patent Application Publication No. 2020-172619, and the compounds represented by Formula 1 described in International Publication No. 2020 / 152120 are all incorporated herein by reference. Specific examples of hexaaryl diimidazole compounds include 2,2',4-tris(2-chlorophenyl)-5-(3,4-dimethoxyphenyl)-4,5-diphenyl-1,1'-diimidazole, etc. Commercially available α-hydroxy ketone compounds include Omnirad 184, Omnirad 1173, Omnirad 2959, Omnirad 127 (all manufactured by IGM Resins BV), and Irgacure 184, Irgacure 1173, Irgacure 2959, and Irgacure 127 (all manufactured by BASF). Commercially available α-amino ketone compounds include Omnirad 907, Omnirad 369, Omnirad 369E, Omnirad 379EG (all manufactured by IGM Resins BV), and Irgacure 907, Irgacure 369, Irgacure 369E, and Irgacure 379EG (all manufactured by BASF). Commercially available acetylglucosinolate compounds include Omnirad 819, Omnirad TPO (both manufactured by IGM Resins BV), Irgacure 819, and Irgacure TPO (both manufactured by BASF). Examples of oxime compounds include those described in Japanese Patent Application Publication No. 2001-233842, Japanese Patent Application Publication No. 2000-080068, Japanese Patent Application Publication No. 2006-342166, JCS Perkin II (1979, pp. 1653-1660), JCS Perkin II (1979, pp. 156-162), and the Journal of Photopolymer Science and... The compounds described in Technology (1995, pp. 202-232), the compounds described in Japanese Patent Application Publication No. 2000-066385, the compounds described in Japanese Patent Application Publication No. 2004-534797, the compounds described in Japanese Patent Application Publication No. 2017-019766, the compounds described in Japanese Patent Publication No. 6065596, and the compounds described in International Publication No. 2015 / 152153 Compounds, compounds described in International Publication No. 2017 / 051680, compounds described in Japanese Patent Application Publication No. 2017-198865, compounds described in paragraphs 0025 to 0038 of International Publication No. 2017 / 164127, compounds described in International Publication No. 2013 / 167515, compounds described in Japanese Patent No. 5430746, compounds described in Japanese Patent No. 5647738, etc. Specific examples of oxime compounds include 3-benzoxyloxyiminobutane-2-one, 3-acetoxyiminobutane-2-one, 3-propoxyiminobutane-2-one, 2-acetoxyiminopentane-3-one, 2-acetoxyimino-1-phenylpropane-1-one, 2-benzoxyloxyimino-1-phenylpropane-1-one, 3-(4-toluenesulfonoxy)iminobutane-2-one, 2-ethoxycarbonyloxyimino-1-phenylpropane-1-one, and 1-[4-(phenylthio)phenyl]-3-cyclohexyl-propane-1,2-dione-2-(O-acetyloxime), etc. Commercially available products include Irgacure-OXE01, Irgacure-OXE02, Irgacure-OXE03, Irgacure-OXE04 (all manufactured by BASF), TR-PBG-304, TR-PBG-327 (manufactured by TRONLY), and Adeka Optomer N-1919 (manufactured by ADEKA CORPORATION, a photopolymerization initiator 2 as described in Japanese Patent Application Publication No. 2012-014052). Oxime compounds having a cyclohexane ring can also be used as other photopolymerization initiators. Specific examples of oxime compounds having a cyclohexane ring include the compound described in Japanese Patent Application Publication No. 2014-137466, the compound described in Japanese Patent No. 6636081, and the compound described in Korean Patent Publication No. 10-2016-0109444. As other photopolymerization initiators, oxime compounds with at least one benzene ring having a carbazole ring as the backbone of a naphthalene ring can also be used. Specific examples of such oxime compounds include the compound described in International Publication No. 2013 / 083505. Oxime compounds containing fluorine atoms can also be used as other photopolymerization initiators. Specific examples of oxime compounds containing fluorine atoms 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 compound (C-3) described in Japanese Patent Application Publication No. 2013-164471. Nitro-containing oxime compounds can be used as other photopolymerization initiators. It is also preferable that the nitro-containing oxime compound is a dimer. Specific examples of nitro-containing oxime compounds include the compounds described in paragraphs 0031 to 0047 of Japanese Patent Application Publication No. 2013-114249, paragraphs 0008 to 0012 and 0070 to 0079 of Japanese Patent Application Publication No. 2014-137466, the compounds described in paragraphs 0007 to 0025 of Japanese Patent Application No. 4223071, and ADEKA ARKLS NCI-831 (manufactured by ADEKA CORPORATION). Oxime compounds having a benzofuran skeleton can also be used as other photopolymerization initiators. Specific examples include OE-01 to OE-75 as described in International Publication No. 2015 / 036910. Specific examples of oxime compounds used as initiators of other photopolymerization include the compounds shown below. [Chemical Formula 20] [Chemical Formula 21] [Chemical Formula 22] Oxidime compounds are preferably those with maximum absorption wavelengths in the range of 350–500 nm, and even more preferably those with maximum absorption wavelengths in the range of 360–480 nm. Furthermore, from a sensitivity point of view, it is preferable for oxime compounds to have high molar absorptivity at wavelengths of 365 nm or 405 nm, with 1000–300000 being more preferred, 2000–300000 being further preferred, and 5000–200000 being particularly preferred. The molar absorptivity of the compound can be determined using known methods. For example, it is preferable to use a spectrophotometer (Varian Cary-5 spectrophotometer) with ethyl acetate solvent at a concentration of 0.01 g / L. As other photopolymerization initiators, difunctional or trifunctional or higher photopolymerization initiators can be used. By using such photopolymerization initiators, two or more free radicals are generated from one molecule of the photopolymerization initiator, thus obtaining good sensitivity. Furthermore, in the case of using compounds with asymmetric structures, crystallinity decreases while solubility in solvents and the like increases, making it less likely to precipitate over time, thereby improving the long-term stability of the colored composition. Specific examples of photopolymerization initiators with two or more functionalities include dimers of oxime compounds described in Japanese Patent Application Publication No. 2010-527339, Japanese Patent Application Publication No. 2011-524436, International Publication No. 2015 / 004565, Japanese Patent Application Publication No. 2016-532675 (paragraphs 0407-0412), and International Publication No. 2017 / 033680 (paragraphs 0039-0055), as well as compound (E) described in Japanese Patent Application Publication No. 2013-522445. And compounds (G), Cmpd1 to 7 as described in International Publication No. 2016 / 034963, oxime ester photoinitiators as described in paragraph 0007 of Japanese Patent Application Publication No. 2017-523465, photoinitiators as described in paragraphs 0020 to 0033 of Japanese Patent Application Publication No. 2017-167399, photopolymerization initiators (A) as described in paragraphs 0017 to 0026 of Japanese Patent Application Publication No. 2017-151342, and oxime ester photoinitiators as described in Japanese Patent Application Publication No. 6469669, etc. The content of the photopolymerization initiator in the total solids composition of the coloring composition is preferably 0.1% to 20% by mass. The lower limit is preferably 0.5% by mass or more, and more preferably 1% by mass or more. The upper limit is preferably 15% by mass or less, and more preferably 10% by mass or less. The content of the specific oxime compound in the total solids composition of the coloring composition is preferably 0.1% to 20% by mass. The lower limit is preferably 0.5% by mass or more, and more preferably 1% by mass or more. The upper limit is preferably 15% by mass or less, and more preferably 10% by mass or less. The content of the specific oxime compound relative to 100 parts by mass of the alicyclic epoxy resin is preferably 10 to 50 parts by mass. The upper limit is preferably 45 parts by mass or less, and more preferably 40 parts by mass or less. The lower limit is preferably 15 parts by mass or more, and more preferably 20 parts by mass or more. The photopolymerization initiator can be of only one type, or of two or more types. When there are two or more types, it is preferable that the total amount of such items is within the above-mentioned range. <<Solvent>> The coloring composition of the present invention contains a solvent. Examples of solvents include organic solvents. The type of solvent is not particularly limited as long as it satisfies the solubility of each component or the coatability of the composition. Examples of organic solvents include ester solvents, ketone solvents, alcohol solvents, amide solvents, ether solvents, and hydrocarbon solvents. For details regarding these, please refer to paragraph 0223 of International Publication No. 2015 / 166779, which is incorporated herein by reference. Furthermore, ester solvents with cyclic alkyl substituted components and ketone solvents with cyclic alkyl substituted components are also preferred. Specific examples of organic solvents include polyethylene glycol monomethyl ether, dichloromethane, methyl 3-ethoxypropionate, ethyl 3-ethoxypropionate, ethyl celecoxib acetate, ethyl lactate, diethylene glycol dimethyl ether, butyl acetate, methyl 3-methoxypropionate, 2-heptanone, 2-pentanone, 3-pentanone, 4-heptanone, cyclohexanone, 2-methylcyclohexanone, 3-methylcyclohexanone, 4-methylcyclohexanone, cycloheptanone, cyclooctanone, cyclohexyl acetate, cyclopentanone, ethyl carbitol acetate, butyl carbitol acetate, propylene glycol monomethyl ether, and propylene glycol. Monomethyl ether acetate, 3-methoxy-N,N-dimethylpropionic acid, 3-butoxy-N,N-dimethylpropionic acid, propylene glycol diacetate, 3-methoxybutanol, methyl ethyl ketone, γ-butyrolactone, cyclobutane, anisole, 1,4-diethoxybutane, diethylene glycol monoethyl ether acetate, 1,3-butanediol diacetate, dipropylene glycol methyl ether acetate, diacetone alcohol (also known as diacetone alcohol, 4-hydroxy-4-methyl-2-pentanone), 2-methoxypropyl acetate, 2-methoxy-1-propanol, isopropanol, etc. However, sometimes for environmental reasons, it is better to reduce the amount of aromatic hydrocarbons (benzene, toluene, xylene, ethylbenzene, etc.) used as organic solvents (for example, relative to the total amount of organic solvents, it can be set to 50 ppm (parts per million) or less, or 10 ppm or less, or 1 ppm or less). In this invention, it is preferable to use organic solvents with low metal content. For example, a metal content of 10 ppb (parts per billion) or less is preferred. Organic solvents at the ppt (parts per trillion) level can be used as needed; such organic solvents are provided, for example, by Toyo Gosei Co., Ltd. (Chemical Industry Daily, November 13, 2015). Methods for removing impurities such as metals from organic solvents include, for example, distillation (molecular distillation, membrane distillation, etc.) or filtration using a filter. For the filter used for filtration, a pore size of 10 μm or less is preferred, 5 μm or less is more preferred, and 3 μm or less is even more preferred. The filter material is preferably polytetrafluoroethylene, polyethylene, or nylon. Organic solvents can contain isomers (compounds with the same number of atoms but different structures). Furthermore, they can contain only one isomer or multiple isomers. It is preferable for the peroxide content in organic solvents to be below 0.8 mmol / L, and even better if there is no peroxide at all. The solvent content in the coloring composition is preferably 10-95% by mass. The upper limit is preferably 92.5% by mass or less, and even more preferably 90% by mass or less. The lower limit is preferably 30% by mass or more, even more preferably 50% by mass or more, further preferably 70% by mass or more, even more preferably 75% by mass or more, and especially preferably 80% by mass or more. From an environmental control perspective, it is preferable that the coloring composition of the present invention is substantially free of environmentally regulated substances. Furthermore, in the present invention, "substantially free of environmentally regulated substances" means that the content of environmentally regulated substances in the coloring composition is 50 ppm by mass or less, preferably 30 ppm by mass or less, further preferably 10 ppm by mass or less, and especially preferably 1 ppm by mass or less. Examples of environmentally regulated substances include benzene; alkylbenzenes such as toluene and xylene; and halogenated benzenes such as chlorobenzene. These substances are registered as environmentally regulated substances under REACH (Registration Evaluation Authorization and Restriction of Chemicals) regulations, PRTR (Pollutant Release and Transfer Register) law, and VOC (Volatile Organic Compounds) regulations, and their usage and treatment methods are strictly regulated. These compounds are sometimes used as solvents in the manufacture of other components used in the coloring composition, and sometimes they are mixed into the coloring composition as residual solvents. From the perspective of human safety and environmental considerations, it is preferable to minimize the amount of such substances. One method for reducing environmentally regulated substances is to heat or reduce the pressure of the system to above the boiling point of the substance, thereby removing it by distillation. Furthermore, in cases where only small amounts of environmentally regulated substances are to be removed by distillation, it is useful to azeotropically distill the substance with a solvent having the same boiling point as the original solvent to improve efficiency. Additionally, in cases involving compounds with free radical polymerization potential, polymerization inhibitors can be added to inhibit intermolecular cross-linking caused by free radical polymerization during vacuum distillation. These distillation removal methods can be performed at any stage, including the raw material stage, the product stage (e.g., a polymerized resin solution or a multifunctional monomer solution), or the stage where the compounds are mixed to form a colored composition. <<Other Compounds with Cyclic Ether Groups>> The coloring composition of the present invention can contain compounds with cyclic ether groups other than the alicyclic epoxy resins described above (also referred to as other compounds with cyclic ether groups). By combining alicyclic epoxy compounds with other compounds having cyclic ether groups, the formation of developing residues can be further suppressed. Furthermore, it is preferable that the coloring composition of the present invention is substantially free of other compounds having cyclic ether groups. According to this specification, heat shrinkage resistance can be further improved. Moreover, in this specification, "substantially free of other compounds having cyclic ether groups" means that the content of other compounds having cyclic ether groups in the total solids composition of the coloring composition is 0.1% by mass or less, preferably 0.01% by mass or less, and even more preferably free of other compounds having cyclic ether groups. Examples of compounds with cyclic ether groups other than alicyclic epoxy resins include compounds having groups represented by formula (e-2). [Chemical Formula 23] In equation (e-2), R e2 This indicates a hydrogen atom or an alkyl group, n represents 0 or 1, and * represents a bond. R e2 The number of carbon atoms in the alkoxy group is preferably 1 to 20, more preferably 1 to 10, further preferably 1 to 5, and especially preferably 1 to 3. R e2 It is preferred that the alkyl group represented is straight-chain or branched, with straight-chain being more preferred. When n is 0, R e2 Hydrogen atoms are preferred. When n is 1, R e2 It is preferred to have hydrogen atoms or alkyl groups having 1 to 3 carbon atoms. Other compounds with cyclic ether groups can be monomers or polymers. When these compounds are monomers, it is preferable that their molecular weight is less than 1500, more preferably 100–1250, and further preferably 300–1000. When these compounds are polymers, it is preferable that their weight average molecular weight is 1500 or higher, more preferably 1750 or higher, and further preferably 2000 or higher. An upper limit of 100,000 or less is preferable, 50,000 or less is more preferably, and 10,000 or less is further preferably. Epoxy resins can be preferentially used as other compounds having cyclic ether groups. Examples of epoxy resins include: epoxy resins that are epoxypropyl etherified compounds of phenolic compounds, epoxy resins that are epoxypropyl etherified compounds of various phenolic varnish resins, aliphatic epoxy resins, glycidyl ester-based epoxy resins, epoxypropylamine-based epoxy resins, epoxy resins that are epoxypropylated from halogenated phenols, condensates of silicone compounds having epoxy groups and other silicone compounds, and copolymers of polymerizable unsaturated compounds having epoxy groups and other polymerizable unsaturated compounds. Other commercially available compounds containing cyclic ether groups include, for example, naphthalene-modified epoxy resins such as EPICLON HP5000 and EPICLON HP4032D (manufactured by DIC Corporation). Alkyl diphenol type epoxy resins include EPICLON 820 (manufactured by DIC Corporation). Bisphenol A type epoxy resins include jER825, jER827, jER828, jER834, jER1001, jER1002, jER1003, jER1055, jER1007, jER1009, jER1010 (manufactured by Mitsubishi Chemical Corporation), EPICLON860, EPICLON1050, EPICLON1051, and EPICLON1055 (manufactured by DIC Corporation). Examples of bisphenol F type epoxy resins include jER806, jER807, jER4004, jER4005, jER4007, jER4010 (manufactured by Mitsubishi Chemical Corporation), EPICLON830, EPICLON835 (manufactured by DIC Corporation), LCE-21, and RE-602S (manufactured by Nippon Kayaku Co., Ltd.). Examples of phenolic varnish type epoxy resins include jER152, jER154, jER157S70, jER157S65 (manufactured by Mitsubishi Chemical Corporation), EPICLON N-740, EPICLON N-770, and EPICLON N-775 (manufactured by DIC Corporation). Examples of cresol-phenolic varnish-type epoxy resins include EPICLON N-660, EPICLON N-665, EPICLON N-670, EPICLON N-673, EPICLON N-680, EPICLON N-690, and EPICLON N-695 (all manufactured by DIC Corporation), and EOCN-1020 (manufactured by Nippon Kayaku Co., Ltd.).Examples of aliphatic epoxy resins include ADEKA RESIN EP-4080S, ADEKA RESIN EP-4085S, ADEKA RESIN EP-4088S (manufactured by ADEKA CORPORATION), CELLOXIDE2021P, CELLOXIDE2081, CELLOXIDE2083, CELLOXIDE2085, EHPE3150, EPOLEAD PB 3600, EPOLEAD PB 4700 (manufactured by Daicel Corporation), and DENACOL EX-212L, EX-214L, EX-216L, EX-321L, and EX-850L (manufactured by Nagase ChemteX Corporation). Furthermore, examples of compounds containing oxocyclic butyl groups include OXT-101, OXT-121, OXT-212, OXT-221 (all manufactured by TOAGOSEI CO., LTD.), OXE-10, and OXE-30 (all manufactured by OSAKA ORGANIC CHEMICAL IND. LTD.). Furthermore, as other compounds having cyclic ether groups, compounds described in paragraphs 0034 to 0036 of Japanese Patent Application Publication No. 2013-011869, compounds described in paragraphs 0147 to 0156 of Japanese Patent Application Publication No. 2014-043556, compounds described in paragraphs 0085 to 0092 of Japanese Patent Application Publication No. 2014-089408, compounds described in Japanese Patent Application Publication No. 2017-179172, and compounds described in paragraphs 0117 to 0120 of Japanese Patent Application Publication No. 2020-515680 may also be used. When the coloring composition contains other compounds having cyclic ether groups, the content of the other compounds having cyclic ether groups is preferably 5 to 30 parts by weight relative to 100 parts by weight of the alicyclic epoxy resin. A lower limit of 7 parts by weight or more is preferred, and 10 parts by weight or more is even more preferred. An upper limit of 25 parts by weight or less is preferred, and 20 parts by weight or less is even more preferred. The coloring composition of the present invention may contain only one other compound having cyclic ether groups, or it may contain two or more other compounds having cyclic ether groups. When it contains two or more other compounds having cyclic ether groups, the total amount of these compounds is preferably within the above-mentioned range. <<Pigment Derivatives>> The coloring composition of the present invention can contain pigment derivatives. When the coloring agent used in the coloring composition of the present invention contains a pigment, it is preferable that the coloring composition of the present invention contains a pigment derivative. Pigment derivatives can be used, for example, as dispersing agents. Dispersing agents are materials used to improve the dispersibility of pigments in a coloring composition. Examples of pigment derivatives include compounds having a structure in which acid groups or base groups are bonded to the pigment backbone. Examples of pigment skeletons constituting pigment derivatives include quinoline pigment skeletons, benzimidazolone pigment skeletons, benzisoindole pigment skeletons, benzothiazole pigment skeletons, imine pigment skeletons, squaric acid cyanine pigment skeletons, ketoneonium pigment skeletons, oxacyanine pigment skeletons, pyrrolopyrrole pigment skeletons, diketopyrrolopyrrole pigment skeletons, azo pigment skeletons, methylimine pigment skeletons, phthalocyanine pigment skeletons, naphthylphthalocyanine pigment skeletons, anthraquinone pigment skeletons, quinacridone pigment skeletons, diazonium pigment skeletons, violet ketone pigment skeletons, perylene pigment skeletons, thioindole pigment skeletons, isoindoline pigment skeletons, isoindoline ketone pigment skeletons, quinoline yellow pigment skeletons, dithiol pigment skeletons, triarylmethane pigment skeletons, and pyrrole methylene pigment skeletons. Examples of acid groups include carboxyl, sulfonyl, phosphate, borate, carboxylic acid amide, sulfonic acid amide, amide imine, and their salts. Examples of atoms or groups constituting salts include alkali metal ions (Li...). + Na + K + (etc.), alkaline earth metal ions (Ca 2+ Mg 2+ (etc.), ammonium ions, imidazolium ions, pyridinium ions, phosphonium ions, etc. As a carboxylic acid amino group, it is formed by -NHCOR X1 The indicated group is preferred. As a sulfonic acid amino group, it is represented by -NHSO 2R X2 The indicated group is preferred. As an imine group, it is represented by -SO 2NHSO 2R X3 -CONHSO 2R X4 -CONHCOR X5 or -SO 2NHCOR X6 The indicated group is preferred, -SO 2NHSO 2R X3 For better. X1 ~R X6 Each can be represented independently as either alkyl or aryl. R X1 ~R X6 The alkyl and aryl groups may have substituents. Halogen atoms are preferred as substituents, and fluorine atoms are even more preferred. Examples of bases include amino groups, pyridyl groups and their salts, ammonium salts, and phthalimide methyl groups. Examples of atoms or groups that constitute salts include hydroxide ions, halide ions, carboxylic acid ions, sulfonic acid ions, and phenoxide ions. Pigment derivatives with excellent visible transparency (hereinafter also referred to as transparent pigment derivatives) can also be used. The maximum molar absorptivity (εmax) of transparent pigment derivatives in the wavelength region of 400–700 nm is 3000 L·mol⁻¹. -1 ・cm -1 The following is preferred, 1000 L·mol -1 ・cm -1 The following is preferred, 100L·mol -1 ・cm -1 The following is a further preferred option. The lower limit of εmax is, for example, 1 L·mol⁻¹. -1 ・cm -1 The above can be 10 L·mol -1 ・cm -1 above. Specific examples of pigment derivatives include compounds described in Japanese Patent Application Publication No. 56-118462, Japanese Patent Application Publication No. 63-264674, Japanese Patent Application Publication No. 01-217077, Japanese Patent Application Publication No. 03-009961, Japanese Patent Application Publication No. 03-026767, Japanese Patent Application Publication No. 03-153780, Japanese Patent Application Publication No. 03-045662, and Japanese Patent Application Publication No. 04-285669. The compounds described in the following publications: Japanese Patent Application Publication No. 06-145546, Japanese Patent Application Publication No. 06-212088, Japanese Patent Application Publication No. 06-240158, Japanese Patent Application Publication No. 10-030063, Japanese Patent Application Publication No. 10-195326, compounds described in paragraphs 0086 to 0098 of International Publication No. 2011 / 024896, and compounds described in paragraphs 0063 to 0094 of International Publication No. 2012 / 102399. Compounds, compounds described in paragraph 0082 of International Publication No. 2017 / 038252, compounds described in paragraph 0171 of Japanese Patent Application Publication No. 2015-151530, compounds described in paragraphs 0162-0183 of Japanese Patent Application Publication No. 2011-252065, compounds described in Japanese Patent Application Publication No. 2003-081972, compounds described in Japanese Patent Application Publication No. 5299151, compounds described in Japanese Patent Application Publication No. 2015-172732, compounds described in Japanese Patent Application Publication No. 2014-199308, and Japanese... The compounds described in Japanese Patent Application Publication No. 2014-085562, the compounds described in Japanese Patent Application Publication No. 2014-035351, the compounds described in Japanese Patent Application Publication No. 2008-081565, the compounds described in Japanese Patent Application Publication No. 2019-109512, the compounds described in Japanese Patent Application Publication No. 2019-133154, the diketopyrrolopyrrole compounds having a thiol linker described in International Publication No. 2020 / 002106, the benzimidazolone compounds described in Japanese Patent Application Publication No. 2018-168244, or salts thereof. Relative to 100 parts by weight of pigment, the content of pigment derivative is preferably 1 to 30 parts by weight, and more preferably 3 to 20 parts by weight. Furthermore, the total content of pigment derivative and colorant in the total solids of the coloring composition is preferably 30% by weight or more, more preferably 35% by weight or more, and more preferably 40% by weight or more. The upper limit is preferably 80% by weight or less, more preferably 70% by weight or less, and more preferably 65% ​​by weight or less. The coloring composition of the present invention may contain only one pigment derivative, or it may contain two or more pigment derivatives. When containing two or more pigment derivatives, the total amount of these is preferably within the above-mentioned range. <<Polyalkylimine>> The coloring composition of the present invention may also contain polyalkylimine. Polyalkylimine is used, for example, as a dispersing agent for pigments. Polyalkylimine refers to a polymer formed by ring-opening polymerization of alkylimine. Polyalkylimine is preferably a polymer having at least a secondary amino group. In addition to secondary amino groups, polyalkylimine may also contain primary or tertiary amino groups. Polyalkylimine is preferably a polymer having a branched structure containing primary, secondary, and tertiary amino groups respectively. The number of carbon atoms in the alkylimine is preferably 2 to 6, more preferably 2 to 4, further preferably 2 or 3, and especially preferably 2. The molecular weight of polyalkylimide is preferably 200 or higher, and more preferably 250 or higher. An upper limit of 100,000 or lower is preferred, 50,000 or lower is even better, 10,000 or lower is further preferred, and 2,000 or lower is especially preferred. Furthermore, regarding the molecular weight of polyalkylimide, when the molecular weight can be calculated from the structural formula, the molecular weight of the polyalkylimide is the value calculated from the structural formula. On the other hand, when the molecular weight of a specific amine compound cannot be calculated from the structural formula or is difficult to calculate, the number-average molecular weight determined by the boiling point rise method is used. Also, when the boiling point rise method is not feasible or difficult to determine, the number-average molecular weight determined by the viscosity method is used. Furthermore, when the viscosity method is not feasible or difficult to determine, the number-average molecular weight of the polystyrene equivalent determined by GPC (gel permeation chromatography) is used. The amine value of polyalkylimide is preferably 5 mmol / g or higher, more preferably 10 mmol / g or higher, and even more preferably 15 mmol / g or higher. Specific examples of polyalkylimides include ethyleneimide, propyleneimide, 1,2-butylimide, and 2,3-butylimide, with ethyleneimide or propyleneimide being preferred, and ethyleneimide being even more preferred. Polyethyleneimide is particularly preferred among polyalkylimides. Furthermore, relative to the total number of primary, secondary, and tertiary amino groups, it is preferable for polyethyleneimide to contain 10 mol% or more of primary amino groups, even more preferable to contain 20 mol% or more of primary amino groups, and further preferable to contain 30 mol% or more of primary amino groups. Commercially available polyethyleneimides include EPOMIN SP-003, SP-006, SP-012, SP-018, SP-200, and P-1000 (all manufactured by NIPPON SHOKUBAI CO., LTD.). The content of polyalkylimide in the total solids of the coloring composition is preferably 0.1 to 5% by mass. A lower limit of 0.2% by mass or more is preferred, 0.5% by mass or more is more preferred, and 1% by mass or more is further preferred. An upper limit of 4.5% by mass or less is preferred, 4% by mass or less is more preferred, and 3% by mass or less is further preferred. Furthermore, relative to 100 parts by mass of pigment, the content of polyalkylimide is preferably 0.5 to 20 parts by mass. A lower limit of 0.6 parts by mass or more is preferred, 1 part by mass or more is more preferred, and 2 parts by mass or more is further preferred. An upper limit of 10 parts by mass or less is preferred, and 8 parts by mass or less is more preferred. Only one type of polyalkylimide may be used, or two or more types may be used. When two or more types are used, the total amount within the above-mentioned range is preferred. <<Curing Accelerator>> The coloring composition of the present invention can contain a curing accelerator. Examples of curing accelerators include thiols, hydroxymethyl compounds, amine compounds, phosphonium salts, amidine salts, amide compounds, alkane-generating agents, isocyanate compounds, alkoxysilane compounds, and onium salts. Specific examples of curing accelerators include compounds described in paragraphs 0094 to 0097 of International Publication No. 2018 / 056189, compounds described in paragraphs 0246 to 0253 of Japanese Patent Application Publication No. 2015-034963, compounds described in paragraphs 0186 to 0251 of Japanese Patent Application Publication No. 2013-041165, and compounds described in Japanese Patent Application Publication No. 2014-055114. The compounds include, but are not limited to, compounds described in paragraphs 0071 to 0080 of Japanese Patent Application Publication No. 2012-150180, alkoxysilane compounds with epoxy groups described in Japanese Patent Application Publication No. 2011-253054, compounds described in paragraphs 0085 to 0092 of Japanese Patent Application No. 5765059, and epoxy curing agents containing carboxyl groups described in Japanese Patent Application Publication No. 2017-036379. The content of the curing accelerator in the total solids of the coloring composition is preferably 0.3 to 8.9% by mass, and more preferably 0.8 to 6.4% by mass. <<Ultraviolet Absorbers>> The coloring composition of the present invention can contain ultraviolet absorbers. Examples of ultraviolet absorbers include conjugated diene compounds, amino diene compounds, salicylate compounds, benzophenone compounds, benzotriazole compounds, acrylonitrile compounds, hydroxyphenyl trioxide compounds, indole compounds, trioxide compounds, and dibenzoxyl compounds. Specific examples of such compounds include those described in Japanese Patent Application Publication No. 2009-217221 (paragraphs 0038-0052), Japanese Patent Application Publication No. 2012-208374 (paragraphs 0052-0072), Japanese Patent Application Publication No. 2013-068814 (paragraphs 0317-0334), Japanese Patent Application Publication No. 2016-162946 (paragraphs 0061-0080), International Publication No. 2021 / 131355 (paragraphs 0052 and 0074), and International Publication No. 2021 / 132247 (paragraphs 0022-0024), the contents of which are incorporated herein by reference. Specific examples of ultraviolet absorbers include compounds with the following structures. Commercially available ultraviolet absorbers include, for example, UV-503 (manufactured by DAITO CHEMICAL CO.,LTD.), the Tinuvin series and Uvinul series manufactured by BASF, and the Sumisorb series manufactured by Sumika Chemtex Company, Limited. Also, as benzotriazole compounds, the MYUA series manufactured by MIYOSHI OIL & FAT CO.,LTD. can be cited (Chemical Industry Daily, February 1, 2016). Furthermore, ultraviolet absorbers can also use compounds described in paragraphs 0049-0059 of Japanese Patent No. 6268967, compounds described in paragraphs 0059-0076 of International Publication No. 2016 / 181987, and thioaryl-substituted benzotriazole type ultraviolet absorbers described in International Publication No. 2020 / 137819. [Chemical Formula 24] The content of ultraviolet absorber in the total solids of the coloring composition is preferably 0.01 to 10% by mass, and more preferably 0.01 to 5% by mass. There may be only one type of ultraviolet absorber, or there may be two or more types. When there are two or more types, the total amount of these absorbers is preferably within the above range. <<Polymerization Inhibitors>> The coloring composition of the present invention can contain polymerization inhibitors. Examples of polymerization inhibitors include hydroquinone, p-methoxyphenol, di- and tri-butyl-p-cresol, gallnutol, tri-butylcatechol, benzoquinone, 4,4'-thiobis(3-methyl-6-tri-butylphenol), 2,2'-methylenebis(4-methyl-6-tri-butylphenol), and N-nitrosophenylhydroxylamine salts (ammonium salts, cerium salts, etc.). Among these, p-methoxyphenol is preferred. The content of polymerization inhibitors in the total solids of the coloring composition is preferably 0.0001 to 5% by mass. There may be only one type of polymerization inhibitor, or there may be two or more types. When there are two or more types, the total amount of these 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 other functional groups. Furthermore, a hydrolyzable group refers to a substituent that directly bonds to a silicon atom and can generate a siloxane bond through at least one of a hydrolysis reaction and a condensation reaction. Examples of hydrolyzable groups include halogen atoms, alkoxy groups, and aceoxy groups, with alkoxy groups being preferred. That is, a silane coupling agent is preferably a compound having an alkoxysilyl group. Furthermore, examples of functional groups other than the hydrolyzable group include vinyl, (meth)allyl, (meth)acrylyl, mercapto, epoxy, oxetyl, amino, urea, thioether, isocyanate, and phenyl groups, with amino, (meth)acrylyl, and epoxy groups being preferred. Specific examples of silane coupling agents include N-β-aminoethyl-γ-aminopropylmethyldimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., trade name KBM-602), N-β-aminoethyl-γ-aminopropyltrimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., trade name KBM-603), N-β-aminoethyl-γ-aminopropyltriethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., trade name KBE-602), γ-aminopropyltrimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., trade name KBM-903), and γ-aminopropyltriethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., trade name KBM-903). (Manufactured by Shin-Etsu Chemical Co., Ltd., trade name KBE-903), 3-methylpropenoxypropylmethyldimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., trade name KBM-502), 3-methylpropenoxypropyltrimethoxysilane (manufactured by Shin-Etsu Chemical Co., Ltd., trade name KBM-503), etc. Specific examples of silane coupling agents include compounds described in paragraphs 0018 to 0036 of Japanese Patent Application Publication No. 2009-288703 and compounds described in paragraphs 0056 to 0066 of Japanese Patent Application Publication No. 2009-242604, the contents of which are incorporated herein by reference. The content of silane coupling agent in the total solids of the coloring composition is preferably 0.01 to 15.0% by mass, and more preferably 0.05 to 10.0% by mass. The silane coupling agent may be of only one type or of two or more types. When there are two or more types, it is preferable that their total amount be within the range described above. <<Surfactants>> The coloring composition of the present invention can contain surfactants. Various surfactants, such as fluorinated surfactants, nonionic surfactants, cationic surfactants, anionic surfactants, and polysiloxane surfactants, can be used as surfactants. Polysiloxane surfactants or fluorinated surfactants are preferred. For information on surfactants, please refer to paragraphs 0238 to 0245 of International Publication No. 2015 / 166779, which is incorporated herein by reference. Examples of fluorinated surfactants include those described in Japanese Patent Application Publication No. 2014-041318 (paragraphs 0060-0064 of the corresponding International Publication No. 2014 / 017669), Japanese Patent Application Publication No. 2011-132503 (paragraphs 0117-0132), and Japanese Patent Application Publication No. 2020-008634, all of which are incorporated herein by reference. Commercially available fluorinated surfactants include, 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-560, 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, R-43, TF-1956, RS-90, R-94, RS-72-K, DS-21 (the above are DIC) FLUORAD FC430, FC431, FC171 (manufactured by Sumitomo 3M Limited), SURFLON S-382, SC-101, SC-103, SC-104, SC-105, SC-1068, SC-381, SC-383, S-393, KH-40 (manufactured by AGC INC.), PolyFox PF636, PF656, PF6320, PF6520, PF7002 (manufactured by OMNOVA SOLUTIONS INC.), Futurgent 208G, 215M, 245F, 601AD, 601ADH2, 602A, 610FM, 710FL, 710FM, 710FS, FTX-218 (manufactured by NEOS COMPANY LIMITED), etc. Fluorinated surfactants can also be used more effectively with acrylic compounds, which have a molecular structure containing functional groups with fluorine atoms, and whose functional groups with fluorine atoms are cleaved upon heating, causing the fluorine atoms to volatilize. Examples of such fluorinated surfactants include the MEGAFACE DS series manufactured by DIC Corporation (Chemical Industry Daily (February 22, 2016), Nikkei Industrial News (February 23, 2016)), such as MEGAFACE DS-21. Fluorinated surfactants are preferably polymers of fluorinated vinyl ether compounds having fluorinated alkyl or fluorinated alkyl ether groups and hydrophilic vinyl ether compounds. Examples of such fluorinated surfactants include those described in Japanese Patent Application Publication No. 2016-216602, the contents of which are incorporated herein by reference. Fluorinated surfactants can also be used with block polymers. Fluorinated surfactants can also preferably use fluorinated polymers containing: repeating units derived from (meth)acrylate compounds having fluorine atoms; and repeating units derived from (meth)acrylate compounds having two or more (preferably five or more) alkoxy groups (preferably ethoxy or propoxy). Furthermore, the fluorinated surfactants described in paragraphs 0016 to 0037 of Japanese Patent Application Publication No. 2010-032698, or the compounds described below, can also be exemplified as fluorinated surfactants used in this invention. [Chemical Formula 25] The weight-average molecular weight of the above compounds is preferably 3,000 to 50,000, for example, 14,000. In the above compounds, the percentage of repeating units is expressed in moles. Furthermore, fluorinated surfactants can also be used on fluoropolymers with ethylene-unsaturated groups on their side chains. Specific examples include compounds described in paragraphs 0050-0090 and 0289-0295 of Japanese Patent Application Publication No. 2010-164965, and MEGAFACE RS-101, RS-102, RS-718K, and RS-72-K manufactured by DIC Corporation. Additionally, compounds described in paragraphs 0015-0158 of Japanese Patent Application Publication No. 2015-117327 can also be used as fluorinated surfactants. Furthermore, from an environmental regulation perspective, it is preferable to use the surfactants described in International Publication No. 2020 / 084854 as substitutes for surfactants with perfluoroalkyl groups having 6 or more carbon atoms. Furthermore, fluoroimidide salt compounds represented by formula (fi-1) are also preferred as surfactants. [Chemical Formula 26] In equation (fi-1), m represents 1 or 2, n represents an integer from 1 to 4, a represents 1 or 2, and X represents... a+ This represents α-valent metal ions, primary ammonium ions, secondary ammonium ions, tertiary ammonium ions, quaternary ammonium ions, or NH4+ ions. 4 + . Examples of nonionic surfactants include glycerol, trimethylolpropane, trimethylolethane, and their ethoxylated and propoxylated derivatives (e.g., glycerol propoxylated, glycerol ethoxylated, etc.), polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene oil ether, polyoxyethylene octylphenyl ether, polyoxyethylene nonylphenyl ether, polyethylene glycol dilaurate, polyethylene glycol distearate, sorbitol fatty acid esters, Pluronic L10, L31, L61, L62, 10R5, 17R2, 25R2 (manufactured by BASF), Tetronic 304, 701, 704, 901, 904, 150R1 (manufactured by BASF), and SOLSPERSE 20000 (Japan Lubrizol). (Manufactured by FUJIFILMWako Pure Chemical Corporation), NCW-101, NCW-1001, NCW-1002 (manufactured by FUJIFILMWako 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 polysiloxane-based surfactants include DOWSIL SH8400, SH8400 FLUID, FZ-2122, 67 Additive, 74 Additive, M Additive, SF 8419 OIL (manufactured by Dow Corning Toray Co., Ltd.), TSF-4300, TSF-4445, TSF-4460, TSF-4452 (manufactured by Momentive Performance Materials Inc.), KP-341, KF-6000, KF-6001, KF-6002, and KF-6003 (manufactured by Shin-Etsu Chemical). BYK-307, BYK-322, BYK-323, BYK-330, BYK-333, BYK-3760, BYK-UV3510 (all manufactured by BYK-Chemie GmbH), etc. Furthermore, polysiloxane surfactants can also utilize compounds with the following structure: [Chemical Formula 27] The content of surfactant in the total solids component of the coloring composition is preferably 0.001% to 5.0% by mass, and more preferably 0.005% to 3.0% by mass. There may be only one type of surfactant, or there may be two or more types. When there are two or more types, the total amount within the above range is preferred. <<Cyclic Silicon Oxide Compounds>> The coloring composition of the present invention can contain cyclic silicon oxide compounds. When the coloring composition of the present invention contains a polysiloxane surfactant, it is preferable that the coloring composition further contains cyclic silicon oxide compounds. By containing cyclic silicon oxide compounds, the film thickness uniformity during coating can be further improved, and a film with excellent surface smoothness can be formed. Here, cyclic silicon oxide compounds refer to cyclic compounds formed by silicon oxide bonds. Cyclic siloxane compounds represented by formula (Si-1) are preferred. [Chemical Formula 28] In equation (Si-1), R 1 and R 2 Each can be used to represent a hydrogen atom or a substituent, and m can be an integer from 3 to 20. R as in equation (Si-1) 1 and R 2 Examples of substituents include alkyl and aryl groups, with alkyl being preferred. The alkyl group preferably has 1 to 10 carbon atoms, more preferably 1 to 5, further preferably 1 to 3, and most preferably 1. The alkyl group can be either straight-chain or branched, but straight-chain is preferred. The aryl group preferably has 6 to 20 carbon atoms, more preferably 6 to 12, and most preferably 6. 1 and R 2 It is preferable that the atoms are hydrogen atoms, methyl or phenyl atoms, and methyl is even better. In formula (Si-1), m represents an integer from 3 to 20, an integer from 3 to 10 is preferred, an integer from 3 to 8 is even better, an integer from 3 to 6 is further preferred, and an integer from 4 to 6 is especially preferred. The molecular weight of the cyclic silicate compound is preferably below 1000, more preferably below 800, and further preferably below 600. The lower limit can be set above 100. Specific examples of cyclic siloxane compounds include octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecylcyclohexasiloxane, and hexamethylcyclotrisiloxane, with at least one selected from octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecylcyclohexasiloxane being preferred. The coloring composition of the present invention may contain only one cyclic silicate compound, but it is preferable to contain two or more cyclic silicate compounds. When containing two or more cyclic silicate compounds, it is preferable to contain compounds of formula (1) with m being 3 or 4 (preferably compounds with m being 4) and compounds of formula (1) with m being an integer of 5 or more (preferably compounds with m being an integer of 5 to 10, more preferably compounds with m being an integer of 5 to 8, and even more preferably compounds with m being 5 or 6). Furthermore, regarding the ratio of compounds in formula (Si-1) where m is an integer of 3 or 4 to compounds in formula (Si-1) where m is an integer of 5 or more, it is preferable that the amount of compounds in formula (Si-1) where m is an integer of 3 or 4 is 10 to 1000 parts by mass relative to 100 parts by mass of compounds in formula (Si-1) where m is an integer of 5 or more, more preferably 25 to 750 parts by mass, and even more preferably 50 to 500 parts by mass. The cyclic silicate compound is preferably selected from at least one of octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecylcyclohexasiloxane, and is even more preferably composed of octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecylcyclohexasiloxane. Furthermore, the cyclic silicate compound is preferably selected from at least one of octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecylcyclohexasiloxane, and is even more preferably composed of octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecylcyclohexasiloxane. When using cyclic siloxane compounds containing octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecylcyclohexasiloxane, the following ratios are preferred: 1 to 100 parts by weight of octamethylcyclotetrasiloxane and 50 to 200 parts by weight of decamethylcyclopentasiloxane relative to 100 parts by weight of dodecylcyclohexasiloxane. More preferably, 10 to 50 parts by weight of octamethylcyclotetrasiloxane relative to 100 parts by weight of dodecylcyclohexasiloxane. More preferably, 1 to 200 parts by weight of decamethylcyclopentasiloxane relative to 100 parts by weight of dodecylcyclohexasiloxane. The content of cyclic siloxanes in the total solids of the coloring composition is preferably 0.001 to 1% by mass, and even more preferably 0.0015 to 0.5% by mass. When the coloring composition contains a polysiloxane surfactant and a cyclic silicate compound, the content of the cyclic silicate compound is preferably 0.01 to 10 parts by weight relative to 100 parts by weight of the polysiloxane surfactant. A lower limit of 0.1 parts by weight or more is preferred, and 0.5 parts by weight or more is more preferred. An upper limit of 5 parts by weight or less is preferred, 4 parts by weight or less is more preferred, and 3 parts by weight or less is further preferred. When the composition of the present invention contains two or more cyclic silicate compounds, the total amount of these compounds is preferably within the above-mentioned range. <<Antioxidants>> The coloring composition of the present invention can contain antioxidants. Examples of antioxidants include phenolic antioxidants, amine antioxidants, phosphorus antioxidants, and sulfur antioxidants. Examples of phenolic antioxidants include hindered phenolic compounds. Phenolic antioxidants are preferably compounds having a substituent at the ortho position adjacent to the phenolic hydroxyl group. As the aforementioned substituent, substituted or unsubstituted alkyl groups having 1 to 22 carbon atoms are preferred. Furthermore, antioxidants containing both a phenolic group and a phosphite group within the same molecule are also preferred. Phosphorus antioxidants are also preferably used as antioxidants. Examples of phosphorus-based antioxidants include tris[2-[[2,4,8,10-tetra(1,1-dimethylethyl)dibenzo[d,f][1,3,2]dioxaphosphonium-heptacyclic-6-yl]oxy]ethyl]amine, tris[2-[(4,6,9,11-tetra-tertiary-butyldibenzo[d,f][1,3,2]dioxaphosphonium-heptacyclic-2-yl)oxy]ethyl]amine, and ethyl bis(2,4-di-tertiary-butyl-6-methylphenyl) phosphite. Commercially available antioxidants include, for example, ADEKA STAB AO-20, ADEKA STAB AO-30, ADEKA STAB AO-40, ADEKA STAB AO-50, ADEKA STAB AO-50F, ADEKA STAB AO-60, ADEKA STAB AO-60G, ADEKA STAB AO-80, and ADEKA STAB AO-330 (all manufactured by ADEKA CORPORATION). Furthermore, antioxidants can also include compounds described in paragraphs 0023-0048 of Japanese Patent No. 6268967, compounds described in International Publication No. 2017 / 006600, compounds described in International Publication No. 2017 / 164024, and compounds described in Korean Patent Publication No. 10-2019-0059371. The antioxidant content in the total solids of the coloring composition is preferably 0.01–20% by mass, and more preferably 0.3–15% by mass. Only one type of antioxidant may be used, or two or more types may be used. When two or more types are used, the total amount within the above range is preferred. <<Other Ingredients>> The coloring composition of the present invention may, as needed, contain sensitizers, curing accelerators, fillers, thermosetting accelerators, plasticizers, and other additives (e.g., conductive particles, defoamers, flame retardants, leveling agents, peeling accelerators, fragrances, surface tension modifiers, chain transfer agents, etc.). By appropriately containing these ingredients, the physical properties of the film can be adjusted. Regarding these ingredients, for example, reference can be made to paragraphs 0183 onwards in Japanese Patent Application Publication No. 2012-003225 (corresponding to paragraph 0237 of U.S. Patent Application Publication No. 2013 / 0034812), and paragraphs 0101-0104, 0107-0109 of Japanese Patent Application Publication No. 2008-250074, the contents of which are incorporated herein by reference. Furthermore, the coloring composition of the present invention may, as needed, contain potential antioxidants. Compounds that act as potential antioxidants include those whose antioxidant sites are protected by a protecting group, and whose antioxidant function is achieved by heating at 100–250°C or at 80–200°C in the presence of an acid / base catalyst, after which the protecting group is removed. Compounds described in International Patent Publication No. 2014 / 021023, International Patent Publication No. 2017 / 030005, and Japanese Patent Application Publication No. 2017-008219 are examples of potential antioxidants. Commercially available products that act as potential antioxidants include ADEKA ARKLS GPA-5001 (manufactured by ADEKA CORPORATION). To adjust the refractive index of the obtained film, the coloring composition of the present invention may contain a metal oxide. Examples of metal oxides include TiO₂. 2. ZrO 2. Al 2O 3. SiO 2. The primary particle size of the metal oxide is preferably 1–100 nm, more preferably 3–70 nm, and further preferably 5–50 nm. The metal oxide can have a core-shell structure. Furthermore, in this case, the core can be hollow. The coloring composition of the present invention may contain a lightfastness modifier. Examples of lightfastness modifiers include compounds described in paragraphs 0036-0037 of Japanese Patent Application Publication No. 2017-198787, compounds described in paragraphs 0029-0034 of Japanese Patent Application Publication No. 2017-146350, compounds described in paragraphs 0036-0037 and 0049-0052 of Japanese Patent Application Publication No. 2017-129774, and compounds described in Japanese Patent Application Publication No. 20... Compounds described in paragraphs 0031-0034 and 0058-0059 of Japanese Patent Application Publication No. 17-129674, compounds described in paragraphs 0036-0037 and 0051-0054 of Japanese Patent Application Publication No. 2017-122803, compounds described in paragraphs 0025-0039 of International Patent Application Publication No. 2017 / 164127, and Japanese Patent Application Publication No. 2017-186546. The compounds described in paragraphs 0034 to 0047 of Japanese Patent Application Publication No. 2015-025116, the compounds described in paragraphs 0019 to 0041 of Japanese Patent Application Publication No. 2012-145604, the compounds described in paragraphs 0101 to 0125 of Japanese Patent Application Publication No. 2012-103475, the compounds described in paragraphs 0018 to 0021 of Japanese Patent Application Publication No. 2011, and the compounds described in Japanese Patent Application Publication No. 2011 The compounds described in paragraphs 0015 to 0018 of Japanese Patent Application Publication No. 257591, the compounds described in paragraphs 0017 to 0021 of Japanese Patent Application Publication No. 2011-191483, the compounds described in paragraphs 0108 to 0116 of Japanese Patent Application Publication No. 2011-145668, and the compounds described in paragraphs 0103 to 0153 of Japanese Patent Application Publication No. 2011-253174, etc. It is also preferable that the coloring composition of the present invention is substantially free of terephthalate. Here, "substantially free" means that the content of terephthalate in the total amount of the coloring composition is less than 1000 ppb by mass, less than 100 ppb by mass is more preferred, and 0 is even more preferred. In the coloring composition of the present invention, it is preferable that the free metal content is 100 ppm or less, and more preferably 50 ppm or less. The type of metal is not particularly limited, and examples include alkali metals, alkaline earth metals, transition metals, Al, Sn, Pb, Bi, etc. Furthermore, it is preferable that the free halogen content is 100 ppm or less, and more preferably 50 ppm or less. Methods for reducing free metals or halogens in the coloring composition include washing with ion-exchanged water, filtration, ultrafiltration, and purification using ion-exchange resins. From an environmental control perspective, the use of perfluoroalkyl sulfonic acids and their salts, as well as perfluoroalkyl carboxylic acids and their salts, is sometimes regulated. In the coloring composition of the present invention, when reducing the content of the above-mentioned compounds, the content of perfluoroalkyl sulfonic acids (especially perfluoroalkyl sulfonic acids with 6 to 8 carbon atoms in the perfluoroalkyl group) and their salts, and perfluoroalkyl carboxylic acids (especially perfluoroalkyl carboxylic acids with 6 to 8 carbon atoms in the perfluoroalkyl group) and their salts, relative to the total solids content of the coloring composition, is 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 can be substantially free of perfluoroalkyl sulfonic acids and their salts, and perfluoroalkyl carboxylic acids and their salts. For example, by using compounds that can replace perfluoroalkyl sulfonic acids and their salts, and compounds that can replace perfluoroalkyl carboxylic acids and their salts, a coloring composition substantially free of perfluoroalkyl sulfonic acids and their salts can be selected. As alternatives to regulated compounds, examples include compounds excluded from regulation due to differences in the number of carbon atoms in the perfluoroalkyl group. However, the above does not preclude the use of perfluoroalkyl sulfonic acids and their salts, or perfluoroalkyl carboxylic acids and their salts. The coloring compositions of the present invention may contain perfluoroalkyl sulfonic acids and their salts, or perfluoroalkyl carboxylic acids and their salts, to the maximum permissible extent. The water content of the coloring composition of the present invention is generally less than 3% by mass, preferably 0.01 to 1.5% by mass, and more preferably 0.1 to 1.0% by mass. The water content can be determined using the Karl Fischer method. The coloring composition of the present invention can be used to adjust the viscosity for purposes such as adjusting film surface (flatness, etc.) and film thickness. The viscosity value can be appropriately selected as needed; for example, 0.3 mPa·s to 50 mPa·s is preferred at 25°C, and 0.5 mPa·s to 20 mPa·s is more preferred. As a method for measuring viscosity, for example, a cone-plate viscometer can be used to perform the measurement at a temperature of 25°C. <<Containing Container>> There are no particular restrictions on the type of container used for containing the coloring composition; known containers can be used. However, for the purpose of preventing impurities from contaminating the raw materials or coloring composition, multi-layered bottles with an inner wall composed of six layers of six different resins, or bottles with a seven-layer structure of the six resins, are preferred. For example, the container described in Japanese Patent Application Publication No. 2015-123351 can be cited as such a container. Furthermore, for the purpose of preventing metal leaching from the inner wall of the container, improving the storage stability of the coloring composition, or inhibiting component deterioration, glass or stainless steel are also preferred. <Preparation Method of Coloring Composition> The coloring composition of the present invention can be prepared by mixing the aforementioned components. When preparing the coloring composition, all components can be dissolved and / or dispersed in a solvent simultaneously to prepare the coloring composition, or, as needed, each component can be appropriately prepared into a solution or dispersion of 2 or more parts, which are then mixed during use (coating) to prepare the composition. When preparing coloring compositions, processes including the dispersion of pigments are preferred. In the process of dispersing pigments, mechanical forces used for dispersing the pigments can include compression, extrusion, impact, shearing, and pitting. Specific examples of such processes include bead milling, sand milling, roller milling, ball milling, coating agitation, microjet milling, high-speed impeller milling, sand mixing, jet mixing, high-pressure wet microparticle formation, and ultrasonic dispersion. Furthermore, when pulverizing pigments in a sand mill (bead mill), it is preferable to perform the process under conditions that improve pulverization efficiency by using small-diameter microbeads and increasing the microbead filling rate. After pulverization, it is preferable to remove coarse particles by filtration, centrifugation, or other methods. Furthermore, regarding the manufacturing process and dispersing equipment for disperse pigments, the processes and dispersing equipment described in "Complete Collection of Dispersion Technology, JOHOKIKO CO.,LTD., July 15, 2005" or "Comprehensive Data Collection on Dispersion Technology and Practical Industrial Applications Centered on Suspension (Solid / Liquid Dispersion Systems), Business Development Center Publishing Department, October 10, 1978" and paragraph 0022 of Japanese Patent Application Publication No. 2015-157893 are preferred. Additionally, in the manufacturing process of disperse pigments, particle refinement can be achieved through a salt milling step. For the materials, equipment, and processing conditions used in the salt milling step, please refer to, for example, Japanese Patent Application Publication Nos. 2015-194521 and 2012-046629. Examples of materials used for dispersing beads include zirconium dioxide, agate, quartz, titanium dioxide, tungsten carbide, silicon nitride, aluminum oxide, stainless steel, and glass. Furthermore, inorganic compounds with a Mohs hardness of 2 or higher can also be used for the beads. The composition may contain 1 to 10,000 ppm of the aforementioned beads. When preparing a coloring composition, it is preferable to filter the coloring composition using a filter for the purpose of removing impurities and reducing defects. As long as the filter is one that has been used for filtration purposes, it can be used without particular restriction. Examples of filters made from materials such as fluoropolymers like polytetrafluoroethylene (PTFE) and polyvinylidene fluoride (PVDF), polyamide resins like nylon (e.g., nylon-6, nylon-6,6), and polyolefin resins like polyethylene and polypropylene (PP) (including high-density and ultra-high molecular weight polyolefin resins) are also acceptable. Among these materials, polypropylene (including high-density polypropylene) and nylon are preferred. A filter pore size of 0.01–7.0 μm is preferred, 0.01–3.0 μm is more preferred, and 0.05–0.5 μm is even more preferred. If the filter pore size is within the above range, fine foreign matter can be removed more effectively. For filter pore size values, refer to the filter manufacturer's specifications. Various filters supplied by Nihon Pall Ltd. (DFA4201NIEY, DFA4201NAEY, DFA4201J006P, etc.), Advantec Toyo Kaisha, Ltd., Nihon Entegris KK (Formerly Nippon Mykrolis Corporation), and KITZ MICROFILTER Corporation can be used. Furthermore, fibrous filter media are preferred as filters. Examples of fibrous filter media include polypropylene fiber, nylon fiber, and glass fiber. Commercially available products include the SBP series (SBP008, etc.), TPR series (TPR002, TPR005, etc.), and SHPX series (SHPX003, etc.) manufactured by ROKI TECHNO CO.,LTD. When using filters, different filters can be combined (e.g., a first filter and a second filter, etc.). In this case, filtration using each filter can be performed only once or more. Furthermore, filters with different pore sizes can be combined within the above-mentioned range. Also, the dispersion can be filtered only with the first filter, and then filtered with the second filter after mixing other components. Furthermore, the filter can be appropriately selected based on the hydrophilicity or hydrophobicity of the coloring composition. <Membrane> The membrane of the present invention is a membrane obtained from the coloring composition of the present invention described above. The membrane of the present invention can be used in filters such as color filters or infrared transmission filters. The film thickness of the membrane of the present invention can be appropriately adjusted according to the purpose. For example, a film thickness of 20 μm or less is preferred, 10 μm or less is more preferred, and 5 μm or less is even more preferred. A lower limit of 0.1 μm or more is preferred, 0.2 μm or more is more preferred, and 0.3 μm or more is even more preferred. When the film of the present invention is used as a color filter, it is preferable that the film has a green, red, blue, cyan, magenta, or yellow hue, and even more preferably, a green, red, or yellow hue. Furthermore, the film of the present invention can be preferably used as a colored pixel in a color filter. Examples of colored pixels include red pixels, green pixels, blue pixels, magenta pixels, cyan pixels, and yellow pixels. When the membrane of the present invention is used as an infrared transmission filter, it is preferable that the membrane of the present invention has any one of the following (1) to (4) spectral characteristics. (1): The maximum transmittance of the membrane in the thickness direction in the wavelength range of 400 to 640 nm is 20% or less (preferably 15% or less, more preferably 10% or less) and the minimum transmittance of the membrane in the thickness direction in the wavelength range of 800 to 1300 nm is 70% or more (preferably 75% or more, more preferably 80% or more). A membrane having such spectral characteristics can block light in the wavelength range of 400 to 640 nm, while allowing light with a wavelength exceeding 700 nm to pass through. (2): A film whose transmittance in the thickness direction is at most 20% (preferably 15% or less, more preferably 10%) in the wavelength range of 400 to 750 nm and at least 70% (preferably 75% or more, more preferably 80% or more) in the wavelength range of 900 to 1300 nm. A film with this spectral dispersive property can block light in the wavelength range of 400 to 750 nm, while allowing light with wavelengths exceeding 850 nm to pass through. (3): A film whose transmittance in the thickness direction is at most 20% (preferably 15% or less, more preferably 10%) in the wavelength range of 400 to 830 nm and at least 70% (preferably 75% or more, more preferably 80% or more) in the wavelength range of 1000 to 1300 nm. A film with this spectral dispersive property can block light in the wavelength range of 400–830 nm, while allowing light with a wavelength exceeding 940 nm to pass through. (4): A film whose maximum transmittance in the thickness direction in the wavelength range of 400–950 nm is 20% or less (preferably 15% or less, more preferably 10% or less) and whose minimum transmittance in the thickness direction in the wavelength range of 1100–1300 nm is 70% or more (preferably 75% or more, more preferably 80% or more). A film with this spectral dispersive property can block light in the wavelength range of 400–950 nm, while allowing light with a wavelength exceeding 1040 nm to pass through. <Pixel Manufacturing Method> A method for manufacturing pixels using the coloring composition of the present invention will be described. The pixel manufacturing method preferably includes the following steps: forming a coloring composition layer on a support using the coloring composition of the present invention; exposing the coloring composition layer in a patterned manner; and developing to remove the unexposed portions of the coloring composition layer to form a pattern (pixel). If necessary, a step of baking the coloring composition layer (pre-baking step) and a step of baking the developed pattern (pixel) can be provided (post-baking step). In the step of forming the color composition layer, the color composition layer of the present invention is formed on a support. There are no particular limitations on the support, and it can be appropriately selected according to the application. For example, glass substrates, silicon substrates, etc., are possible, with silicon substrates being preferred. Furthermore, charge-coupled devices (CCDs), complementary metal-oxide-semiconductor (CMOS) films, transparent conductive films, etc., can also be formed on silicon substrates. Also, sometimes a black matrix is ​​formed on a silicon substrate to isolate each pixel. Furthermore, a base layer for improving adhesion to the upper layer, preventing material diffusion, or planarizing the substrate surface can also be provided on the silicon substrate. Regarding the surface contact angle of the base layer, when measured with diiodomethane, 20–70° is preferred. When measured with water, 30–80° is preferred. As a coating method for the coloring composition, known methods can be used. Examples include drop casting; slot coating; spraying; roller coating; spin coating; cast coating; slot spin coating; pre-wetting (e.g., the method described in Japanese Patent Application Publication No. 2009-145395); inkjet printing (e.g., on-demand, piezoelectric, thermal), nozzle jetting and other ejection systems; flexographic printing; screen printing; gravure printing; reverse offset printing; metal mask printing and other similar methods; transfer printing using molds; nanoimprinting, etc. There are no particular limitations on the application methods in inkjet printing. For example, the methods described in "Expansion and Use of Inkjet Printing - Infinite Possibilities Appearing in Patents - Published February 2005, Sumitbe Techon Research Co., Ltd." (especially pages 115-133) or those described in Japanese Patent Application Publication Nos. 2003-262716, 2003-185831, 2003-261827, 2012-126830, and 2006-169325 can be cited. Furthermore, regarding the coating method of the coloring composition, please refer to International Publication Nos. 2017 / 030174 and 2017 / 018419, the contents of which are incorporated herein by reference. The colored composition layer formed on the support can be dried (pre-baked). When manufacturing the film using a low-temperature process, pre-baking is not necessary. When pre-baking is performed, a pre-baking temperature below 150°C is preferred, below 120°C is more preferred, and below 110°C is even more preferred. The lower limit can be set to, for example, above 50°C, or above 80°C. A pre-baking time of 10–300 seconds is preferred, 40–250 seconds is more preferred, and 80–220 seconds is even more preferred. Pre-baking can be performed using a heating plate, oven, or similar equipment. Next, the coloring composition layer is exposed in a pattern (exposure step). For example, using a stepper or scanning exposure machine, the coloring composition layer is exposed through a mask with a predetermined mask pattern, thereby enabling patterned exposure. This allows the exposed portion to harden. Examples of radiation (light) that can be used during exposure include gamma rays and i-rays. Light with wavelengths below 300 nm can also be used (preferably light with wavelengths of 180–300 nm). Examples of light with wavelengths below 300 nm include KrF rays (wavelength 248 nm) and ArF rays (wavelength 193 nm), with KrF rays (wavelength 248 nm) being preferred. Furthermore, light sources with wavelengths above 300 nm can also be used. Furthermore, during exposure, light can be continuously irradiated for exposure, or pulsed irradiation can be performed for exposure (pulse exposure). In addition, pulse exposure refers to an exposure method in which light is repeatedly irradiated and paused in a short period of time (e.g., less than milliseconds). For example, the exposure dose (irradiation dose) is 0.03–2.5 J / cm². 2 For optimal performance, the concentration is 0.05–1.0 J / cm³. 2 For even better results, the oxygen concentration during exposure can be appropriately selected. Besides exposure under atmospheric conditions, it can be performed in low-oxygen environments (e.g., 15% or 5% by volume, or virtually oxygen-free) or in high-oxygen environments (e.g., 22%, 30%, or 50% by volume) with an oxygen concentration exceeding 21% by volume. Furthermore, the exposure illuminance can be appropriately set, typically selecting 1000 W / m². 2 ~100000W / m 2 (For example, 5000W / m) 2 15000W / m 2 Or 35000W / m 2 The range of oxygen concentration and exposure illuminance can be appropriately combined; for example, it can be set to an oxygen concentration of 10% by volume and an illuminance of 10,000 W / m². 2 The oxygen concentration is 35% by volume and the illuminance is 20,000 W / m². 2 wait. Next, development removes the unexposed portions of the color composition layer to form a pattern (pixels). The unexposed portions of the color composition layer can be removed using a developing solution. In this way, the unexposed portions of the color composition layer from the exposure step dissolve into the developing solution, leaving only the photocured portion. For example, a developing solution temperature of 20–30°C is preferred. A developing time of 20–180 seconds is preferred. Furthermore, to improve residue removal, the process of repeatedly discarding the developing solution every 60 seconds and then supplying fresh developing solution can be repeated several times. Developers can be organic solvents or alkaline developers, with alkaline developers being preferred. An alkaline aqueous solution (alkaline developer) obtained by diluting an alkaline agent with pure water is preferred. Examples of alkaline agents include, for example, ammonia, ethylamine, diethylamine, dimethylethanolamine, diethylene glycolamine, diethanolamine, hydroxylamine, 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, and other organic alkaline compounds, or inorganic alkaline compounds such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium bicarbonate, sodium silicate, and sodium metasilicate. From an environmental and safety perspective, alkaline agents with high molecular weight compounds are preferred. The concentration of the alkaline agent in the alkaline aqueous solution is preferably 0.001 to 10% by mass, and more preferably 0.01 to 1% by mass. Furthermore, the developer may further contain a surfactant. From the viewpoint of ease of transportation and storage, the developer can be prepared as a concentrate and diluted to the required concentration before use. The dilution ratio is not particularly limited, and can be set in the range of 1.5 to 100 times. It is also preferable to rinse (wash) with pure water after development. Furthermore, rinsing is preferably performed as follows: while rotating the support on which the developed colored composition layer has formed, rinsing solution is supplied to the developed colored composition layer. It is also preferable to perform rinsing by moving the nozzle that sprays the rinsing solution from the center of the support to the periphery of the support. In this case, when moving the nozzle from the center of the support to the periphery, the moving speed of the nozzle can be gradually reduced. By rinsing in this way, in-plane unevenness in rinsing can be suppressed. Alternatively, the same effect can be achieved by gradually reducing the rotational speed of the support while moving the nozzle from the center to the periphery of the support. After development, it is preferable to perform additional exposure and heating treatment (post-baking) after drying. This additional exposure and post-baking is a post-development curing process to ensure complete hardening. The heating temperature during post-baking is preferably 100–300°C, and more preferably 200–270°C. To achieve these conditions, heating mechanisms such as heating plates, convection ovens (hot air circulating dryers), or high-frequency heaters can be used to perform post-baking on the developed film continuously or intermittently. When performing additional exposure, it is preferable to use light with a wavelength of 400 nm or less. Furthermore, the additional exposure process can be performed using the method described in Korean Patent Publication No. 10-2017-0122130. <Filter> The filter of the present invention has the film of the present invention as described above. Examples of filters include color filters and infrared transmission filters, with color filters being preferred. It is preferable that the color filter has the film of the present invention as its coloring pixel. In the filter, the film thickness of the membrane of the present invention can be appropriately adjusted according to the purpose. A film thickness of 20 μm or less is preferred, 10 μm or less is more preferred, and 5 μm or less is further preferred. A lower limit of 0.1 μm or more is preferred, 0.2 μm or more is more preferred, and 0.3 μm or more is further preferred. The width of the pixels contained in the filter is preferably 0.4 to 10.0 μm. A lower limit of 0.4 μm or more is preferred, 0.5 μm or more is even more preferred, and 0.6 μm or more is further preferred. An upper limit of 5.0 μm or less is preferred, 2.0 μm or less is even more preferred, 1.0 μm or less is further preferred, and 0.8 μm is even more preferred. Furthermore, the Young's modulus of the pixel is preferably 0.5 to 20 GPa, and 2.5 to 15 GPa is even more preferred. The pixels contained in the filter preferably have high flatness. Specifically, a pixel surface roughness Ra of 100 nm or less is preferred, 40 nm or less is more preferred, and 15 nm or less is even more preferred. There is no specified lower limit, but for example, 0.1 nm or more is preferred. The pixel surface roughness can be measured, for example, using a Veeco Instruments Inc. AFM (Atomic Force Microscope) Dimension 3100. Furthermore, the water contact angle on the pixel can be appropriately set to a preferred value, but typically in the range of 50–110°. The contact angle can be measured, for example, using a contact angle meter CV-DT・A type (manufactured by Kyowa Interface Science Co., Ltd.). Also, a high pixel volume resistivity is preferred. Specifically, a pixel volume resistivity of 10... 9 Ω・cm or higher is preferred, 10 11Ω・cm or higher is preferred. There is no upper limit, but for example, 10 14 Ω・cm or less is preferred. The volume resistivity of a pixel can be measured using an ultra-high resistance meter 5410 (manufactured by Advantest Corporation). In a filter, a protective layer can be provided on the surface of the membrane of the present invention. By providing a protective layer, various functions can be imparted, such as blocking oxidation, reducing reflectivity, hydrophilicity / hydrophobicity, and blocking light of specific wavelengths (ultraviolet, near-infrared, etc.). The thickness of the protective layer is preferably 0.01 to 10 μm, and more preferably 0.1 to 5 μm. Methods for forming the protective layer include methods of coating a composition for forming a protective layer, chemical vapor deposition, and methods of attaching a pre-formed resin with an adhesive material. Examples of components constituting the protective layer include (meth)acrylic resin, olefin-thiol resin, polycarbonate resin, polyether resin, polyaryl ester resin, polyurethane resin, polyether ester resin, polystyrene resin, polyaryl ether phosphine oxide resin, polyimide resin, polyamide-amide resin, polyolefin resin, cyclic olefin resin, polyester resin, styrene resin, polyol resin, polyvinylidene chloride resin, melamine resin, amine ester resin, polyarylamide resin, polyamide resin, alkyd resin, epoxy resin, modified polysiloxane resin, fluoropolymer resin, polyacrylonitrile resin, cellulose resin, Si, C, W, and Al. 2O 3. Mo, SiO 2. Si 2N Grade 4 may contain two or more of these components. For example, in the case of a protective layer intended to prevent oxidation, the protective layer contains polyol resin, SiO2, etc. 2 and Si 2N Option 4 is preferred. Furthermore, in the case of a protective layer intended for low reflectivity, it is preferable that the protective layer contains (meth)acrylic resin and fluoropolymer resin. Depending on the requirements, the protective layer may contain additives such as organic / inorganic microparticles, absorbers for specific wavelengths of light (e.g., ultraviolet, near-infrared, etc.), refractive index modifiers, antioxidants, adhesives, and surfactants. Examples of organic / inorganic microparticles include, for instance, polymeric microparticles (e.g., polysiloxane microparticles, polystyrene microparticles, melamine resin microparticles), titanium dioxide, zinc oxide, zirconium oxide, indium oxide, aluminum oxide, titanium nitride, titanium oxynitride, magnesium fluoride, hollow silica, silicon dioxide, calcium carbonate, and barium sulfate. Known absorbers can be used for the specific wavelengths of light. The content of these additives can be appropriately adjusted, but 0.1–70% by mass relative to the total mass of the protective layer is preferred, and 1–60% by mass is further preferred. Furthermore, as a protective layer, the protective layer described in paragraphs 0073 to 0092 of Japanese Patent Application Publication No. 2017-151176 can also be used. The filter can also have the following structure: each pixel is embedded in a space divided into, for example, a grid by partitions. <Solid-State Imaging Element> The solid-state imaging element of the present invention has the film of the present invention as described above. The structure of the solid-state imaging element is not particularly limited as long as it is a structure that functions as a solid-state imaging element; for example, the following structures can be cited. A solid-state imaging element has the following structure: On a substrate, there are multiple photodiodes constituting the light-receiving area of ​​a solid-state imaging element (CCD (charge-coupled device) image sensor, CMOS (complementary metal oxide semiconductor) image sensor, etc.) and a transmission electrode made of silicon or the like; on the photodiodes and transmission electrodes, there is a light-shielding film with openings only in the light-receiving portion of the photodiodes; on the light-shielding film, there is an element protective film made of silicon nitride or the like, formed to cover the entire light-shielding film and the light-receiving portion of the photodiodes; and on the element protective film, there is a color filter. Furthermore, it can also be a structure with a light-gathering mechanism (e.g., a microlens, etc. hereinafter the same) on the element protective film and below the color filter (closer to the substrate side), or a structure with a light-gathering mechanism on the color filter. Also, the color filter can have a structure in which pixels are embedded in spaces divided into, for example, a grid pattern by partitions. In this case, it is preferable that the refractive index of the partitions is lower than that of each colored pixel. Examples of camera devices with this structure include those described in Japanese Patent Application Publication No. 2012-227478, Japanese Patent Application Publication No. 2014-179577, and International Publication No. 2018 / 043654. Furthermore, as shown in Japanese Patent Application Publication No. 2019-211559, an ultraviolet absorption layer can be provided within the structure of the solid-state camera element to improve lightfastness. Camera devices equipped with the solid-state camera element of the present invention can be used not only in digital cameras or electronic devices with camera functions (such as mobile phones), but also as dashcams or surveillance cameras. <Image Display Device> The image display device of the present invention includes the film of the present invention described above. Examples of image display devices include liquid crystal display devices and organic electroluminescent display devices. Definitions of image display devices and detailed descriptions of various image display devices are described, for example, in "Electronic Display Devices" (by Akio Sasaki, published by Kogyo Chosakai Publishing Co., Ltd., 1990) and "Display Devices" (by Junsho Ibuki, published by Sangyo Tosho Publishing Co., Ltd., 1989). Regarding liquid crystal display devices, for example, they are described in "Next-Generation Liquid Crystal Display Technology" (edited by Tatsuo Uchida, published by Kogyo Chosakai Publishing Co., Ltd., 1994). There are no particular limitations on the liquid crystal display devices to which the present invention can be applied; for example, liquid crystal display devices of various types described in "Next-Generation Liquid Crystal Display Technology" can be applied. [Examples] The present invention will be described in more detail below with examples. The materials, amounts, proportions, processing contents, and processing order shown in the following examples can be appropriately modified without departing from the spirit of the invention. Therefore, the scope of the present invention is not limited to the specific examples shown below. Furthermore, in the structural formulas shown below, Et represents ethyl, and iPr represents isopropyl. <Preparation of the Dispersion> The mixture obtained by mixing the materials listed in the table below was mixed and dispersed for 3 hours using a bead mill (zirconia with a diameter of 0.1 mm). Next, a high-pressure disperser NANO-3000-10 (manufactured by Nippon BEE Co., Ltd.) with a pressure reduction mechanism was used at a pressure of 2000 kg / cm². 2 The dispersion was performed at a flow rate of 500 g / min. This dispersion was repeated 10 times to obtain a dispersion. Furthermore, in the table below, the values ​​listed in the blending amount column are in parts by mass. [Table 1] The materials listed in the table above using abbreviations are as follows. (Colorants) PY139: CI Pigment Yellow 139 PY150: CI Pigment Yellow 150 PY185: CI Pigment Yellow 185 PB15:4: CI Pigment Blue 15:4 PB15:6: CI Pigment Blue 15:6 PG7: CI Pigment Green 7 PG36: CI Pigment Green 36 PG58: CI Pigment Green 58 PG59: CI Pigment Green 59 PR122: CI Pigment Red 122 PR254: CI Pigment Red 254 PR264: CI Pigment Red 264 PR272: CI Pigment Red 272 PR291: CI Pigment Red 291 PV23: CI Pigment Violet 23 (Dispersant) A-1: ​​Resin synthesized by the following method (resin containing alicyclic epoxy groups with polycyclic aliphatic hydrocarbon rings) In a flask equipped with a reflux condenser, dropping funnel, and stirrer, a suitable amount of nitrogen gas was introduced to replace the nitrogen atmosphere, and 340 parts by weight of propylene glycol monomethyl ether acetate (PGMEA) were added, while stirring and heating to 80°C. Then, over 5 hours, 57 parts by weight of acrylic acid and 54 parts by weight of 3,4-epoxy tricyclic [5.2.1.0] were added dropwise. 2,6 ] Decane-8-yl acrylate and 3,4-epoxy tricyclic [5.2.1.0] 2 ， 6 A mixture of decane-9-yl acrylate (containing a molar ratio of 1:1), 239 parts by mass of benzyl methacrylate, and 73 parts by mass of PGMEA was prepared. Next, a solution obtained by dissolving 40 parts by mass of a polymerization initiator (2,2-azobis(2,4-dimethylpentanonitrile)) in 197 parts by mass of PGMEA was added dropwise over 6 hours. After the addition of the polymerization initiator solution was completed, the solution was maintained at 80°C for 3 hours and then cooled to room temperature to obtain a resin with the following structure. The obtained resin had a weight average molecular weight of 9400, a dispersion of 1.89, and an acid value of 114 mg KOH / g. [Chemical Formula 29] A-2: Resins with the following structure (values ​​on the main chain are molar ratios, values ​​on the side chains are the number of repeating units. Weight average molecular weight 24000) [Chemical Formula 30] A-3: Resins with the following structure (values ​​on the main chain are in molar ratios. Weight average molecular weight 11000) [Chemical Formula 31] A-4: Resins with the following structure (values ​​on the main chain are molar ratios, values ​​on the side chains are the number of repeating units. Weight average molecular weight 20,000) [Chemical Formula 32] A-5: Resins with the following structure (values ​​on the main chain are molar ratios, values ​​on the side chains are the number of repeating units. Weight average molecular weight 16000) [Chemical Formula 33] A-6: Resins with the following structure (the values ​​on the side chains indicate the number of repeating units. Weight average molecular weight 20,000) [Chemical Formula 34] A-7: Resins with the following structure (values ​​on the main chain are molar ratios, values ​​on the side chains are the number of repeating units. Weight average molecular weight 20,000) [Chemical Formula 35] A-8: Resins with the following structure (values ​​on the main chain are molar ratios, values ​​on the side chains are the number of repeating units. Weight average molecular weight 7000) [Chemical Formula 36] A-9: A resin synthesized by the following method (a resin with alicyclic epoxy groups). In the synthesis of resin A-1, 3,4-epoxytricyclic [5.2.1.0] is used. 2 ， 6 ] Decane-8-yl acrylate and 3,4-epoxy tricyclic [5.2.1.0] 2 ， 6 The mixture of decane-9-yl acrylate was replaced with methyl 3,4-epoxycyclohexyl methacrylate, and otherwise, a resin with the following structure was obtained by the same method as resin A-1. The weight average molecular weight of the obtained resin was 10,000. [Chemical Formula 37] (Solvent) Z-1: Propylene glycol monomethyl ether acetate (PGMEA) <Preparation of Dye Solutions> Dye solutions X-1 to X-3 were prepared by mixing the materials listed in the table below. Furthermore, in the table below, the values ​​listed in the "Amount of Admixture" column are in parts by mass. [Table 2] The materials listed in the table above using abbreviations are as follows. (Dye) Dye 1: Koyama-kojima dye with the following structure [Chemical Formula 38] Dye 2: Koyama-kojima dye with the following structure [Chemical Formula 39] Dye 3: Koyama-kojima dye with the following structure (weight average molecular weight 10000) [Chemical Formula 40] (Solvent) Z-4: Cyclohexanone <Preparation of the Coloring Composition> The coloring composition was prepared by mixing the raw materials listed in the table below. Furthermore, in the table below, the values ​​listed in the amount of admixture column are in parts by mass. [Table 3] [Table 4] [Table 5] [Table 6] [Table 7] [Table 8] [Table 9] [Table 10] The raw materials listed in the table above using abbreviations are as follows. (Dispersions) DY-1~DY-14: Dispersions DY-1~DY-14 mentioned above DB-1, DB-2: Dispersions DB-1, DB-2 mentioned above DG-1~DG-4: Dispersions DG-1~DG-4 mentioned above DR-1~DR-5: Dispersions DR-1~DR-5 mentioned above DV-1: Dispersion DV-1 mentioned above (Dye solutions) X-1 to X-3: The dye solutions X-1 to X-3 mentioned above. (Adhesive) B-1: A PGMEA solution (solid content concentration 40% by mass) of a resin synthesized by the following method (containing an alicyclic epoxy group with a polycyclic aliphatic hydrocarbon ring). In a 1L flask equipped with a reflux condenser, dropping funnel, and stirrer, a suitable amount of nitrogen gas was introduced to replace the nitrogen atmosphere, and 371 parts by mass of PGMEA were added. The mixture was heated to 85°C while stirring. Then, over 4 hours, 54 parts by mass of acrylic acid, 225 parts by mass of 3,4-epoxy resin, and 54 parts by mass of 0% 3,4-epoxy resin were added dropwise. 2 ， 6A mixture of decane-8 and / or 9-yl acrylate, 81 parts by mass of vinyltoluene (a mixture of isomers), and 80 parts by mass of PGMEA were prepared. Next, a solution obtained by dissolving 30 parts by mass of a polymerization initiator (2,2-azobis(2,4-dimethylpentanonitrile)) in 160 parts by mass of PGMEA was added dropwise over 5 hours. After the addition of the polymerization initiator solution was completed, the solution was maintained at the same temperature for 4 hours, and then cooled to room temperature to obtain the target resin. The obtained resin had a weight average molecular weight of 10600 and a dispersion of 2.01. B-2: A PGMEA solution (40% by mass) of a resin with the following structure (values ​​on the main chain are in molar ratios; weight average molecular weight 11000) [Chemical Formula 41] B-3: A PGMEA solution (40% by mass) of a resin with the following structure (values ​​on the main chain are in molar ratios; weight average molecular weight 30,000) [Chemical Formula 42] B-4: A PGMEA solution (solids concentration 40% by mass) of the following resin structure (values ​​on the main chain are mass percentages; weight average molecular weight 14600) [Chemical Formula 43] B-5: A PGMEA solution (solids concentration 40% by mass) of a resin with the following structure (weight average molecular weight 10600) [Chemical Formula 44] BM: A mixture obtained by mixing equal amounts of the above adhesives B-1 to B-5 (solid component concentration 40% by mass). (Photopolymerization initiator) C-1: Compounds with the following structures (containing hydroxyl oxime compounds) C-2: Compounds with the following structures (containing hydroxyl oxime compounds) C-3: Compounds with the following structures (containing hydroxyl and thioether oxime compounds) C-4: Compounds with the following structures (containing hydroxyl and thioether oxime compounds) C-5: Compounds with the following structures (containing hydroxyl and thioether oxime compounds) C-6: Compounds with the following structures (containing hydroxyl oxime compounds) C-7: Compounds with the following structures (containing hydroxyl and thioether oxime compounds) C-8: Compounds with the following structures (containing hydroxyl and thioether oxime compounds) C-9: Compounds with the following structures (containing hydroxyl and thioether oxime compounds) C-10: Compounds with the following structures (containing hydroxyl oxime compounds) [Chemical Formula 45] C-11~C-14: Compounds with the following structures (excluding hydroxyl oxime compounds) [Chemical Formula 46] C-15: 2,2',4-Tris(2-chlorophenyl)-5-(3,4-dimethoxyphenyl)-4,5-diphenyl-1,1'-bisimidazole; CM: A mixture obtained by mixing equal amounts of the above photopolymerization initiators C-1 to C-10. (Polymerizable compounds) D-1: Compounds with the following structure [Chemical Formula 47] D-2: NK Ester M-DPH-6E (ethoxylated dipentylenetetroxide hexamethacrylate, manufactured by SHIN-NAKAMURA CHEMICAL Co., Ltd.) D-3: A mixture of compounds with the following structure (a mixture of the left-hand compound (a 6-functional (meth)acrylate compound) and the right-hand compound (a 5-functional (meth)acrylate compound) in a molar ratio of 7:3) [Chemical Formula 48] D-4: Compounds with the following structure [Chemical Formula 49] D-5: Trimethylolpropane ethyleneoxy modified triacrylate (manufactured by TOAGOSEI CO., LTD., ARONIX M-350) D-6: EBECRYL80 (manufactured by DAICEL-ALLNEX LTD., an amine-containing 4-functional acrylate) DM: A mixture obtained by mixing equal amounts of the above polymerizable compounds D-1 to D-6 (Additive) E-1: A compound with the following structure (UV absorber) [Chemical Formula 50] E-2: Compounds with the following structure (weight average molecular weight 3500) [Chemical Formula 51] E-3: Compounds with the following structure (weight average molecular weight 2300) [Chemical Formula 52] E-4: Compounds with the following structure (silane coupling agents) [Chemical Formula 53] E-5: 3-Methylpropenoxypropylmethyldimethoxysilane (KBM-502, manufactured by Shin-Etsu Chemical Co., Ltd., silane coupling agent) E-6: 3-Methylpropenoxypropyltrimethoxysilane (KBM-503, manufactured by Shin-Etsu Chemical Co., Ltd., silane coupling agent) E-7: ADEKA STAB AO-80 (manufactured by ADEKA CORPORATION, antioxidant) EM: A mixture obtained by mixing equal amounts of the above compounds E-1 to E-7 (Surfactants) F-1: SH-8400 (manufactured by DuPont Toray Specialty Materials KK, polysiloxane surfactant) F-2: Compounds with the following structure (polysiloxane surfactant, hydroxyl value 62 mgKOH / g). [Chemical Formula 54] F-3: MEGAFACE F-551 (manufactured by DIC Corporation, fluorinated surfactant) F-4: DISPERBYK BYK-330 (manufactured by BYK Corporation, polysiloxane surfactant) F-5: EMULGEN103 (manufactured by Kao Corporation, nonionic surfactant) F-6: A mixture obtained by mixing equal amounts of octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecylcyclohexasiloxane (cyclic siloxane compound) FM: A mixture obtained by mixing equal amounts of the above surfactants F-1 to F-5 (Polymerization inhibitor) G-1: p-Methoxyphenol (Solvents) Z-1: Propylene glycol monomethyl ether acetate (PGMEA) Z-2: Propylene glycol monomethyl ether (PGME) Z-3: Cyclopentanone Z-4: Cyclohexanone Z-5: Anisole Z-6: Diacetone alcohol Z-7: Cyclohexyl acetate Z-8: Propylene glycol diacetate Z-9: 3-Methoxybutanol ZM: Mixture obtained by mixing equal amounts of the above solvents Z-1 to Z-6 <Evaluation of Developing Residue> On a silicon wafer, each coloring composition was coated using a spin coater (manufactured by MIKASA CO., LTD) to achieve a post-baking film thickness of 1.0 μm. Then, the composition layer was obtained by heating at 100°C for 2 minutes using a hot plate. Next, this composition layer was exposed using an i-ray stepper FPA-3000i5+ (manufactured by Canon Inc.) through a mask with a 1 μm square Bayer pattern at 1000 mJ / cm². 2The silicon wafer with the exposed composition layer was exposed to light at a wavelength of 365 nm. Next, the silicon wafer with the exposed composition layer was placed on the horizontal rotating stage of a spin / spray developer (DW-30 type, manufactured by CHEMITRONICS CO., LTD.), and subjected to a 60-second spin-immersion development using a 0.3% by mass aqueous solution of tetramethylammonium hydroxide (TMAH) at 23°C. Afterward, the silicon wafer was fixed to the horizontal rotating stage using a vacuum chuck, and while rotating at 50 rpm, it was rinsed with pure water from a spray nozzle above the center of rotation. The wafer was then heated (post-baked) at 200°C for 5 minutes using a heating plate to form pixels (colored patterns). The unexposed areas between the patterns were observed using a scanning electron microscope (SEM, magnification: 10000), and the development residue was evaluated according to the following evaluation criteria. 5: No residue was found in the unexposed area. 4: In the unexposed area, averaging across 10 locations, one residue with a diameter less than 200 nm was found. 3: In the unexposed area, averaging across 10 locations, 2 to 5 residues with a diameter less than 200 nm were found. 2: In the unexposed area, averaging across 10 locations, 6 or more residues with a diameter less than 200 nm were found. 1: In the unexposed area, residues with a diameter greater than 200 nm were found, or the unexposed area showed almost no dissolution. <Evaluation of Heat Shrinkage Resistance> Pixels (colored patterns) prepared for evaluating developer residue were heated at 260°C for 30 minutes using a heating plate. The film thickness of the pixels before and after heating was measured using a Dektak (manufactured by Bruker), and heat shrinkage resistance was evaluated according to the following criteria. The film thickness of the pixels was the average of 5 samples (pixels). 5: (film thickness of the pixel after heating / film thickness of the pixel before heating) is 0.9 or higher. 4: (film thickness of the pixel after heating / film thickness of the pixel before heating) is 0.88 or higher but less than 0.9. 3: (film thickness of the pixel after heating / film thickness of the pixel before heating) is 0.85 or higher but less than 0.88. 2: (film thickness of the pixel after heating / film thickness of the pixel before heating) is 0.8 or higher but less than 0.85. 1: (film thickness of the pixel after heating / film thickness of the pixel before heating) is less than 0.8. <Evaluation of Moisture Resistance> A constant temperature and humidity test was conducted on pixels (colored patterns) created for evaluating developer residue at 50°C and 85% humidity for 2000 hours. After the constant temperature and humidity test, the cross-sections of the pixels were observed at 40,000x magnification using a transmission electron microscope. The void generation rate of the pixels (number of pixels with voids within the pixel / number of observed pixels) was calculated, and the moisture resistance was evaluated according to the following criteria. Furthermore, cross-sections at 20 randomly selected locations were examined, and the presence or absence of voids was observed in 10 pixels at each cross-section. The void generation rate was calculated by observing the boundaries of a total of 200 locations. Generation rate = Number of pixels with gaps within a pixel / Number of observed pixels. 5: Gap generation rate is 0. 4: Gap generation rate is greater than 0 and less than 0.1. 3: Gap generation rate is greater than 0.1 and less than 0.2. 2: Gap generation rate is greater than 0.2 and less than 0.5. 1: Gap generation rate is greater than 0.5 and less than 1.0. [Table 11] [Table 12] [Table 13] [Table 14] As shown in the table above, the coloring composition of the embodiments has less residue and excellent heat shrinkage resistance and moisture resistance. Furthermore, the surface smoothness of the film formed using the coloring composition of Example 50 is particularly excellent. none

Claims

1. A coloring composition comprising a colorant, a resin, a polymerizable compound, a photopolymerization initiator, and a solvent, wherein the photopolymerization initiator comprises an oxime compound having a hydroxyl group, and the resin comprises a resin having an alicyclic epoxy group.

2. The coloring composition as claimed in claim 1, wherein the aforementioned alicyclic epoxy group is a group having a polycyclic aliphatic hydrocarbon ring.

3. The coloring composition as described in claim 1 or claim 2, wherein the aforementioned polymeric compound contains an alkylene oxide-modified (meth)acrylate compound.

4. The coloring composition as described in claim 1 or claim 2, wherein the aforementioned oxime compound having a hydroxyl group is an oxime compound containing a hydroxyl group and a thioether group.

5. The coloring composition as described in claim 1 or claim 2, wherein the aforementioned photopolymerization initiator further contains a photopolymerization initiator other than the aforementioned oxime compound having a hydroxyl group.

6. The coloring composition as described in claim 1 or claim 2, further comprising a cyclic silicate compound.

7. A membrane obtained using a coloring composition as described in any one of claims 1 to 6.

8. A filter having the membrane described in claim 7.

9. A solid-state imaging element having the film described in claim 7.

10. An image display device having the film described in claim 7.