Active light sensitive or radiation sensitive resin composition, resist film, pattern forming method, method for producing electronic device, and compound

Abstract

Provided are: an active light sensitive or radiation sensitive resin composition which contains a resin and a compound that has a specific structure and an iodine atom; a resist film which is formed using the active light sensitive or radiation sensitive resin composition; a pattern forming method and a method for producing an electronic device, each using the active light sensitive or radiation sensitive resin composition; and a compound which has a specific structure and an iodine atom.

Description

Actinic ray- or radiation-sensitive resin composition, resist film, pattern forming method, electronic device manufacturing method, and compound

[0001] The present invention relates to an actinic ray-sensitive or radiation-sensitive resin composition, a resist film, a pattern forming method, a method for manufacturing an electronic device, and a compound. More specifically, the present invention relates to an actinic ray-sensitive or radiation-sensitive resin composition, a resist film, a pattern forming method, and a method for manufacturing an electronic device that can be suitably used in an ultra-microlithography process applicable to processes for manufacturing VLSI (Large Scale Integration) and high-capacity microchips, processes for creating molds for nanoimprinting, and processes for manufacturing high-density information recording media, as well as other photofabrication processes.

[0002] Conventionally, in the manufacturing process of semiconductor devices such as ICs (Integrated Circuits) and LSIs (Large Scale Integration), microfabrication is performed by lithography using resist compositions. In recent years, with the increasing integration density of integrated circuits, there has been a demand for ultrafine pattern formation in the submicron or quarter-micron range. Accordingly, there has been a trend toward shorter exposure wavelengths, from g-line to i-line and then to KrF excimer laser light, and currently, exposure machines using ArF excimer lasers with a wavelength of 193 nm as a light source have been developed. Furthermore, as a technique for further improving resolution, the so-called immersion method, in which a high refractive index liquid (hereinafter also referred to as "immersion liquid") is filled between the projection lens and the sample, has been developed.

[0003] Currently, in addition to excimer laser light, lithography using electron beams (EB), X-rays, extreme ultraviolet rays (EUV), etc. is also being developed. Accordingly, resist compositions that are effectively sensitive to various types of actinic rays or radiation have been developed.

[0004] Patent Document 1 describes a resist material containing a base polymer and an acid generator containing a sulfonium salt or iodonium salt having a specific structure.

[0005] Japanese Patent Application Publication No. 2018-5224

[0006] Recently, the performance required of resist compositions has been increasing. In particular, when forming a fine pattern (for example, a 1:1 line and space pattern with a line width of 30 nm or less), it is required that the resist composition be capable of forming a pattern with excellent pattern shape (pattern rectangularity). Furthermore, although resist compositions may be stored for a certain period after preparation, even when pattern formation is performed after the resist composition has been stored for a certain period, it is required that the resist composition be capable of forming a pattern with excellent pattern shape (rectangularity) (i.e., excellent stability over time).

[0007] An object of the present invention is to provide an actinic ray-sensitive or radiation-sensitive resin composition that can form a pattern with excellent shape and has excellent stability over time. Another object of the present invention is to provide a resist film formed using the actinic ray-sensitive or radiation-sensitive resin composition, a pattern formation method and an electronic device manufacturing method that use the actinic ray-sensitive or radiation-sensitive resin composition, and a compound that can be used in the actinic ray-sensitive or radiation-sensitive resin composition.

[0008] The present inventors have found that the above problems can be solved by the following configuration.

[0009] [1] An actinic ray-sensitive or radiation-sensitive resin composition containing a compound (N) represented by the following formula (1) and a resin:

[0010]

[0011] In formula (1), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ represents an alkylene group, a cycloalkylene group, or an arylene group, provided that Y １ At least one hydrogen atom of the alkylene group, cycloalkylene group or arylene group represented by X is substituted with at least one atom selected from the group consisting of a fluorine atom and a fluoroalkyl group. １represents a single bond or a divalent linking group. １ and V １ Each independently represents an organic group. １ and V １ may be bonded to form a ring. q represents an integer of 1 or more. M ＋ represents a cation. [2] The actinic ray-sensitive or radiation-sensitive resin composition according to [1], wherein the compound (N) is represented by the following formula (2):

[0012]

[0013] In formula (2), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ Rf each independently represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ When there are a plurality of Rf １ and multiple Rf ２ may be the same or different. p represents an integer of 1 or more. W １ and V １ Each independently represents an organic group. １ and V １ may be bonded to form a ring. q represents an integer of 1 or more. M ＋ represents a cation. [3] The actinic ray-sensitive or radiation-sensitive resin composition according to [1] or [2], wherein the compound (N) is represented by the following formula (3):

[0014]

[0015] In formula (3), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ and Rf ２Rf each independently represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ When there are a plurality of Rf １ and multiple Rf ２ may be the same or different, and p represents an integer of 1 or more. １ represents an organic group. ２ represents a hydrocarbon group. ２ and V １ may be bonded to form a ring. １ represents an organic group having an iodine atom. q1 and q2 each independently represent an integer of 0 or more, provided that at least one of q1 and q2 represents an integer of 1 or more. P １ represents an organic group having no iodine atom; q3 represents an integer of 0 or more; M ＋ represents a cation. [4] W in the above formula (3) ２ and V １ [5] The actinic ray-sensitive or radiation-sensitive resin composition according to [3], wherein W in the formula (3) is bonded to form a ring. ２ [6] The actinic ray-sensitive or radiation-sensitive resin composition according to any one of [3] to [5], wherein R in formula (3) represents a saturated hydrocarbon group or an aromatic hydrocarbon group. [7] The actinic ray-sensitive or radiation-sensitive resin composition according to any one of [3] to [5], wherein R in formula (3) represents an integer of 1 or more. １ At least one of the groups is -CO-O-R ２ , —O—CO—R ２ , -O-CO-OR ２ , -SO ２ -R ２ or -SO ３ -R ２ represents R ２ [8] The actinic ray-sensitive or radiation-sensitive resin composition according to any one of [3] to [6], wherein Z in the formula (1) represents an organic group having an iodine atom. １ Ga-SO ３ －[9] The actinic ray-sensitive or radiation-sensitive resin composition according to any one of [1] to [7], wherein p in the above formula (2) represents an integer of 1 to 3.

[10] The actinic ray-sensitive or radiation-sensitive resin composition according to any one of [1] to [9], wherein compound (N) is represented by the following formula (4):

[0016]

[0017] In formula (4), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ Rf each independently represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ When there are a plurality of Rf １ and multiple Rf ２ may be the same or different. p represents an integer of 1 or more. K １ represents a ring containing a nitrogen atom as a ring member. １ represents a single bond or a divalent linking group. １ represents an aromatic group. １ represents an organic group having an iodine atom. １ represents an organic group that does not contain an iodine atom. １ and Ar １ may be bonded to form a ring. q4 represents an integer of 1 or more. q5 and q6 each independently represent an integer of 0 or more. M ＋ represents a cation.

[11] M in the above formula (1) ＋

[12] The actinic ray-sensitive or radiation-sensitive resin composition according to any one of [1] to

[10] , wherein M in the formula (1) represents a sulfonium cation or an iodonium cation. ＋

[13] The actinic ray-sensitive or radiation-sensitive resin composition according to any one of [1] to

[12] , wherein W in formula (1) represents a sulfonium cation having one or more fluorine atoms or an iodonium cation having one or more fluorine atoms.

[14] The actinic ray-sensitive or radiation-sensitive resin composition according to any one of [1] to

[13] , wherein q in formula (1) represents an integer of 3 or more.

[15] The actinic ray-sensitive or radiation-sensitive resin composition according to any one of [1] to

[15] , wherein W in formula (1) represents a sulfonium cation having one or more fluorine atoms or an iodonium cation having one or more fluorine atoms. １ has an aromatic group having three or more iodine atoms bonded to the same aromatic ring.

[15] A resist film formed using the actinic ray-sensitive or radiation-sensitive resin composition according to any one of [1] to

[14] .

[16] A pattern forming method comprising the steps of forming a resist film on a substrate using the actinic ray-sensitive or radiation-sensitive resin composition according to any one of [1] to

[14] , exposing the resist film to light, and developing the exposed resist film using a developer.

[17] A method for manufacturing an electronic device, comprising the pattern forming method according to

[16] .

[18] A compound represented by the following formula (3):

[0018]

[0019] In formula (3), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ Rf each independently represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ When there are a plurality of Rf １ and multiple Rf ２ may be the same or different, and p represents an integer of 1 or more. １ represents an organic group. ２ represents a hydrocarbon group. ２ and V １ may be bonded to form a ring. １represents an organic group having an iodine atom. q1 and q2 each independently represent an integer of 0 or more, provided that at least one of q1 and q2 represents an integer of 1 or more. P １ represents an organic group having no iodine atom; q3 represents an integer of 0 or more; M ＋ represents a cation.

[19] W in the above formula (3) ２ and V １ and are bonded to form a ring.

[20] The compound according to

[18] or

[19] , wherein the compound is a compound represented by the following formula (4):

[0020]

[0021] In formula (4), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ Rf each independently represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ When there are a plurality of Rf １ and multiple Rf ２ may be the same or different. p represents an integer of 1 or more. K １ represents a ring containing a nitrogen atom as a ring member. １ represents a single bond or a divalent linking group. １ represents an aromatic group. １ represents an organic group having an iodine atom. １ represents an organic group that does not contain an iodine atom. １ and Ar １ may be bonded to form a ring. q4 represents an integer of 1 or more. q5 and q6 each independently represent an integer of 0 or more. M ＋ represents a cation.

[0022] The present invention provides an actinic ray-sensitive or radiation-sensitive resin composition that can form a pattern with excellent shape and has excellent stability over time. The present invention also provides a resist film formed using the actinic ray-sensitive or radiation-sensitive resin composition, a pattern formation method and an electronic device production method that use the actinic ray-sensitive or radiation-sensitive resin composition, and a compound that can be used in the actinic ray-sensitive or radiation-sensitive resin composition.

[0023] The present invention will be described in detail below. The following description of the components will be based on representative embodiments of the present invention, but the present invention is not limited to such embodiments.

[0024] In this specification, "actinic rays" or "radiation" refers to, for example, the bright line spectrum of a mercury lamp, far ultraviolet rays typified by excimer lasers, extreme ultraviolet rays (EUV), X-rays, soft X-rays, and electron beams (EB). In this specification, "light" refers to actinic rays or radiation. Unless otherwise specified, in this specification, "exposure" includes not only exposure using the bright line spectrum of a mercury lamp, far ultraviolet rays typified by excimer lasers, extreme ultraviolet rays, X-rays, and EUV, but also drawing using particle beams such as electron beams and ion beams. In this specification, the word "to" is used to mean that the numerical values ​​before and after it are included as the lower and upper limits.

[0025] In this specification, (meth)acrylate refers to at least one of acrylate and methacrylate, and (meth)acrylic acid refers to at least one of acrylic acid and methacrylic acid.

[0026] In this specification, the weight average molecular weight (Mw), number average molecular weight (Mn), and dispersity (also referred to as molecular weight distribution) (Mw / Mn) of a resin are defined as polystyrene-equivalent values ​​measured by gel permeation chromatography (GPC) using a GPC apparatus (HLC-8120GPC manufactured by Tosoh Corporation) (solvent: tetrahydrofuran, flow rate (sample injection amount): 10 μL, column: TSK gel Multipore HXL-M manufactured by Tosoh Corporation, column temperature: 40° C., flow rate: 1.0 mL / min, detector: differential refractive index detector).

[0027] In the description of groups (atomic groups) in this specification, unless contrary to the spirit of the present invention, notations that do not specify whether they are substituted or unsubstituted include groups that contain a substituent as well as groups that do not have a substituent. For example, the term "alkyl group" includes not only alkyl groups that do not have a substituent (unsubstituted alkyl groups) but also alkyl groups that have a substituent (substituted alkyl groups). Furthermore, the term "organic group" in this specification refers to a group containing at least one carbon atom. Unless otherwise specified, a monovalent substituent is preferred as the substituent. Examples of the substituent include monovalent non-metallic atomic groups excluding hydrogen atoms, which can be selected, for example, from the following substituents T:

[0028] (Substituent T) Examples of the substituent T include halogen atoms such as a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom; alkoxy groups such as a methoxy group, an ethoxy group, and a tert-butoxy group; a cycloalkyloxy group; an aryloxy group such as a phenoxy group and a p-tolyloxy group; an alkoxycarbonyl group such as a methoxycarbonyl group and a butoxycarbonyl group; a cycloalkyloxycarbonyl group; an aryloxycarbonyl group such as a phenoxycarbonyl group; an acyloxy group such as an acetoxy group, a propionyloxy group, and a benzoyloxy group; an acetyl group, a benzoyl group, an isobutyryl group, Examples of the substituent T include acyl groups such as acryloyl, methacryloyl, and methoxalyl; sulfanyl groups; alkylsulfanyl groups such as methylsulfanyl and tert-butylsulfanyl; arylsulfanyl groups such as phenylsulfanyl and p-tolylsulfanyl; alkyl groups; alkenyl groups; cycloalkyl groups; aryl groups; aromatic heterocyclic groups; hydroxy groups; carboxyl groups; formyl groups; sulfo groups; cyano groups; alkylaminocarbonyl groups; arylaminocarbonyl groups; sulfonamide groups; silyl groups; amino groups; carbamoyl groups; etc. In addition, when these substituents can further have one or more substituents, examples of the substituent T also include groups having one or more substituents selected from the above-mentioned substituents as the further substituents (for example, monoalkylamino groups, dialkylamino groups, arylamino groups, trifluoromethyl groups, etc.).

[0029] In this specification, the bonding direction of a divalent group is not limited unless otherwise specified. For example, when Y is -COO- in a compound represented by the formula "X-Y-Z", Y may be -CO-O- or -O-CO-. The compound may be either "X-CO-O-Z" or "X-O-CO-Z".

[0030] In this specification, the acid dissociation constant (pKa) refers to the pKa in an aqueous solution, and specifically, is a value determined by calculation using the following software package 1 based on a database of Hammett's substituent constants and known literature values. All pKa values ​​described in this specification are values ​​determined by calculation using this software package. Software package 1: Advanced Chemistry Development (ACD / Labs) Software V8.14 for Solaris (1994-2007 ACD / Labs).

[0031] The pKa can also be calculated by molecular orbital calculation. A specific method for this is to calculate the pKa of H in an aqueous solution based on the thermodynamic cycle. ＋ One method is to calculate the dissociation free energy. ＋ The dissociation free energy can be calculated by, for example, DFT (density functional theory), but various other methods have been reported in the literature, and the method is not limited to these. There are several software programs that can perform DFT, and Gaussian 16 is an example.

[0032] In this specification, pKa refers to a value calculated based on a database of Hammett's substituent constants and publicly known literature values ​​using software package 1, as described above, but if pKa cannot be calculated by this method, a value obtained by Gaussian 16 based on DFT (density functional theory) will be adopted. In this specification, pKa refers to "pKa in aqueous solution" as described above, but if pKa in aqueous solution cannot be calculated, "pKa in dimethyl sulfoxide (DMSO) solution" will be adopted.

[0033] In this specification, the term "solid content" refers to components that form a film (preferably a resist film) formed using the actinic ray-sensitive or radiation-sensitive resin composition, and does not include solvents. Furthermore, any component that forms a film (preferably a resist film) formed using the actinic ray-sensitive or radiation-sensitive resin composition is considered to be a solid content even if it is in a liquid state.

[0034] <Actinic ray-sensitive or radiation-sensitive resin composition> The actinic ray-sensitive or radiation-sensitive resin composition of the present invention (also referred to as "the composition of the present invention") is an actinic ray-sensitive or radiation-sensitive resin composition containing a compound (N) represented by the following formula (1) and a resin:

[0035]

[0036] In formula (1), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ represents an alkylene group, a cycloalkylene group, or an arylene group, provided that Y １ At least one hydrogen atom of the alkylene group, cycloalkylene group or arylene group represented by X is substituted with at least one atom selected from the group consisting of a fluorine atom and a fluoroalkyl group. １ represents a single bond or a divalent linking group. １ and V １ Each independently represents an organic group. １ and V １ may be bonded to form a ring. q represents an integer of 1 or more. M ＋ represents a cation.

[0037] The mechanism by which the composition of the present invention can form a pattern with an excellent shape and has excellent stability over time is not clear, but the inventors have hypothesized it as follows. However, the present invention is not limited in any way by the hypothesized mechanism below. Compound (N) contained in the composition of the present invention has a sulfonamide group. Sulfonamide groups tend to interact with resins. This interaction is thought to be based on the polarity of the sulfonamide group. This is thought to suppress acid diffusion and improve (rectangularize) the pattern shape. Furthermore, compound (N) contained in the composition of the present invention has an iodine atom. Iodine atoms have hydrophobic properties, so they have low affinity with other components and tend to aggregate over time. However, compound (N) having a sulfonamide group is thought to alleviate aggregation and significantly improve stability over time.

[0038] The composition of the present invention is typically a resist composition and may be a positive resist composition or a negative resist composition. The composition of the present invention may be a resist composition for alkali development or a resist composition for organic solvent development. The composition of the present invention may be a chemically amplified resist composition or a non-chemically amplified resist composition. The composition of the present invention is preferably a chemically amplified resist composition. An actinic ray-sensitive or radiation-sensitive film can be formed using the composition of the present invention. The actinic ray-sensitive or radiation-sensitive film formed using the composition of the present invention is typically a resist film.

[0039] First, the various components of the composition of the present invention will be described in detail below.

[0040] [Compound (N)] The composition of the present invention contains compound (N) (also simply referred to as "compound (N)") represented by formula (1). Compound (N) is preferably a compound that generates an acid upon irradiation with actinic rays or radiation (a photoacid generator). When compound (N) is a photoacid generator, the pKa of the acid (generated acid) generated from compound (N) upon irradiation with actinic rays or radiation is preferably -2 or less, more preferably -3 or less, and even more preferably -3.4 or less. Furthermore, the pKa of the generated acid is preferably -12 or more, more preferably -11 or more, and even more preferably -10 or more.

[0041] In formula (1), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ represents -Rf. Rf represents a fluorine atom or a fluoroalkyl group. The fluoroalkyl group represented by Rf is an alkyl group having at least one fluorine atom. The fluoroalkyl group may be linear or branched. The number of carbon atoms in the fluoroalkyl group is not particularly limited, and for example, it is preferably a fluoroalkyl group having 1 to 20 carbon atoms, more preferably a fluoroalkyl group having 1 to 15 carbon atoms, even more preferably a fluoroalkyl group having 1 to 10 carbon atoms, and particularly preferably a fluoroalkyl group having 1 to 6 carbon atoms. The fluoroalkyl group represented by Rf is not particularly limited as long as it is an alkyl group having at least one fluorine atom, but a preferred embodiment is a perfluoroalkyl group. The fluoroalkyl group represented by Rf may have a substituent other than a fluorine atom. Rf preferably represents a fluoroalkyl group, and particularly preferably represents a trifluoromethyl group. Z １ Ha-SO ３ － It is preferred that

[0042] In formula (1), Y １ represents an alkylene group, a cycloalkylene group, or an arylene group. １The alkylene group represented by the formula (I) may be linear or branched. The number of carbon atoms in the alkylene group is not particularly limited, and preferably has 1 to 12 carbon atoms, more preferably has 1 to 8 carbon atoms, and further preferably has 1 to 5 carbon atoms. Y １ The cycloalkylene group represented by the formula (I) may be monocyclic or polycyclic. The number of carbon atoms in the cycloalkylene group is not particularly limited, and preferably has 3 to 20 carbon atoms, more preferably has 4 to 12 carbon atoms, and even more preferably has 5 to 10 carbon atoms. Y １ The arylene group represented by the formula (I) may be monocyclic or polycyclic. The number of carbon atoms in the arylene group is not particularly limited, and for example, the number of carbon atoms is preferably 6 to 20, more preferably 6 to 12, and even more preferably 6 to 10.

[0043] Y １ At least one hydrogen atom of the alkylene group, cycloalkylene group or arylene group represented by Y is substituted with at least one atom selected from the group consisting of a fluorine atom and a fluoroalkyl group. １ When Y is substituted with a fluoroalkyl group, the description, specific examples, and preferred range of the fluoroalkyl group are the same as those of the fluoroalkyl group represented by Rf described above. １ The alkylene group, cycloalkylene group or arylene group represented by Y may have a substituent other than a fluorine atom or a fluoroalkyl group. １ The number of fluorine atoms contained in Y is not particularly limited as long as it is 1 or more, but is preferably 2 to 10, and more preferably 2 to 8. １ preferably represents a perfluoroalkylene group, a perfluorocycloalkylene group or a perfluoroarylene group.

[0044] In formula (1), X １ represents a single bond or a divalent linking group. １Examples of the divalent linking group represented by the formula (I) include -CO-, -O-, -COO-, -S-, -SO-, hydrocarbon groups (e.g., alkylene groups, cycloalkylene groups, alkenylene groups, arylene groups, etc.), and linking groups formed by linking a plurality of these groups. The hydrocarbon group may have a substituent. An alkylene group, which is an example of a hydrocarbon group, may be linear or branched. The number of carbon atoms in the alkylene group is not particularly limited, but is preferably 1 to 10, and more preferably 1 to 6. A cycloalkylene group, which is an example of a hydrocarbon group, may be monocyclic or polycyclic. The number of carbon atoms in the cycloalkylene group is not particularly limited, but is preferably 3 to 20, more preferably 4 to 12, and even more preferably 5 to 10. An alkenylene group, which is an example of a hydrocarbon group, may be linear or branched. The number of carbon atoms in the alkenylene group is not particularly limited, but is preferably 2 to 10, and more preferably 2 to 6. An arylene group, which is an example of a hydrocarbon group, may be monocyclic or polycyclic. The number of carbon atoms in the arylene group is not particularly limited, but is preferably 6 to 20, more preferably 6 to 12, and even more preferably 6 to 10.

[0045] In formula (1), W １ represents an organic group. １ The organic group represented by W is not particularly limited. １ The number of carbon atoms in the organic group represented by the formula (I) is preferably 1 to 100, more preferably 3 to 70, and even more preferably 5 to 50. １ The organic group represented by the formula (I) is preferably a hydrocarbon group or a heterocyclic group. The hydrocarbon group is not particularly limited, and examples thereof include an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, and an aryl group. The hydrocarbon group and the heterocyclic group may have a substituent. In addition, W １ The organic group represented by the formula (I) may be a group in which at least two groups selected from hydrocarbon groups (e.g., alkyl groups, alkenyl groups, alkynyl groups, cycloalkyl groups, and aryl groups) and heterocyclic groups are bonded together via a direct bond or a linking group. １The organic group represented by the formula (I) is preferably a group having at least one aromatic ring. The aromatic ring may be an aromatic hydrocarbon ring or an aromatic hetero ring, but is preferably an aromatic hydrocarbon ring. The number of carbon atoms in the aromatic hydrocarbon ring is preferably 6 to 20, more preferably 6 to 15, and even more preferably 6 to 10. The aromatic hetero ring preferably contains at least one heteroatom selected from the group consisting of a nitrogen atom, an oxygen atom, and a sulfur atom as a ring member. The number of ring atoms in the aromatic hetero ring is not particularly limited, but is preferably 3 to 30, and more preferably 4 to 20. The number of carbon atoms in the aromatic hetero ring is not particularly limited, but is preferably 2 to 20, and more preferably 3 to 15. W １ The organic group represented by the formula (I) may have a substituent other than an iodine atom. １ When the organic group represented by the formula (I) is a group having an aromatic ring, the iodine atom may be bonded to the aromatic ring, or the iodine atom may be bonded to a substituent bonded to the aromatic ring. １ Preferably, the aromatic group has three or more iodine atoms bonded to the same aromatic ring.

[0046] In formula (1), V １ represents an organic group. １ The organic group represented by the formula V is not particularly limited. １ The number of carbon atoms in the organic group represented by the formula (V) is preferably 1 to 50, more preferably 1 to 30, and even more preferably 1 to 10. １ The organic group represented by the formula (I) is preferably a hydrocarbon group which may have a substituent. The hydrocarbon group is not particularly limited, and examples thereof include an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, and an aryl group, and is preferably an alkyl group.

[0047] W １ and V １ may be bonded to form a ring, W １ and V １ and preferably bond to form a ring.

[0048] In formula (1), q represents an integer of 1 or more, preferably an integer of 2 or more, and more preferably an integer of 3 or more. Furthermore, q preferably represents an integer of 20 or less, more preferably an integer of 10 or less, and even more preferably an integer of 8 or less.

[0049] In formula (1), M ＋ represents a cation, preferably an organic cation, more preferably a sulfonium cation or an iodonium cation. ＋ The cation represented by formula (ZaI) is not particularly limited. The valence of the cation may be monovalent or divalent or higher. As the cation, a cation represented by formula (ZaI) below (hereinafter also referred to as "cation (ZaI)") or a cation represented by formula (ZaII) below (hereinafter also referred to as "cation (ZaII)") is preferred.

[0050]

[0051] In the above formula (ZaI), R ２０１ , R ２０２ and R ２０３ R each independently represents an organic group. ２０１ , R ２０２ and R ２０３ The number of carbon atoms in the organic group represented by R is preferably 1 to 30, and more preferably 1 to 20. ２０１ ~R ２０３ Two of these may be bonded to form a ring structure, and the ring may contain an oxygen atom, a sulfur atom, an ester group, an amide group, or a carbonyl group. ２０１ ~R ２０３ Examples of groups formed by combining two of these include alkylene groups (e.g., butylene and pentylene groups) and —CH ２ -CH ２ -O-CH ２ -CH ２ - are listed.

[0052] Suitable embodiments of the organic cation in formula (ZaI) include cation (ZaI-1), cation (ZaI-2), cation (ZaI-3b), and cation (ZaI-4b) described below.

[0053] First, the cation (ZaI-1) will be described. The cation (ZaI-1) is R in the above formula (ZaI). ２０１ ~R ２０３ is an arylsulfonium cation, in which at least one of R is an aryl group. ２０１ ~R ２０３ may all be aryl groups, or R ２０１ ~R ２０３ A part of R may be an aryl group, and the rest may be an alkyl group or a cycloalkyl group. ２０１ ~R ２０３ is an aryl group, and R ２０１ ~R ２０３ The remaining two of R may be bonded to form a ring structure, and the ring may contain an oxygen atom, a sulfur atom, an ester group, an amide group, or a carbonyl group. ２０１ ~R ２０３ Examples of groups formed by combining two of the above include alkylene groups in which one or more methylene groups may be substituted with an oxygen atom, a sulfur atom, an ester group, an amide group, and / or a carbonyl group (e.g., butylene group, pentylene group, and —CH ２ -CH ２ -O-CH ２ -CH ２ The arylsulfonium cations include triarylsulfonium cations, diarylalkylsulfonium cations, aryldialkylsulfonium cations, diarylcycloalkylsulfonium cations, and aryldicycloalkylsulfonium cations.

[0054] The aryl group contained in the arylsulfonium cation is preferably a phenyl group or a naphthyl group, and more preferably a phenyl group. The aryl group may be an aryl group having a heterocyclic structure containing an oxygen atom, a nitrogen atom, or a sulfur atom. Examples of heterocyclic structures include pyrrole residues, furan residues, thiophene residues, indole residues, benzofuran residues, and benzothiophene residues. When the arylsulfonium cation has two or more aryl groups, the two or more aryl groups may be the same or different. The alkyl group or cycloalkyl group optionally contained in the arylsulfonium cation is preferably a linear alkyl group having 1 to 15 carbon atoms, a branched alkyl group having 3 to 15 carbon atoms, or a cycloalkyl group having 3 to 15 carbon atoms, and more preferably a methyl group, an ethyl group, a propyl group, an n-butyl group, a sec-butyl group, a t-butyl group, a cyclopropyl group, a cyclobutyl group, or a cyclohexyl group.

[0055] R ２０１ ~R ２０３ Preferred substituents that the aryl group, alkyl group, and cycloalkyl group may have include alkyl groups (e.g., having 1 to 15 carbon atoms), cycloalkyl groups (e.g., having 3 to 15 carbon atoms), aryl groups (e.g., having 6 to 14 carbon atoms), alkoxy groups (e.g., having 1 to 15 carbon atoms), cycloalkylalkoxy groups (e.g., having 1 to 15 carbon atoms), halogen atoms other than fluorine atoms (e.g., chlorine atoms, bromine atoms, iodine atoms), hydroxyl groups, carboxyl groups, ester groups, sulfinyl groups, sulfonyl groups, alkylthio groups, and phenylthio groups. The above substituents may further have substituents, if possible. It is also preferred that the above substituents form an acid-decomposable group in any combination.

[0056] Next, the cation (ZaI-2) will be described. The cation (ZaI-2) is a cation represented by the formula (ZaI) R ２０１ ~R ２０３ are each independently a cation representing an organic group that does not have an aromatic ring. The aromatic ring also includes an aromatic ring containing a heteroatom. ２０１ ~R ２０３The number of carbon atoms of the organic group not having an aromatic ring as R is preferably 1 to 30, and more preferably 1 to 20. ２０１ ~R ２０３ are each independently preferably an alkyl group, a cycloalkyl group, an allyl group, or a vinyl group, more preferably a linear or branched 2-oxoalkyl group, a 2-oxocycloalkyl group, or an alkoxycarbonylmethyl group, and still more preferably a linear or branched 2-oxoalkyl group.

[0057] R ２０１ ~R ２０３ Examples of the alkyl group and cycloalkyl group in R include linear alkyl groups having 1 to 10 carbon atoms or branched alkyl groups having 3 to 10 carbon atoms (e.g., methyl, ethyl, propyl, butyl, and pentyl groups), and cycloalkyl groups having 3 to 10 carbon atoms (e.g., cyclopentyl, cyclohexyl, and norbornyl groups). ２０１ ~R ２０３ may be further substituted with a halogen atom other than a fluorine atom, an alkoxy group (for example, having 1 to 5 carbon atoms), a hydroxyl group, a cyano group, or a nitro group. ２０１ ~R ２０３ It is also preferred that the substituents independently form an acid-decomposable group by any combination of the substituents.

[0058] Next, the cation (ZaI-3b) will be described. The cation (ZaI-3b) is a cation represented by the following formula (ZaI-3b).

[0059]

[0060] In formula (ZaI-3b), R １ｃ ~R ５ｃ R each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an alkoxy group, an aryloxy group, an alkoxycarbonyl group, an alkylcarbonyloxy group, a cycloalkylcarbonyloxy group, a halogen atom other than a fluorine atom, a hydroxyl group, a nitro group, an alkylthio group, or an arylthio group. ６ｃ and R ７ｃR each independently represents a hydrogen atom, an alkyl group (for example, a t-butyl group), a cycloalkyl group, a halogen atom other than a fluorine atom, a cyano group, or an aryl group. ｘ and R ｙ R each independently represents an alkyl group, a cycloalkyl group, a 2-oxoalkyl group, a 2-oxocycloalkyl group, an alkoxycarbonylalkyl group, an allyl group, or a vinyl group. １ｃ ~R ７ｃ , and R ｘ and R ｙ It is also preferred that the substituents independently form an acid-decomposable group by any combination of the substituents.

[0061] R １ｃ ~R ５ｃ Two or more of the following, R ５ｃ and R ６ｃ , R ６ｃ and R ７ｃ , R ５ｃ and R ｘ , and R ｘ and R ｙ may be bonded to each other to form a ring, and each of these rings may independently contain an oxygen atom, a sulfur atom, a ketone group, an ester bond, or an amide bond. Examples of the ring include aromatic or non-aromatic hydrocarbon rings, aromatic or non-aromatic heterocycles, and polycyclic fused rings formed by combining two or more of these rings. Examples of the ring include 3- to 10-membered rings, preferably 4- to 8-membered rings, and more preferably 5- or 6-membered rings.

[0062] R １ｃ ~R ５ｃ Two or more of the following, R ６ｃ and R ７ｃ , and R ｘ and R ｙ Examples of the group formed by bonding of R include alkylene groups such as butylene and pentylene. A methylene group in this alkylene group may be substituted with a heteroatom such as an oxygen atom. ５ｃ and R ６ｃ , and R ５ｃ and R ｘThe group formed by bonding is preferably a single bond or an alkylene group. Examples of the alkylene group include a methylene group and an ethylene group.

[0063] R １ｃ ~R ５ｃ , R ６ｃ , R ７ｃ , R ｘ , R ｙ , and R １ｃ ~R ５ｃ Two or more of the following, R ５ｃ and R ６ｃ , R ６ｃ and R ７ｃ , R ５ｃ and R ｘ , and R ｘ and R ｙ The ring formed by bonding together may have a substituent.

[0064] Next, the cation (ZaI-4b) will be described. The cation (ZaI-4b) is a cation represented by the following formula (ZaI-4b).

[0065]

[0066] In formula (ZaI-4b), l represents an integer of 0 to 2, and r represents an integer of 0 to 8. １３ represents a hydrogen atom, a halogen atom other than a fluorine atom (for example, a chlorine atom, a bromine atom, or an iodine atom), a hydroxyl group, an alkyl group, a halogenated alkyl group other than a fluorine atom, an alkoxy group, a carboxyl group, an alkoxycarbonyl group, or a group containing a cycloalkyl group (which may be a cycloalkyl group itself or a group containing a cycloalkyl group as a part). These groups may have a substituent. R １４ represents a hydroxyl group, a halogen atom other than a fluorine atom (for example, a chlorine atom, a bromine atom, or an iodine atom), an alkyl group, a halogenated alkyl group other than a fluorine atom, an alkoxy group, an alkoxycarbonyl group, an alkylcarbonyl group, an alkylsulfonyl group, a cycloalkylsulfonyl group, or a group containing a cycloalkyl group (which may be a cycloalkyl group itself or a group containing a cycloalkyl group as a part). These groups may have a substituent. R １４When a plurality of R are present, each independently represents the above group such as a hydroxyl group. １５ each independently represents an alkyl group, a cycloalkyl group, or a naphthyl group. １５ may be bonded to each other to form a ring. １５ When two R are bonded to each other to form a ring, the ring skeleton may contain a heteroatom such as an oxygen atom or a nitrogen atom. １５ are preferably alkylene groups and bonded to each other to form a ring structure. １５ The ring formed by bonding together may have a substituent.

[0067] In formula (ZaI-4b), R １３ , R １４ , and R １５ The alkyl group in R may be linear or branched. The number of carbon atoms in the alkyl group is preferably 1 to 10. The alkyl group is preferably a methyl group, an ethyl group, an n-butyl group, a t-butyl group, or the like. １３ ~R １５ , and R ｘ and R ｙ It is also preferred that each of the substituents independently form an acid-decomposable group by any combination of the substituents.

[0068] Next, formula (ZaII) will be described. In formula (ZaII), R ２０４ and R ２０５ R each independently represents an aryl group, an alkyl group, or a cycloalkyl group. ２０４ and R ２０５ The aryl group in R is preferably a phenyl group or a naphthyl group, and more preferably a phenyl group. ２０４ and R ２０５ The aryl group in R may be an aryl group having a heterocycle containing an oxygen atom, a nitrogen atom, a sulfur atom, or the like. Examples of the skeleton of the aryl group having a heterocycle include pyrrole, furan, thiophene, indole, benzofuran, and benzothiophene. ２０４ and R ２０５The alkyl group and cycloalkyl group are preferably a linear alkyl group having 1 to 10 carbon atoms or a branched alkyl group having 3 to 10 carbon atoms (e.g., methyl, ethyl, propyl, butyl, or pentyl), or a cycloalkyl group having 3 to 10 carbon atoms (e.g., cyclopentyl, cyclohexyl, or norbornyl).

[0069] R ２０４ and R ２０５ The aryl group, alkyl group, and cycloalkyl group in R may each independently have a substituent. ２０４ and R ２０５ Examples of the substituent that the aryl group, alkyl group, and cycloalkyl group may have include an alkyl group (e.g., having 1 to 15 carbon atoms), a cycloalkyl group (e.g., having 3 to 15 carbon atoms), an aryl group (e.g., having 6 to 15 carbon atoms), an alkoxy group (e.g., having 1 to 15 carbon atoms), a halogen atom other than a fluorine atom, a hydroxyl group, and a phenylthio group. ２０４ and R ２０５ It is also preferred that the substituents independently form an acid-decomposable group by any combination of the substituents.

[0070] M ＋preferably represents a sulfonium cation having one or more fluorine atoms or an iodonium cation having one or more fluorine atoms. Examples of sulfonium cations having one or more fluorine atoms include sulfonium cations having at least one selected from the group consisting of fluorine atoms and fluoroalkyl groups. The fluoroalkyl group is an alkyl group having at least one fluorine atom and may be linear or branched. The number of carbon atoms in the fluoroalkyl group is not particularly limited, and for example, a fluoroalkyl group having 1 to 20 carbon atoms is preferred, a fluoroalkyl group having 1 to 15 carbon atoms is more preferred, a fluoroalkyl group having 1 to 10 carbon atoms is even more preferred, and a fluoroalkyl group having 1 to 6 carbon atoms is particularly preferred. The fluoroalkyl group may be a perfluoroalkyl group. Examples of iodonium cations having one or more fluorine atoms include iodonium cations having at least one selected from the group consisting of fluorine atoms and fluoroalkyl groups. The fluoroalkyl group is an alkyl group having at least one fluorine atom and may be linear or branched. The number of carbon atoms in the fluoroalkyl group is not particularly limited, and for example, it is preferably a fluoroalkyl group having 1 to 20 carbon atoms, more preferably a fluoroalkyl group having 1 to 15 carbon atoms, even more preferably a fluoroalkyl group having 1 to 10 carbon atoms, and particularly preferably a fluoroalkyl group having 1 to 6 carbon atoms. The fluoroalkyl group may be a perfluoroalkyl group.

[0071] Below is M ＋ Specific examples of the cation represented by the formula (I) are shown below, but the present invention is not limited thereto.

[0072]

[0073]

[0074] The compound (N) is preferably represented by the following formula (2).

[0075]

[0076] In formula (2), Z １ Ha-SO ３－ or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ Rf each independently represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ When there are a plurality of Rf １ and multiple Rf ２ may be the same or different. p represents an integer of 1 or more. W １ and V １ Each independently represents an organic group. １ and V １ may be bonded to form a ring. q represents an integer of 1 or more. M ＋ represents a cation.

[0077] Z in formula (2) １ , Rf, W １ , V １ , q and M ＋ The explanation, specific examples and preferred ranges of Z in the above formula (1) are １ , Rf, W １ , V １ , q and M ＋ It is the same as in

[0078] In formula (2), Rf １ and Rf ２ Rf each independently represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ When there are a plurality of Rf １ and multiple Rf ２ may be the same or different. １ and Rf ２ The explanation, specific examples, and preferred ranges for the fluoroalkyl group (an alkyl group having at least one fluorine atom) represented by the formula (I) are the same as those for the fluoroalkyl group represented by Rf described above. １ and Rf ２ preferably represents a fluorine atom.

[0079] In formula (2), p represents an integer of 1 or more, preferably an integer of 1 to 10, more preferably an integer of 1 to 6, and even more preferably an integer of 1 to 3.

[0080] The compound (N) is preferably represented by the following formula (3).

[0081]

[0082] In formula (3), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ Rf each independently represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ When there are a plurality of Rf １ and multiple Rf ２ may be the same or different, and p represents an integer of 1 or more. １ represents an organic group. ２ represents a hydrocarbon group. ２ and V １ may be bonded to form a ring. １ represents an organic group having an iodine atom. q1 and q2 each independently represent an integer of 0 or more, provided that at least one of q1 and q2 represents an integer of 1 or more. P １ represents an organic group having no iodine atom; q3 represents an integer of 0 or more; M ＋ represents a cation.

[0083] Z in formula (3) １ , Rf, V １ and M ＋ The explanation, specific examples and preferred ranges of Z in the above formula (1) are １ , Rf, V １ and M ＋ It is the same as in

[0084] Rf in formula (3) １ , Rf ２The description, specific examples and preferred ranges of p and p are respectively based on Rf in formula (2) described above. １ , Rf ２ and the same as in p.

[0085] In formula (3), W ２ represents a hydrocarbon group. ２ The hydrocarbon group represented by the formula (I) is preferably a saturated hydrocarbon group or an aromatic hydrocarbon group. The saturated hydrocarbon group may be linear, branched, or cyclic. The saturated hydrocarbon group is preferably an alkyl group, a cycloalkyl group, or an alkyl group substituted with a cycloalkyl group. The saturated hydrocarbon group preferably has 1 to 15 carbon atoms, more preferably 1 to 10 carbon atoms. The aromatic hydrocarbon group (aryl group) preferably has 6 to 15 carbon atoms, more preferably 6 to 10 carbon atoms. The aromatic hydrocarbon group is preferably a phenyl group, a naphthyl group, or an anthryl group, more preferably a phenyl group or a naphthyl group, and particularly preferably a phenyl group.

[0086] W in formula (3) ２ and V １ and preferably bond to form a ring.

[0087] In formula (3), R １ represents an organic group having an iodine atom. １ The organic group represented by R is not particularly limited except that it has an iodine atom (i.e., is substituted with an iodine atom). １ The number of carbon atoms in the organic group represented by R is preferably 1 to 50, more preferably 1 to 40, and even more preferably 1 to 30. １ The organic group represented by may have a substituent other than an iodine atom. １ The organic group represented by R is preferably a hydrocarbon group or a heterocyclic group. The hydrocarbon group is not particularly limited, and examples thereof include an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, and an aryl group. The hydrocarbon group and the heterocyclic group may have a substituent. １The organic group represented by may or may not have an aromatic ring. The aromatic ring may be an aromatic hydrocarbon ring or an aromatic hetero ring, but is preferably an aromatic hydrocarbon ring. The number of carbon atoms in the aromatic hydrocarbon ring is preferably 6 to 20, more preferably 6 to 15, and even more preferably 6 to 10. The aromatic hetero ring preferably contains at least one hetero atom selected from the group consisting of a nitrogen atom, an oxygen atom, and a sulfur atom as a ring member. The number of ring atoms in the aromatic hetero ring is not particularly limited, but is preferably 3 to 30, and more preferably 4 to 20. The number of carbon atoms in the aromatic hetero ring is not particularly limited, but is preferably 2 to 20, and more preferably 3 to 15. R １ A preferred embodiment of the organic group represented by R １ In this embodiment, the organic group represented by the formula (I) does not have an aromatic ring.

[0088] R １ The number of iodine atoms contained in the organic group represented by the formula (I) is 1 or more, preferably 1 to 8, more preferably 1 to 6, and even more preferably 1 to 4.

[0089] When q2 in formula (3) represents an integer of 1 or more, R １ At least one of is -O-R ２ , -CO-O-R ２ , —O—CO—R ２ , -O-CO-OR ２ , -SO ２ -R ２ or -SO ３ -R ２ Preferably, it represents —CO—O—R ２ , —O—CO—R ２ , -O-CO-OR ２ , -SO ２ -R ２ or -SO ３ -R ２ More preferably, it represents —CO—O—R ２ , —O—CO—R ２ or -O-CO-O-R ２ It is more preferable that R ２ represents an organic group having an iodine atom. ２The organic group represented by R is not particularly limited except that it has an iodine atom (i.e., is substituted with an iodine atom). ２ The number of carbon atoms in the organic group represented by R is preferably 1 to 40, more preferably 1 to 30, and even more preferably 1 to 20. ２ Examples of the organic group represented by R include an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, an aryl group, and a group formed by combining two or more of these groups. ２ The organic group represented by the formula (I) is preferably an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, an aryl group, or a group formed by combining two or more of these, and more preferably an alkyl group, a cycloalkyl group, an aryl group, or a group formed by combining two or more of these.

[0090] R ２ When the organic group represented by R ２ When the organic group represented by the formula (I) contains an alkyl group, the alkyl group may be linear or branched. The number of carbon atoms in the alkyl group is not particularly limited, and is, for example, preferably 1 to 20, more preferably 1 to 15, and even more preferably 1 to 10. The alkyl group may have a substituent other than an iodine atom. The alkyl group may also contain an ether bond (—O—) in the chain. Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a t-butyl group, a pentyl group, a neopentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, an undecyl group, a dodecyl group, a tridecyl group, a tetradecyl group, a pentadecyl group, a hexadecyl group, a heptadecyl group, an octadecyl group, a nonadecyl group, and an eicosyl group.

[0091] R ２ When the organic group represented by R ２When the organic group represented by the formula (I) contains an alkenyl group, the alkenyl group may be linear or branched. The number of carbon atoms in the alkenyl group is not particularly limited, and is preferably 2 to 20, more preferably 2 to 15, and even more preferably 2 to 10. The alkenyl group may have a substituent other than an iodine atom. The alkenyl group may also contain an ether bond in the chain. Examples of the alkenyl group include a vinyl group and an allyl group.

[0092] R ２ When the organic group represented by R ２ When the organic group represented by the formula (I) contains an alkynyl group, the alkynyl group may be linear or branched. The number of carbon atoms in the alkynyl group is not particularly limited, and is preferably 2 to 20, more preferably 2 to 15, and even more preferably 2 to 10. The alkynyl group may have a substituent other than an iodine atom. Furthermore, the alkynyl group may contain an ether bond in the chain. Examples of the alkynyl group include an ethynyl group.

[0093] R ２ When the organic group represented by R ２ When the organic group represented by the formula (I) contains a cycloalkyl group, the cycloalkyl group may be monocyclic or polycyclic. The number of carbon atoms in the cycloalkyl group is not particularly limited, and is preferably 3 to 20, more preferably 4 to 15, and even more preferably 5 to 10. The cycloalkyl group may have a substituent other than an iodine atom. In the cycloalkyl group, for example, one of the methylene groups constituting the ring may be replaced with a heteroatom such as an oxygen atom, a group containing a heteroatom such as a carbonyl group, or a vinylidene group. In addition, in the cycloalkyl group, one or more of the ethylene groups constituting the cycloalkane ring may be replaced with a vinylene group. Examples of the cycloalkyl group include a cyclopentyl group, a cyclohexyl group, a norbornyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, and an adamantyl group.

[0094] R ２ When the organic group represented by R ２When the organic group represented by the formula (I) contains an aryl group, the number of carbon atoms in the aryl group is not particularly limited, and is, for example, preferably 6 to 20, more preferably 6 to 15, and even more preferably 6 to 10. The aryl group may have a substituent other than an iodine atom. Examples of the aryl group include a phenyl group, a naphthyl group, and an anthryl group.

[0095] R ２ The number of iodine atoms contained in the organic group represented by the formula (I) is 1 or more, preferably 1 to 8, more preferably 1 to 5, and even more preferably 1 to 4.

[0096] In formula (3), q1 and q2 each independently represent an integer of 0 or greater. However, at least one of q1 and q2 represents an integer of 1 or greater. q1 more preferably represents an integer of 0 to 8, even more preferably represents an integer of 0 to 5, and particularly preferably represents an integer of 0 to 4. q2 preferably represents an integer of 1 or greater, more preferably represents an integer of 1 to 8, even more preferably represents an integer of 1 to 5, and particularly preferably represents an integer of 1 to 3.

[0097] In formula (3), P １ represents an organic group that does not contain an iodine atom. １ The number of carbon atoms in the organic group represented by the formula (I) is preferably 1 to 50, more preferably 1 to 40, and even more preferably 1 to 30. １ The organic group represented by the formula (I) may have a substituent other than an iodine atom. １ The organic group represented by the formula (I) is preferably a hydrocarbon group or a heterocyclic group. The hydrocarbon group is not particularly limited, and examples thereof include an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, and an aryl group. The hydrocarbon group and the heterocyclic group may have a substituent. １The organic group represented by may or may not have an aromatic ring. The aromatic ring may be an aromatic hydrocarbon ring or an aromatic hetero ring, but is preferably an aromatic hydrocarbon ring. The number of carbon atoms in the aromatic hydrocarbon ring is preferably 6 to 20, more preferably 6 to 15, and even more preferably 6 to 10. The aromatic hetero ring preferably contains at least one hetero atom selected from the group consisting of a nitrogen atom, an oxygen atom, and a sulfur atom as a ring member. The number of ring atoms in the aromatic hetero ring is not particularly limited, but is preferably 3 to 30, and more preferably 4 to 20. The number of carbon atoms in the aromatic hetero ring is not particularly limited, but is preferably 2 to 20, and more preferably 3 to 15. P １ It is preferable that the organic group represented by the formula (I) does not have an aromatic ring.

[0098] When q3 in formula (3) represents an integer of 1 or more, P １ At least one of is -O-P ２ , -CO-O-P ２ , —O—CO—P ２ , -O-CO-O-P ２ , -SO ２ -P ２ or -SO ３ -P ２ Preferably, it represents -CO-O-P ２ , —O—CO—P ２ , -O-CO-O-P ２ , -SO ２ -P ２ or -SO ３ -P ２ More preferably, it represents -CO-O-P ２ , —O—CO—P ２ or -O-CO-O-P ２ It is more preferred that P ２ represents an organic group that does not contain an iodine atom. ２ The number of carbon atoms in the organic group represented by P is preferably 1 to 40, more preferably 1 to 30, and even more preferably 1 to 20. ２ Examples of the organic group represented by the formula (I) include an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, an aryl group, and a group formed by combining two or more of these groups. ２The organic group represented by the formula (I) is preferably an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, or a group formed by combining two or more of these, and more preferably an alkyl group, a cycloalkyl group, or a group formed by combining two or more of these.

[0099] P ２ When the organic group represented by P ２ When the organic group represented by the formula (I) contains an alkyl group, the alkyl group may be linear or branched. The number of carbon atoms in the alkyl group is not particularly limited, and is, for example, preferably 1 to 20, more preferably 1 to 15, and even more preferably 1 to 10. The alkyl group may have a substituent other than an iodine atom. The alkyl group may also contain an ether bond (—O—) in the chain. Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a t-butyl group, a pentyl group, a neopentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, an undecyl group, a dodecyl group, a tridecyl group, a tetradecyl group, a pentadecyl group, a hexadecyl group, a heptadecyl group, an octadecyl group, a nonadecyl group, and an eicosyl group.

[0100] P ２ When the organic group represented by P is an alkenyl group, ２ When the organic group represented by the formula (I) contains an alkenyl group, the alkenyl group may be linear or branched. The number of carbon atoms in the alkenyl group is not particularly limited, and is preferably 2 to 20, more preferably 2 to 15, and even more preferably 2 to 10. The alkenyl group may have a substituent other than an iodine atom. The alkenyl group may also contain an ether bond in the chain. Examples of the alkenyl group include a vinyl group and an allyl group.

[0101] P ２ When the organic group represented by P is an alkynyl group, ２When the organic group represented by the formula (I) contains an alkynyl group, the alkynyl group may be linear or branched. The number of carbon atoms in the alkynyl group is not particularly limited, and is preferably 2 to 20, more preferably 2 to 15, and even more preferably 2 to 10. The alkynyl group may have a substituent other than an iodine atom. Furthermore, the alkynyl group may contain an ether bond in the chain. Examples of the alkynyl group include an ethynyl group.

[0102] P ２ When the organic group represented by P ２ When the organic group represented by the formula (I) contains a cycloalkyl group, the cycloalkyl group may be monocyclic or polycyclic. The number of carbon atoms in the cycloalkyl group is not particularly limited, and is preferably 3 to 20, more preferably 4 to 15, and even more preferably 5 to 10. The cycloalkyl group may have a substituent other than an iodine atom. In the cycloalkyl group, for example, one of the methylene groups constituting the ring may be replaced with a heteroatom such as an oxygen atom, a group containing a heteroatom such as a carbonyl group, or a vinylidene group. In addition, in the cycloalkyl group, one or more of the ethylene groups constituting the cycloalkane ring may be replaced with a vinylene group. Examples of the cycloalkyl group include a cyclopentyl group, a cyclohexyl group, a norbornyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, and an adamantyl group.

[0103] P ２ When the organic group represented by ２ When the organic group represented by the formula (I) contains an aryl group, the number of carbon atoms in the aryl group is not particularly limited, and is, for example, preferably 6 to 20, more preferably 6 to 15, and even more preferably 6 to 10. The aryl group may have a substituent other than an iodine atom. Examples of the aryl group include a phenyl group, a naphthyl group, and an anthryl group.

[0104] In formula (3), q3 represents an integer of 0 or more, more preferably an integer of 0 to 8, even more preferably an integer of 0 to 5, and particularly preferably an integer of 0 to 3.

[0105] The compound (N) is preferably represented by the following formula (4).

[0106]

[0107] In formula (4), Z １ Ha-SO ３ － or -SO ２ -N － -SO ２ -Rf represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ Rf each independently represents a fluorine atom or a fluoroalkyl group. １ and Rf ２ When there are a plurality of Rf １ and multiple Rf ２ may be the same or different. p represents an integer of 1 or more. K １ represents a ring containing a nitrogen atom as a ring member. １ represents a single bond or a divalent linking group. １ represents an aromatic group. １ represents an organic group having an iodine atom. １ represents an organic group that does not contain an iodine atom. １ and Ar １ may be bonded to form a ring. q4 represents an integer of 1 or more. q5 and q6 each independently represent an integer of 0 or more. M ＋ represents a cation.

[0108] Z in formula (4) １ , Rf and M ＋ The explanation, specific examples and preferred ranges of Z in the above formula (1) are １ , Rf and M ＋ It is the same as in

[0109] Rf in formula (4) １ , Rf ２ The description, specific examples and preferred ranges of p and p are respectively based on Rf in formula (2) described above. １ , Rf ２ and the same as in p.

[0110] R in formula (4) １ and P １The explanation, specific examples and preferred ranges of R in the above formula (3) are as follows: １ and P １ It is the same as in

[0111] In formula (4), K １ is a ring containing a nitrogen atom as a ring member ("ring K"). １ ") Ring K １ may be a monocyclic or polycyclic ring. １ is preferably a ring having 3 to 20 ring atoms, more preferably a ring having 4 to 15 ring atoms, even more preferably a ring having 5 to 10 ring atoms, and particularly preferably a 5- or 6-membered ring. １ Preferably, the ring K contains at least one atom selected from a carbon atom, an oxygen atom, and a sulfur atom in addition to a nitrogen atom, and more preferably contains a carbon atom. １ may be an aromatic ring or a non-aromatic ring, but is preferably a non-aromatic ring (alicyclic ring). １ When is a non-aromatic ring, ring K １ may or may not contain an unsaturated bond in the ring.

[0112] In formula (4), L １ represents a single bond or a divalent linking group. １ Examples of the divalent linking group represented by the formula (I) include -CO-, -O-, -COO-, -S-, -SO-, hydrocarbon groups (e.g., alkylene groups, cycloalkylene groups, alkenylene groups, arylene groups, etc.), and linking groups in which a plurality of these groups are linked together. The hydrocarbon group may have a substituent. When the hydrocarbon group has a substituent, the substituent may be Ar １and may bond to form a ring. An alkylene group, which is an example of a hydrocarbon group, may be linear or branched. The number of carbon atoms in the alkylene group is not particularly limited, but is preferably 1 to 10, and more preferably 1 to 6. A cycloalkylene group, which is an example of a hydrocarbon group, may be monocyclic or polycyclic. The number of carbon atoms in the cycloalkylene group is not particularly limited, but is preferably 3 to 20, more preferably 4 to 12, and even more preferably 5 to 10. An alkenylene group, which is an example of a hydrocarbon group, may be linear or branched. The number of carbon atoms in the alkenylene group is not particularly limited, but is preferably 2 to 10, and more preferably 2 to 6. An arylene group, which is an example of a hydrocarbon group, may be monocyclic or polycyclic. The number of carbon atoms in the arylene group is not particularly limited, but is preferably 6 to 20, more preferably 6 to 12, and even more preferably 6 to 10. L １ The divalent linking group represented by the formula (I) is preferably —CO—, —O—, —COO—, an alkylene group, or a linking group in which a plurality of these groups are linked together, more preferably —CO—, —O—, or —COO—, and even more preferably —COO—.

[0113] In formula (4), Ar １ represents an aromatic group. １ The aromatic group represented by Ar may be an aromatic hydrocarbon group (aryl group) or an aromatic heterocyclic group. １ The aromatic group represented by the formula (I) may have a substituent other than an iodine atom. １ When Ar represents an aryl group, the aryl group is preferably an aryl group having 6 to 30 carbon atoms, more preferably an aryl group having 6 to 20 carbon atoms, still more preferably a phenyl group, a naphthyl group or an anthryl group, particularly preferably a phenyl group or a naphthyl group, and most preferably a phenyl group. １When Ar represents an aromatic heterocyclic group, it is preferable that the aromatic heterocyclic group contains at least one heteroatom selected from the group consisting of a nitrogen atom, an oxygen atom, and a sulfur atom as a ring member. The number of ring atoms in the aromatic heterocyclic group is not particularly limited, but is preferably 3 to 30, more preferably 4 to 20. The number of carbon atoms in the aromatic heterocyclic group is not particularly limited, but is preferably 2 to 20, more preferably 3 to 15. １ The aromatic group represented by the formula (I) may be a fused ring group having a structure in which at least one of the aromatic hydrocarbon ring and the aromatic heterocycle is fused with at least one selected from the group consisting of cycloalkanes (for example, monocyclic or polycyclic cycloalkanes having 3 to 12 carbon atoms such as cyclopentane and cyclohexane), cycloalkenes (for example, monocyclic or polycyclic cycloalkenes having 3 to 12 carbon atoms such as cyclohexene), and non-aromatic heterocyclic compounds (for example, five-membered ring non-aromatic heterocyclic compounds such as pyrrolidine, pyrroline, 2-oxazolidone, tetrahydrofuran, and tetrahydrothiophene, and six-membered ring non-aromatic heterocyclic compounds such as morpholine, piperidine, piperazine, tetrahydropyran, and 1,4-dioxane). １ preferably represents an aryl group.

[0114] In formula (4), q4 represents an integer of 1 or greater, preferably an integer of 2 or greater, and more preferably an integer of 3 or greater. Furthermore, q4 preferably represents an integer of 10 or less, and more preferably an integer of 8 or less. In formula (4), q5 and q6 each independently represent an integer of 0 or greater, preferably an integer of 0 to 8, more preferably an integer of 0 to 5, and particularly preferably an integer of 0 to 3.

[0115] The molecular weight of the compound (N) is preferably 600 or more, more preferably 700 or more, and even more preferably 800 or more. The molecular weight of the compound (N) is preferably 2,300 or less, more preferably 2,000 or less, and even more preferably 1,800 or less.

[0116] Compound (N) can be synthesized by a known method, and a synthesis example of compound (N) will be described in the Examples below.

[0117] Specific examples of compound (N) include, but are not limited to, (I)-1 to (I)-21 used in the examples described below.

[0118] The content of compound (N) in the composition of the present invention is not particularly limited, but is preferably 1% by mass or more, more preferably 5% by mass or more, and even more preferably 10% by mass or more, based on the total solid content of the composition of the present invention. Furthermore, the content of compound (N) is preferably 50% by mass or less, more preferably 45% by mass or less, and even more preferably 40% by mass or less, based on the total solid content of the composition of the present invention. Compound (N) may be used alone, or two or more types may be used. When two or more types are used, the total content is preferably within the above-mentioned preferred content range.

[0119] [Resin] The composition of the present invention contains a resin. The composition of the present invention preferably contains a resin (also referred to as "resin (A)") whose polarity increases under the action of acid. The resin (A) preferably contains a group (also referred to as "acid-decomposable group") that decomposes under the action of acid and increases its polarity, and contains a repeating unit having an acid-decomposable group. When the resin (A) has an acid-decomposable group, in a pattern formation method using the composition of the present invention, typically, a positive pattern is preferably formed when an alkaline developer is used as the developer, and a negative pattern is preferably formed when an organic developer is used as the developer. As the repeating unit having an acid-decomposable group, in addition to a repeating unit having an acid-decomposable group, a repeating unit having an acid-decomposable group containing an unsaturated bond is preferred.

[0120] (Repeating unit having an acid-decomposable group) The acid-decomposable group refers to a group that decomposes under the action of an acid to generate a polar group. The acid-decomposable group preferably has a structure in which a polar group is protected with a group (leaving group) that is released under the action of an acid. In other words, the resin (A) has a repeating unit that decomposes under the action of an acid to generate a polar group. The polarity of a resin having this repeating unit increases under the action of an acid, increasing its solubility in an alkaline developer and decreasing its solubility in an organic solvent. The polar group is preferably an alkali-soluble group, such as a carboxyl group, a phenolic hydroxyl group, a fluorinated alcohol group, a sulfonic acid group, a phosphate group, a sulfonamide group, a sulfonylimide group, a (alkylsulfonyl) (alkylcarbonyl) methylene group, a (alkylsulfonyl) (alkylcarbonyl) imide group, a bis(alkylcarbonyl) methylene group, a bis(alkylcarbonyl) imide group, a bis(alkylsulfonyl) methylene group, a bis(alkylsulfonyl) imide group, a tris(alkylcarbonyl) methylene group, and an acidic group such as a tris(alkylsulfonyl) methylene group, and an alcoholic hydroxyl group. Among these, the polar group is preferably a carboxyl group, a phenolic hydroxyl group, a fluorinated alcohol group (preferably a hexafluoroisopropanol group), or a sulfonic acid group.

[0121] Examples of the group that is eliminated by the action of an acid include groups represented by formulae (Y1) to (Y4). Formula (Y1): —C(Rx １ ) (Rx ２ ) (Rx ３ ) Formula (Y2): -C(=O)OC(Rx １ ) (Rx ２ ) (Rx ３ ) Formula (Y3): -C(R ３６ ) (R ３７ ) (OR ３８ ) Formula (Y4): -C(Rn)(H)(Ar)

[0122] In formula (Y1) and formula (Y2), Rx １ ~Rx ３Rx each independently represents an alkyl group (linear or branched), a cycloalkyl group (monocyclic or polycyclic), an alkenyl group (linear or branched), or an aryl group (monocyclic or polycyclic). １ ~Rx ３ When all of Rx are alkyl groups (linear or branched), １ ~Rx ３ At least two of Rx are preferably methyl groups. １ ~Rx ３ each independently preferably represents a linear or branched alkyl group, and Rx １ ~Rx ３ More preferably, Rx each independently represents a linear alkyl group. １ ~Rx ３ may be bonded to form a monocyclic or polycyclic ring. １ ~Rx ３ The alkyl group of Rx is preferably an alkyl group having 1 to 5 carbon atoms, such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, or a t-butyl group. １ ~Rx ３ The cycloalkyl group of Rx is preferably a monocyclic cycloalkyl group such as a cyclopentyl group or a cyclohexyl group, or a polycyclic cycloalkyl group such as a norbornyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, or an adamantyl group. １ ~Rx ３ The aryl group in Rx is preferably an aryl group having 6 to 10 carbon atoms, and examples thereof include a phenyl group, a naphthyl group, and an anthryl group. １ ~Rx ３ The alkenyl group of Rx is preferably a vinyl group. １ ~Rx ３ The ring formed by combining the two is preferably a cycloalkyl group. １ ~Rx ３The cycloalkyl group formed by bonding the two is preferably a monocyclic cycloalkyl group such as a cyclopentyl group or a cyclohexyl group, or a polycyclic cycloalkyl group such as a norbornyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, or an adamantyl group, and more preferably a monocyclic cycloalkyl group having 5 to 6 carbon atoms. １ ~Rx ３ In the cycloalkyl group formed by bonding these two, one of the methylene groups constituting the ring may be replaced with a heteroatom such as an oxygen atom, a group containing a heteroatom such as a carbonyl group, or a vinylidene group. In these cycloalkyl groups, one or more of the ethylene groups constituting the cycloalkane ring may be replaced with a vinylene group. The group represented by formula (Y1) or formula (Y2) can be, for example, Rx １ is a methyl group or an ethyl group, and Rx ２ and Rx ３ and Rx are preferably bonded to form the above-mentioned cycloalkyl group. When the actinic ray-sensitive or radiation-sensitive resin composition is, for example, a resist composition for EUV exposure, １ ~Rx ３ an alkyl group, a cycloalkyl group, an alkenyl group, an aryl group, and Rx １ ~Rx ３ The ring formed by bonding these two groups preferably further has a fluorine atom or an iodine atom as a substituent.

[0123] In formula (Y3), R ３６ ~R ３８ R each independently represents a hydrogen atom or a monovalent organic group. ３７ and R ３８ may be bonded to each other to form a ring. Examples of the monovalent organic group include an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, and an alkenyl group. ３６is also preferably a hydrogen atom. The alkyl group, cycloalkyl group, aryl group, and aralkyl group may contain a heteroatom such as an oxygen atom and / or a group containing a heteroatom such as a carbonyl group. For example, in the alkyl group, cycloalkyl group, aryl group, and aralkyl group, one or more methylene groups may be replaced with a heteroatom such as an oxygen atom and / or a group containing a heteroatom such as a carbonyl group. R ３８ may bond with another substituent on the main chain of the repeating unit to form a ring. ３８ The group formed by bonding together R and another substituent on the main chain of the repeating unit is preferably an alkylene group such as a methylene group. ３６ ~R ３８ and a monovalent organic group represented by R ３７ and R ３８ It is also preferable that the ring formed by bonding these groups together further has a fluorine atom or an iodine atom as a substituent.

[0124] Formula (Y3) is preferably a group represented by the following formula (Y3-1).

[0125]

[0126] Here, L １ and L ２ Each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, or a group combining these (for example, a group combining an alkyl group and an aryl group). M represents a single bond or a divalent linking group. Q represents an alkyl group that may contain a heteroatom, a cycloalkyl group that may contain a heteroatom, an aryl group that may contain a heteroatom, an amino group, an ammonium group, a mercapto group, a cyano group, an aldehyde group, or a group combining these (for example, a group combining an alkyl group and a cycloalkyl group). In the alkyl group and the cycloalkyl group, for example, one of the methylene groups may be replaced with a heteroatom such as an oxygen atom, or a group containing a heteroatom such as a carbonyl group. In addition, L １ and L２ It is preferred that one of Q, M, and L is a hydrogen atom, and the other is an alkyl group, a cycloalkyl group, an aryl group, or a group in which an alkylene group and an aryl group are combined. １ At least two of the groups may be bonded to form a ring (preferably a 5- or 6-membered ring). ２ is preferably a secondary or tertiary alkyl group, and more preferably a tertiary alkyl group. Examples of secondary alkyl groups include an isopropyl group, a cyclohexyl group, and a norbornyl group, and examples of tertiary alkyl groups include a tert-butyl group and an adamantane group. In these embodiments, the Tg (glass transition temperature) and activation energy are increased, thereby ensuring film strength and suppressing fogging.

[0127] When the composition of the present invention is, for example, a resist composition for EUV exposure, L １ and L ２ It is also preferable that the alkyl group, cycloalkyl group, aryl group, and combinations thereof represented by the formula (I) further have a fluorine atom or an iodine atom as a substituent. The alkyl group, cycloalkyl group, aryl group, and aralkyl group preferably contain a heteroatom such as an oxygen atom in addition to the fluorine atom and iodine atom. Specifically, in the alkyl group, cycloalkyl group, aryl group, and aralkyl group, for example, one of the methylene groups may be replaced with a heteroatom such as an oxygen atom, or a group containing a heteroatom such as a carbonyl group. When the composition of the present invention is, for example, a resist composition for EUV exposure, in the alkyl group which may contain a heteroatom, cycloalkyl group which may contain a heteroatom, aryl group which may contain a heteroatom, amino group, ammonium group, mercapto group, cyano group, aldehyde group, and combinations thereof represented by Q, the heteroatom is preferably selected from the group consisting of a fluorine atom, an iodine atom, and an oxygen atom.

[0128] In formula (Y4), Ar represents an aromatic ring group. Rn represents an alkyl group, a cycloalkyl group, or an aryl group. Rn and Ar may be bonded to each other to form a non-aromatic ring. Ar is preferably an aryl group. When the composition of the present invention is, for example, a resist composition for EUV exposure, it is also preferable that the aromatic ring group represented by Ar and the alkyl group, cycloalkyl group, and aryl group represented by Rn have a fluorine atom or an iodine atom as a substituent.

[0129] In terms of excellent acid decomposition properties of the repeating unit, when a non-aromatic ring is directly bonded to the polar group (or a residue thereof) in the leaving group protecting the polar group, it is also preferable that the ring atom in the non-aromatic ring adjacent to the ring atom directly bonded to the polar group (or a residue thereof) does not have a halogen atom such as a fluorine atom as a substituent.

[0130] The group that is eliminated by the action of an acid may also be a 2-cyclopentenyl group having a substituent (such as an alkyl group), such as a 3-methyl-2-cyclopentenyl group, or a cyclohexyl group having a substituent (such as an alkyl group), such as a 1,1,4,4-tetramethylcyclohexyl group.

[0131] The repeating unit having an acid-decomposable group is also preferably a repeating unit represented by formula (A).

[0132]

[0133] L １ represents a divalent linking group which may have a fluorine atom or an iodine atom, R １ represents a hydrogen atom, a fluorine atom, an iodine atom, an alkyl group which may have a fluorine atom or an iodine atom, or an aryl group which may have a fluorine atom or an iodine atom; R ２ represents a leaving group which is eliminated by the action of an acid and which may have a fluorine atom or an iodine atom. １ , R １ , and R ２ At least one of L has a fluorine atom or an iodine atom. １Examples of the divalent linking group which may have a fluorine atom or an iodine atom and is represented by the formula: ２ -, hydrocarbon groups which may have a fluorine atom or an iodine atom (for example, alkylene groups, cycloalkylene groups, alkenylene groups, arylene groups, etc.), and linking groups in which a plurality of these groups are linked together. １ As the alkylene group, -CO-, an arylene group, or -arylene group-alkylene group having a fluorine atom or an iodine atom- is preferred, and -CO- or -arylene group-alkylene group having a fluorine atom or an iodine atom- is more preferred. As the arylene group, a phenylene group is preferred. The alkylene group may be linear or branched. The number of carbon atoms in the alkylene group is not particularly limited, but is preferably 1 to 10, and more preferably 1 to 3. The total number of fluorine atoms and iodine atoms contained in the alkylene group having a fluorine atom or an iodine atom is not particularly limited, but is preferably 2 or more, more preferably 2 to 10, and even more preferably 3 to 6.

[0134] R １ The alkyl group represented by R may be linear or branched. The number of carbon atoms in the alkyl group is not particularly limited, but is preferably 1 to 10, and more preferably 1 to 3. １ The total number of fluorine atoms and iodine atoms contained in the alkyl group having a fluorine atom or an iodine atom, represented by the formula (I), is not particularly limited, but is preferably 1 or more, more preferably 1 to 5, and even more preferably 1 to 3. １ The alkyl group represented by the formula (I) may contain a heteroatom other than a halogen atom, such as an oxygen atom.

[0135] R ２ Examples of the leaving group represented by the formulae (Y1) to (Y4) above and which may have a fluorine atom or an iodine atom include leaving groups represented by the formulae (Y1) to (Y4) above and which have a fluorine atom or an iodine atom.

[0136] The repeating unit having an acid-decomposable group is also preferably a repeating unit represented by formula (AI).

[0137]

[0138] In formula (AI), Xa １ represents a hydrogen atom or an alkyl group which may have a substituent. T represents a single bond or a divalent linking group. Rx １ ~Rx ３ each independently represents an alkyl group (linear or branched), a cycloalkyl group (monocyclic or polycyclic), an alkenyl group (linear or branched), or an aryl group (monocyclic or polycyclic). １ ~Rx ３ When all of Rx are alkyl groups (linear or branched), １ ~Rx ３ Preferably, at least two of Rx are methyl groups. １ ~Rx ３ may be bonded to form a monocyclic or polycyclic ring (such as a monocyclic or polycyclic cycloalkyl group).

[0139] Xa １ Examples of the alkyl group represented by the formula (I) which may have a substituent include a methyl group or a —CH ２ -R １１ Examples of the group include a group represented by R １１ represents a halogen atom (such as a fluorine atom), a hydroxyl group, or a monovalent organic group. １１ Examples of the monovalent organic group represented by the formula (I) include an alkyl group having 5 or less carbon atoms which may be substituted with a halogen atom, an acyl group having 5 or less carbon atoms which may be substituted with a halogen atom, and an alkoxy group having 5 or less carbon atoms which may be substituted with a halogen atom, and an alkyl group having 3 or less carbon atoms is preferred, and a methyl group is more preferred. １ is preferably a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

[0140] Examples of the divalent linking group for T include an alkylene group, an aromatic ring group, a -COO-Rt- group, and a -O-Rt- group. In the formula, Rt represents an alkylene group or a cycloalkylene group. T is preferably a single bond or a -COO-Rt- group. When T represents a -COO-Rt- group, Rt is preferably an alkylene group having 1 to 5 carbon atoms, and is preferably a -CH ２- group, -(CH ２ ) ２ - group or -(CH ２ ) ３ The - group is more preferred.

[0141] Rx １ ~Rx ３ The alkyl group of Rx is preferably an alkyl group having 1 to 4 carbon atoms, such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, or a t-butyl group. １ ~Rx ３ The cycloalkyl group of Rx is preferably a monocyclic cycloalkyl group such as a cyclopentyl group or a cyclohexyl group, or a polycyclic cycloalkyl group such as a norbornyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, or an adamantyl group. １ ~Rx ３ The aryl group in Rx is preferably an aryl group having 6 to 10 carbon atoms, and examples thereof include a phenyl group, a naphthyl group, and an anthryl group. １ ~Rx ３ The alkenyl group of Rx is preferably a vinyl group. １ ~Rx ３ As the cycloalkyl group formed by combining the above two, a monocyclic cycloalkyl group such as a cyclopentyl group or a cyclohexyl group is preferred. Polycyclic cycloalkyl groups such as a norbornyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, and an adamantyl group are also preferred. Among these, a monocyclic cycloalkyl group having 5 to 6 carbon atoms is preferred. Rx １ ~Rx ３ The cycloalkyl group formed by bonding these two may have, for example, one of the methylene groups constituting the ring replaced with a heteroatom such as an oxygen atom, a group containing a heteroatom such as a carbonyl group, or a vinylidene group. Furthermore, in these cycloalkyl groups, one or more of the ethylene groups constituting the cycloalkane ring may be replaced with a vinylene group. The repeating unit represented by formula (AI) can be, for example, Rx １ is a methyl group or an ethyl group, and Rx ２ and Rx ３and are preferably bonded to form the above-mentioned cycloalkyl group.

[0142] When each of the above groups has a substituent, examples of the substituent include an alkyl group (having 1 to 4 carbon atoms), a halogen atom, a hydroxyl group, an alkoxy group (having 1 to 4 carbon atoms), a carboxyl group, and an alkoxycarbonyl group (having 2 to 6 carbon atoms). The number of carbon atoms in the substituent is preferably 8 or less.

[0143] The repeating unit represented by formula (AI) may be an acid-decomposable (meth)acrylic acid tertiary alkyl ester repeating unit (Xa １ represents a hydrogen atom or a methyl group, and T represents a single bond).

[0144] The resin (A) may have a repeating unit having an acid-decomposable group containing an unsaturated bond as a repeating unit having an acid-decomposable group. As the repeating unit having an acid-decomposable group containing an unsaturated bond, a repeating unit represented by formula (B) is preferred.

[0145]

[0146] In formula (B), Xb represents a hydrogen atom, a halogen atom, or an alkyl group which may have a substituent. L represents a single bond or a divalent linking group which may have a substituent. Ry １ ~Ry ３ each independently represents a linear or branched alkyl group, a monocyclic or polycyclic cycloalkyl group, an alkenyl group, an alkynyl group, or a monocyclic or polycyclic aryl group, provided that Ry １ ~Ry ３ At least one of R represents an alkenyl group, an alkynyl group, a monocyclic or polycyclic cycloalkenyl group, or a monocyclic or polycyclic aryl group. １ ~Ry ３ may be bonded to form a monocyclic or polycyclic ring (such as a monocyclic or polycyclic cycloalkyl group or cycloalkenyl group).

[0147] The alkyl group represented by Xb, which may have a substituent, is, for example, a methyl group or —CH ２ -R １１Examples of the group include a group represented by R １１ represents a halogen atom (such as a fluorine atom), a hydroxyl group, or a monovalent organic group, and examples thereof include an alkyl group having 5 or less carbon atoms which may be substituted with a halogen atom, an acyl group having 5 or less carbon atoms which may be substituted with a halogen atom, and an alkoxy group having 5 or less carbon atoms which may be substituted with a halogen atom, preferably an alkyl group having 3 or less carbon atoms, and more preferably a methyl group. Xb is preferably a hydrogen atom, a fluorine atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

[0148] Examples of the divalent linking group for L include a -Rt- group, a -CO- group, a -COO-Rt- group, a -COO-Rt-CO- group, a -Rt-CO- group, and a -O-Rt- group. In the formula, Rt represents an alkylene group, a cycloalkylene group, or an aromatic ring group, and an aromatic ring group is preferable. L is preferably a -Rt- group, a -CO- group, a -COO-Rt-CO- group, or a -Rt-CO- group. Rt may have a substituent such as a halogen atom, a hydroxyl group, or an alkoxy group.

[0149] Ry １ ~Ry ３ The alkyl group of Ry is preferably an alkyl group having 1 to 4 carbon atoms, such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, or a t-butyl group. １ ~Ry ３ The cycloalkyl group of Ry is preferably a monocyclic cycloalkyl group such as a cyclopentyl group or a cyclohexyl group, or a polycyclic cycloalkyl group such as a norbornyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, or an adamantyl group. １ ~Ry ３ The aryl group in Ry is preferably an aryl group having 6 to 10 carbon atoms, and examples thereof include a phenyl group, a naphthyl group, and an anthryl group. １ ~Ry ３ The alkenyl group in Ry is preferably a vinyl group. １ ~Ry ３ The alkynyl group in Ry is preferably an ethynyl group. １ ~Ry ３The cycloalkenyl group of Ry is preferably a monocyclic cycloalkyl group such as a cyclopentyl group or a cyclohexyl group, which has a double bond in part thereof. １ ~Ry ３ The cycloalkyl group formed by combining the above two groups is preferably a monocyclic cycloalkyl group such as a cyclopentyl group or a cyclohexyl group, or a polycyclic cycloalkyl group such as a norbornyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, or an adamantyl group. Among these, a monocyclic cycloalkyl group having 5 to 6 carbon atoms is more preferred. １ ~Ry ３ The cycloalkyl group or cycloalkenyl group formed by bonding two of the above is, for example, a group in which one of the methylene groups constituting the ring is substituted with a heteroatom such as an oxygen atom, a carbonyl group, or —SO ２ - group and -SO ３ The repeating unit represented by formula (B) may be substituted with a group containing a hetero atom such as a - group, a vinylidene group, or a combination thereof. In addition, in these cycloalkyl groups or cycloalkenyl groups, one or more ethylene groups constituting the cycloalkane ring or cycloalkene ring may be substituted with a vinylene group. １ is a methyl group, an ethyl group, a vinyl group, an allyl group, or an aryl group, and Ry ２ and Ry ３ and are bonded to form the above-mentioned cycloalkyl group or cycloalkenyl group.

[0150] When each of the above groups has a substituent, examples of the substituent include an alkyl group (having 1 to 4 carbon atoms), a halogen atom, a hydroxyl group, an alkoxy group (having 1 to 4 carbon atoms), a carboxyl group, and an alkoxycarbonyl group (having 2 to 6 carbon atoms). The number of carbon atoms in the substituent is preferably 8 or less.

[0151] The repeating unit represented by formula (B) is preferably an acid-decomposable (meth)acrylic acid tertiary ester repeating unit (a repeating unit in which Xb represents a hydrogen atom or a methyl group and L represents a —CO— group), an acid-decomposable hydroxystyrene tertiary alkyl ether repeating unit (a repeating unit in which Xb represents a hydrogen atom or a methyl group and L represents a phenyl group), or an acid-decomposable styrene carboxylic acid tertiary ester repeating unit (a repeating unit in which Xb represents a hydrogen atom or a methyl group and L represents a —Rt—CO— group (Rt is an aromatic group)).

[0152] The content of the repeating unit having an acid-decomposable group containing an unsaturated bond is preferably 15 mol% or more, more preferably 20 mol% or more, and even more preferably 30 mol% or more, relative to all repeating units in the resin (A). The upper limit is preferably 80 mol% or less, more preferably 70 mol% or less, and even more preferably 60 mol% or less, relative to all repeating units in the resin (A). Specific examples of repeating units having an acid-decomposable group containing an unsaturated bond include the repeating units described in paragraphs

[0067] to

[0071] of WO 2022 / 024928. The above descriptions are incorporated herein by reference.

[0153] Specific examples of repeating units having an acid-decomposable group are shown below, but are not limited to these.

[0154]

[0155] The content of the repeating units having an acid-decomposable group is preferably 15 mol% or more, more preferably 20 mol% or more, and even more preferably 30 mol% or more, based on the total repeating units in the resin (A), and the upper limit thereof is preferably 90 mol% or less, more preferably 80 mol% or less, even more preferably 70 mol% or less, and particularly preferably 60 mol% or less, based on the total repeating units in the resin (A).

[0156] Resin (A) may contain at least one repeating unit selected from the group consisting of Group A below, and / or at least one repeating unit selected from the group consisting of Group B below. Group A: A group consisting of the following repeating units (20) to (25). (20) A repeating unit having an acid group, as described below. (21) A repeating unit having neither an acid-decomposable group nor an acid group, and having a fluorine atom, a bromine atom, or an iodine atom, as described below. (22) A repeating unit having a lactone group, a sultone group, or a carbonate group, as described below. (23) A repeating unit having a photoacid-generating group, as described below. (24) A repeating unit represented by Formula (V-1) or Formula (V-2), as described below. (25) A repeating unit for reducing main chain mobility. The repeating units represented by Formulas (A) to (E), as described below, correspond to (25) A repeating unit for reducing main chain mobility. Group B: A group consisting of the following repeating units (30) to (32). (30) A repeating unit having at least one group selected from a lactone group, a sultone group, a carbonate group, a hydroxyl group, a cyano group, and an alkali-soluble group, as described below. (31) A repeating unit having an alicyclic hydrocarbon structure and not exhibiting acid decomposability, as described below. (32) A repeating unit represented by formula (III), as described below, having neither a hydroxyl group nor a cyano group.

[0157] The resin (A) preferably has an acid group, and as described below, preferably contains a repeating unit having an acid group. The acid group will be described later together with preferred embodiments of the repeating unit having an acid group. When the resin (A) has an acid group, the interaction between the resin (A) and the acid generated from the photoacid generator is more excellent. As a result, the diffusion of the acid is further suppressed, and the cross-sectional shape of the formed pattern can be more rectangular.

[0158] The resin (A) may have at least one repeating unit selected from the group consisting of Group A. When the composition of the present invention is used as an actinic ray-sensitive or radiation-sensitive resin composition for EUV exposure, the resin (A) preferably has at least one repeating unit selected from the group consisting of Group A. The resin (A) may contain at least one of a fluorine atom and an iodine atom. When the composition of the present invention is used as an actinic ray-sensitive or radiation-sensitive resin composition for EUV exposure, the resin (A) preferably contains at least one of a fluorine atom and an iodine atom. When the resin (A) contains both a fluorine atom and an iodine atom, the resin (A) may have one repeating unit containing both a fluorine atom and an iodine atom, or the resin (A) may contain two repeating units, one containing a fluorine atom and one containing an iodine atom. The resin (A) may have a repeating unit containing an aromatic group. When the composition of the present invention is used as an actinic ray-sensitive or radiation-sensitive resin composition for EUV exposure, the resin (A) also preferably has a repeating unit containing an aromatic group. Resin (A) may have at least one repeating unit selected from the group consisting of Group B. When the composition of the present invention is used as an actinic ray-sensitive or radiation-sensitive resin composition for ArF, resin (A) preferably has at least one repeating unit selected from the group consisting of Group B. When the composition of the present invention is used as an actinic ray-sensitive or radiation-sensitive resin composition for ArF, resin (A) preferably contains neither a fluorine atom nor a silicon atom. When the composition of the present invention is used as an actinic ray-sensitive or radiation-sensitive resin composition for ArF, resin (A) preferably does not have an aromatic group.

[0159] (Repeating Unit Having an Acid Group) The resin (A) may have a repeating unit having an acid group. The acid group preferably has a pKa of 13 or less. The acid dissociation constant of the acid group is preferably 13 or less, more preferably 3 to 13, and even more preferably 5 to 10. When the resin (A) has an acid group having a pKa of 13 or less, the content of the acid group in the resin (A) is not particularly limited, but is often 0.2 to 6.0 mmol / g. Of these, 0.8 to 6.0 mmol / g is preferred, 1.2 to 5.0 mmol / g is more preferred, and 1.6 to 4.0 mmol / g is even more preferred. When the content of the acid group is within the above range, development proceeds smoothly, and the formed pattern shape is excellent, and resolution is also excellent. Examples of the acid group that may be preferred include a carboxyl group, a phenolic hydroxyl group, a fluorinated alcohol group (preferably a hexafluoroisopropanol group), a sulfonic acid group, a sulfonamide group, and an isopropanol group. In the hexafluoroisopropanol group, one or more (preferably one to two) fluorine atoms may be substituted with a group other than a fluorine atom (such as an alkoxycarbonyl group). The acid group may be —C(CF ３ )(OH)—CF ２ In addition, one or more fluorine atoms are substituted with a group other than a fluorine atom to form -C(CF ３ )(OH)—CF ２ - may form a ring containing the repeating unit. The repeating unit having an acid group is preferably a repeating unit different from the repeating unit having a structure in which a polar group is protected by a group that is cleaved by the action of an acid described above, and the repeating unit having a lactone group, a sultone group, or a carbonate group described below. The repeating unit having an acid group may have a fluorine atom or an iodine atom. Specific examples of the repeating unit having an acid group include the repeating units described in paragraphs

[0088] to

[0089] and

[0103] to

[0110] of WO 2022 / 024928. The above descriptions are incorporated herein by reference.

[0160] The repeating unit having an acid group is preferably a repeating unit having a phenolic hydroxyl group. The repeating unit having a phenolic hydroxyl group is preferably a repeating unit different from the repeating unit having an acid-decomposable group described above. The repeating unit having a phenolic hydroxyl group is preferably a repeating unit represented by the following formula (Pa2):

[0161]

[0162] In formula (Pa2), R １０１ , R １０２ and R １０３ R each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, a halogen atom, a cyano group, or an alkoxycarbonyl group. １０２ is Ar Ａ may be bonded to form a ring, in which case R １０２ represents a single bond or an alkylene group. Ａ represents a single bond or a divalent linking group. Ａ represents an aromatic ring group, and k represents an integer of 1 to 5.

[0163] R in formula (Pa2) １０１ , R １０２ and R １０３ R each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, a halogen atom, a cyano group, or an alkoxycarbonyl group. １０１ , R １０２ and R １０３ The alkyl group in R may be either linear or branched. The number of carbon atoms in the alkyl group is not particularly limited, but is preferably 1 to 10, more preferably 1 to 5, and particularly preferably 1 to 3. Examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, and a t-butyl group. １０１ , R １０２ and R １０３ The number of carbon atoms in the cycloalkyl group is not particularly limited, but is preferably 3 to 20, and more preferably 5 to 15. １０１ , R １０２ and R １０３The cycloalkyl group of R is preferably a monocyclic cycloalkyl group such as a cyclopentyl group or a cyclohexyl group, or a polycyclic cycloalkyl group such as a norbornyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, or an adamantyl group. １０１ , R １０２ and R １０３ Examples of the halogen atom in R include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom, and a fluorine atom or an iodine atom is preferred. １０１ , R １０２ and R １０３ The alkyl group contained in the alkoxycarbonyl group may be either linear or branched. The number of carbon atoms in the alkyl group contained in the alkoxycarbonyl group is not particularly limited, but is preferably 1 to 5, and more preferably 1 to 3.

[0164] Ar in formula (Pa2) Ａ represents an aromatic ring group, more specifically, a (k+1)-valent aromatic ring group. When k is 1, the divalent aromatic ring group is preferably an arylene group having 6 to 18 carbon atoms, such as a phenylene group, a tolylene group, a naphthylene group, or an anthracenylene group, or a divalent aromatic ring group containing a heterocycle, such as a thiophene ring, a furan ring, a pyrrole ring, a benzothiophene ring, a benzofuran ring, a benzopyrrole ring, a triazine ring, an imidazole ring, a benzimidazole ring, a triazole ring, a thiadiazole ring, or a thiazole ring. The aromatic ring group may have a substituent. When k is an integer of 2 or more, specific examples of the (k+1)-valent aromatic ring group include groups obtained by removing any (k-1) hydrogen atoms from the above-mentioned specific examples of the divalent aromatic ring group. The (k+1)-valent aromatic ring group may further have a substituent. The substituent that the (k+1)-valent aromatic ring group may have is not particularly limited, and examples thereof include alkyl groups such as methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, hexyl, 2-ethylhexyl, octyl, and dodecyl; alkoxy groups such as methoxy, ethoxy, hydroxyethoxy, propoxy, hydroxypropoxy, and butoxy; and aryl groups such as phenyl. Ａpreferably represents an aromatic ring group having 6 to 18 carbon atoms, and more preferably represents a benzene ring group, a naphthalene ring group or a biphenylene ring group.

[0165] L in formula (Pa2) Ａ represents a single bond or a divalent linking group. Ａ The divalent linking group represented by is not particularly limited, but examples thereof include -COO-, -CONR １０４ -, an alkylene group, or a group formed by combining two or more of these groups. １０４ represents a hydrogen atom or an alkyl group. The alkylene group is not particularly limited, but is preferably an alkylene group having 1 to 8 carbon atoms, such as a methylene group, an ethylene group, a propylene group, a butylene group, a hexylene group, or an octylene group. R １０４ When represents an alkyl group, examples of the alkyl group include alkyl groups having 20 or less carbon atoms, such as a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, a hexyl group, a 2-ethylhexyl group, an octyl group, and a dodecyl group, and alkyl groups having 8 or less carbon atoms are preferred.

[0166] The repeating unit represented by formula (Pa2) preferably has a hydroxystyrene structure. Ａ preferably represents a benzene ring group. k preferably represents an integer of 1 to 3, and more preferably represents 1 or 2.

[0167] Specific examples of repeating units having an acid group are shown below, but are not limited to these. １ and G ２ each independently represents a hydrogen atom, a methyl group, a fluorine atom, a chlorine atom, a trifluoromethyl group, a cyano group, a hydroxy group, or a hydroxymethyl group. f1 represents an integer of 1 to 3.

[0168]

[0169] When the resin (A) contains a repeating unit having an acid group, the content of the repeating unit having an acid group is preferably 10 mol% or more, more preferably 15 mol% or more, based on the total repeating units in the resin (A), and the upper limit thereof is preferably 70 mol% or less, more preferably 65 mol% or less, and even more preferably 60 mol% or less, based on the total repeating units in the resin (A).

[0170] (Repeating units having neither an acid-decomposable group nor an acid group, and having a fluorine atom, a bromine atom, or an iodine atom) In addition to the above-mentioned <repeating units having an acid-decomposable group> and <repeating units having an acid group>, the resin (A) may have a repeating unit having neither an acid-decomposable group nor an acid group, and having a fluorine atom, a bromine atom, or an iodine atom (hereinafter also referred to as unit X). The <repeating units having neither an acid-decomposable group nor an acid group, and having a fluorine atom, a bromine atom, or an iodine atom> referred to here is preferably different from other types of repeating units belonging to Group A, such as the <repeating units having a lactone group, a sultone group, or a carbonate group> and the <repeating units having a photoacid-generating group> described below.

[0171] The unit X is preferably a repeating unit represented by formula (C).

[0172]

[0173] L ５ represents a single bond or an ester group. ９ represents a hydrogen atom or an alkyl group which may have a fluorine atom or an iodine atom. １０ represents a hydrogen atom, an alkyl group which may have a fluorine atom or an iodine atom, a cycloalkyl group which may have a fluorine atom or an iodine atom, an aryl group which may have a fluorine atom or an iodine atom, or a group combining these. Specific examples of repeating units having a fluorine atom or an iodine atom include the repeating units described in paragraphs

[0116] to

[0117] of WO 2022 / 024928. The above descriptions are incorporated herein by reference.

[0174] The content of the units X is preferably 0 mol% or more, more preferably 5 mol% or more, and even more preferably 10 mol% or more, based on all repeating units in the resin (A), and the upper limit thereof is preferably 50 mol% or less, more preferably 45 mol% or less, and even more preferably 40 mol% or less, based on all repeating units in the resin (A).

[0175] Among the repeating units of the resin (A), the total content of repeating units containing at least one of a fluorine atom, a bromine atom, and an iodine atom is preferably 10 mol% or more, more preferably 20 mol% or more, even more preferably 30 mol% or more, and particularly preferably 40 mol% or more, based on the total repeating units of the resin (A). The upper limit is not particularly limited, but is, for example, 100 mol% or less, based on the total repeating units of the resin (A). Examples of repeating units containing at least one of a fluorine atom, a bromine atom, and an iodine atom include repeating units having a fluorine atom, a bromine atom, or an iodine atom and an acid-decomposable group, repeating units having a fluorine atom, a bromine atom, or an iodine atom and an acid group, and repeating units having a fluorine atom, a bromine atom, or an iodine atom.

[0176] (Repeating unit having a lactone group, a sultone group, or a carbonate group) The resin (A) may have a repeating unit (hereinafter also referred to as "unit Y") having at least one selected from the group consisting of a lactone group, a sultone group, and a carbonate group. It is also preferable that unit Y does not have a hydroxyl group or an acid group such as a hexafluoropropanol group.

[0177] The lactone group or sultone group may have a lactone structure or a sultone structure. The lactone structure or sultone structure is preferably a 5- to 7-membered cyclic lactone structure or a 5- to 7-membered cyclic sultone structure. Among these, a 5- to 7-membered cyclic lactone structure to which another ring structure is fused in the form of a bicyclo or spiro structure, or a 5- to 7-membered cyclic sultone structure to which another ring structure is fused in the form of a bicyclo or spiro structure, is more preferred. Resin (A) preferably has a repeating unit having a lactone group, sultone group, or carbonate group obtained by removing one or more hydrogen atoms from a ring atom of a lactone structure represented by any one of formulas (LC1-1) to (LC1-22) below, a sultone structure represented by any one of formulas (SL1-1) to (SL1-3) below, or a cyclic carbonate ester structure represented by any one of formulas (CC1-1) to (CC1-2) below, and the lactone group, sultone group, or carbonate group may be directly bonded to the main chain. For example, ring atoms of a lactone group, a sultone group, or a carbonate group may constitute the main chain of the resin (A). The lactone group, the sultone group, and the carbonate group may have a substituent.

[0178] R in the following structural formula Ｌ represents a substituent. Ｌ If there are multiple R Ｌ may be the same or different. Ｌ Examples of R include an alkyl group having 1 to 8 carbon atoms, a cycloalkyl group having 4 to 10 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 2 to 8 carbon atoms, a carboxyl group, a halogen atom, a cyano group, and an acid-decomposable group. e1 represents an integer of 0 to 4. When multiple e1s are present, the multiple e1s may be the same or different. When e1 is 2 or more, the multiple R Ｌ may be the same or different, and multiple R Ｌ They may be bonded to each other to form a ring.

[0179]

[0180] Examples of repeating units having a lactone group, a sultone group, or a carbonate group include repeating units represented by the following formula (AI-2).

[0181]

[0182] In formula (AI-2), Rb ０ represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 4 carbon atoms. ０ Preferred substituents that the alkyl group of Rb may have include a hydroxyl group and a halogen atom. ０ Examples of the halogen atom in Rb include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. ０ is preferably a hydrogen atom or a methyl group. Ab represents a single bond, an alkylene group, a divalent linking group having a monocyclic or polycyclic alicyclic hydrocarbon structure, an ether group, an ester group, a carbonyl group, a carboxyl group, or a divalent linking group formed by combining these. Among these, Ab is preferably a single bond or -Ab １ -CO ２ A linking group represented by - is preferred. １ is a linear or branched alkylene group, or a monocyclic or polycyclic cycloalkylene group, and is preferably a methylene group, an ethylene group, a cyclohexylene group, an adamantylene group, or a norbornylene group. V is a group obtained by removing one hydrogen atom from a ring member atom of a lactone structure represented by any of formulas (LC1-1) to (LC1-22), a group obtained by removing one hydrogen atom from a ring member atom of a sultone structure represented by any of formulas (SL1-1) to (SL1-3), or a group obtained by removing one hydrogen atom from a ring member atom of a cyclic carbonate structure represented by any of formulas (CC1-1) to (CC1-2).

[0183] When optical isomers exist in the repeating unit having a lactone group or a sultone group, any optical isomer may be used. One optical isomer may be used alone, or multiple optical isomers may be used in combination. When one optical isomer is primarily used, its optical purity (ee) is preferably 90 or more, more preferably 95 or more.

[0184] The carbonate group is preferably a cyclic carbonate ester group. For repeating units having a cyclic carbonate ester group, see, for example, paragraphs

[0127] to

[0133] of WO 2022 / 024928. The above description is incorporated herein by reference.

[0185] When the resin (A) contains the unit Y, the content of the unit Y is preferably 1 mol% or more, more preferably 10 mol% or more, based on all repeating units in the resin (A), and the upper limit thereof is preferably 85 mol% or less, more preferably 80 mol% or less, even more preferably 70 mol% or less, and particularly preferably 60 mol% or less, based on all repeating units in the resin (A).

[0186] (Repeating unit having a photoacid generating group) The resin (A) may have, as a repeating unit other than those described above, a repeating unit having a group that generates an acid upon irradiation with actinic rays or radiation (also referred to as a "photoacid generating group"). Examples of the repeating unit having a photoacid generating group include a repeating unit represented by formula (40).

[0187]

[0188] R ４１ represents a hydrogen atom or a methyl group. ４１ represents a single bond or a divalent linking group. ４２ represents a divalent linking group. ４０ represents a structural moiety that decomposes upon irradiation with actinic rays or radiation to generate an acid in a side chain. Specific examples of repeating units having a photoacid generating group include the repeating units described in

[0094] to

[0105] of JP 2014-041327 A, the repeating unit described in

[0094] of WO 2018 / 193954 A, and the repeating unit described in

[0138] of WO 2022 / 024928 A. The above descriptions are incorporated herein by reference.

[0189] Examples of the repeating unit represented by formula (40) include the repeating units described in paragraphs

[0094] to

[0105] of JP 2014-041327 A and the repeating unit described in paragraph

[0094] of WO 2018 / 193954 A.

[0190] The content of the repeating unit having a photoacid generating group is preferably 1 mol% or more, more preferably 5 mol% or more, based on the total repeating units in the resin (A), and the upper limit thereof is preferably 40 mol% or less, more preferably 35 mol% or less, and even more preferably 30 mol% or less, based on the total repeating units in the resin (A).

[0191] (Repeating unit represented by formula (V-1) or formula (V-2)) The resin (A) may have a repeating unit represented by the following formula (V-1) or formula (V-2). The repeating units represented by the following formula (V-1) and formula (V-2) are preferably repeating units different from the above-mentioned repeating units.

[0192]

[0193] In the formula, R ６ and R ７ each independently represents a hydrogen atom, a hydroxyl group, an alkyl group, an alkoxy group, an acyloxy group, a cyano group, a nitro group, an amino group, a halogen atom, an ester group (-OCOR or -COOR: R is an alkyl group or a fluorinated alkyl group having 1 to 6 carbon atoms), or a carboxyl group. As the alkyl group, a linear, branched or cyclic alkyl group having 1 to 10 carbon atoms is preferred. ３ represents an integer of 0 to 6. ４ represents an integer of 0 to 4. ４ is a methylene group, an oxygen atom, or a sulfur atom. Examples of repeating units represented by formula (V-1) or (V-2) are shown below. Examples of repeating units represented by formula (V-1) or (V-2) include the repeating units described in paragraph

[0100] of WO 2018 / 193954.

[0194] (Repeating Unit for Reducing Mobility of Main Chain) Resin (A) preferably has a high glass transition temperature (Tg) in order to suppress excessive diffusion of generated acid or pattern collapse during development. Tg is preferably higher than 90°C, more preferably higher than 100°C, even more preferably higher than 110°C, and particularly preferably higher than 125°C. In order to achieve an excellent dissolution rate in a developer, Tg is preferably 400°C or lower, more preferably 350°C or lower. In this specification, the glass transition temperature (Tg) of a polymer such as resin (A) (hereinafter referred to as "Tg of repeating unit") is calculated by the following method. First, the Tg of a homopolymer consisting of only each repeating unit contained in the polymer is calculated using the Bicerano method. Next, the mass proportion (%) of each repeating unit relative to all repeating units in the polymer is calculated. Next, the Tg at each mass ratio is calculated using the Fox formula (described in Materials Letters 62 (2008) 3152, etc.), and the sum of these values ​​is used to determine the Tg (°C) of the polymer. The Bicerano method is described in "Prediction of Polymer Properties," Marcel Dekker Inc., New York (1993). Calculation of Tg by the Bicerano method can be performed using polymer property estimation software MDL Polymer (MDL Information Systems, Inc.).

[0195] In order to increase the Tg of resin (A) (preferably to make the Tg greater than 90°C), it is preferable to reduce the mobility of the main chain of resin (A). Methods for reducing the mobility of the main chain of resin (A) include the following methods (a) to (e): (a) Introduction of a bulky substituent into the main chain; (b) Introduction of multiple substituents into the main chain; (c) Introduction of a substituent that induces interactions between resins (A) near the main chain; (d) Formation of a main chain with a cyclic structure; (e) Linking of a cyclic structure to the main chain. It is preferable that resin (A) has a repeating unit that exhibits a homopolymer Tg of 130°C or higher. The type of repeating unit that exhibits a homopolymer Tg of 130°C or higher is not particularly limited, and it is sufficient that the repeating unit exhibits a homopolymer Tg of 130°C or higher as calculated by the Bicerano method. It is to be noted that depending on the type of functional group in the repeating units represented by formulas (A) to (E) described below, it may be considered a repeating unit that exhibits a homopolymer Tg of 130°C or higher.

[0196] One example of a specific means for achieving the above (a) is to introduce a repeating unit represented by formula (A) into resin (A).

[0197]

[0198] Formula (A), R Ａ represents a group containing a polycyclic structure. ｘ represents a hydrogen atom, a methyl group, or an ethyl group. A group containing a polycyclic structure is a group containing multiple ring structures, and the multiple ring structures may be condensed or not condensed. Specific examples of the repeating unit represented by formula (A) include those described in paragraphs

[0107] to

[0119] of WO 2018 / 193954.

[0199] One example of a specific means for achieving the above (b) is to introduce a repeating unit represented by formula (B) into resin (A).

[0200]

[0201] In formula (B), R ｂ１ ~R ｂ４ each independently represents a hydrogen atom or an organic group; R ｂ１ ~R ｂ４At least two of the above represent organic groups. When at least one of the organic groups is a group in which a ring structure is directly linked to the main chain in the repeating unit, the type of the other organic groups is not particularly limited. Furthermore, when none of the organic groups is a group in which a ring structure is directly linked to the main chain in the repeating unit, at least two of the organic groups are substituents having three or more constituent atoms excluding hydrogen atoms. Specific examples of the repeating unit represented by formula (B) include those described in paragraphs

[0113] to

[0115] of WO 2018 / 193954.

[0202] One example of a specific means for achieving the above (c) is to introduce a repeating unit represented by formula (C) into resin (A).

[0203]

[0204] In formula (C), R ｃ１ ~R ｃ４ each independently represents a hydrogen atom or an organic group; R ｃ１ ~R ｃ４ At least one of the repeating units represented by formula (C) is a group containing a hydrogen-bonding hydrogen atom within three atoms from the main chain carbon. In particular, in order to induce interactions between the main chains of resin (A), it is preferable to have a hydrogen-bonding hydrogen atom within two atoms (closer to the main chain). Specific examples of the repeating unit represented by formula (C) include those described in paragraphs

[0119] to

[0121] of WO 2018 / 193954.

[0205] One example of a specific means for achieving the above (d) is to introduce a repeating unit represented by formula (D) into resin (A).

[0206]

[0207] In formula (D), "Cyclic" represents a group that forms a main chain with a cyclic structure. The number of constituent atoms of the ring is not particularly limited. Specific examples of the repeating unit represented by formula (D) include those described in paragraphs

[0126] to

[0127] of WO 2018 / 193954.

[0208] One example of a specific means for achieving the above (e) is to introduce a repeating unit represented by formula (E) into resin (A).

[0209]

[0210] In formula (E), Re each independently represents a hydrogen atom or an organic group. Examples of the organic group include an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, and an alkenyl group, each of which may have a substituent. "Cyclic" refers to a cyclic group containing carbon atoms in the main chain. The number of atoms contained in the cyclic group is not particularly limited. Specific examples of the repeating unit represented by formula (E) include those described in paragraphs

[0131] to

[0133] of WO 2018 / 193954.

[0211] (Repeating unit having at least one group selected from a lactone group, a sultone group, a carbonate group, a hydroxyl group, a cyano group, and an alkali-soluble group) The resin (A) may have a repeating unit having at least one group selected from a lactone group, a sultone group, a carbonate group, a hydroxyl group, a cyano group, and an alkali-soluble group. Examples of the repeating unit having a lactone group, a sultone group, or a carbonate group contained in the resin (A) include the repeating units described above in <Repeating unit having a lactone group, a sultone group, or a carbonate group>. The preferred content is also as described above in <Repeating unit having a lactone group, a sultone group, or a carbonate group>.

[0212] The resin (A) may have a repeating unit having a hydroxyl group or a cyano group. This improves substrate adhesion and developer affinity. The repeating unit having a hydroxyl group or a cyano group is preferably a repeating unit having an alicyclic hydrocarbon structure substituted with a hydroxyl group or a cyano group. The repeating unit having a hydroxyl group or a cyano group preferably does not have an acid-decomposable group. Examples of repeating units having a hydroxyl group or a cyano group include those described in paragraphs

[0081] to

[0084] of JP 2014-098921 A.

[0213] The resin (A) may have a repeating unit having an alkali-soluble group. Examples of the alkali-soluble group include a carboxyl group, a sulfonamide group, a sulfonylimide group, a bissulfonylimide group, and an aliphatic alcohol group (e.g., a hexafluoroisopropanol group) substituted at the α-position with an electron-withdrawing group, with a carboxyl group being preferred. When the resin (A) contains a repeating unit having an alkali-soluble group, the resolution in contact hole applications is improved. Examples of repeating units having an alkali-soluble group include those described in paragraphs

[0085] and

[0086] of JP 2014-098921 A.

[0214] (Repeating unit having an alicyclic hydrocarbon structure and not exhibiting acid decomposability) Resin (A) may have a repeating unit having an alicyclic hydrocarbon structure and not exhibiting acid decomposability. This can reduce elution of low-molecular-weight components from the resist film into the immersion liquid during immersion exposure. Examples of repeating units having an alicyclic hydrocarbon structure and not exhibiting acid decomposability include repeating units derived from 1-adamantyl(meth)acrylate, diamantyl(meth)acrylate, tricyclodecanyl(meth)acrylate, or cyclohexyl(meth)acrylate.

[0215] (Repeating Unit Represented by Formula (III) Having Neither a Hydroxyl Group nor a Cyano Group) The resin (A) may have a repeating unit represented by formula (III) having neither a hydroxyl group nor a cyano group.

[0216]

[0217] In formula (III), R ５ represents a hydrocarbon group having at least one cyclic structure and having neither a hydroxyl group nor a cyano group. Ra represents a hydrogen atom, an alkyl group, or a —CH ２ -O-Ra ２ represents a group. ２ represents a hydrogen atom, an alkyl group, or an acyl group. Examples of the repeating unit represented by formula (III) that does not have either a hydroxyl group or a cyano group include those described in paragraphs

[0087] to

[0094] of JP 2014-098921 A.

[0218] (Other Repeating Units) Furthermore, the resin (A) may have a repeating unit other than the repeating units described above. For example, the resin (A) may have a repeating unit selected from the group consisting of a repeating unit having an oxathiane ring group, a repeating unit having an oxazolone ring group, a repeating unit having a dioxane ring group, and a repeating unit having a hydantoin ring group.

[0219] In addition to the repeating structural units described above, the resin (A) may have various repeating structural units for the purpose of adjusting dry etching resistance, suitability for a standard developer, substrate adhesion, resist profile, resolution, heat resistance, sensitivity, and the like.

[0220] As the resin (A), particularly when the composition of the present invention is used as an actinic ray-sensitive or radiation-sensitive resin composition for ArF, it is preferable that all of the repeating units are composed of repeating units derived from a compound having an ethylenically unsaturated bond. In particular, it is also preferable that all of the repeating units are composed of (meth)acrylate repeating units. When all of the repeating units are composed of (meth)acrylate repeating units, any of those in which all of the repeating units are methacrylate repeating units, all of the repeating units are acrylate repeating units, or all of the repeating units are a combination of methacrylate repeating units and acrylate repeating units can be used, and it is preferable that the acrylate repeating units account for 50 mol% or less of the total repeating units.

[0221] Resin (A) can be synthesized according to a conventional method (e.g., radical polymerization). The weight average molecular weight (Mw) of resin (A), as measured by GPC in terms of polystyrene, is preferably 30,000 or less, more preferably 1,000 to 30,000, even more preferably 3,000 to 30,000, and particularly preferably 5,000 to 15,000. The dispersity (molecular weight distribution, Mw / Mn) of resin (A) is preferably 1 to 5, more preferably 1 to 3, even more preferably 1.2 to 3.0, and particularly preferably 1.2 to 2.0. The smaller the dispersity, the better the resolution and resist shape, and furthermore, the smoother the sidewalls of the resist pattern and the better the roughness.

[0222] The content of resin (A) in the composition of the present invention is preferably 30.0 to 99.9 mass%, more preferably 40.0 to 99.9 mass%, and even more preferably 60.0 to 90.0 mass%, based on the total solid content of the composition of the present invention. Resin (A) may be used alone or in combination of two or more. When two or more types are used, the total content thereof is preferably within the above-mentioned preferred content range.

[0223] [Compound (B) that generates an acid upon irradiation with actinic rays or radiation] The composition of the present invention may further contain a compound (B) that generates an acid upon irradiation with actinic rays or radiation, and that is different from compound (N). Compound (B) may be in the form of a low molecular weight compound, or may be incorporated into a part of a polymer. Furthermore, the form of a low molecular weight compound and the form of being incorporated into a part of a polymer may be used in combination. When compound (B) is in the form of a low molecular weight compound, the molecular weight of compound (B) is preferably 5,000 or less, more preferably 4,000 or less, and even more preferably 3,000 or less. The lower limit is not particularly limited, but is preferably 100 or more. When compound (B) is in the form of being incorporated into a part of a polymer, it may be incorporated into a part of resin (A) or into a resin different from resin (A). Compound (B) is preferably in the form of a low molecular weight compound.

[0224] Examples of the compound (B) include "M ＋ X － ", and it is preferably a compound that generates an organic acid upon exposure. Examples of the organic acid include sulfonic acids (aliphatic sulfonic acids, aromatic sulfonic acids, camphorsulfonic acids, etc.), carboxylic acids (aliphatic carboxylic acids, aromatic carboxylic acids, aralkyl carboxylic acids, etc.), carbonylsulfonylimide acids, bis(alkylsulfonyl)imide acids, and tris(alkylsulfonyl)methide acids.

[0225] "M ＋ X － In the compound represented by the formula ", M ＋represents a cation, and preferably represents an organic cation. ＋ The description, specific examples and preferred ranges of M in the above formula (1) are ＋ It is similar to that in

[0226] "M ＋ X － In the compound represented by the formula "X － represents an anion, preferably an organic anion. The organic anion is not particularly limited, and examples thereof include monovalent or divalent or higher organic anions. The organic anion is preferably an anion having a significantly low ability to cause a nucleophilic reaction, and more preferably a non-nucleophilic anion.

[0227] Examples of non-nucleophilic anions include sulfonate anions (aliphatic sulfonate anions, aromatic sulfonate anions, camphorsulfonate anions, etc.), carboxylate anions (aliphatic carboxylate anions, aromatic carboxylate anions, aralkyl carboxylate anions, etc.), sulfonylimide anions, bis(alkylsulfonyl)imide anions, and tris(alkylsulfonyl)methide anions.

[0228] The aliphatic moiety in the aliphatic sulfonate anion and the aliphatic carboxylate anion may be a linear or branched alkyl group or a cycloalkyl group, and is preferably a linear or branched alkyl group having 1 to 30 carbon atoms or a cycloalkyl group having 3 to 30 carbon atoms. The alkyl group may be, for example, a fluoroalkyl group (which may have a substituent other than a fluorine atom, or may be a perfluoroalkyl group).

[0229] The aryl group in the aromatic sulfonate anion and aromatic carboxylate anion is preferably an aryl group having 6 to 14 carbon atoms, and examples thereof include a phenyl group, a tolyl group, and a naphthyl group.

[0230] The alkyl group, cycloalkyl group, and aryl group mentioned above may have a substituent. The substituent is not particularly limited, but examples thereof include a nitro group, a halogen atom such as a fluorine atom or a chlorine atom, a carboxyl group, a hydroxyl group, an amino group, a cyano group, an alkoxy group (preferably having 1 to 15 carbon atoms), an alkyl group (preferably having 1 to 10 carbon atoms), a cycloalkyl group (preferably having 3 to 15 carbon atoms), an aryl group (preferably having 6 to 14 carbon atoms), an alkoxycarbonyl group (preferably having 2 to 7 carbon atoms), an acyl group (preferably having 2 to 12 carbon atoms), an alkoxycarbonyloxy group (preferably having 2 to 7 carbon atoms), an alkylthio group (preferably having 1 to 15 carbon atoms), an alkylsulfonyl group (preferably having 1 to 15 carbon atoms), an alkyliminosulfonyl group (preferably having 1 to 15 carbon atoms), and an aryloxysulfonyl group (preferably having 6 to 20 carbon atoms).

[0231] The aralkyl group in the aralkyl carboxylate anion is preferably an aralkyl group having 7 to 14 carbon atoms. Examples of the aralkyl group having 7 to 14 carbon atoms include a benzyl group, a phenethyl group, a naphthylmethyl group, a naphthylethyl group, and a naphthylbutyl group.

[0232] An example of the sulfonylimide anion is a saccharin anion.

[0233] The alkyl group in the bis(alkylsulfonyl)imide anion and the tris(alkylsulfonyl)methide anion is preferably an alkyl group having 1 to 5 carbon atoms. Substituents for these alkyl groups include halogen atoms, alkyl groups substituted with halogen atoms, alkoxy groups, alkylthio groups, alkyloxysulfonyl groups, aryloxysulfonyl groups, and cycloalkylaryloxysulfonyl groups, with fluorine atoms or alkyl groups substituted with fluorine atoms being preferred. Furthermore, the alkyl groups in the bis(alkylsulfonyl)imide anion may be bonded to each other to form a ring structure, which increases the acid strength.

[0234] Other non-nucleophilic anions include, for example, phosphorus fluorides (e.g., PF ６－ ), boron fluorides (e.g., BF ４ － ), and antimony fluorides (e.g., SbF ６ － ) are listed.

[0235] The non-nucleophilic anion is also preferably an anion represented by the following formula (AN1).

[0236]

[0237] In formula (AN1), R １ and R ２ each independently represents a hydrogen atom or a substituent. The substituent is not particularly limited, but a group that is not an electron-withdrawing group is preferred. Examples of groups that are not electron-withdrawing groups include hydrocarbon groups, hydroxyl groups, oxyhydrocarbon groups, oxycarbonyl hydrocarbon groups, amino groups, hydrocarbon-substituted amino groups, and hydrocarbon-substituted amide groups. Examples of groups that are not electron-withdrawing groups include, each independently, -R', -OH, -OR', -OCOR', -NH ２ , -NR' ２ , —NHR′, or —NHCOR′ is preferred, where R′ is a monovalent hydrocarbon group.

[0238] Examples of the monovalent hydrocarbon group represented by R' include monovalent linear or branched hydrocarbon groups such as alkyl groups such as methyl, ethyl, propyl, and butyl; alkenyl groups such as ethenyl, propenyl, and butenyl; alkynyl groups such as ethynyl, propynyl, and butynyl; cycloalkyl groups such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, norbornyl, and adamantyl; monovalent alicyclic hydrocarbon groups such as cycloalkenyl groups such as cyclopropenyl, cyclobutenyl, cyclopentenyl, and norbornenyl; aryl groups such as phenyl, tolyl, xylyl, mesityl, naphthyl, methylnaphthyl, anthryl, and methylanthryl; and aralkyl groups such as benzyl, phenethyl, phenylpropyl, naphthylmethyl, and anthrylmethyl. Among these, R １ and R２ are each independently preferably a hydrocarbon group (preferably a cycloalkyl group) or a hydrogen atom.

[0239] L represents a divalent linking group. When a plurality of L's are present, they may be the same or different. Examples of the divalent linking group include -O-CO-O-, -COO-, -CONH-, -CO-, -O-, -S-, -SO-, and -SO ２ Examples of the divalent linking group include -, an alkylene group (preferably having 1 to 6 carbon atoms), a cycloalkylene group (preferably having 3 to 15 carbon atoms), an alkenylene group (preferably having 2 to 6 carbon atoms), and a divalent linking group formed by combining a plurality of these groups. Among these, examples of the divalent linking group include -O-CO-O-, -COO-, -CONH-, -CO-, -O-, and -SO ２ -, -O-CO-O-alkylene group-, -COO-alkylene group-, or -CONH-alkylene group- is preferred, and -O-CO-O-, -O-CO-O-alkylene group-, -COO-, -CONH-, or -SO ２ - or -COO-alkylene group- is more preferred.

[0240] As L, for example, a group represented by the following formula (AN1-1) is preferable: ａ - (CR ２ａ ２ ) Ｘ -Q-(CR ２ｂ ２ ) Ｙ -* ｂ (AN1-1)

[0241] In formula (AN1-1), * ａ is R in formula (AN1). ３ Represents the bonding position with * ｂ represents -C(R １ ) (R ２ X and Y each independently represent an integer of 0 to 10, preferably an integer of 0 to 3. R ２ａ and R ２ｂ R each independently represents a hydrogen atom or a substituent. ２ａ and R ２ｂ When there are multiple R２ａ and R ２ｂ may be the same or different, provided that when Y is 1 or more, -C(R １ ) (R ２ )- and CR directly bonded ２ｂ ２ R in ２ｂ is other than a fluorine atom. Q is * Ａ -O-CO-O-* Ｂ , * Ａ -CO-* Ｂ , * Ａ -CO-O-* Ｂ , * Ａ -O-CO-* Ｂ , * Ａ -O-* Ｂ , * Ａ -S-* Ｂ , or * Ａ -SO ２ -* Ｂ where X+Y in formula (AN1-1) is 1 or more, and R ２ａ and R ２ｂ are all hydrogen atoms, Q is * Ａ -O-CO-O-* Ｂ , * Ａ -CO-* Ｂ , * Ａ -O-CO-* Ｂ , * Ａ -O-* Ｂ , * Ａ -S-* Ｂ , or * Ａ -SO ２ -* Ｂ Represents. Ａ is R in formula (AN1). ３ represents the bonding position on the side, and * Ｂ represents -SO in formula (AN1). ３ － represents the bonding position on the side.

[0242] In formula (AN1), R ３represents an organic group. The organic group is not particularly limited as long as it has one or more carbon atoms, and may be a linear group (for example, a linear alkyl group), a branched group (for example, a branched alkyl group such as a t-butyl group), or a cyclic group. The organic group may or may not have a substituent. The organic group may or may not have a heteroatom (such as an oxygen atom, a sulfur atom, and / or a nitrogen atom).

[0243] Among them, R ３ is preferably an organic group having a cyclic structure. The cyclic structure may be monocyclic or polycyclic and may have a substituent. The ring in the organic group having a cyclic structure is preferably directly bonded to L in formula (AN1). The organic group having a cyclic structure may or may not have a heteroatom (oxygen atom, sulfur atom, and / or nitrogen atom, etc.). The heteroatom may be substituted for one or more of the carbon atoms forming the cyclic structure. The organic group having a cyclic structure is preferably, for example, a hydrocarbon group having a cyclic structure, a lactone ring group, or a sultone ring group. Among these, the organic group having a cyclic structure is preferably a hydrocarbon group having a cyclic structure. The hydrocarbon group having a cyclic structure is preferably a monocyclic or polycyclic cycloalkyl group. These groups may have a substituent. The cycloalkyl group may be monocyclic (e.g., a cyclohexyl group) or polycyclic (e.g., an adamantyl group), and preferably has 5 to 12 carbon atoms. As the lactone group and sultone group, for example, a group in which one hydrogen atom has been removed from a ring member atom constituting the lactone structure or sultone structure in any of the structures represented by the above-mentioned formulae (LC1-1) to (LC1-22) and the structures represented by the above-mentioned formulae (SL1-1) to (SL1-3) is preferred.

[0244] The non-nucleophilic anion may be a benzenesulfonate anion, and is preferably a benzenesulfonate anion substituted with a branched alkyl group or a cycloalkyl group.

[0245] The non-nucleophilic anion is also preferably an anion represented by the following formula (AN2).

[0246]

[0247] In formula (AN2), o represents an integer of 1 to 3. p represents an integer of 0 to 10. q represents an integer of 0 to 10.

[0248] Xf represents a hydrogen atom, a fluorine atom, an alkyl group substituted with at least one fluorine atom, or an organic group having no fluorine atoms. The number of carbon atoms in this alkyl group is preferably 1 to 10, more preferably 1 to 4. The alkyl group substituted with at least one fluorine atom is preferably a perfluoroalkyl group. Xf is preferably a fluorine atom or a perfluoroalkyl group having 1 to 4 carbon atoms, and is preferably a fluorine atom or CF ３ It is more preferable that both Xf's are fluorine atoms.

[0249] R ４ and R ５ R each independently represents a hydrogen atom, a fluorine atom, an alkyl group, or an alkyl group substituted with at least one fluorine atom. ４ and R ５ If there are multiple ４ and R ５ may be the same or different. ４ and R ５ The alkyl group represented by the formula (I) preferably has 1 to 4 carbon atoms. The alkyl group may have a substituent. ４ and R ５ is preferably a hydrogen atom.

[0250] L represents a divalent linking group, and is defined as L in formula (AN1).

[0251] W represents an organic group containing a cyclic structure. Among these, a cyclic organic group is preferred. Examples of the cyclic organic group include an alicyclic group, an aryl group, and a heterocyclic group. The alicyclic group may be monocyclic or polycyclic. Examples of the monocyclic alicyclic group include a monocyclic cycloalkyl group such as a cyclopentyl group, a cyclohexyl group, and a cyclooctyl group. Examples of the polycyclic alicyclic group include a polycyclic cycloalkyl group such as a norbornyl group, a tricyclodecanyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, and an adamantyl group. Among these, alicyclic groups having a bulky structure with 7 or more carbon atoms, such as a norbornyl group, a tricyclodecanyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, and an adamantyl group, are preferred.

[0252] The aryl group may be monocyclic or polycyclic. Examples of the aryl group include a phenyl group, a naphthyl group, a phenanthryl group, and an anthryl group. The heterocyclic group may be monocyclic or polycyclic. In particular, a polycyclic heterocyclic group can further suppress the diffusion of acid. The heterocyclic group may or may not have aromaticity. Examples of heterocyclic rings having aromaticity include a furan ring, a thiophene ring, a benzofuran ring, a benzothiophene ring, a dibenzofuran ring, a dibenzothiophene ring, and a pyridine ring. Examples of heterocyclic rings having no aromaticity include a tetrahydropyran ring, a lactone ring, a sultone ring, and a decahydroisoquinoline ring. The heterocyclic ring in the heterocyclic group is preferably a furan ring, a thiophene ring, a pyridine ring, or a decahydroisoquinoline ring.

[0253] The cyclic organic group may have a substituent. Examples of the substituent include an alkyl group (which may be either linear or branched, and preferably has 1 to 12 carbon atoms), a cycloalkyl group (which may be either monocyclic, polycyclic, or spirocyclic, and preferably has 3 to 20 carbon atoms), an aryl group (which preferably has 6 to 14 carbon atoms), a hydroxyl group, an alkoxy group, an ester group, an amide group, a urethane group, a ureido group, a thioether group, a sulfonamide group, and a sulfonate ester group. The carbon constituting the cyclic organic group (the carbon that contributes to ring formation) may be a carbonyl carbon.

[0254] The anion represented by formula (AN2) is SO ３ － -CF ２ -CH ２ -OCO-(L) ｑ’ -W, SO ３ － -CF ２ -CHF-CH ２ -OCO-(L) ｑ’ -W, SO ３ － -CF ２ -COO-(L) ｑ’ -W, SO ３ － -CF ２ -CF ２ -CH ２ -CH ２ - (L) ｑ -W or SO ３ － -CF ２ -CH(CF ３ ) -OCO-(L) ｑ’ -W is preferred. Here, L, q and W are the same as those in formula (AN2). q' represents an integer of 0 to 10.

[0255] The non-nucleophilic anion is also preferably an aromatic sulfonate anion represented by the following formula (AN3).

[0256]

[0257] In formula (AN3), Ar represents an aryl group (such as a phenyl group) and may further have a substituent other than the sulfonate anion and the -(D-B) group. Examples of the substituent that may further be had include a fluorine atom and a hydroxyl group. n represents an integer of 0 or greater. n is preferably 1 to 4, more preferably 2 to 3, and even more preferably 3.

[0258] D represents a single bond or a divalent linking group. Examples of the divalent linking group include an ether group, a thioether group, a carbonyl group, a sulfoxide group, a sulfone group, a sulfonate ester group, an ester group, and a group formed by combining two or more of these groups.

[0259] B represents a hydrocarbon group. B is preferably an aliphatic hydrocarbon group, and more preferably an isopropyl group, a cyclohexyl group, or an aryl group which may further have a substituent (such as a tricyclohexylphenyl group).

[0260] As the non-nucleophilic anion, a disulfonamide anion is also preferred. The disulfonamide anion is, for example, N － (SO ２ -R ｑ ) ２ where R ｑ represents an alkyl group which may have a substituent, preferably a fluoroalkyl group, more preferably a perfluoroalkyl group. ｑ may be bonded to each other to form a ring. ｑ The group formed by bonding together is preferably an alkylene group which may have a substituent, more preferably a fluoroalkylene group, and even more preferably a perfluoroalkylene group. The alkylene group preferably has 2 to 4 carbon atoms.

[0261] It is also preferable that the compound (B) is at least one selected from the group consisting of the compounds (I) to (II).

[0262] (Compound (I)) Compound (I) is a compound having one or more structural moieties X and one or more structural moieties Y, which generates an acid containing the first acidic moiety derived from the structural moiety X and the second acidic moiety derived from the structural moiety Y when irradiated with actinic rays or radiation. Structural moiety X: Anionic moiety A １ － and the cationic moiety M １ ＋ and by irradiation with actinic rays or radiation, HA １ Structural moiety Y: anionic moiety A, which forms a first acidic moiety represented by the formula: ２ － and the cationic moiety M ２ ＋ and by irradiation with actinic rays or radiation, HA ２ The compound (I) satisfies the following condition I:

[0263] Condition I: In the compound (I), the cationic moiety M in the structural moiety X １ ＋ and the cationic moiety M in the structural moiety Y ２ ＋ H ＋ The compound PI in which the cation moiety M in the structural moiety X is replaced by １ ＋ H ＋ HA is replaced by １ and the cationic moiety M in the structural moiety Y. ２ ＋ H ＋ HA is replaced by ２ and an acid dissociation constant a2 derived from the acidic site represented by the formula (I), and the acid dissociation constant a2 is greater than the acid dissociation constant a1.

[0264] Condition I will be explained in more detail below. For example, when compound (I) is an acid-generating compound having one of the first acidic sites derived from the structural moiety X and one of the second acidic sites derived from the structural moiety Y, compound PI is "HA １ and H.A.２ The acid dissociation constant a1 and the acid dissociation constant a2 of the compound PI correspond to "a compound having the following structure." More specifically, when the acid dissociation constant of the compound PI is calculated, the acid dissociation constant a1 and the acid dissociation constant a2 of the compound PI correspond to "a compound having the following structure." １ － and H.A. ２ The pKa at which the compound becomes "a compound having the above formula (A)" is the acid dissociation constant a1, １ － and H.A. ２ "A compound having １ － and A ２ － The pKa at which the compound becomes "a compound having the above formula (I)" is the acid dissociation constant a2.

[0265] For example, when compound (I) is an acid-generating compound having two of the first acidic sites derived from the structural site X and one of the second acidic sites derived from the structural site Y, compound PI is a compound having two HAs. １ and one HA ２ When the acid dissociation constant of compound PI is calculated, compound PI corresponds to "a compound having one A １ － and one HA １ and one HA ２ and the acid dissociation constant when "a compound having one A １ － and one HA １ and one HA ２ "Compound having two A １ － and one HA ２ The acid dissociation constant when the compound is a compound having two A's corresponds to the acid dissociation constant a1 described above. １ － and one HA ２ "Compound having two A １ － and A ２ － In other words, in the case of compound PI, the acid dissociation constant when the compound becomes a compound having the cation moiety M in the structural moiety X corresponds to the acid dissociation constant a2. １ ＋ H ＋ HA is replaced by１ When the compound PI has a plurality of acid dissociation constants derived from the acidic moiety represented by the formula (I), the value of the acid dissociation constant a2 is larger than the largest value of the plurality of acid dissociation constants a1. １ － and one HA １ and one HA ２ The acid dissociation constant when the compound is aa is defined as "a compound having one A １ － and one HA １ and one HA ２ "Compound having two A １ － and one HA ２ When the acid dissociation constant when the compound becomes "a compound having the formula (I)" is ab, the relationship between aa and ab satisfies aa<ab.

[0266] The acid dissociation constants a1 and a2 are determined by the above-mentioned method for measuring an acid dissociation constant. The compound PI corresponds to an acid generated when compound (I) is irradiated with actinic rays or radiation. When compound (I) has two or more structural moieties X, the structural moieties X may be the same or different. In addition, when two or more of the above A １ － and two or more of the above M １ ＋ In compound (I), the above A １ － and the above A ２ － , and the above M １ ＋ and the above M ２ ＋ may be the same or different, but １ － and the above A ２ － are preferably different from each other.

[0267] In the compound PI, the difference (absolute value) between the acid dissociation constant a1 (the maximum value when there are multiple acid dissociation constants a1) and the acid dissociation constant a2 is preferably 0.1 or more, more preferably 0.5 or more, and even more preferably 1.0 or more. The upper limit of the difference (absolute value) between the acid dissociation constant a1 (the maximum value when there are multiple acid dissociation constants a1) and the acid dissociation constant a2 is not particularly limited, but is, for example, 16 or less.

[0268] In the compound PI, the acid dissociation constant a2 is preferably not more than 20, more preferably not more than 15. The lower limit of the acid dissociation constant a2 is preferably not less than −4.0.

[0269] In the compound PI, the acid dissociation constant a1 is preferably 2.0 or less, and more preferably 0 or less. The lower limit of the acid dissociation constant a1 is preferably −20.0 or more.

[0270] Anion site A １ － and anionic moiety A ２ － is a structural moiety containing a negatively charged atom or atomic group, and examples thereof include structural moieties selected from the group consisting of formulae (AA-1) to (AA-3) and formulae (BB-1) to (BB-6) shown below. １ － As the anionic moiety A, those capable of forming an acidic moiety with a small acid dissociation constant are preferred, and among these, any of formulas (AA-1) to (AA-3) is more preferred, and any of formulas (AA-1) and (AA-3) is even more preferred. ２ － As the anion moiety A １ － Preferably, it is one that can form an acidic site with a larger acid dissociation constant than the above, more preferably any of formulas (BB-1) to (BB-6), and even more preferably any of formulas (BB-1) and (BB-4). In the following formulas (AA-1) to (AA-3) and formulas (BB-1) to (BB-6), * represents a bonding position. In formula (AA-2), R Ａ represents a monovalent organic group. ＡThe monovalent organic group represented by the formula (I) is not particularly limited, but examples thereof include a cyano group, a trifluoromethyl group, and a methanesulfonyl group.

[0271]

[0272]

[0273] Cationic moiety M １ ＋ and cationic moiety M ２ ＋ is a structural moiety containing a positively charged atom or atomic group, and examples thereof include monovalent organic cations. ＋ Examples of the organic cation include those represented by the following formula:

[0274] (Compound (II)) Compound (II) is a compound having two or more of the above structural moieties X and one or more of the following structural moieties Z, which generates an acid containing two or more of the first acidic moieties derived from the structural moiety X and the structural moiety Z upon irradiation with actinic rays or radiation. Structural moiety Z: a ​​nonionic moiety capable of neutralizing an acid

[0275] In compound (II), the definition of the structural moiety X and A １ － and M １ ＋ The definition of the structural moiety X in the compound (I) and the definition of A １ － and M １ ＋ The definition and preferred embodiments are also the same.

[0276] In the compound (II), the cation moiety M in the structural moiety X １ ＋ H ＋ In the compound PII, the cationic moiety M in the structural moiety X is replaced by １ ＋ H ＋ HA is replaced by １The preferred range of the acid dissociation constant a1 derived from the acidic moiety represented by the formula (I) is the same as the acid dissociation constant a1 in the compound PI. In addition, when the compound (II) is, for example, a compound that generates an acid having two of the first acidic moieties derived from the structural moiety X and the structural moiety Z, the compound PII is a compound that generates an acid having two HAs. １ When the acid dissociation constant of this compound PII was calculated, it was found that the compound PII has "one A １ － and one HA １ and the acid dissociation constant when "a compound having one A １ － and one HA １ "Compound having two A １ － The acid dissociation constant when the compound becomes "a compound having the formula (I)" corresponds to the acid dissociation constant a1.

[0277] The acid dissociation constant a1 is determined by the above-mentioned method for measuring an acid dissociation constant. The compound PII corresponds to the acid generated when the compound (II) is irradiated with actinic rays or radiation. The two or more structural moieties X may be the same or different. １ － and two or more of the above M １ ＋ may be the same or different.

[0278] The nonionic moiety capable of neutralizing an acid in the structural moiety Z is not particularly limited, and is preferably, for example, a moiety containing a group capable of electrostatically interacting with a proton or a functional group having electrons. Examples of the group capable of electrostatically interacting with a proton or the functional group having electrons include functional groups having a macrocyclic structure such as cyclic polyethers, and functional groups having a nitrogen atom with an unshared electron pair that does not contribute to π-conjugation. The nitrogen atom with an unshared electron pair that does not contribute to π-conjugation is, for example, a nitrogen atom having a partial structure shown in the following formula:

[0279]

[0280] Examples of the partial structure of a functional group having a group or electron capable of electrostatically interacting with a proton include a crown ether structure, an azacrown ether structure, a primary amine structure, a secondary amine structure, a tertiary amine structure, a pyridine structure, an imidazole structure, and a pyrazine structure. Of these, a primary amine structure, a secondary amine structure, a tertiary amine structure, and a tertiary amine structure are preferred.

[0281] Examples of moieties other than cations that Compound (I) and Compound (II) may have are shown below.

[0282]

[0283]

[0284] Specific examples of compound (B) include the compounds described in paragraphs

[0320] to

[0321] of WO 2022 / 172715. The above descriptions are incorporated herein by reference.

[0285] The composition of the present invention may or may not contain compound (B). When the composition of the present invention contains compound (B), the content of compound (B) is not particularly limited, but is preferably 0.1% by mass or more, more preferably 1% by mass or more, based on the total solid content of the composition of the present invention. When the composition of the present invention contains compound (B), the content of compound (B) is preferably 30% by mass or less, more preferably 20% by mass or less, based on the total solid content of the composition of the present invention. Compound (B) may be used alone, or two or more types may be used. When two or more types are used, the total content is preferably within the above-mentioned preferred content range.

[0286] [Acid Diffusion Controller] The composition of the present invention may further contain an acid diffusion controller (also referred to as "compound (C)"). Compound (C) is preferably a compound different from compound (N), resin (A), and compound (B). The acid diffusion controller traps acid generated from a photoacid generator or the like upon exposure and acts as a quencher to suppress the reaction of the resin, which becomes more polar due to the action of excess acid generated in unexposed areas. The type of compound (C) is not particularly limited, and examples include basic compounds (CA), low-molecular-weight compounds (CB) having a nitrogen atom and a group that is cleaved by the action of an acid, and compounds (CC) whose acid diffusion control ability is reduced or eliminated by exposure to actinic rays or radiation. Examples of compound (CC) include onium salt compounds (CD) that are weakly acidic relative to the photoacid generator, and basic compounds (CE) whose basicity is reduced or eliminated by exposure to actinic rays or radiation. Specific examples of the basic compound (CA) include those described in paragraphs

[0132] to

[0136] of WO 2020 / 066824, and specific examples of the basic compound (CE) whose basicity is reduced or eliminated by irradiation with actinic rays or radiation include those described in paragraphs

[0137] to

[0155] of WO 2020 / 066824, and those described in paragraph

[0164] of WO 2020 / 066824. Specific examples of the low molecular weight compound (CB) having a nitrogen atom and having a group that leaves under the action of an acid include those described in paragraphs

[0156] to

[0163] of WO 2020 / 066824. Specific examples of the onium salt compound (CD) that is a weak acid relative to the photoacid generator include those described in paragraphs

[0305] to

[0314] of WO 2020 / 158337.

[0287] In addition to the above, for example, known compounds disclosed in paragraphs

[0627] to

[0664] of U.S. Patent Application Publication No. 2016 / 0070167A1, paragraphs

[0095] to

[0187] of U.S. Patent Application Publication No. 2015 / 0004544A1, paragraphs

[0403] to

[0423] of U.S. Patent Application Publication No. 2016 / 0237190A1, and paragraphs

[0259] to

[0328] of U.S. Patent Application Publication No. 2016 / 0274458A1 can be suitably used as the acid diffusion controller.

[0288] The composition of the present invention may or may not contain compound (C). When compound (C) is contained in the composition of the present invention, the content of compound (C) is preferably 0.01 to 30 mass%, more preferably 0.05 to 20 mass%, and even more preferably 0.1 to 15 mass%, based on the total solid content of the composition of the present invention. Compound (C) may be used alone, or two or more types may be used. When two or more types are used, the total content thereof is preferably within the above-mentioned preferred content range.

[0289] [Hydrophobic Resin] The composition of the present invention may further contain a hydrophobic resin (also referred to as "hydrophobic resin") different from resin (A). The hydrophobic resin is preferably designed so as to be unevenly distributed on the surface of the resist film, but unlike surfactants, it does not necessarily have to have a hydrophilic group in the molecule, and it does not necessarily have to contribute to uniform mixing of polar and non-polar substances. Effects of adding a hydrophobic resin include control of the static and dynamic contact angles of water on the resist film surface and suppression of outgassing.

[0290] The hydrophobic resin contains fluorine atoms, silicon atoms, and CH atoms contained in the side chain portion of the resin in order to be unevenly distributed on the surface layer of the film. ３ It is preferable to have one or more of the partial structures, and more preferably two or more. The hydrophobic resin preferably has a hydrocarbon group having 5 or more carbon atoms. These groups may be present in the main chain of the resin or may be substituted on a side chain. Examples of hydrophobic resins include the compounds described in paragraphs

[0275] to

[0279] of WO 2020 / 004306.

[0291] The composition of the present invention may or may not contain a hydrophobic resin. When the composition of the present invention contains a hydrophobic resin, the content of the hydrophobic resin is preferably 0.01 to 20 mass %, more preferably 0.1 to 15 mass %, based on the total solid content of the composition of the present invention. The hydrophobic resin may be used alone, or two or more types may be used. When two or more types are used, the total content thereof is preferably within the above-mentioned preferred content range.

[0292] [Surfactant] The composition of the present invention may contain a surfactant. When a surfactant is contained, a pattern with better adhesion and fewer development defects can be formed. The surfactant is preferably a fluorine-based and / or silicon-based surfactant. Examples of the fluorine-based and / or silicon-based surfactant include the surfactants disclosed in paragraphs

[0218] and

[0219] of WO 2018 / 193954.

[0293] The surfactant may be used alone or in combination of two or more.

[0294] The composition of the present invention may or may not contain a surfactant. When the composition of the present invention contains a surfactant, the content of the surfactant is preferably 0.0001 to 2.0 mass%, more preferably 0.0005 to 1.0 mass%, and even more preferably 0.1 to 1.0 mass%, based on the total solid content of the composition of the present invention. The surfactant may be used alone, or two or more types may be used. When two or more types are used, the total content thereof is preferably within the above-mentioned preferred content range.

[0295] [Solvent] The composition of the present invention preferably contains a solvent. The solvent preferably contains (M1) propylene glycol monoalkyl ether carboxylate and (M2) at least one selected from the group consisting of propylene glycol monoalkyl ether, lactate ester, acetate ester, alkoxypropionate ester, linear ketone, cyclic ketone, lactone, and alkylene carbonate. The solvent may further contain components other than components (M1) and (M2).

[0296] Combining the above-mentioned solvent with the above-mentioned resin is preferable in terms of improving the coatability of the composition of the present invention and reducing the number of development defects in the pattern. The above-mentioned solvent has a good balance of the solubility, boiling point, and viscosity of the above-mentioned resin, and therefore can suppress unevenness in the film thickness of the resist film and the occurrence of precipitates during spin coating. Details of component (M1) and component (M2) are described in paragraphs

[0218] to

[0226] of WO 2020 / 004306, the contents of which are incorporated herein by reference.

[0297] When the solvent further contains components other than the components (M1) and (M2), the content of the components other than the components (M1) and (M2) is preferably 5 to 30 mass % based on the total amount of the solvent.

[0298] The content of the solvent in the composition of the present invention is preferably determined so that the solids concentration is 0.5 to 30% by mass, more preferably 1 to 20% by mass, which further improves the coatability of the composition of the present invention.

[0299] [Other Additives] The composition of the present invention may further contain a dissolution inhibiting compound, a dye, a plasticizer, a photosensitizer, a light absorber, and / or a compound that promotes solubility in a developer (for example, a phenol compound having a molecular weight of 1,000 or less, or an alicyclic or aliphatic compound containing a carboxyl group).

[0300] The "dissolution inhibiting compound" is a compound having a molecular weight of 3,000 or less, which is decomposed by the action of an acid and has a reduced solubility in an organic developer.

[0301] The content of fluorine atoms in the total solid content of the composition of the present invention is preferably 1% by mass or less, more preferably 0.5% by mass or less, and even more preferably 0.1% by mass or less.

[0302] The composition of the present invention is also suitable as a photosensitive composition for EUV exposure.

[0303] <Actinic ray- or radiation-sensitive film, pattern forming method> The present invention also relates to an actinic ray- or radiation-sensitive film formed from the composition of the present invention. The actinic ray- or radiation-sensitive film of the present invention is preferably a resist film. The procedure of the pattern forming method using the composition of the present invention is not particularly limited, but preferably includes the following steps: Step 1: forming a resist film on a substrate using the composition of the present invention; Step 2: exposing the resist film; Step 3: developing the exposed resist film using a developer. The procedure of each of the above steps will be described in detail below.

[0304] (Step 1: Resist Film Forming Step) Step 1 is a step of forming a resist film on a substrate using the composition of the present invention.

[0305] A method for forming a resist film on a substrate using the composition of the present invention includes, for example, applying the composition of the present invention to a substrate. It is preferable to filter the composition of the present invention before application, if necessary. The pore size of the filter is preferably 0.1 μm or less, more preferably 0.05 μm or less, and even more preferably 0.03 μm or less. The filter is preferably made of polytetrafluoroethylene, polyethylene, or nylon.

[0306] The composition of the present invention can be applied onto a substrate (e.g., silicon, silicon coated with silicon dioxide) such as those used in the manufacture of integrated circuit elements by an appropriate application method such as a spinner or coater. Spin application using a spinner is preferred. The rotation speed during spin application using a spinner is preferably 1,000 to 3,000 rpm (rotations per minute). After application of the composition of the present invention, the substrate may be dried to form a resist film. If necessary, various undercoating films (inorganic film, organic film, anti-reflective film) may be formed below the resist film.

[0307] An example of a drying method is a method of drying by heating. Heating can be performed by means provided in a normal exposure machine and / or developing machine, and may also be performed using a hot plate or the like. The heating temperature is preferably 80 to 150°C, more preferably 80 to 140°C, and even more preferably 80 to 130°C. The heating time is preferably 30 to 1,000 seconds, more preferably 60 to 800 seconds, and even more preferably 60 to 600 seconds.

[0308] The thickness of the resist film is not particularly limited, but is preferably 10 to 120 nm from the viewpoint of forming a finer pattern with higher precision. In particular, when EUV exposure is used, the thickness of the resist film is more preferably 10 to 65 nm, and even more preferably 15 to 50 nm. When ArF immersion exposure is used, the thickness of the resist film is more preferably 10 to 120 nm, and even more preferably 15 to 90 nm.

[0309] A top coat may be formed on the resist film using a top coat composition. It is preferable that the top coat composition does not mix with the resist film and can be uniformly applied to the resist film. The top coat is not particularly limited, and a conventionally known top coat can be formed by a conventionally known method. For example, a top coat can be formed based on the description in paragraphs

[0072] to

[0082] of JP 2014-059543 A. For example, a top coat containing a basic compound such as that described in JP 2013-61648 A is preferably formed on the resist film. Specific examples of basic compounds that may be contained in the top coat include the basic compounds that may be contained in the composition of the present invention. It is also preferable that the top coat contain a compound containing at least one group or bond selected from the group consisting of an ether bond, a thioether bond, a hydroxyl group, a thiol group, a carbonyl bond, and an ester bond.

[0310] (Step 2: Exposure Step) Step 2 is a step of exposing the resist film to light. Examples of exposure methods include irradiating the formed resist film with actinic rays or radiation through a predetermined mask. Examples of actinic rays or radiation include infrared rays, visible rays, ultraviolet rays, far ultraviolet rays, extreme ultraviolet rays, X-rays, and electron beams. Actinic rays or radiation preferably have a wavelength of 250 nm or less, more preferably a wavelength of 220 nm or less, and particularly preferably far ultraviolet rays with a wavelength of 1 to 200 nm. Specific examples include KrF excimer laser (248 nm), ArF excimer laser (193 nm), and F ２ These are excimer laser (157 nm), EUV (13.5 nm), X-ray, and electron beam.

[0311] After exposure, it is preferable to bake (heat) the film before developing. Baking promotes the reaction of the exposed areas, resulting in better sensitivity and pattern shape. The heating temperature is preferably 80 to 150°C, more preferably 80 to 140°C, and even more preferably 80 to 130°C. The heating time is preferably 10 to 1,000 seconds, more preferably 10 to 180 seconds, and even more preferably 30 to 120 seconds. Heating can be performed using means provided in a typical exposure machine and / or development machine, and may also be performed using a hot plate or the like. This process is also called post-exposure baking.

[0312] (Step 3: Development Step) Step 3 is a step of developing the exposed resist film using a developer to form a pattern. The developer may be an alkaline developer or a developer containing an organic solvent (also referred to as an "organic developer").

[0313] Examples of development methods include a method in which a substrate is immersed in a tank filled with a developer for a certain period of time (dip method), a method in which a developer is piled up on the surface of a substrate by surface tension and left to stand for a certain period of time for development (puddle method), a method in which a developer is sprayed onto the surface of the substrate (spray method), and a method in which a developer is continuously dispensed onto a substrate rotating at a constant speed while a developer dispense nozzle is scanned at a constant speed (dynamic dispense method). Furthermore, after the development step, a step of stopping development while replacing the solvent with another solvent may be carried out. The development time is not particularly limited as long as it is long enough to sufficiently dissolve the resin in the unexposed areas, and is preferably 10 to 300 seconds, more preferably 20 to 120 seconds. The temperature of the developer is preferably 0 to 50°C, more preferably 15 to 35°C.

[0314] The alkaline developer is preferably an aqueous alkaline solution containing an alkali. The type of alkaline aqueous solution is not particularly limited, but examples include aqueous alkaline solutions containing a quaternary ammonium salt, such as tetramethylammonium hydroxide, an inorganic alkali, a primary amine, a secondary amine, a tertiary amine, an alcohol amine, or a cyclic amine. Of these, the alkaline developer is preferably an aqueous solution of a quaternary ammonium salt, such as tetramethylammonium hydroxide (TMAH). Appropriate amounts of alcohols, surfactants, and the like may be added to the alkaline developer. The alkaline concentration of the alkaline developer is usually preferably 0.1 to 20% by mass. The pH of the alkaline developer is usually preferably 10.0 to 15.0.

[0315] The organic developer is preferably a developer containing at least one organic solvent selected from the group consisting of ketone-based solvents, ester-based solvents, alcohol-based solvents, amide-based solvents, ether-based solvents, and hydrocarbon-based solvents.

[0316] The above-mentioned solvents may be mixed in plural, or may be mixed with a solvent other than the above or water. The water content of the developer as a whole is preferably less than 50% by mass, more preferably less than 20% by mass, even more preferably less than 10% by mass, and particularly preferably substantially free of water. The content of the organic solvent in the organic developer is preferably 50% by mass or more and 100% by mass or less, more preferably 80% by mass or more and 100% by mass or less, even more preferably 90% by mass or more and 100% by mass or less, and particularly preferably 95% by mass or more and 100% by mass or less, based on the total amount of the developer.

[0317] Preferred embodiments of the organic developer include the following embodiments (OD1) and (OD2). (OD1) An embodiment in which the organic developer is n-butyl acetate. (OD2) An embodiment in which the organic developer is a mixed solvent of n-butyl acetate and a hydrocarbon having 11 or more carbon atoms. The mixed solvent of (OD2) above is also referred to as mixed solvent (OD2). The hydrocarbon having 11 or more carbon atoms in mixed solvent (OD2) is preferably an alkane, more preferably an alkane having 11 to 15 carbon atoms, even more preferably an alkane having 11 to 13 carbon atoms, particularly preferably undecane or dodecane, and most preferably undecane. Note that when structural isomers exist, such as undecane and dodecane, the hydrocarbon having 11 or more carbon atoms may contain the structural isomer. The hydrocarbon having 11 or more carbon atoms contained in mixed solvent (OD2) may be one type or two or more types. The content of hydrocarbons having 11 or more carbon atoms in the mixed solvent (OD2) (the total amount when multiple hydrocarbons having 11 or more carbon atoms are contained) is preferably 1% by mass or more and 35% by mass or less, more preferably 5% by mass or more and 30% by mass or less, and even more preferably 10% by mass or more and 25% by mass or less, based on 100% by mass of the entire mixed solvent (OD2).

[0318] The content of n-butyl acetate in the mixed solvent (OD2) is preferably 65% ​​by mass or more and 99% by mass or less, more preferably 70% by mass or more and 95% by mass or less, and even more preferably 75% by mass or more and 90% by mass or less, with the entire mixed solvent (OD2) being 100% by mass.

[0319] A particularly preferred embodiment of the mixed solvent (OD2) is one containing n-butyl acetate and undecane, with the mass ratio of "n-butyl acetate / undecane" being "90 / 10".

[0320] The developer may contain other components in addition to the components described above. Examples of other components include surfactants, antioxidants, basic compounds, etc. The content of other components in the developer is preferably 0% by mass or more and 5% by mass or less, more preferably 0% by mass or more and 1% by mass or less, even more preferably 0% by mass or more and 0.5% by mass or less, based on 100% by mass of the entire developer, and particularly preferably 0% by mass (i.e., no other components are contained).

[0321] (Other Steps) The pattern formation method preferably includes, after step 3, a step of cleaning with a rinse liquid.

[0322] The rinse liquid used in the rinse step after the development step using an alkaline developer can be, for example, pure water. A suitable amount of surfactant may be added to the pure water. A suitable amount of surfactant may be added to the rinse liquid.

[0323] The rinse liquid used in the rinse step after the development step using an organic developer is not particularly limited as long as it does not dissolve the pattern, and a solution containing a general organic solvent can be used. The rinse liquid is preferably a rinse liquid containing at least one organic solvent selected from the group consisting of hydrocarbon solvents, ketone solvents, ester solvents, alcohol solvents, amide solvents, and ether solvents.

[0324] The method for the rinsing step is not particularly limited, and examples include a method in which a rinsing solution is continuously discharged onto a substrate rotating at a constant speed (spin coating method), a method in which a substrate is immersed in a tank filled with the rinsing solution for a certain period of time (dipping method), and a method in which the rinsing solution is sprayed onto the substrate surface (spray method). The pattern formation method may also include a heating step (post-bake) after the rinsing step. This step removes the developer and rinsing solution remaining between and within the pattern by baking. This step also has the effect of annealing the resist pattern and improving the surface roughness of the pattern. The heating step after the rinsing step is typically performed at 40 to 250°C (preferably 90 to 200°C) for typically 10 seconds to 3 minutes (preferably 30 to 120 seconds).

[0325] Alternatively, the substrate may be etched using the formed pattern as a mask. That is, the substrate (or the underlayer film and the substrate) may be processed using the pattern formed in step 3 as a mask to form a pattern on the substrate. The method for processing the substrate (or the underlayer film and the substrate) is not particularly limited, but a method of forming a pattern on the substrate by dry etching the substrate (or the underlayer film and the substrate) using the pattern formed in step 3 as a mask is preferred. The dry etching is preferably oxygen plasma etching.

[0326] The composition of the present invention and various materials used in the pattern formation method (e.g., solvents, developers, rinse solutions, anti-reflective coating compositions, top coat compositions, etc.) preferably do not contain impurities such as metals. The content of impurities contained in these materials is preferably 1 mass ppm (parts per million) or less, more preferably 10 mass ppb (parts per billion) or less, even more preferably 100 mass ppt or less, particularly preferably 10 mass ppt or less, and most preferably 1 mass ppt or less. There is no particular lower limit, and 0 mass ppt or more is preferred. Here, examples of metal impurities include Na, K, Ca, Fe, Cu, Mg, Al, Li, Cr, Ni, Sn, Ag, As, Au, Ba, Cd, Co, Pb, Ti, V, W, and Zn.

[0327] Examples of methods for removing impurities such as metals from various materials include filtration using a filter. Details of filtration using a filter are described in paragraph

[0321] of WO 2020 / 004306.

[0328] Methods for reducing impurities such as metals contained in various materials include, for example, selecting raw materials with a low metal content as raw materials for the various materials, filtering the raw materials for the various materials, and performing distillation under conditions that minimize contamination as much as possible, for example by lining the inside of the apparatus with Teflon (registered trademark).

[0329] In addition to filter filtration, impurities may be removed using an adsorbent, or a combination of filter filtration and an adsorbent may be used. Known adsorbents can be used as the adsorbent, including inorganic adsorbents such as silica gel and zeolite, and organic adsorbents such as activated carbon. In order to reduce impurities such as metals contained in the various materials, it is necessary to prevent the incorporation of metal impurities during the manufacturing process. Whether metal impurities have been sufficiently removed from the manufacturing equipment can be confirmed by measuring the content of metal components contained in the cleaning solution used to clean the manufacturing equipment. The content of metal components contained in the used cleaning solution is preferably 100 parts per trillion (ppt) by mass or less, more preferably 10 ppt by mass or less, and even more preferably 1 ppt by mass or less. There is no particular lower limit, and 0 ppt by mass or more is preferred.

[0330] A conductive compound may be added to an organic processing liquid such as a rinse solution to prevent breakdown of the chemical solution piping and various parts (filters, O-rings, tubes, etc.) due to static charging and subsequent electrostatic discharge. The conductive compound is not particularly limited, but examples include methanol. The amount added is not particularly limited, but in order to maintain favorable development or rinsing characteristics, it is preferably 10% by mass or less, more preferably 5% by mass or less. There is no particular lower limit, but 0.01% by mass or more is preferred. For the chemical solution piping, for example, stainless steel (SUS), or various piping coated with antistatically treated polyethylene, polypropylene, or fluororesin (such as polytetrafluoroethylene or perfluoroalkoxy resin), can be used. Similarly, for the filters and O-rings, antistatically treated polyethylene, polypropylene, or fluororesin (such as polytetrafluoroethylene or perfluoroalkoxy resin), can be used.

[0331] <Method for manufacturing an electronic device> The present invention also relates to a method for manufacturing an electronic device, including the above-mentioned pattern formation method, and an electronic device manufactured by this manufacturing method. A preferred embodiment of the electronic device of the present invention is one that is installed in electrical and electronic equipment (such as home appliances, office automation (OA), media-related equipment, optical equipment, and communication equipment).

[0332] The present invention will be described in more detail below with reference to the following examples. The materials, amounts used, ratios, treatment details, and treatment procedures shown in the following examples can be appropriately changed without departing from the spirit of the present invention. Therefore, the scope of the present invention should not be construed as being limited by the following examples.

[0333] The various components used in the resist compositions of the examples and comparative examples are shown below.

[0334] <Compound (N)> Compounds (I)-1 to (I)-21 were used as compounds (N). (I)-1 to (I)-21 can function as photoacid generators. In addition, (Z)-1 and (Z)-2 were used as photoacid generators other than compound (N). In Table 4 below, (Z)-1 and (Z)-2 are also listed in the column for compound (N) for convenience.

[0335]

[0336]

[0337]

[0338] A synthesis example of the compound (N) is shown below.

[0339] (Synthesis of (I)-1)

[0340]

[0341] In a three-neck flask, 150 g of 2,3,5-triiodobenzoic acid (Tokyo Chemical Industry Co., Ltd.), 200 mL of toluene, and 5.9 g of N,N-dimethylformamide were mixed under a nitrogen atmosphere and heated to 60°C. Thionyl chloride (Fujifilm Wako Pure Chemical Industries, Ltd.) was added dropwise over 1 hour, and the mixture was stirred for 3 hours. The reaction solution was evaporated under reduced pressure, and then 100 mL of toluene was added and evaporated again under reduced pressure, yielding 150 g of (I)-1-A as a yellow solid. In a three-neck flask under a nitrogen atmosphere, 18 g of 1-BOC-4-hydroxypiperidine (1-(tert-butoxycarbonyl)-4-hydroxypiperidine) (manufactured by FUJIFILM Wako Pure Chemical Industries, Ltd.), 180 mL of dichloromethane, 50 mL of triethylamine, and 21.9 g of 4-dimethylaminopyridine (DMAP) (manufactured by FUJIFILM Wako Pure Chemical Industries, Ltd.) were mixed (reaction solution 1). 70 g of (I)-1-A was dissolved in 360 mL of dichloromethane (reaction solution 2). Reaction solution 1 was cooled to 5°C, and reaction solution 2 was added dropwise over 30 minutes. The liquid temperature was then raised to 20°C and stirred for 20 hours. The reaction solution was cooled to 10°C, and 500 mL of saturated aqueous sodium bicarbonate solution was added, and the organic layer was extracted using a separatory funnel. The obtained organic layer was further washed with 1 mol / L hydrochloric acid (1N HCl), 1 mol / L aqueous sodium hydroxide solution (1N NaOH), and saturated saline, and then the solvent was distilled off to obtain 50 g of (I)-1-B as a white solid. In a three-necked flask, 25 g of (I)-1-B and 50 mL of dichloromethane were mixed under a nitrogen atmosphere and cooled to 5°C. 25 g of trifluoroacetic acid (Tokyo Chemical Industry Co., Ltd.) was added dropwise over 20 minutes, and then the temperature was raised to 20°C and stirred for 8 hours. The reaction solution was dissolved in a saturated aqueous sodium bicarbonate solution (NaHCO ３aq), and the organic layer was extracted using a separatory funnel. The organic layer was washed with saturated saline, and the solvent was then distilled off to obtain 16.7 g of (I)-1-C as a colorless, transparent liquid. In a three-neck flask, 3.1 g of (I)-1-D and 15 g of tetrahydrofuran (THF) were mixed under a nitrogen atmosphere (Reaction Solution 3). 16.7 g of (I)-1-C and 46 g of THF were mixed to obtain a homogeneous solution (Reaction Solution 4). Reaction Solution 3 was cooled to -15°C, and Reaction Solution 4 was added dropwise over 1 hour, followed by stirring for an additional 1 hour. The mixture was heated to 20°C and stirred for 2 hours. After that, 45 mL of distilled water, 21 mL of ethyl acetate, and 21 mL of hexane were added, and the organic layer was extracted using a separatory funnel. The organic layer was washed with 1 N HCl and saturated sodium bicarbonate. After distilling off the solvent, the residue was purified by silica gel column chromatography using a mixture of ethyl acetate and hexane as an eluent, yielding 3.9 g of (I)-1-E as a white solid. In a three-neck flask, 3.5 g of (I)-1-E, 30 g of THF, 0.9 g of sodium bicarbonate, and 18 g of distilled water were mixed under a nitrogen atmosphere, heated to 60°C, and stirred for 3 hours. 5 mL of 1N HCl and 10 mL of distilled water were added, followed by the addition of 30 mL of saturated aqueous sodium bicarbonate solution. 40 mL of ethyl acetate and 20 mL of hexane were added, and the solid precipitated by stirring was collected by filtration, yielding 3.5 g of (I)-1-F as a white solid.

[0342]

[0343] In a three-necked flask, 2.1 g of (I)-1-G, 3.3 g of (I)-1-F, 29 g of distilled water, and 44 g of methylene chloride were mixed under a nitrogen atmosphere and stirred at 20°C for 3 hours. After removing the aqueous layer using a separatory funnel, the organic layer was washed twice with 50 mL of ion-exchanged water. After distilling off the solvent from the washed organic layer under reduced pressure, crystallization was performed using diisopropyl ether to obtain 4.6 g of (I)-1 as a white solid. The resulting (I)-1 was identified as follows: １ H-NMR (nuclear magnetic resonance) and １９ F-NMR was used. １H-NMR (400 MHz, acetone-d6) d = 8.43 (d, 1H), 8.38 (d, 6H), 8.23 ​​(d, 6H), 7.89 (d, 1H), 6.20 (s, 1H), 3.46-3.81 (m, 4H), 1.81-2.20 (m, 4H) ppm １９ F-NMR (376.6 MHz, acetone-d6) d = -63.9, -101.6 ppm

[0344] (I)-2 to (I)-21 were synthesized according to the synthesis method of (I)-1.

[0345] <Resin (A)> A-1 to A-35 were used as resins (A) (resins whose polarity increases under the action of acid). A-1 to A-35 were synthesized according to known methods. Table 1 below shows the content (mol %), weight average molecular weight (Mw), and dispersity (Mw / Mn) of each repeating unit contained in each resin. The content of a repeating unit is the ratio (molar ratio) of each repeating unit to all repeating units contained in each resin. Each repeating unit is shown by the structure of the corresponding monomer. The weight average molecular weight (Mw) and dispersity (Mw / Mn) of the resin were measured by GPC (carrier: tetrahydrofuran (THF)) (amounts converted into polystyrene). The content of a repeating unit was １３ Measurement was performed by C-NMR (nuclear magnetic resonance).

[0346]

[0347] The structural formulae of the monomers (corresponding to each repeating unit) listed in Table 1 are shown below.

[0348]

[0349]

[0350]

[0351] <Compound (B)> As the compound (B), B-1 to B-19 were used.

[0352]

[0353]

[0354]

[0355]

[0356] <Compound (C)> Compounds (C) (acid diffusion controllers) used were C-1 to C-14 and D-1 to D-5.

[0357]

[0358]

[0359]

[0360] <Hydrophobic Resin> E-1 to E-8 were used as hydrophobic resins. The structural formula of each repeating unit contained in E-1 to E-8 is shown below. For each resin, the content (mol %; corresponding in order from left to right) of each repeating unit relative to the total repeating units contained, the weight average molecular weight (Mw), and the dispersity (Mw / Mn) are shown in Table 2 below. The content of each repeating unit is the content ratio (molar ratio) of each repeating unit relative to the total repeating units contained in each resin. The weight average molecular weight (Mw) and dispersity (Mw / Mn) of the resin were measured by GPC (carrier: tetrahydrofuran (THF)) (polystyrene equivalent). The content of the repeating unit was １３ Measurement was performed by C-NMR.

[0361]

[0362]

[0363] <Surfactants> The surfactants used are as follows: F-1: Megafac F176 (manufactured by DIC Corporation, fluorochemical surfactant) F-2: Megafac R08 (manufactured by DIC Corporation, fluorine and silicon surfactant) F-3: PF656 (manufactured by OMNOVA, fluorochemical surfactant)

[0364] <Solvents> The solvents used are as follows: G-1: Propylene glycol monomethyl ether acetate (PGMEA) G-2: Propylene glycol monomethyl ether (PGME) G-3: Propylene glycol monoethyl ether (PGEE) G-4: Cyclohexanone G-5: Cyclopentanone G-6: 2-heptanone G-7: Ethyl lactate G-8: γ-butyrolactone G-9: Propylene carbonate

[0365] <Preparation and Coating of Resist Compositions> The components shown in Tables 3 and 4 below were mixed to a solids concentration of 2% by mass. The resulting mixture was filtered through a polyethylene filter with a pore size of 0.02 μm to prepare each resist composition. "Solids" refers to components other than the solvent. These resist compositions were applied to a 6-inch Si (silicon) wafer previously treated with hexamethyldisilazane (HMDS) using a Tokyo Electron "Mark 8" spin coater, and dried on a hot plate at 130°C for 300 seconds to obtain a resist film with a thickness of 35 nm. Here, 1 inch is 0.0254 m. In Tables 3 and 4, entries separated by " / " in the "Type" column indicate that the wafer contains multiple compounds, and entries separated by " / " in the "Wt%" column indicate the content of multiple compounds in order. In Tables 3 and 4, the "Wt%" column indicates the content (wt%) of each solid component relative to the total solids content. In Tables 3 and 4, the "mixing ratio" column of "solvent" indicates the mixing ratio (mass ratio) of each solvent.

[0366]

[0367]

[0368] [EUV Exposure] The wafer coated with the resist film obtained above was subjected to pattern exposure using an EUV exposure apparatus (Micro Exposure Tool, NA (numerical aperture) 0.3, Quadruple, outer sigma 0.68, inner sigma 0.36) manufactured by Exitech Corp. An exposure mask with a line width of 14 nm and a 1:1 line and space pattern was used.

[0369] The exposed wafer was developed and evaluated by the following method.

[0370] [Alkali Development (Examples 1-1 to 1-42, and Comparative Examples 1-1 and 1-2)] The exposed wafer was heated on a hot plate at 100°C for 90 seconds, then immersed in a 2.38% by mass aqueous solution of tetramethylammonium hydroxide (TMAH) for 60 seconds, and then rinsed with water for 30 seconds. The wafer was then rotated at 4000 rpm for 30 seconds, baked at 95°C for 60 seconds, and dried to obtain a positive resist pattern. In this manner, the resist patterns of Examples 1-1 to 1-42 and Comparative Examples 1-1 and 1-2 were obtained. The resist compositions used are shown in Table 5.

[0371] <Evaluation of Pattern Shape (Cross-Sectional Rectangularity) (Part 1)> The resist patterns of each Example and Comparative Example (Examples 1-1 to 1-42, and Comparative Examples 1-1 and 1-2) obtained by alkali development were evaluated according to the following procedure. The cross-sectional shape of the resulting line pattern of each Example and Comparative Example, with an average line width of 14 nm, was observed using a critical dimension scanning electron microscope (SEM, S-9380II manufactured by Hitachi, Ltd.), and the pattern line width Lb at the bottom of the resist pattern and the pattern line width La at the top of the resist pattern were measured. Using the value of Lb / La as an index, the cross-sectional rectangularity of the pattern shape was evaluated according to the following criteria: S is the best, and F is the worst. In practical terms, a rating of D or higher is desirable. The results are shown in Table 5.

[0372] [Evaluation Criteria] S: 1.00≦(Lb / La)≦1.01 A: 1.01<(Lb / La)≦1.02 B: 1.02<(Lb / La)≦1.03 C: 1.03<(Lb / La)≦1.04 D: 1.04<(Lb / La)≦1.05 E: 1.05<(Lb / La)≦1.06 F:1.06<(Lb / La)

[0373] <Evaluation of Stability Over Time (Part 1)> The pattern shape (cross-sectional rectangularity) was evaluated in the same manner as in <Evaluation of Pattern Shape (Cross-Sectional Rectangularity) (Part 1)> above, except that the resist composition was stored at 4°C for 6 months. The evaluation criteria were also the same as those described above. The results are shown in Table 5.

[0374]

[0375] [Organic Solvent Development (Examples 2-1 to 2-42, Comparative Examples 2-1 and 2-2, Examples 3-1 to 3-42, and Comparative Examples 3-1 and 3-2)] Wafers exposed by the method described in [EUV Exposure] above were heated on a hot plate at 90°C for 60 seconds, then developed for 30 seconds with the developers shown in Tables 6 and 7, and spin-dried to obtain negative resist patterns. In this manner, resist patterns for Examples 2-1 to 2-42, Comparative Examples 2-1 and 2-2, Examples 3-1 to 3-42, and Comparative Examples 3-1 and 3-2 were obtained. The resist compositions used are shown in Tables 6 and 7. The developers (J-1 and J-2) shown in Tables 6 and 7 are as follows: J-1: n-butyl acetate J-2: n-butyl acetate / undecane=90 / 10 (mass ratio)

[0376] <Evaluation of Pattern Shape (Cross-Sectional Rectangularity) (Part 2)> The resist patterns of each of the Examples and Comparative Examples (Examples 2-1 to 2-42, Comparative Examples 2-1 and 2-2, Examples 3-1 to 3-42, and Comparative Examples 3-1 and 3-2) obtained by organic solvent development were evaluated according to the following procedure. The cross-sectional shape of the resulting line pattern of each of the Examples and Comparative Examples, each having an average line width of 14 nm, was observed using a length-measuring scanning electron microscope (SEM, S-9380II manufactured by Hitachi, Ltd.), and the pattern line width Lb at the bottom of the resist pattern and the pattern line width La at the top of the resist pattern were measured. Using the value of La / Lb as an index, the cross-sectional rectangularity of the pattern shape was evaluated according to the following criteria: S is the best, and F is the worst. In practical terms, a rating of D or higher is desirable. The results are shown in Tables 6 and 7.

[0377] [Evaluation Criteria] S: 1.00≦(La / Lb)≦1.01 A: 1.01<(La / Lb)≦1.02 B: 1.02<(La / Lb)≦1.03 C: 1.03<(La / Lb)≦1.04 D: 1.04<(La / Lb)≦1.05 E: 1.05<(La / Lb)≦1.06 F:1.06<(La / Lb)

[0378] <Evaluation of temporal stability> The pattern shape (cross-sectional rectangularity) was evaluated in the same manner as in <Evaluation of pattern shape (cross-sectional rectangularity) (part 2)> above, except that the resist composition was stored at 4°C for 6 months. The evaluation criteria were also the same as those described above. The results are shown in Tables 6 and 7.

[0379]

[0380]

[0381] The results in Tables 5 to 7 show that the resist compositions used in the examples are capable of forming patterns with excellent shape and have excellent stability over time.

[0382] The present invention provides an actinic ray-sensitive or radiation-sensitive resin composition that can form a pattern with excellent shape and has excellent stability over time. The present invention also provides a resist film formed using the actinic ray-sensitive or radiation-sensitive resin composition, a pattern formation method and an electronic device production method that use the actinic ray-sensitive or radiation-sensitive resin composition, and a compound that can be used in the actinic ray-sensitive or radiation-sensitive resin composition.

[0383] Although the present invention has been described in detail and with reference to specific embodiments, it will be apparent to those skilled in the art that various changes and modifications can be made without departing from the spirit and scope of the present invention. This application is based on a Japanese patent application (Patent Application No. 2024-000144) filed on January 4, 2024, the contents of which are incorporated herein by reference.

Claims

1. A radiation-sensitive or radiation-sensitive resin composition containing a compound (N) represented by the following formula (1) and a resin. In formula (1), Z １ represents -SO ３ － or -SO ２ -N － -SO ２ -Rf. Rf represents a fluorine atom or a fluoroalkyl group. Y １ represents an alkylene group, a cycloalkylene group or an arylene group. However, at least one of the hydrogen atoms of the alkylene group, cycloalkylene group or arylene group represented by Y １ is substituted with at least one selected from the group consisting of a fluorine atom and a fluoroalkyl group. X １ represents a single bond or a divalent linking group. W １ and V １ each independently represent an organic group. W １ and V １ may combine to form a ring. q represents an integer of 1 or more. M ＋ represents a cation.

2. The radiation-sensitive or radiation-sensitive resin composition according to claim 1, wherein the compound (N) is represented by the following formula (2). In formula (2), Z １ is -SO ３ － or -SO ２ -N － -SO ２ -Rf represents. Rf represents a fluorine atom or a fluoroalkyl group. Rf １ and Rf ２ each independently represent a fluorine atom or a fluoroalkyl group. Rf １ and Rf ２ When there are a plurality of them, the plurality of Rf １ and the plurality of Rf ２ may be the same or different from each other. p represents an integer of 1 or more. W １ and V １ each independently represent an organic group. W １ and V １ may combine to form a ring. q represents an integer of 1 or more. M ＋ represents a cation.

3. The radiation-sensitive or radiation-sensitive resin composition according to claim 1, wherein the compound (N) is represented by the following formula (3). In formula (3), Z １ is -SO ３ － or -SO ２ -N － -SO ２ -Rf represents. Rf represents a fluorine atom or a fluoroalkyl group. Rf １ and Rf ２ each independently represents a fluorine atom or a fluoroalkyl group. Rf １ and Rf ２ When there are a plurality of them, the plurality of Rf １ and the plurality of Rf ２ may be the same or different from each other. p represents an integer of 1 or more. V １ represents an organic group. W ２ represents a hydrocarbon group. W ２ and V １ may combine to form a ring. R １ represents an organic group having an iodine atom. q1 and q2 each independently represent an integer of 0 or more. However, at least one of q1 and q2 represents an integer of 1 or more. P １ represents an organic group having no iodine atom. q3 represents an integer of 0 or more. M ＋ represents a cation.

4. W in the formula (3) ２ and V １ are combined to form a ring, and the radiation-sensitive or radiation-sensitive resin composition according to claim 3.

5. W in the formula (3) ２ The radiation-sensitive or radiation-sensitive resin composition according to claim 3, wherein represents a saturated hydrocarbon group or an aromatic hydrocarbon group.

6. The radiation-sensitive or actinic ray-sensitive resin composition according to claim 3, wherein q2 in the formula (3) represents an integer of 1 or more.

7. R in the formula (3) １ At least one of them is —CO—O—R ２ , —O—CO—R ２ , —O—CO—O—R ２ , —SO ２ —R ２ or —SO ３ —R ２ represents, and R ２ represents an organic group having an iodine atom. The radiation-sensitive or radiation-sensitive resin composition according to claim 6.

8. Z in the formula (1) １ represents -SO ３ － The photosensitive or radiation-sensitive resin composition according to claim 1.

9. The radiation-sensitive or actinic ray-sensitive resin composition according to claim 2, wherein p in the formula (2) represents an integer of 1 to 3.

10. The radiation-sensitive or radiation-sensitive resin composition according to claim 1, wherein the compound (N) is represented by the following formula (4). In formula (4), Z １ is -SO ３ － or -SO ２ -N － -SO ２ -Rf represents. Rf represents a fluorine atom or a fluoroalkyl group. Rf １ and Rf ２ each independently represent a fluorine atom or a fluoroalkyl group. Rf １ and Rf ２ When a plurality of them are present, the plurality of Rf １ and the plurality of Rf ２ may be the same or different from each other. p represents an integer of 1 or more. K １ represents a ring containing a nitrogen atom in the ring members. L １ represents a single bond or a divalent linking group. Ar １ represents an aromatic group. R １ represents an organic group having an iodine atom. P １ represents an organic group having no iodine atom. P １ and Ar １ may combine to form a ring. q4 represents an integer of 1 or more. q5 and q6 each independently represent an integer of 0 or more. M ＋ represents a cation.

11. M in the formula (1) ＋ The radiation-sensitive or actinic ray-sensitive resin composition according to claim 1, wherein M represents a sulfonium cation or an iodonium cation.

12. M in the formula (1) ＋ represents a sulfonium cation having one or more fluorine atoms or an iodonium cation having one or more fluorine atoms, The active ray-sensitive or radiation-sensitive resin composition according to claim 1.

13. The radiation-sensitive or actinic ray-sensitive resin composition according to claim 1, wherein q in the formula (1) represents an integer of 3 or more.

14. W in the formula (1) １ The radiation-sensitive or radiation-sensitive resin composition according to claim 1, which has an aromatic group in which three or more iodine atoms are bonded to the same aromatic ring.

15. A resist film formed using the radiation-sensitive or actinic ray-sensitive resin composition according to any one of claims 1 to 14.

16. A pattern forming method comprising: a step of forming a resist film on a substrate using the radiation-sensitive or actinic ray-sensitive resin composition according to any one of claims 1 to 14; a step of exposing the resist film; and a step of developing the exposed resist film using a developer.

17. A method for manufacturing an electronic device, including the pattern forming method according to claim 16.

18. A compound represented by the following formula (3). In formula (3), Z １ represents -SO ３ － or -SO ２ -N － -SO ２ -Rf. Rf represents a fluorine atom or a fluoroalkyl group. Rf １ and Rf ２ each independently represent a fluorine atom or a fluoroalkyl group. When there are a plurality of Rf １ and a plurality of Rf ２ are present, the plurality of Rf １ and the plurality of Rf ２ may be the same or different from each other. p represents an integer of 1 or more. V １ represents an organic group. W ２ represents a hydrocarbon group. W ２ and V １ may combine to form a ring. R １ represents an organic group having an iodine atom. q1 and q2 each independently represent an integer of 0 or more. However, at least one of q1 and q2 represents an integer of 1 or more. P １ represents an organic group having no iodine atom. q3 represents an integer of 0 or more. M ＋ represents a cation.

19. W in the formula (3) ２ and V １ are combined to form a ring, and the compound according to claim 18 20. The compound according to claim 18, wherein the compound is a compound represented by the following formula (4). In formula (4), Z １ represents -SO ３ － or -SO ２ -N － -SO ２ -Rf. Rf represents a fluorine atom or a fluoroalkyl group. Rf １ and Rf ２ each independently represents a fluorine atom or a fluoroalkyl group. When there are a plurality of Rf １ and a plurality of Rf ２ exist, the plurality of Rf １ and the plurality of Rf ２ may be the same or different from each other. p represents an integer of 1 or more. K １ represents a ring containing a nitrogen atom in the ring members. L １ represents a single bond or a divalent linking group. Ar １ represents an aromatic group. R １ represents an organic group having an iodine atom. P １ represents an organic group having no iodine atom. P １ and Ar １ may combine to form a ring. q4 represents an integer of 1 or more. q5 and q6 each independently represent an integer of 0 or more. M ＋ represents a cation.

Images