TW202212368A - Colored curable resin composition, color filter, and display device wherein the colored curable resin composition contains colorant, resin, polymerizable compound and polymerization initiator - Google Patents

Abstract

The object of the present invention is to provide a colored curable resin composition and the like which can provide a color filter with excellent dark effect. The colored curable resin composition is characterized by containing colorant (A), resin (B), polymerizable compound (C) and polymerization initiator (D). As for the resin (B), it contains a polymer whose constituent units include (meth)acrylate unit (a1) containing tertiary carbon and unsaturated monomer unit (b1) with acid group.

Description

Colored curable resin composition, color filter, and display device

The present invention relates to a colored curable resin composition, a color filter and a display device.

In recent years, with regard to display displays, development for expanding the displayable color reproduction area has been advanced, and as a part of this, color filters are also required to have darker colors. As a method of darkening a color filter, a method of increasing the colorant concentration in the color filter is exemplified. However, when the colorant concentration is increased, the pattern shape is deteriorated, and the performance is insufficient. In addition, in order to have target color characteristics, the color filter needs to be formed into a thick film, but when applied to a liquid crystal display device, since color mixing with light from adjacent pixels occurs, thickening of the film is also unfavorable.

For example, Patent Document 1 describes a colorable curable resin composition containing a colorant, a resin, a predetermined polymerizable compound, a polymerization initiator, and a thiol compound, but it is desired to further improve darkening (dark effect) . [Prior Art Literature] [Patent Literature]

[Patent Document 1] Japanese Patent Laid-Open No. 2020-041154

[The problem to be solved by the invention]

Therefore, the present invention has disclosed as an object to provide a colorable curable resin composition and the like capable of providing a color filter having an excellent dark color effect. [Means of Solving Problems]

That is, the colored curable resin composition, color filter, and display device of the present invention have the following points. [1] A colored curable resin composition characterized by comprising a colorant (A), a resin (B), a polymerizable compound (C) and a polymerization initiator (D), As the resin (B), a polymer containing a tertiary carbon-containing (meth)acrylate unit (a1) and an acid group-containing unsaturated monomer unit (b1) as a constituent unit is contained. [2] The colored curable resin composition according to [1], wherein the (b1) unsaturated monomer having an acid group is at least one selected from acrylic acid and methacrylic acid. [3] The colored curable resin composition according to [1] or [2], wherein the resin (B) has an acid value exceeding 80 mgKOH/g and a weight average molecular weight of 9000 or less. [4] The colorable curable resin composition according to any one of [1] to [3], wherein the colorant (A) contains at least a green colorant. [5] The colorable curable resin composition according to [4], wherein the green colorant is at least one selected from the group consisting of C.I. Pigment Green 58 and C.I. Pigment Green 59. [6] The colored curable resin composition according to any one of [1] to [5], wherein the colorant (A) further includes a yellow colorant selected from C.I. Pigment Yellow 138 , at least one of C.I. Pigment Yellow 139, C.I. Pigment Yellow 150, and C.I. Pigment Yellow 185. [7] A color filter formed of the colorable curable resin composition according to any one of [1] to [6]. [8] A display device including the color filter described in [7]. [Effect of invention]

ADVANTAGE OF THE INVENTION According to this invention, the colorable curable resin composition which forms the color filter excellent in the dark color effect can be provided.

The colorable curable resin composition of the present invention contains a colorant (hereinafter, sometimes referred to as a colorant (A)) and a resin (hereinafter, sometimes referred to as a resin (B)). The colored curable resin composition of the present invention may contain a polymerizable compound (hereinafter, sometimes referred to as a polymerizable compound (C)), a polymerization initiator (hereinafter, sometimes referred to as a polymerization initiator (D)), A solvent (hereinafter, sometimes referred to as a solvent (E)), and a polymerization initiation aid (hereinafter, may be referred to as a polymerization initiation aid (D1)). The colored curable resin composition of the present invention may contain a leveling agent (hereinafter, sometimes referred to as a leveling agent (F)). In the present invention, the dark color effect means that a difference in color change occurs between the coloring composition layer after pre-baking and the color filter after post-baking, and the color becomes darker per predetermined film thickness.

The colored curable resin composition of the present invention is characterized in that it contains a colorant (A), a resin (B), a polymerizable compound (C), and a polymerization initiator (D), and as the resin (B), contains a structural unit A polymer comprising a tertiary carbon-containing (meth)acrylate unit (a1) and an acid group-containing unsaturated monomer unit (b1). In addition, in this specification, "(meth)acrylate" means at least 1 sort(s) chosen from the group which consists of an acrylate and a methacrylate. Expressions such as "(meth)acryloyl" and "(meth)acrylic acid" also have the same meaning.

In this specification, unless otherwise specified, the compounds exemplified as the respective components can be used alone or in combination of two or more.

＜Colorant (A)＞ The colorable curable resin composition of the present invention contains a colorant (A), and the colorant (A) preferably contains at least a green colorant. The green colorant can be any one of a pigment and a dye, preferably a pigment, more preferably a zinc phthalocyanine, more preferably a polyhalogenated zinc phthalocyanine, more preferably a polychlorinated zinc phthalocyanine, and a polybrominated zinc phthalocyanine , particularly preferably selected from C.I. Pigment Green 58 and C.I. Pigment Green 59.

For green colorants (preferably zinc phthalocyanine, more preferably polyhalogenated zinc phthalocyanine), if necessary, rosin treatment, surface treatment using a pigment derivative into which an acidic group or a basic group is introduced, etc., using a polymer Grafting of compounds, etc. on the surface of pigments, micronization by sulfuric acid micronization, etc., or cleaning by organic solvents or water to remove impurities, and removal of ionic impurities by ion exchange, etc. .

The green colorant (preferably zinc phthalocyanine, more preferably polyhalogenated zinc phthalocyanine) is preferably used in the state of a dispersion liquid uniformly dispersed in a solvent, and the dispersion liquid can be used by mixing the green colorant in the solvent (preferably zinc phthalocyanine, more preferably polyhalogenated zinc phthalocyanine). A dispersant can also be mixed as desired.

The dispersant may be any one of cationic, anionic, and amphoteric dispersants, and examples thereof include polyester-based, polyamine-based, and acrylic-based dispersants. These dispersants may be used alone or in combination of two or more. As the dispersing agent, trade names can be listed: KP (manufactured by Shin-Etsu Chemical Industry Co., Ltd.), Flowlen (manufactured by Kyeisha Chemical Co., Ltd.), Solsperse (Zeneca Co., Ltd.) ) (stock), EFKA (BASF), Ajisper (Ajinomoto Fine-Techno (stock)), Disperbyk (manufactured by BYK-chemie), etc. As a dispersing agent, the resin (B) (preferably resin (B1)) mentioned later can be used from the viewpoint of the dispersibility of a colorant and the compatibility with resin (B). When a dispersant is used, its usage amount is preferably 100 parts by mass or less, more preferably 5 parts by mass or more and 50 parts by mass or less, with respect to 100 parts by mass of the pigment. When the usage-amount of a pigment dispersant is in the said range, there exists a tendency for the pigment dispersion liquid in which a pigment is uniformly dispersed in a solvent to be obtained.

Although it does not specifically limit as a solvent, The same solvent as the solvent (E) in the colored curable resin composition of this invention is mentioned. Among them, propylene glycol monomethyl ether acetate, ethyl lactate, propylene glycol monomethyl ether, 3-ethoxy ethyl propionate, ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, diethylene glycol are preferred. Alcohol monoethyl ether, 3-methoxybutyl acetate, 3-methoxy-1-butanol, 4-hydroxy-4-methyl-2-pentanone, N,N-dimethylformamide etc., more preferably propylene glycol monomethyl ether acetate, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether acetate, ethyl lactate, 3-methoxybutyl acetate, 3-methoxy-1-butane alcohol, ethyl 3-ethoxypropionate, etc. The amount of the solvent to be used is not particularly limited, and it can be adjusted and used so that the concentration of the solid content in the solvent and the pigment dispersion liquid is 3 to 30 mass %, more preferably 5 to 25 mass % quantity.

Furthermore, as the colorant (A), pigments such as a yellow colorant and a blue colorant, which are second colorants other than the green colorant (preferably zinc phthalocyanine, more preferably polyhalogenated zinc phthalocyanine), may be contained. and or dyes. The colorant (A) preferably further includes a yellow colorant.

Examples of the pigment include organic pigments and inorganic pigments, and examples thereof include compounds classified as pigments in the Color Index (published by The Society of Dyers and Colourists). Examples of organic pigments include: C.I. 117, 125, 128, 137, 138, 139, 147, 148, 150, 153, 154, 166, 173, 185, 194, 214 and other yellow pigments; C.I. Pigment Blue 15, 15:3, 15:4, 15:6, 60 and other blue pigments; C.I. Pigment Violet 1, 19, 23, 29, 32, 36, 38 and other purple pigments; C.I. Pigment green (pigment green) 7, 36 and other green pigments other than polyhalogenated zinc phthalocyanine; Wait.

Among them, as the pigment, it is preferable to contain at least one or more selected from the group consisting of green pigments other than zinc phthalocyanine, yellow pigments, and blue pigments. The green colorant (preferably a green pigment) and the blue colorant (preferably a blue pigment) are preferably C.I. Pigment Blue 15:3, C.I. Pigment Blue 15:6, C.I. Pigment Green 7, C.I. Pigment Green 36. The yellow colorant, preferably a yellow pigment, is preferably selected from the group consisting of C.I. Pigment Yellow 138, C.I. Pigment Yellow 139, C.I. Pigment Yellow 150 and C.I. Pigment Yellow 185. Two or more of these pigments can be used.

The pigment may be subjected to rosin treatment, surface treatment using a pigment derivative into which an acidic group or basic group is introduced or a pigment dispersant, etc., grafting treatment of the pigment surface with a polymer compound or the like, and sulfuric acid treatment, if necessary. Micronization treatment such as atomization method, cleaning treatment with organic solvent, water, etc. for removing impurities, removal treatment of ionic impurities by ion exchange method, etc., and the like. In addition, the pigment preferably has a uniform particle size. By containing a pigment dispersant and performing dispersion treatment, a pigment dispersion liquid in a state in which the pigment is uniformly dispersed in the solution can be obtained.

As the pigment dispersant, commercially available surfactants can be used, and examples include silicone-based, fluorine-based, ester-based, cationic, anionic, nonionic, amphoteric, polyester-based, polyamine-based, and acrylic-based and other surfactants. Examples of the surfactant include polyoxyethylene alkyl ethers, polyoxyethylene alkyl phenyl ethers, polyethylene glycol diesters, sorbitan fatty acid esters, and fatty acid-modified polyesters. In addition to urethanes, tertiary amine-modified polyurethanes, polyethyleneimine, etc., KP (Shin-Etsu Chemical Industry Co., Ltd.), Flowlen (Kyoeisha Chemical Co., Ltd.) (stock), Solsperse (made by Zeneca (stock)), EFKA (manufactured by BASF Japan (stock)), Ajisper (registered trademark) (manufactured by Ajinomoto Fine-Techno (stock)), Disperbyk (manufactured by BYK-Chemie), etc. These can be used individually or in combination of 2 or more types, respectively.

When a pigment dispersant is used, its usage amount is preferably 100 parts by mass or less with respect to the pigment, and more preferably 1 part by mass to 50 parts by mass. When the usage-amount of a pigment dispersing agent exists in the said range, there exists a tendency for the pigment dispersion liquid of a uniform dispersion state to be obtained.

The dye is not particularly limited, and known dyes can be used, and examples thereof include solvent dyes, acid dyes, direct dyes, mordant dyes, and the like. Examples of dyes include compounds classified as having hues other than pigments in the Color Index (published by The Society of Dyers and Colourists), or dyeing notes (colors). Well-known dyes described in Shikisensha Co., Ltd.). In addition, according to the chemical structure, azo dyes, cyanine dyes, triphenylmethane dyes, xanthene dyes, phthalocyanine dyes, anthraquinone dyes, naphthoquinone dyes, quinoneimine dyes, methine dyes, Azomethine dyes, squaraine dyes, acridine dyes, styryl dyes, coumarin dyes, quinoline dyes and nitro dyes, etc. Of these, organic solvent-soluble dyes are preferred.

From the viewpoint of the dark color effect, the content rate of all colorants is 45.5 mass % or more, preferably 46.0 mass % or more, more preferably 46.5 mass % or more with respect to the solid content of the colored curable resin composition, and further, Preferably it is 65 mass % or less, More preferably, it is 63 mass % or less, More preferably, it is 61 mass % or less.

The content rate of the green colorant can be appropriately adjusted to obtain a desired chromaticity. From the viewpoint of the dark color effect, it is preferably 35% by mass or more and 99.9% by mass or less with respect to the solid content of all the colorants. The lower limit value of the content rate of the green colorant is more preferably 40% by mass or more, more preferably 50% by mass or more, and still more preferably 60% by mass or more. Moreover, as for the upper limit of the content rate of a green coloring agent, 98 mass % or less is more preferable, 95 mass % or less is more preferable, and 90 mass % or less is more preferable. From the viewpoint of the dark color effect, the content of the green colorant is preferably 5 mass % or more and 60 mass % or less, more preferably 10 mass % or more and 55 mass % with respect to the solid content of the colored curable resin composition. Below, it is more preferable that it is 15 mass % or more and 50 mass % or less, and it is still more preferable that it is 20 mass % or more and 45 mass % or less.

When the colorant contains both C.I. Pigment Green 59 and C.I. Pigment Green 58, the content ratio of C.I. Pigment Green 59 and C.I. Pigment Green 58 expressed by "content of C.I. Pigment Green 59: Content of C.I. Pigment Green 58" is 0.1 -99.9:99.9-0.1 should just be in the range, Preferably it is 1-99:99-1. The content ratio of these can be appropriately adjusted according to the desired color.

When green pigments other than zinc phthalocyanine are contained, the usage-amount of the green pigments other than zinc phthalocyanine is preferably 0.1 part by mass or more, more preferably 1 part by mass or more, and still more preferably 10 parts by mass with respect to 100 parts by mass of zinc phthalocyanine part or more, preferably 2000 parts by mass or less, more preferably 300 parts by mass or less, still more preferably 100 parts by mass or less.

The yellow colorant may be any of a yellow pigment and a yellow dye, preferably a yellow pigment. The content of all yellow pigments is preferably 5% by mass or more and 40% by mass or less, more preferably 10% by mass or more, more preferably 15% by mass or more, and still more preferably 20% by mass with respect to the solid content of all the colorants. above. The content of the entire yellow pigment is preferably 1 mass % or more and 30 mass % or less, more preferably 25 mass % or less, and still more preferably 20 mass % or less with respect to the solid content of the entire colored curable resin composition.

The blue colorant may be any one of a blue pigment and a blue dye, preferably a blue pigment. The content of all blue pigments is preferably 0.1% by mass or more and 30% by mass or less, more preferably 1% by mass or more and 25% by mass or less, and still more preferably 3% by mass or more, with respect to the solid content of all the colorants. 20 mass % or less. The content of all blue pigments is preferably 1 mass % or more and 30 mass % or less, more preferably 25 mass % or less, and still more preferably 20 mass % or less with respect to the solid content of the entire colored curable resin composition. When the colorant (A) contains both the green colorant and the yellow colorant, the content of the yellow colorant is preferably 1 part by mass to 100 parts by mass, more preferably 2 parts by mass to 100 parts by mass of the green colorant. 80 parts by mass, more preferably 5 parts by mass to 60 parts by mass, still more preferably 8 parts by mass to 40 parts by mass.

The total amount of the colorant (A) is preferably 25% by mass to 65% by mass, more preferably 30% by mass to 60% by mass, and still more preferably 35% by mass in 100% by mass of the solid content of the coloring curable resin composition. % to 55% by mass.

＜Resin (B)＞ The resin (B) used in the present invention may be an alkali-soluble resin. The resin (B) contains a polymer (B1) (hereinafter, sometimes referred to as a polymer including a tertiary carbon-containing (meth)acrylate unit (a1) and an acid group-containing unsaturated monomer unit (b1) as a constituent unit) is resin (B1)).

The resin (B1) is a resin that does not contain both a monomer unit having a cyclic ether structure having 2 to 4 carbon atoms and an ethylenically unsaturated bond, and a unit derived from the monomer unit.

As the tertiary carbon-containing (meth)acrylate unit (a1), the tertiary carbon-containing (meth)acrylate may be, for example, a compound represented by the following general formula (1): CH ₂ =C(R )-C(=O)-OC(R ¹ )(R ² )(R ³ ) (1) (R represents a hydrogen atom or a methyl group. R ¹ , R ² and R ³ represent a bonding position with a carbon atom A monovalent organic group having a carbon atom, at least one of R ¹ , R ² and R ³ has one or more hydrogen atoms on the carbon atom at the bonding position to the carbon atom. Among R ¹ , R ² and R ³ , R ¹ and R ² , R ² and R ³ , or R ¹ and R ³ may together form a ring.)

The R ¹ , R ² and R ³ are the same or different, preferably a hydrocarbon group having 1 to 30 carbon atoms, more preferably a saturated hydrocarbon group having 1 to 15 carbon atoms, more preferably a saturated hydrocarbon group having 1 to 10 carbon atoms, and further A saturated hydrocarbon group having 1 to 5 carbon atoms is more preferred, and a saturated hydrocarbon group having 1 to 3 carbon atoms is particularly preferred. The hydrocarbon group may be a saturated hydrocarbon group or an unsaturated hydrocarbon group.

Examples of the hydrocarbon group having 1 to 30 carbon atoms represented by R ¹ , R ² and R ³ include methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, and decyl. base, eleven bases, twelve bases, thirteen bases, fourteen bases, fifteen bases, sixteen bases, seventeen bases, eighteen bases, nineteen bases, twenty bases, twenty-one bases, twenty-two bases base, 23 base, 24 base, 25 base, 26 base, 27 base, 28 base, 29 base, 30 base and other linear alkyl groups; isopropyl , isobutyl, 2-butyl, 3-butyl, 1-methylbutyl, 1-ethylpropyl, 3-methylbutyl, neopentyl, 1,1-dimethylpropyl, 2-methylpentyl, 3-ethylpentyl, 2-propylpentyl, 1-methylpentyl, 4-methylpentyl, 4-methylhexyl, 5-methylhexyl, 2-ethyl 1-methylhexyl, 1-methylhexyl, 1-ethylpentyl, 1-propylbutyl, 3-ethylheptyl, 1-methylheptyl, 1-ethylhexyl, 1-propylpentyl, 1-Methyloctyl, 1-ethylheptyl, 1-propylhexyl, 1-butylpentyl, 1-methylnonyl, 1-ethyloctyl, 1-propylheptyl and 1- Branched chain alkyl such as butylhexyl; cyclopropyl, 1-methylcyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, 1-methylcyclohexyl, 2-methylcyclohexyl , 3-methylcyclohexyl, 4-methylcyclohexyl, 1,2-dimethylcyclohexyl, 1,3-dimethylcyclohexyl, 1,4-dimethylcyclohexyl, 2,3-dimethylcyclohexyl Methylcyclohexyl, 2,4-dimethylcyclohexyl, 2,5-dimethylcyclohexyl, 2,6-dimethylcyclohexyl, 3,4-dimethylcyclohexyl, 3,5-dimethylcyclohexyl Methylcyclohexyl, 2,2-dimethylcyclohexyl, 3,3-dimethylcyclohexyl, 4,4-dimethylcyclohexyl, cyclooctyl, 4-pentylcyclohexyl, 4-octyl Cyclohexyl and alicyclic hydrocarbon groups such as 4-cyclohexylcyclohexyl, decalinyl, norbornyl, adamantyl, bicyclo[2.2.2]octyl; phenyl, o-tolyl, m-tolyl, p-toluene base, 2-ethylphenyl, 3-ethylphenyl, 4-ethylphenyl, 2,3-dimethylphenyl, 2,4-dimethylphenyl, 2,5-dimethylphenyl Phenyl, 2,6-dimethylphenyl, 3,4-dimethylphenyl, 3,5-dimethylphenyl, 4-vinylphenyl, o-isopropylphenyl, m-isopropyl phenyl, p-isopropylphenyl, 4-butylphenyl, 4-pentylphenyl, 1-naphthyl, 2-naphthyl, 6-methyl-2-naphthyl, 5,6,7 ,8-tetrahydro-1-naphthyl, 5,6,7,8-tetrahydro-2-naphthyl, fluorenyl, phenanthrenyl, anthracenyl, 2-dodecylphenyl, 3-dodecylbenzene base, 4-dodecylphenyl group, perylene group, tetramethyl group and aromatic hydrocarbon group such as pyrenyl group, etc. The hydrocarbon group having 1 to 30 carbon atoms represented by R ¹ , R ² and R ³ may be two selected from the group consisting of the straight-chain alkyl group, branched-chain alkyl group, alicyclic hydrocarbon group, and aromatic hydrocarbon group combined. Among them, straight-chain alkyl groups, branched-chain alkyl groups, and alicyclic hydrocarbon groups are preferred, and branched-chain alkyl groups and alicyclic hydrocarbon groups are more preferred.

The ring which R ¹ and R ² , R ² and R ³ , or R ¹ and R ³ may form together includes the same groups as those listed as the above-mentioned alicyclic hydrocarbon group.

Specific examples of the tertiary carbon-containing (meth)acrylate unit (a1) include the following structural units (a1-0) to (a1-2).

[式（a1-0）、式（a1-1）及式（a1-2）中， L ^a01、L ^a1及L ^a2分別獨立地表示氧原子或*-O-(CH ₂) _k1-CO-O-，k1表示1～7的任一整數，*表示與-CO-的鍵結部位。 R ^a01、R ^a4及R ^a5分別獨立地表示氫原子或甲基。 R ^a02、R ^a03及R ^a04分別獨立地表示碳數1～8的烷基、碳數3～18的脂環式烴基或將該些組合而成的基。 R ^a6及R ^a7分別獨立地表示碳數1～8的烷基、碳數3～18的脂環式烴基或藉由將該些組合而形成的基。 m1表示0～14的任一整數。 n1表示0～10的任一整數。 n1'表示0～3的任一整數。]

[In formula (a1-0), formula (a1-1) and formula (a1-2), L ^a01 , L ^a1 and L ^a2 each independently represent an oxygen atom or *-O-(CH ₂ ) _k1 -CO- O-, k1 represents any integer from 1 to 7, and * represents a bonding site with -CO-. R ^a01 , R ^a4 and R ^a5 each independently represent a hydrogen atom or a methyl group. R ^a02 , R ^a03 and R ^a04 each independently represent an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or a group formed by combining these. R ^a6 and R ^a7 each independently represent an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or a group formed by combining these. m1 represents any integer from 0 to 14. n1 represents any integer of 0-10. n1' represents any integer of 0-3. ]

R ^a01 , R ^a4 and R ^a5 are preferably hydrogen atoms. L ^a01 , L ^a1 and L ^a2 are preferably oxygen atoms or *-O-(CH ₂ ) _k01 -CO-O- (wherein, k01 is preferably any integer from 1 to 4, more preferably 1), more Preferably it is an oxygen atom. Examples of the alkyl group in R ^a02 , R ^a03 , R ^a04 , R ^a6 and R ^a7 include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, and an octyl group. The alicyclic hydrocarbon group in R ^a02 , R ^a03 , R ^a04 , R ^a6 and R ^a7 may be either monocyclic or polycyclic. Examples of the monocyclic alicyclic hydrocarbon group include cycloalkyl groups such as cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl. As a polycyclic alicyclic hydrocarbon group, a decalinyl group, an adamantyl group, a norbornyl group, the following group (* represents a bonding site), etc. are mentioned.

Examples of groups obtained by combining an alkyl group among R ^a02 , R ^a03 , R ^a04 , R ^a6 , and R ^a7 with an alicyclic hydrocarbon group include methylcyclohexyl, dimethylcyclohexyl, and methylnorbornyl. group, cyclohexylmethyl, adamantylmethyl, adamantyldimethyl, norbornylethyl, etc.

The number of carbon atoms in the alkyl group in R ^a02 , R ^a03 , and R ^a04 is preferably 1-6, more preferably 1-4, still more preferably 1-2. The number of carbon atoms in the alkyl group in R ^a6 and R ^a7 is preferably 1-6, more preferably 1-4, and still more preferably 2-3. 5-12 are preferable, and, as for carbon number of the alicyclic hydrocarbon group of R ^a02 , R ^a03 , and R ^a04 , 5-10 are more preferable. Regarding a group formed by combining an alkyl group and an alicyclic hydrocarbon group, the total number of carbon atoms in the combination of these alkyl groups and the alicyclic hydrocarbon group is preferably 18 or less.

R ^a02 and R ^a03 are preferably an alkyl group having 1 to 6 carbon atoms, more preferably a methyl group or an ethyl group, and still more preferably a methyl group. R ^a04 is preferably an alkyl group having 1 to 6 carbon atoms or an alicyclic hydrocarbon group having 5 to 12 carbon atoms, more preferably a methyl group, an ethyl group, a cyclohexyl group or an adamantyl group. R ^a6 and R ^a7 are preferably an alkyl group having 1 to 6 carbon atoms, more preferably a methyl group, an ethyl group or an isopropyl group, and still more preferably an ethyl group or an isopropyl group.

m1 is preferably any integer of 0 to 3, more preferably 0 or 1. n1 is preferably any integer of 0 to 3, more preferably 0 or 1. n1' is preferably 0 or 1.

As a structural unit (a1-0), any of formula (a1-0-1) - formula (a1-0-12) and formula (a1-0-13) - formula (a1-0-24) can be mentioned, for example The structural unit represented by the .

As a structural unit (a1-1), any of formula (a1-1-1) - formula (a1-1-4) and formula (a1-1-5) - formula (a1-1-8) can be mentioned, for example The structural unit represented by the .

As a structural unit (a1-2), any one of formula (a2-2-1) to formula (a1-2-6) and formula (a1-2-7) to formula (a1-2-12) can be mentioned represented structural unit.

Among them, the (meth)acrylate unit (a1) containing tertiary carbon is preferably a structural unit represented by formula (a1-0), more preferably formula (a1-0-1)～(a1-0-24) ), more preferably the structural units represented by the formulae (a1-0-13) to (a1-0-24), and still more preferably the structural units represented by the formula (a1-0-13).

The content of the tertiary carbon-containing (meth)acrylate unit (a1) is preferably 1 mass % or more and less than 100 mass % in 100 mass % of the constituent units of the resin (B1). In addition, the resin (B1) may contain a polymer containing the tertiary carbon-containing (meth)acrylate unit (a1) in an amount exceeding 80% by mass in 100% by mass of the constituent units of the resin (B1). .

As the unsaturated monomer unit (b1) having an acid group, the unsaturated monomer having an acid group is preferably at least one selected from acrylic acid and methacrylic acid, and more preferably acrylic acid.

The content of the unsaturated monomer unit (b1) having an acid group is preferably more than 0% by mass and 99% by mass or less in 100% by mass of the constituent units of the resin (B1).

The resin (B) (preferably the resin (B1)) preferably has an acid value exceeding 80 mgKOH/g and a weight average molecular weight of 9000 or less.

The acid value of the resin (B1) is preferably more than 80 mgKOH/g, more preferably 85 mgKOH/g or more, more preferably 95 mgKOH/g or more, more preferably 105 mgKOH/g or more, more preferably 300 mgKOH/g g or less, more preferably 250 mgKOH/g or less, still more preferably 200 mgKOH/g or less. The acid value is a value measured as the amount (mg) of potassium hydroxide required to neutralize 1 g of resin, and can be determined, for example, by titration using an aqueous potassium hydroxide solution.

The weight average molecular weight in terms of polystyrene of the resin (B1) is preferably 9,000 or less, more preferably 8,500 or less, still more preferably 8,000 or less, still more preferably 7,500 or less, preferably 1,000 or more, more preferably 1,500 or more, More preferably, it is 2000 or more, and still more preferably 2500 or more.

The content of the resin (B1) is preferably 40 to 100% by mass, more preferably 50 to 95% by mass, and still more preferably 60 to 90% by mass in 100% by mass of the resin (B). The content of the resin (B1) is preferably 1 to 50% by mass, more preferably 2 to 45% by mass, and still more preferably 5% by mass in 100% by mass of the solid content of the colored curable resin composition. to 40 mass %, more preferably 8 to 35 mass %.

Resin (B) may contain resin (B2) (hereinafter, sometimes referred to as resin (B2)) different from resin (B1). As resin (B2), the following resin [K1] - resin [K6] etc. are mentioned. Resin [K1]: has a structural unit derived from at least one monomer (a2) selected from the group consisting of unsaturated carboxylic acid and unsaturated carboxylic acid anhydride (hereinafter referred to as “(a2)”) , a copolymer with a structural unit derived from a monomer (b2) having a cyclic ether structure of 2 to 4 carbon atoms and an ethylenically unsaturated bond (hereinafter referred to as "(b2)"); Resin [K2]: having a structural unit derived from (a2), a structural unit derived from (b2), and a monomer (c2) derived from a copolymerizable monomer with (a2) (wherein, with (a2) and (b2) different) (hereinafter referred to as "(c2)") structural units of the copolymer; Resin [K3]: a copolymer having a structural unit derived from (a2) and a structural unit derived from (c2); Resin [K4]: a copolymer having a structural unit obtained by adding (b2) to a structural unit derived from (a2) and a structural unit derived from (c2); Resin [K5]: a copolymer having a structural unit obtained by adding (a2) to a structural unit derived from (b2) and a structural unit derived from (c2); Resin [K6]: A copolymer having a structural unit obtained by adding (a2) to a structural unit derived from (b2) and further adding a carboxylic acid anhydride, and a structural unit derived from (c2).

Specific examples of (a2) include unsaturated monocarboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, o-vinyl benzoic acid, m-vinyl benzoic acid, and p-vinyl benzoic acid; Maleic acid, fumaric acid, citraconic acid, mesaconic acid, itaconic acid, 3-vinylphthalic acid, 4-vinylphthalic acid, 3,4,5,6-tetrahydro Phthalic acid, 1,2,3,6-tetrahydrophthalic acid, dimethyltetrahydrophthalic acid, 1,4-cyclohexenedicarboxylic acid and other unsaturated dicarboxylic acids; Methyl-5-norbornene-2,3-dicarboxylic acid, 5-carboxybicyclo[2.2.1]hept-2-ene, 5,6-dicarboxybicyclo[2.2.1]hept-2-ene, 5-Carboxy-5-methylbicyclo[2.2.1]hept-2-ene, 5-carboxy-5-ethylbicyclo[2.2.1]hept-2-ene, 5-carboxy-6-methylbicyclo[ 2.2.1] Hept-2-ene, 5-carboxy-6-ethylbicyclo[2.2.1]hept-2-ene and other bicyclic unsaturated compounds containing carboxyl groups; Maleic anhydride, citraconic anhydride, itaconic anhydride, 3-vinylphthalic anhydride, 4-vinylphthalic anhydride, 3,4,5,6-tetrahydrophthalic anhydride, Unsaturated dicarboxylic acids such as 1,2,3,6-tetrahydrophthalic anhydride, dimethyltetrahydrophthalic anhydride, 5,6-dicarboxybicyclo[2.2.1]hept-2-ene anhydride acid anhydrides; Divalent or higher polycarboxylic acids such as mono[2-(meth)acryloyloxyethyl] succinate and mono[2-(meth)acryloyloxyethyl] phthalate Unsaturated mono[(meth)acryloyloxyalkyl]esters; Unsaturated acrylates etc. which contain a hydroxyl group and a carboxyl group in the same molecule like α-(hydroxymeth)acrylic acid. Among these, acrylic acid, methacrylic acid, maleic anhydride, etc. are preferable in terms of the copolymerization reactivity or the solubility of the obtained resin in an alkaline aqueous solution.

(b2) means, for example, having a cyclic ether structure having 2 to 4 carbon atoms (for example, at least one selected from the group consisting of an oxirane ring, an oxetane ring, and a tetrahydrofuran ring) and an ethylenic A polymerizable compound with an unsaturated bond. (b2) Preferably, it is a monomer which has a C2-C4 cyclic ether and a (meth)acryloyloxy group.

Examples of (b2) include a monomer (b2-1) (hereinafter, sometimes referred to as "(b2-1)") having an oxiranyl group and an ethylenically unsaturated bond, an oxetane having a Monomer (b2-2) (hereinafter, sometimes referred to as "(b2-2)") having an alkyl group and an ethylenically unsaturated bond, and a monomer (b2-3) having a tetrahydrofuran group and an ethylenically unsaturated bond ( Hereinafter, sometimes referred to as "(b2-3)").

Examples of (b2-1) include monomers (b2-1-1) having a structure in which linear or branched aliphatic unsaturated hydrocarbons are epoxidized (hereinafter, sometimes referred to as "( b2-1-1)"), a monomer (b2-1-2) having a structure in which an alicyclic unsaturated hydrocarbon is epoxidized (hereinafter, sometimes referred to as "(b2-1-2)") .

As (b2-1-1), glycidyl (meth)acrylate, β-methyl glycidyl (meth)acrylate, β-ethyl glycidyl (meth)acrylate, glycidyl (meth)acrylate can be mentioned. vinyl ether, o-vinylbenzyl glycidyl ether, m-vinylbenzyl glycidyl ether, p-vinylbenzyl glycidyl ether, alpha-methyl-o-vinylbenzyl glycidyl ether, alpha-methyl- m-vinylbenzyl glycidyl ether, α-methyl-p-vinylbenzyl glycidyl ether, 2,3-bis(glycidyloxymethyl)styrene, 2,4-bis(glycidyloxymethyl) bis(glycidyloxymethyl)styrene, 2,5-bis(glycidyloxymethyl)styrene, 2,6-bis(glycidyloxymethyl)styrene, 2,3,4-tris(glycidyl)styrene Glyceryloxymethyl)styrene, 2,3,5-tris(glycidyloxymethyl)styrene, 2,3,6-tris(glycidyloxymethyl)styrene, 3, 4,5-tris(glycidyloxymethyl)styrene, 2,4,6-tris(glycidyloxymethyl)styrene and the like.

As (b2-1-2), vinylcyclohexene monooxide, 1,2-epoxy-4-vinylcyclohexane (for example, Celloxide 2000; Daicel ( Daicel) (stock), 3,4-epoxycyclohexylmethyl (meth)acrylate (eg, Cyclomer A400; Daicel (stock)), (meth)acrylic acid 3 ,4-Epoxycyclohexylmethyl ester (for example, Cyclomer M100; manufactured by Daicel Co., Ltd.), the compound represented by the formula (I), the compound represented by the formula (II), and the like.

[In formula (I) and formula (II), R ^a and R ^b represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, and the hydrogen atom contained in the alkyl group may be substituted with a hydroxyl group. X ^a and X ^b represent a single bond, *-R ^c -, *-R ^c -O-, *-R ^c -S- or *-R ^c -NH-. R ^c represents an alkanediyl group with 1 to 6 carbon atoms; * represents a bond with O]

Examples of the alkyl group having 1 to 4 carbon atoms include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, a tert-butyl group, and the like. Examples of the alkyl group in which a hydrogen atom is substituted with a hydroxyl group include hydroxymethyl, 1-hydroxyethyl, 2-hydroxyethyl, 1-hydroxypropyl, 2-hydroxypropyl, 3-hydroxypropyl, 1-hydroxypropyl, -Hydroxy-1-methylethyl, 2-hydroxy-1-methylethyl, 1-hydroxybutyl, 2-hydroxybutyl, 3-hydroxybutyl, 4-hydroxybutyl, etc. Preferable examples of R ^a and R ^b include a hydrogen atom, a methyl group, a hydroxymethyl group, a 1-hydroxyethyl group, and a 2-hydroxyethyl group, and more preferable examples include a hydrogen atom and a methyl group.

Examples of the alkanediyl group include methylene group, ethylidene group, propane-1,2-diyl group, propane-1,3-diyl group, butane-1,4-diyl group, and pentane-1,5-diyl group. -diyl, hexane-1,6-diyl, etc. Preferable examples of X ^a and X ^b include a single bond, a methylene group, an ethylidene group, *-CH ₂ -O- and *-CH ₂ CH ₂ -O-, more preferably a single bond , *-CH ₂ CH ₂ -O- (* represents the bond with O).

As a compound represented by Formula (I), the compound etc. which are represented by any one of Formula (I-1) - Formula (I-15) are mentioned. Among them, formula (I-1), formula (I-3), formula (I-5), formula (I-7), formula (I-9) or formula (I-11) to formula (I-11) are preferred. The compound represented by -15) is more preferably a compound represented by formula (I-1), formula (I-7), formula (I-9) or formula (I-15).

As a compound represented by Formula (II), the compound etc. which are represented by any one of Formula (II-1) - Formula (II-15) are mentioned. Among them, formula (II-1), formula (II-3), formula (II-5), formula (II-7), formula (II-9) or formula (II-11) to formula (II) are preferred The compound represented by -15) is more preferably a compound represented by formula (II-1), formula (II-7), formula (II-9) or formula (II-15).

The compound represented by formula (I) and the compound represented by formula (II) may be used independently, respectively, or two or more of them may be used in combination. When the compound represented by the formula (I) and the compound represented by the formula (II) are used together, the content ratio of these [the compound represented by the formula (I): the compound represented by the formula (II)] is in moles The reference value is preferably 5:95 to 95:5, more preferably 20:80 to 80:20.

As (b2-2), a monomer having an oxetanyl group and a (meth)acryloyloxy group is more preferable. As (b2-2), 3-methyl-3-methacryloyloxymethyloxetane, 3-methyl-3-acryloyloxymethyloxetane, Alkane, 3-ethyl-3-methacryloyloxymethyl oxetane, 3-ethyl-3-propenyloxymethyl oxetane, 3-methyl-3 - Methacryloyloxyethyl oxetane, 3-methyl-3-acryloyloxyethyl oxetane, 3-ethyl-3-methacryloyloxy Ethyloxetane, 3-ethyl-3-propenyloxyethyloxetane, etc.

As (b2-3), a monomer having a tetrahydrofuran group and a (meth)acryloyloxy group is more preferable. Specific examples of (b2-3) include tetrahydrofurfuryl acrylate (for example, Viscoat V#150, manufactured by Osaka Organic Chemical Industry Co., Ltd.), tetrahydrofurfuryl methacrylate Wait.

As (b2), (b2-1) is preferable from the viewpoint of further improving reliability such as heat resistance and chemical resistance of the obtained color filter. Furthermore, (b2-1-2) is more preferable at the point which is excellent in the storage stability of a colored curable resin composition.

As (c2), methyl (meth)acrylate, ethyl (meth)acrylate, n-butyl (meth)acrylate, second butyl (meth)acrylate, third (meth)acrylate Butyl, 2-ethylhexyl (meth)acrylate, dodecyl (meth)acrylate, lauryl (meth)acrylate, stearyl (meth)acrylate, ring (meth)acrylate Amyl ester, cyclohexyl (meth)acrylate, 2-methylcyclohexyl (meth)acrylate, tricyclo[5.2.1.0 ^2,6 ]decan-8-yl (meth)acrylate (in this In the technical field, as a common name, it is called "dicyclopentyl (meth)acrylate"; in addition, it may be called "(meth)acrylate tricyclodecyl"), (meth)acrylate tricyclo [5.2.1.0 ^2,6 ] Decen-8-yl ester (in this technical field, it is called "(meth)acrylic acid dicyclopentenyl ester" as a common name), (meth)acrylic acid dicyclopentenyl ester Alkyloxyethyl ester, isobornyl (meth)acrylate, adamantyl (meth)acrylate, allyl (meth)acrylate, propargyl (meth)acrylate, (meth)acrylate ) (meth)acrylates such as phenyl acrylate, naphthyl (meth)acrylate, benzyl (meth)acrylate; 2-hydroxyethyl (meth)acrylate, 2-hydroxyethyl (meth)acrylate Hydroxypropyl ester and other hydroxyl-containing (meth)acrylates; Diethyl maleate, diethyl fumarate, diethyl itaconic acid and other dicarboxylic acid diesters; Bicyclo[2.2.1] Hept-2-ene, 5-methylbicyclo[2.2.1]hept-2-ene, 5-ethylbicyclo[2.2.1]hept-2-ene, 5-hydroxybicyclo[2.2.1]hept-2 -ene, 5-hydroxymethylbicyclo[2.2.1]hept-2-ene, 5-(2'-hydroxyethyl)bicyclo[2.2.1]hept-2-ene, 5-methoxybicyclo[2.2 .1] Hept-2-ene, 5-ethoxybicyclo[2.2.1]hept-2-ene, 5,6-dihydroxybicyclo[2.2.1]hept-2-ene and other bicyclic unsaturated compounds; N-Phenylmaleimide, N-Cyclohexylmaleimide, N-benzylmaleimide, N-succinimidyl-3-maleimide Succinimidyl benzoate, N-succinimidyl-4-maleimidobutyrate, N-succinimidyl-6-maleimidohexanoate, Dicarbonyl imide derivatives such as N-succinimidyl-3-maleimide propionate, N-(9-acridyl) maleimide; Styrene, α-Methylstyrene, m-methylstyrene, p-methylstyrene, vinyltoluene, p-methoxystyrene, acrylonitrile, methacrylonitrile, vinyl chloride, vinylidene chloride, acrylamide, Methacrylamide, vinyl acetate, 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, etc. Among these, in terms of copolymerization reactivity and heat resistance, 2-hydroxyethyl (meth)acrylate, styrene, vinyltoluene, N-phenylmaleimide, N -Cyclohexylmaleimide, N-benzylmaleimide, bicyclo[2.2.1]hept-2-ene, etc.

Among all the structural units constituting the resin [K1], the ratio of the structural units derived from each in the resin [K1] is preferably: Structural units derived from (a2): 2 mol% to 60 mol%; Structural units derived from (b2): 40 mol% to 98 mol%; better Structural units derived from (a2): 10 mol% to 50 mol%; Structural units derived from (b2): 50 mol% to 90 mol%; When the ratio of the structural unit of the resin [K1] is within the above-mentioned range, the storage stability of the colored curable resin composition, the developability at the time of forming the colored pattern, and the solvent resistance of the obtained color filter can be improved Excellent.

For resin [K1], for example, reference can be made to the method described in the document "Experimental Methods for Polymer Synthesis" (Otsu Takayuki Chemical Doujin Publishing Co., Ltd., 1st edition, 1st printing, March 1, 1972) and the method described in this document. Manufactured from the cited references.

Specifically, a method of creating a deoxidized environment by placing predetermined amounts of (a2) and (b2), a polymerization initiator, a solvent, and the like in a reaction vessel, and replacing oxygen with nitrogen, for example, can be used. , and heating and heat preservation were performed while stirring. In addition, the polymerization initiator, solvent, etc. used here are not specifically limited, Those generally used in this field can be used. For example, as the polymerization initiator, azo compounds (2,2'-azobisisobutyronitrile, 2,2'-azobis(2,4-dimethylvaleronitrile), etc.) or organic peroxides can be mentioned. The oxide (benzyl peroxide, etc.) may be used as a solvent as long as it dissolves each monomer, and examples thereof include the solvent (E) described later as the solvent (E) of the colored curable resin composition of the present invention.

In addition, the obtained copolymer may use the solution after reaction as it is, may use the concentrated or diluted solution, may also use what was extracted as a solid (powder) by methods, such as reprecipitation. In particular, by using the solvent contained in the colored curable resin composition of the present invention as a solvent during the polymerization, the solution after the reaction can be directly used for the preparation of the colored curable resin composition of the present invention, so it is possible to The manufacturing process of the coloring curable resin composition of this invention is simplified.

Among all the structural units constituting the resin [K2], the ratio of the structural units derived from each in the resin [K2] is preferably: Structural units derived from (a2): 2 mol% to 45 mol%; Structural units derived from (b2): 2 mol% to 95 mol%; Structural units derived from (c2): 1 mol% to 65 mol%; better Structural units derived from (a2): 5 mol% to 40 mol%; Structural unit derived from (b2): 5 mol% to 80 mol%; Structural unit derived from (c2): 5 mol% to 60 mol%; When the ratio of the structural unit of the resin [K2] is within the above range, the storage stability of the colored curable resin composition, the developability at the time of forming a colored pattern, and the solvent resistance of the obtained color filter can be improved , excellent heat resistance and mechanical strength.

The resin [K2] can be produced, for example, in the same manner as the method described as the production method of the resin [K1].

Among all the structural units constituting the resin [K3], the ratio of the structural units derived from each in the resin [K3] is preferably: Structural units derived from (a2): 2 mol% to 60 mol%; Structural units derived from (c2): 40 mol% to 98 mol%; better Structural units derived from (a2): 10 mol% to 50 mol%; Structural units derived from (c2): 50 mol% to 90 mol%; The resin [K3] can be produced, for example, in the same manner as the method described as the production method of the resin [K1].

Resin [K4] can be obtained by obtaining a copolymer of (a2) and (c2) and adding the cyclic ether having 2 to 4 carbon atoms contained in (b2) to the carboxylic acid and/or carboxylic acid contained in (a2) Manufactured from acid anhydride. First, the copolymer of (a2) and (c2) is produced in the same manner as the method described as the production method of resin [K1]. In this case, it is preferable that the ratio of the structural unit derived from each monomer is the same ratio as enumerated in resin [K3].

Next, the cyclic ether having 2 to 4 carbon atoms contained in (b2) and a part of the carboxylic acid and/or carboxylic acid anhydride derived from (a2) in the copolymer are reacted. Following the production of the copolymer of (a2) and (c2), the atmosphere in the flask is replaced from nitrogen to air, and the reaction catalyst (for example, tris(dimethyl) of (b2), carboxylic acid or carboxylic anhydride and cyclic ether Aminomethyl)phenol, etc.) and a polymerization inhibitor (for example, hydroquinone, etc.), etc., are put into a flask, and the reaction is carried out at 60°C to 130°C for 1 hour to 10 hours, whereby resin [K4 ]. The amount of (b2) used is preferably 5 mol to 80 mol, more preferably 10 mol to 75 mol, relative to 100 mol of (a). By setting it as this range, the storage stability of a colored curable resin composition, the developability at the time of pattern formation, and the solvent resistance of the obtained pattern, heat resistance, mechanical strength, and the balance of sensitivity can be made favorable. As the (b2) used for the resin [K4], (b2-1) is preferable, and (b2-1) is more preferable in terms of the high reactivity of the cyclic ether and the difficulty in remaining unreacted (b2). -1). The amount of the reaction catalyst used is preferably 0.001 to 5 parts by mass relative to 100 parts by mass of the total amount of (a2), (b2) and (c2). The amount of the polymerization inhibitor used is preferably 0.001 to 5 parts by mass relative to 100 parts by mass of the total amount of (a2), (b2) and (c2). The reaction conditions such as the charging method, the reaction temperature, and the time can be appropriately adjusted in consideration of the production facility, the calorific value due to the polymerization, and the like. In addition, similarly to the polymerization conditions, the charging method and the reaction temperature can be appropriately adjusted in consideration of the production facility, the heat generation due to the polymerization, and the like.

Regarding the resin [K5], as the first stage, a copolymer of (b2) and (c2) was obtained in the same manner as in the production method of the resin [K1]. In the same manner as described above, the obtained copolymer may be used as it is in the solution after the reaction, may be used as a concentrated or diluted solution, or may be taken out as a solid (powder) by a method such as reprecipitation. The ratios of the structural units derived from (b2) and (c2) with respect to the total number of moles of all the structural units constituting the copolymer are preferably: Structural units derived from (b2): 5 mol% to 95 mol%; Structural units derived from (c2): 5 mol% to 95 mol%; better Structural units derived from (b2): 10 mol% to 90 mol%; Structural units derived from (c2): 10 mol% to 90 mol%;

Furthermore, the carboxylic acid or carboxylic anhydride contained in (a2) and the cyclic ether derived from (b2) contained in the copolymer of (b2) and (c2) were prepared under the same conditions as in the production method of resin [K4]. reaction, whereby resin [K5] can be obtained. The amount of (a2) used to react with the copolymer is preferably 5 mol to 80 mol relative to 100 mol of (b2). As the (b2) used for the resin [K5], (b2-1) is preferable, and (b2-1) is more preferable in that the cyclic ether has high reactivity and it is difficult for unreacted (b2) to remain. -1).

Resin [K6] is a resin obtained by further reacting carboxylic anhydride and resin [K5]. The carboxylic acid anhydride is reacted with the hydroxyl group generated by the reaction of the cyclic ether with the carboxylic acid or the carboxylic acid anhydride. Examples of the carboxylic anhydride include maleic anhydride, citraconic anhydride, itaconic anhydride, 3-vinylphthalic anhydride, 4-vinylphthalic anhydride, 3,4,5,6-tetrakis Hydrophthalic anhydride, 1,2,3,6-tetrahydrophthalic anhydride, dimethyltetrahydrophthalic anhydride, 5,6-dicarboxybicyclo[2.2.1]hept-2- alkene anhydride, etc. The usage-amount of the carboxylic anhydride is preferably 0.5 mol to 1 mol per 1 mol of the usage-amount of (a2).

Specific examples of the resin (B2) include: (meth)acrylic acid 3,4-epoxycyclohexylmethyl/(meth)acrylic acid copolymer, acrylic acid 3,4-epoxytricyclo[5.2.1.0 ^2,6 ] Resin [K1] such as decyl ester/(meth)acrylic acid copolymer; Glycidyl (meth)acrylate/(meth)acrylate/(meth)acrylic acid copolymer, (meth)acrylic Glycidyl ester/styrene/(meth)acrylic acid copolymer, 3,4-epoxytricyclo[5.2.1.0 ^2,6 ]decyl acrylate/(meth)acrylic acid/N-cyclohexylmaleic acid Imine copolymer, 3,4-epoxytricyclo[5.2.1.0 ^2,6 ]decyl acrylate/(meth)acrylic acid/N-cyclohexylmaleimide/(meth)acrylic acid 2- Resins such as hydroxyethyl ester copolymer, 3-methyl-3-(meth)acryloyloxymethyloxetane/(meth)acrylic acid/styrene copolymer [K2]; (methyl) Acrylate/(meth)acrylic acid copolymer, benzyl (meth)acrylate/(meth)acrylic acid copolymer, styrene/(meth)acrylic acid copolymer and other resins [K3]; benzyl p-(meth)acrylate Resin obtained by adding glycidyl (meth)acrylate to ester/(meth)acrylic acid copolymer, and adding tricyclodecyl p-(meth)acrylate/styrene/(meth)acrylic acid copolymer (methyl) ) resin made of glycidyl acrylate, resin obtained by adding glycidyl (meth)acrylate to tricyclodecyl (meth)acrylate/benzyl (meth)acrylate/(meth)acrylic acid copolymer etc. Resin [K4]; a resin obtained by reacting a copolymer of tricyclodecyl (meth)acrylate/glycidyl (meth)acrylate with (meth)acrylic acid, a resin obtained by reacting tricyclodecyl (meth)acrylate / Resin [K5] such as a resin obtained by reacting a copolymer of styrene/glycidyl (meth)acrylate and (meth)acrylic acid; make tricyclodecyl (meth)acrylate/glycidyl (meth)acrylate Resin [K6] etc., such as the resin which the copolymer of ester and (meth)acrylic acid reacted, and the resin which reacted with tetrahydrophthalic anhydride. Among these, as resin (B2), resin [K1] and resin [K2] are preferable, and resin [K1] is especially preferable.

The polystyrene-equivalent weight average molecular weight of the resin (B2) is preferably 3,000 to 100,000, more preferably 5,000 to 50,000, still more preferably 5,000 to 30,000, still more preferably 9500 to 30,000. When the molecular weight is within the above range, the solubility of the unexposed portion to the developing solution is high, and the residual film ratio or hardness of the obtained pattern tends to be high. The molecular weight distribution [weight average molecular weight (Mw)/number average molecular weight (Mn)] of the resin (B2) is preferably 1.1 to 6, more preferably 1.2 to 4.

The acid value of the solid content of the resin (B2) is preferably 85 mgKOH/g or more, more preferably 100 mgKOH/g or more, and still more preferably 110 mgKOH/g or more. In addition, the acid value of the solid content is preferably 200 mgKOH/g or less, more preferably 180 mgKOH/g or less, and still more preferably 160 mgKOH/g or less. When the solid content acid value of the resin (B2) is within the above-described range, a coloring pattern having a favorable shape tends to be obtained from the colorable curable resin composition. Here, the acid value is a value measured as the amount (mg) of potassium hydroxide required to neutralize 1 g of resin, and can be determined by, for example, titration using an aqueous potassium hydroxide solution.

The content of the resin (B2) is preferably 0 to 60% by mass, more preferably 5 to 50% by mass, and still more preferably 10 to 40% by mass in 100% by mass of the resin (B). The content of the resin (B2) is preferably 1% by mass to 40% by mass, more preferably 2% by mass to 35% by mass, and still more preferably 3% by mass in 100% by mass of the solid content of the colored curable resin composition. ~30% by mass.

The content of the resin (B) (preferably the content of the resin (B1) and the resin (B2)) is preferably 5 to 50 mass % in 100 mass % of the solid content of the colored curable resin composition, more preferably It is 10 mass % - 40 mass %, More preferably, it is 15 mass % - 30 mass %. When the content of the resin (B) is within the above range, the solubility of the unexposed portion to the developing solution tends to be high.

<Polymerizable compound (C)> The polymerizable compound (C) is a compound that can be polymerized by active radicals and/or acids generated from the polymerization initiator (D). As a polymerizable compound (C), the compound which has a polymerizable ethylenically unsaturated bond and a hydroxyl group is mentioned.

Specific examples of the polymerizable compound (C) include pentaerythritol tri(meth)acrylate, pentaerythritol di(meth)acrylate, pentaerythritol mono(meth)acrylate, and ethylene glycol modified pentaerythritol tri(meth)acrylate. base) acrylate, propylene glycol modified pentaerythritol triacrylate, trimethylolpropane di(meth)acrylate, ethylene glycol modified trimethylolpropane di(meth)acrylate, ethylene glycol modified glycerin Di(meth)acrylate, propylene glycol modified glycerol di(meth)acrylate, di-trimethylolpropane tri(meth)acrylate, ethylene glycol modified di-trimethylolpropane tri(meth)acrylate base) acrylate, propylene glycol modified di-trimethylolpropane triacrylate, dipentaerythritol pentaacrylate, Trimethylolpropane tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, dipentaerythritol penta(meth)acrylate, dipentaerythritol hexa(meth)acrylate, tripentaerythritol octa(meth)acrylate ester, pentaerythritol ten (meth)acrylate, tris(2-(meth)acryloyloxyethyl)isocyanurate, ethylene glycol modified pentaerythritol tetra(meth)acrylate, ethylene glycol Alcohol modified dipentaerythritol hexa(meth)acrylate, propylene glycol modified pentaerythritol tetra(meth)acrylate, propylene glycol modified dipentaerythritol hexa(meth)acrylate, caprolactone modified pentaerythritol tetra(meth)acrylic acid Ester, caprolactone modified dipentaerythritol hexa(meth)acrylate, etc.

The content rate of the polymerizable compound (C) is preferably 1 mass % or more, more preferably 2 mass % or more, and further preferably 3 mass % or more with respect to the total amount of the solid content of the colored curable resin composition, and further, Preferably it is 50 mass % or less, More preferably, it is 40 mass % or less, More preferably, it is 30 mass % or less.

<Polymerization initiator (D)> The polymerization initiator (D) is not particularly limited as long as it is a compound that can generate active radicals, an acid, or the like to initiate polymerization by the action of light or heat, and known polymerization initiators can be used. As a polymerization initiator which generate|occur|produces an active radical, a phenalkyl ketone compound, a triazine compound, an acylphosphine oxide compound, an O-acyl oxime compound, and a biimidazole compound are mentioned, for example.

The O-acyl oxime compound is a compound having a partial structure represented by formula (d1). Hereinafter, * represents a bond key.

Examples of the O-acyl oxime compound include N-benzyloxy-1-(4-phenylthiophenyl)butane-1-one-2-imine, N-benzyl Acyloxy-1-(4-phenylthiophenyl)octan-1-one-2-imine, N-benzyloxy-1-(4-phenylthiophenyl)-3 -Cyclopentylpropan-1-one-2-imine, N-acetoxy-1-[9-ethyl-6-(2-methylbenzyl)-9H-carbazole-3- yl]ethane-1-imine, N-acetoxy-1-[9-ethyl-6-{2-methyl-4-(3,3-dimethyl-2,4-dioxo Heterocyclopentylmethyloxy)benzyl}-9H-carbazol-3-yl]ethane-1-imine, N-acetoxy-1-[9-ethyl-6-( 2-Methylbenzyl)-9H-carbazol-3-yl]-3-cyclopentylpropane-1-imine, N-benzyloxy-1-[9-ethyl-6 -(2-Methylbenzyl)-9H-carbazol-3-yl]-3-cyclopentylpropan-1-one-2-imine, N-acetyloxy-1-(4 -Phenylthiophenyl)-3-cyclohexylpropan-1-one-2-imine. Irgacure OXE01, OXE02 (above, manufactured by BASF), N-1919 (manufactured by ADEKA), PBG-327 (manufactured by Changzhou Qiangli Electronic New Materials) can also be used ) and other commercially available products. Wherein, the O-acyl oxime compound is preferably selected from N-benzyloxy-1-(4-phenylthiophenyl)butane-1-one-2-imine, N-benzyloxy-1-(4-phenylthiophenyl)butane-1-one-2-imine, Alkyloxy-1-(4-phenylthiophenyl)octan-1-one-2-imine, N-benzyloxy-1-(4-phenylthiophenyl)-3- Cyclopentylpropan-1-one-2-imine, and N-acetyloxy-1-(4-phenylthiophenyl)-3-cyclohexylpropan-1-one-2-imine At least one of the group consisting of, more preferably selected from N-benzyloxy-1-(4-phenylthiophenyl)octane-1-one-2-imine and N-acetylene at least one of the group consisting of oxy-1-(4-phenylthiophenyl)-3-cyclohexylpropan-1-one-2-imine. With these O-acyl oxime compounds, a high-brightness color filter can be obtained.

The phenylalkyl ketone compound is a compound having a partial structure represented by formula (d2) or a partial structure represented by formula (d3). In these partial structures, the benzene ring may have a substituent.

Examples of compounds having a partial structure represented by formula (d2) include 2-methyl-2-morpholino-1-(4-methylthiophenyl)propan-1-one, 2-dimethylene aminoamino-1-(4-morpholinylphenyl)-2-benzylbutan-1-one, 2-(dimethylamino)-2-[(4-methylphenyl)methyl ]-1-[4-(4-morpholinyl)phenyl]butan-1-one. Commercially available products such as Irgacure 369, 907, and 379 (the above, manufactured by BASF) can also be used. Examples of compounds having a partial structure represented by formula (d3) include 2-hydroxy-2-methyl-1-phenylpropan-1-one, 2-hydroxy-2-methyl-1-[4 -(2-Hydroxyethoxy)phenyl]propan-1-one, 1-hydroxycyclohexylphenyl ketone, 2-hydroxy-2-methyl-1-(4-isopropenylphenyl)propane-1 -Oligomers of ketones, α,α-diethoxyacetophenone, benzil dimethyl ketal. In terms of sensitivity, the phenylalkyl ketone compound is preferably a compound having a partial structure represented by formula (d2).

As the triazine compound, for example, 2,4-bis(trichloromethyl)-6-(4-methoxyphenyl)-1,3,5-triazine, 2,4-bis( Trichloromethyl)-6-(4-methoxynaphthyl)-1,3,5-triazine, 2,4-bis(trichloromethyl)-6-pipronyl-1,3,5- Triazine, 2,4-bis(trichloromethyl)-6-(4-methoxystyryl)-1,3,5-triazine, 2,4-bis(trichloromethyl)-6 -[2-(5-Methylfuran-2-yl)vinyl]-1,3,5-triazine, 2,4-bis(trichloromethyl)-6-[2-(furan-2- yl)vinyl]-1,3,5-triazine, 2,4-bis(trichloromethyl)-6-[2-(4-diethylamino-2-methylphenyl)vinyl ]-1,3,5-triazine, 2,4-bis(trichloromethyl)-6-[2-(3,4-dimethoxyphenyl)vinyl]-1,3,5- Triazine.

As said acyl phosphine oxide compound, 2,4,6- trimethylbenzyl diphenylphosphine oxide etc. are mentioned. Commercially available products such as Irgacure (registered trademark) 819 (manufactured by BASF) can also be used.

As the biimidazole compound, for example, 2,2'-bis(2-chlorophenyl)-4,4',5,5'-tetraphenylbiimidazole, 2,2'-bis(2, 3-dichlorophenyl)-4,4',5,5'-tetraphenylbiimidazole (for example, refer to Japanese Patent Laid-Open No. 6-75372, Japanese Patent Laid-Open No. 6-75373, etc.), 2 ,2'-bis(2-chlorophenyl)-4,4',5,5'-tetraphenylbiimidazole, 2,2'-bis(2-chlorophenyl)-4,4',5, 5'-Tetrakis(alkoxyphenyl)biimidazole, 2,2'-bis(2-chlorophenyl)-4,4',5,5'-tetrakis(dialkoxyphenyl)biimidazole, 2,2'-bis(2-chlorophenyl)-4,4',5,5'-tetrakis(trialkoxyphenyl)biimidazole (for example, refer to Japanese Patent Publication No. 48-38403, Japanese Japanese Patent Laid-Open No. 62-174204, etc.), biimidazole compounds in which the phenyl group at the 4,4', 5,5'-position is substituted with an alkoxycarbonyl group (for example, refer to Japanese Patent Laid-Open No. 7-10913, etc.) .

Further, examples of the polymerization initiator (D) include benzoin compounds such as benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, and benzoin isobutyl ether; benzophenone, methyl o-benzoylbenzoate, etc. , 4-phenylbenzophenone, 4-benzyl-4'-methyldiphenyl sulfide, 3,3',4,4'-tetrakis(tert-butylperoxycarbonyl)diphenyl Benzophenone compounds such as ketone, 2,4,6-trimethylbenzophenone; quinone compounds such as 9,10-phenanthraquinone, 2-ethylanthraquinone, camphorquinone; 10-butyl-2- Chloracridone, benzil, methyl phenylglyoxylate, titanocene compounds, etc. These are preferably used in combination with a polymerization initiator (D1) (especially amines) described later.

As the acid generator, for example, 4-hydroxyphenyldimethylperylene p-toluenesulfonate, 4-hydroxyphenyldimethylperylene hexafluoroantimonate, and 4-acetoxyphenyldimethylene are mentioned. Peri-p-toluenesulfonate, 4-Acetyloxyphenyl·methyl·benzyl perylene hexafluoroantimonate, triphenyl perylene p-toluenesulfonate, triphenyl perylene hexafluoroantimonate, diphenyl perylene hexafluoroantimonate Onium salts such as iodonium p-toluenesulfonate, diphenyl iodonium hexafluoroantimonate, or nitrobenzyl tosylate, benzoin tosylate, and the like.

The polymerization initiator (D) preferably contains at least one selected from the group consisting of a phenylalkyl ketone compound, a triazine compound, an acylphosphine oxide compound, an O-acyl oxime compound, and a biimidazole compound The polymerization initiator is more preferably a polymerization initiator containing an O-acyl oxime compound.

The content of the polymerization initiator (D) is preferably 0.1 part by mass or more and 30 parts by mass or less, more preferably 1 part by mass or more, with respect to 100 parts by mass of the total amount of the resin (B) and the polymerizable compound (C). 20 parts by mass or less. When the content of the polymerization initiator (D) is in the above range, the sensitivity can be increased and the exposure time can be shortened, so that the productivity of the color filter can be improved.

<Polymerization Initiating Auxiliary (D1)> The polymerization initiation adjuvant (D1) is a compound or a sensitizer for accelerating the polymerization of the polymerizable compound whose polymerization is initiated by the polymerization initiator. When a polymerization initiator (D1) is contained, it is used in combination with a polymerization initiator (D). As a polymerization initiation aid (D1), an amine compound, an alkoxyanthracene compound, a thioxanthone compound, a carboxylic acid compound, etc. are mentioned. Among them, a thioxanthone compound is preferable. Two or more kinds of polymerization initiators (D1) may also be contained.

Examples of the amine compound include triethanolamine, methyldiethanolamine, triisopropanolamine, methyl 4-dimethylaminobenzoate, ethyl 4-dimethylaminobenzoate, and 4-dimethylaminobenzoate. Isoamyl aminobenzoate, 2-dimethylaminoethyl benzoate, 2-ethylhexyl 4-dimethylaminobenzoate, N,N-dimethyl-p-toluidine, 4,4 '-Bis(dimethylamino)benzophenone (commonly known as Michler's ketone), 4,4'-bis(diethylamino)benzophenone, 4,4'-bis (Ethylmethylamino)benzophenone, etc. Among them, 4,4'-bis(diethylamino)benzophenone is preferable. Commercially available products such as EAB-F (manufactured by Hodogaya Chemical Industry Co., Ltd.) can also be used.

As the alkoxyanthracene compound, 9,10-dimethoxyanthracene, 2-ethyl-9,10-dimethoxyanthracene, 9,10-diethoxyanthracene, 2-ethyl- 9,10-diethoxyanthracene, 9,10-dibutoxyanthracene, 2-ethyl-9,10-dibutoxyanthracene, etc.

As the thioxanthone compound, 2-isopropylthioxanthone, 4-isopropylthioxanthone, 2,4-diethylthioxanthone, 2,4-dichlorothioxanthone, 1- Chloro-4-propoxythioxanthone, etc.

Examples of the carboxylic acid compound include thiophenylacetic acid, methylphenylthioacetic acid, ethylphenylthioacetic acid, methylethylphenylthioacetic acid, dimethylphenylthioacetic acid, and methoxyphenylthioacetic acid. Acetic acid, dimethoxyphenylthioacetic acid, chlorophenylthioacetic acid, dichlorophenylthioacetic acid, N-phenylglycine, phenoxyacetic acid, naphthylthioacetic acid, N-naphthylglycine , naphthoxyacetic acid, etc.

The content of the polymerization initiator (D1) is preferably 0.1 parts by mass to 30 parts by mass, more preferably 1 part by mass to 20 parts by mass with respect to 100 parts by mass of the total amount of the resin (B) and the polymerizable compound (C1). share. When the amount of the polymerization initiation adjuvant (D1) is in this range, a colored pattern can be further formed with high sensitivity, and the productivity of the color filter tends to be improved.

<Solvent (E)> The colored curable resin composition of the present invention preferably contains a solvent (E). Examples of the solvent (E) include ester solvents (solvents containing -COO-), ether solvents other than ester solvents (solvents containing -O-), ether ester solvents (solvents containing -COO- and -O-), Ketone solvents (solvents containing -CO-) other than ester solvents, alcohol solvents, aromatic hydrocarbon solvents, amide solvents, dimethyl sulfoxide, and the like.

Examples of the ester solvent include methyl lactate, ethyl lactate, butyl lactate, methyl 2-hydroxyisobutyrate, ethyl acetate, n-butyl acetate, isobutyl acetate, amyl formate, and isoamyl acetate , butyl propionate, isopropyl butyrate, ethyl butyrate, butyl butyrate, methyl pyruvate, ethyl pyruvate, propyl pyruvate, methyl acetoacetate, ethyl acetoacetate, cyclic Hexanol acetate and γ-butyrolactone, etc.

As the ether solvent, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monoethyl ether, Ethylene glycol monobutyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, propylene glycol monopropyl ether, propylene glycol monobutyl ether, 3-methoxy-1-butanol, 3-methoxy-3-methyl butanol, Tetrahydrofuran, tetrahydropyran, 1,4-dioxane, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol methyl ethyl ether, diethylene glycol dipropyl ether, diethylene glycol Dibutyl ether, anisole, phenethyl ether and methyl anisole, etc.

Examples of ether ester solvents include methyl methoxyacetate, ethyl methoxyacetate, butyl methoxyacetate, methyl ethoxyacetate, ethyl ethoxyacetate, and 3-methoxypropionic acid. Methyl ester, ethyl 3-methoxypropionate, methyl 3-ethoxypropionate, ethyl 3-ethoxypropionate, methyl 2-methoxypropionate, 2-methoxypropionic acid Ethyl, 2-methoxypropionate, 2-ethoxypropionate, 2-ethoxypropionate, 2-ethoxypropionate, 2-methoxy-2-methylpropionate, 2- Ethoxy-2-methylpropionate ethyl ester, 3-methoxybutyl acetate, 3-methyl-3-methoxybutyl acetate, propylene glycol monomethyl ether acetate, propylene glycol mono Diethyl ether acetate, propylene glycol monopropyl ether acetate, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate acid ester and dipropylene glycol methyl ether acetate, etc.

Examples of the ketone solvent include: 4-hydroxy-4-methyl-2-pentanone, acetone, 2-butanone, 2-heptanone, 3-heptanone, 4-heptanone, 4-methyl-2- Pentanone, cyclopentanone, cyclohexanone and isophorone, etc.

Examples of the alcohol solvent include methanol, ethanol, propanol, butanol, hexanol, cyclohexanol, ethylene glycol, propylene glycol, and glycerin. As an aromatic hydrocarbon solvent, benzene, toluene, xylene, mesitylene, etc. are mentioned. As an amide solvent, N,N- dimethylformamide, N,N- dimethylacetamide, N-methylpyrrolidone, etc. are mentioned.

The solvent (E) may be used in combination of two or more. From the viewpoint of coatability and drying properties, an organic solvent having a boiling point at 1 atm of 120°C or higher and 180°C or lower is preferred. Among them, propylene glycol monomethyl ether acetate, ethyl lactate, propylene glycol monomethyl ether, 3-ethoxy ethyl propionate, ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, diethylene glycol are preferred. Alcohol monoethyl ether, 3-methoxybutyl acetate, 3-methoxy-1-butanol, 4-hydroxy-4-methyl-2-pentanone and N,N-dimethylformamide , more preferably propylene glycol monomethyl ether acetate, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether acetate, ethyl lactate, 3-methoxybutyl acetate, 3-methoxy-1-butanol and ethyl 3-ethoxypropionate.

The content of the solvent (E) is preferably from 70% by mass to 95% by mass, more preferably from 75% by mass to 92% by mass, with respect to the colored curable resin composition. In other words, the solid content of the colored curable resin composition is preferably 5% by mass to 30% by mass, more preferably 8% by mass to 25% by mass. When the content of the solvent (E) is in the above range, the flatness at the time of coating becomes favorable, and the color density at the time of forming the color filter tends not to be insufficient, and the display characteristics tend to become favorable.

＜Leveler (F)＞ As the leveling agent (F), a silicone-based surfactant, a fluorine-based surfactant, a silicone-based surfactant having a fluorine atom, and the like are exemplified. These may also have a polymerizable group in the side chain.

As a silicone type surfactant, the surfactant etc. which have a siloxane bond in a molecule|numerator are mentioned. Specifically, Toray silicone DC3PA, Toray silicone SH7PA, Toray silicone DC11PA, Toray silicone SH21PA, Toray silicone Toray silicone SH28PA, Toray silicone SH29PA, Toray silicone SH30PA, Toray silicone SH8400 (trade name; Toray Dow Corning (stock) ), KP321, KP322, KP323, KP324, KP326, KP340, KP341 (manufactured by Shin-Etsu Chemical Industry Co., Ltd.), TSF400, TSF401, TSF410, TSF4300, TSF4440, TSF4445, TSF4446, TSF4452 and TSF4460 (Japan Momentum High-Tech Materials) (manufactured by Momentive Performance Materials Japan Co., Ltd.), etc.

As a fluorine-type surfactant, the surfactant etc. which have a fluorocarbon chain in a molecule|numerator are mentioned. Specific examples include: Fluorad (registered trademark) FC430, Fluorad (Fluorad) FC431 (manufactured by Sumitomo 3M Co., Ltd.), Megafac (registered trademark) F142D, Megafac (Megafac) F171, Megafac F172, Megafac F173, Megafac F177, Megafac F183, Megafac F554, Megafac R30, Megafac RS-718 -K (manufactured by DIC (stock)), Eftop (registered trademark) EF301, Eftop EF303, Eftop EF351, Eftop EF352 ( Mitsubishi Materials Electronics Co., Ltd. (stock), Surflon (registered trademark) S381, Surflon S382, Surflon SC101, Surflon SC105 (AGC (stock) Manufacturing, former Asahi Glass (stock) and E5844 (Daikin Fine Chemical Research Institute (stock)), etc.

As a silicone type surfactant which has a fluorine atom, the surfactant etc. which have a siloxane bond and a fluorocarbon chain in a molecule|numerator are mentioned. Specifically, Megafac (registered trademark) R08, Megafac BL20, Megafac F475, Megafac F477 and Megafac F443 (DIC) ) (stocks), etc.

The content of the leveling agent (F) is, for example, 0.001 mass % or more and 0.2 mass % or less, preferably 0.002 mass % or more and 0.1 mass % or less, and more preferably 0.005 mass % with respect to the total amount of the colored curable resin composition. % or more and 0.05 mass % or less. Furthermore, the content of the pigment dispersant is not included in this content. When the content rate of the leveling agent (F) is within the above range, the flatness of the color filter can be improved.

<Manufacturing method of dispersion liquid> The colorant (A) may be dispersed in the dispersant and the solvent (E) to form a dispersion. The dispersant is preferably one or both of the acrylic dispersant and the resin (B1), and more preferably both of the acrylic dispersant and the resin (B1). The content of the colorant (A) is preferably 1 to 25% by mass, and more preferably 2 to 20% by mass in 100% by mass of the dispersion. The content of the resin (B1) is preferably 1 to 20% by mass, and more preferably 2 to 15% by mass in 100% by mass of the dispersion. The content of the acrylic dispersant is preferably 0.1 to 10% by mass, and more preferably 0.5 to 8% by mass in 100% by mass of the dispersion.

<Manufacturing method of colored curable resin composition> The coloring curable resin composition of the present invention can be prepared by containing a colorant (A), a resin (B), a polymerizable compound (C), a polymerization initiator (D), and optionally a mixed solvent (E), leveling Agent (F), polymerization initiation aid (D1), and other components are prepared.

<Manufacturing method of color filter> As a method of producing a color filter from the colorable curable resin composition of the present invention, a photolithography method, an inkjet method, a printing method, and the like can be mentioned. Among them, photolithography is preferred. The photolithography method is a method of applying the colored curable resin composition on a substrate, drying it to form a colored composition layer, and exposing and developing the colored composition layer through a light shield. In the photolithography method, a colored coating film that is a cured product of the colored composition layer can be formed by not using a photomask and/or without performing development at the time of exposure. The color filter of the present invention can be colored by prebaking of the colored curable resin composition (colored composition layer), exposure of the colored composition layer (colored coating film), development of the colored coating film (colored pattern), and coloring. It can be obtained by post-baking of the pattern, or it can also be obtained by post-baking of the color coating film, omitting the development of the color coating film as necessary.

As the substrate, glass plates such as quartz glass, borosilicate glass, alumina silicate glass, and soda lime glass whose surface is coated with silica; or polycarbonate, polymethyl methacrylate, poly Resin plates such as ethylene terephthalate; silicon; aluminum, silver, silver/copper/palladium alloy thin films, etc. are formed on the substrate. Other color filter layers, resin layers, transistors, circuits, etc. can also be formed on these substrates. Moreover, the board|substrate which performed the surface treatment by 1,1,1,3,3,3- hexamethyldisilazane etc. on the said board|substrate can also be used.

The formation of each color pixel by the photolithography method can be performed by a well-known or conventional apparatus and conditions. For example, it can be produced as follows. First, a coloring curable resin composition is applied on a substrate, and drying by heating (prebaking) and/or drying under reduced pressure is performed to remove volatile components such as a solvent and dry it to obtain a smooth coloring composition layer. As a coating method, a spin coating method, a slit coating method, a slit and spin coating method, etc. are mentioned. The temperature at the time of heating and drying is preferably 30°C to 120°C, more preferably 50°C to 110°C. In addition, the heating time is preferably from 10 seconds to 5 minutes, more preferably from 30 seconds to 3 minutes. When drying under reduced pressure, it is preferable to carry out in the temperature range of 20 degreeC - 25 degreeC under the pressure of 50 Pa - 150 Pa. The film thickness of the coloring composition layer is not particularly limited, and may be appropriately selected according to the film thickness of the target color filter.

Next, a colored coating film is obtained by exposing the colored composition layer through a photomask for forming a target colored pattern. The pattern on the mask is not particularly limited, and a pattern according to the intended use is used. As a light source used for exposure, a light source that generates light having a wavelength of 250 nm to 450 nm is preferable. For example, for light less than 350 nm, use a filter that cuts off this wavelength range, or for light around 436 nm, around 408 nm, and around 365 nm, use a bandpass filter that takes out these wavelength ranges. Selective removal. Specifically, a mercury lamp, a light emitting diode, a metal halide lamp, a halogen lamp, etc. are mentioned as a light source.

It is preferable to use a mask aligner (proximity exposure machine) and a Exposure devices such as stepper (reduced projection exposure machine). A colored pattern is formed on a board|substrate by contacting the coloring coating film after exposure with a developing solution, and developing. By development, the unexposed portion of the colored coating film is dissolved in the developing solution and removed. As the developer, for example, an aqueous solution of an alkaline compound such as potassium hydroxide, sodium bicarbonate, sodium carbonate, and tetramethylammonium hydroxide is preferable. The concentration of these basic compounds in the aqueous solution is preferably 0.01% by mass to 10% by mass, more preferably 0.03% by mass to 5% by mass. Furthermore, the developer may contain a surfactant. The development method may be any of a liquid coating method, a dipping method, a spray method, and the like. Furthermore, the substrate may be inclined at an arbitrary angle during development. After development, it is preferable to wash with water. Furthermore, it is preferable to post-bake the obtained colored pattern. The post-baking temperature is preferably 80°C to 250°C, more preferably 100°C to 250°C, further preferably 150°C to 250°C, and still more preferably 160°C to 235°C. The post-baking time is preferably 1 minute to 120 minutes, more preferably 2 minutes to 120 minutes, more preferably 10 minutes to 60 minutes, and still more preferably 10 minutes to 30 minutes.

Since the film thickness of the obtained coloring coating film and coloring pattern affects adjacent pixels, it is preferable to be as thin as possible. In particular, when a thick film is used, light from a light source may leak through pixels of two or more colors when a liquid crystal panel is produced, and when the panel is viewed from an oblique direction, the vividness of the color may be lost. The film thickness of the colored coating film and the colored pattern is, for example, preferably 4 μm or less or 3 μm or less, more preferably 2.8 μm or less, still more preferably 2.5 μm or less, and still more preferably 2.3 μm or less. The lower limit of the film thickness of the colored coating film and the colored pattern is not particularly limited, but is usually 0.1 μm or more, preferably 0.2 μm or more, 0.5 μm or more, or 1 μm or more, and may be 1.5 μm or more.

The color filter is formed so that the film thickness after post-baking at a temperature of 230° C. for 30 minutes is 1 μm to 4 μm (preferably 1 μm to 3 μm, more preferably 2.8 μm or less, further preferably 2.5 μm or less, More preferably, it is 2.3 μm or less).

By using the colored curable resin composition of the present invention, a color filter having an excellent dark color effect can be produced. This color filter is useful as a color filter used in display devices (eg, liquid crystal display devices, organic electroluminescence (EL) devices, electronic paper, etc.) and solid-state imaging elements. [Example]

Hereinafter, the present invention will be described in more detail by way of examples. However, the present invention is not limited to the following examples at all, and it goes without saying that the present invention can be implemented by appropriately adding changes within the scope that can be adapted to the above-mentioned and later-mentioned gist. It is included in the technical scope of the present invention. In addition, in the following, unless otherwise specified, "part" means "mass part", and "%" means "mass %".

Synthesis Example 1 100 mass parts of propylene glycol monomethyl ether acetate were added to the flask equipped with a stirring blade, a reflux cooling tube, a thermometer, and a dropping funnel, and it heated to 90 degreeC. A solution obtained by mixing 81 parts by mass of tertiary butyl acrylate, 19 parts by mass of acrylic acid, 15 parts by mass of azobis(isobutyronitrile), and 54 parts by mass of propylene glycol monomethyl ether acetate was started to be continuous by a dropping funnel. Add dropwise to the flask. The temperature in the flask during the dropwise addition of the mixed solution was maintained at 90±1°C, and the dropwise addition was completed in 3 hours. After the completion of the dropwise addition, the temperature in the flask was adjusted to 90 ± 1°C and reacted for 3 hours, the temperature in the flask was raised to 105°C to 110°C, and the reaction was carried out for 1.5 hours to obtain a solid content of 40.3 mass %. (resin B1) solution (hereinafter sometimes referred to as resin solution (B1)). The weight average molecular weight Mw of the produced copolymer was 6100, and the acid value of the solid content was 131 mgKOH/g.

Synthesis Example 2 An appropriate amount of nitrogen gas was circulated in a flask equipped with a reflux cooler, a dropping funnel, and a stirrer, and it was replaced with a nitrogen atmosphere. Then, 58 parts by mass of acrylic acid, 3,4-epoxytricyclo[5.2.1.0 ^2,6 ]decane-8-yl acrylate, and 3,4-epoxytricyclo[5.2.1.0 acrylate were added dropwise over 5 hours. ^2,6 ] 167 parts by mass of a mixture of decan-9-yl esters (the content ratio is 1:1 in molar ratio), 65 parts by mass of 2-ethylhexyl acrylate, and 111 parts by mass of propylene glycol monomethyl ether acetate part of the mixed solution. On the other hand, a mixed solution obtained by dissolving 27 parts by mass of 2,2-azobis(2,4-dimethylvaleronitrile) in 210 parts by mass of propylene glycol monomethyl ether acetate was added dropwise over 6 hours. After completion of the dropwise addition, the solution was kept at 80°C for 5.5 hours, and then cooled to room temperature to obtain a copolymer (resin B2) solution with a B-type viscosity (23°C) of 43 mPa·s and a solid content of 29.8% by mass (hereinafter, sometimes called resin solution (B2)). The solid content acid value of the produced copolymer was 149 mgKOH/g, the weight average molecular weight Mw was 11220, and the degree of dispersion was 2.25.

The measurement of the polystyrene-equivalent weight average molecular weight Mw and the number average molecular weight Mn of the resin obtained in the above-mentioned synthesis example was performed under the following conditions by the GPC method. Device: HLC-8120GPC (manufactured by Tosoh Co., Ltd.) Column: TSK-GELG2000HXL Column temperature: 40℃ Solvent: THF Flow rate: 1.0 mL/min Test liquid solid content concentration: 0.001% by mass to 0.01% by mass Injection volume: 50 μL Detector: Refractive Index (RI) Standard material for calibration: TSK standard polystyrene (STANDARD POLYSTYRENE) F-40, F-4, F-288, A-2500, A-500 (manufactured by Tosoh Co., Ltd.)

[Preparation of dispersion liquid] The dispersion liquid (A-1) to the dispersion liquid (A-3) were prepared by mixing the following components and sufficiently dispersing the pigment using a bead mill. As resin (B1) - resin (B2), the above-mentioned resin solution (B1) - resin solution (B2) were used.

[Preparation of Dispersion (A-1)] C.I. Pigment Green 58     14.0 parts Acrylic pigment dispersant 1.9 parts Resin (B2) (solid content conversion) 6.5 parts Propylene glycol monomethyl ether acetate 77.6 parts

[Preparation of Dispersion (A-2)] C.I. Pigment Green 58     14.0 parts Acrylic pigment dispersant 3.3 parts Resin (B1) (solid content conversion) 5.6 parts Propylene glycol monomethyl ether acetate 77.1 parts

[Preparation of Dispersion (A-3)] C.I. Pigment Yellow 150 12.0 parts Acrylic pigment dispersant 5.4 parts Resin (B2) (solid content conversion) 4.2 parts Propylene glycol monomethyl ether acetate 78.4 parts

Example 1 and Comparative Example 1 [Preparation of Colored Curable Resin Composition] The components described in Table 1 were mixed to obtain a colored curable resin composition.

[Table 1] (parts by mass) Example 1 Comparative Example 1 Colorant (A) Dispersion (A-1) 60.1 Dispersion (A-2) 67.5 Dispersion (A-3) 20.9 18.6 Resin (B) Resin (B1) 1.7 Resin (B2) 2.2 Polymeric compound (C) 1.3 1.3 Polymerization Initiator (D) 1.0 1.0 Solvent (E) 51.2 44.6 Leveler (F) 0.1 0.1 Color change at the same film thickness after PoB Δx -0.0113 -0.0035 Δy 0.0266 0.0083

Each component in Table 1 is as follows. In addition, the usage-amount in a table shows the usage-amount of the following components. Dispersion (A-1) to Dispersion (A-3): the prepared dispersions Resin (B1): Copolymer solution obtained in Synthesis Example 1 Resin (B2): Copolymer solution obtained in Synthesis Example 2 Polymerizable compound (C): Dipentaerythritol polyacrylate (A-9570W; manufactured by Shin-Nakamura Chemical Industry Co., Ltd.) Polymerization initiator (D): IRGACURE (registered trademark) OXE-03: manufactured by BASF; compound represented by formula (d1-24)

溶劑（E）：丙二醇單甲醚乙酸酯 調平劑（F）：聚醚改質矽酮油（SH8400；東麗道康寧（Toray Dow Corning）股份有限公司製造、固體成分10%的丙二醇單甲醚乙酸酯溶液）

Solvent (E): propylene glycol monomethyl ether acetate Leveling agent (F): polyether-modified silicone oil (SH8400; manufactured by Toray Dow Corning Co., Ltd., 10% solid content of propylene glycol monomethyl) ether acetate solution)

<Preparation of color filter> The colored curable resin composition was applied by spin coating on a 2-inch-square glass substrate (Eagle XG; manufactured by Corning), and then heated at 100°C. It was pre-baked for 3 minutes to form a coloring composition layer. After standing to cool, the distance between the substrate on which the coloring composition layer was formed and the mask made of quartz glass was set to 100 μm, and an exposure machine (TME-150RSK; manufactured by Topcon Co., Ltd.) was used in an atmospheric environment. Light irradiation was performed at an exposure of 150 mJ/ ^cm2 (365 nm reference). As a photomask, one formed with a 50 μm line and space pattern was used. The colored coating film after light irradiation was immersed and developed in an aqueous developer containing 0.12% of nonionic surfactant and 0.04% of potassium hydroxide at 24°C for 60 seconds, washed with water, and then carried out in an oven at 230°C After 20 minutes, it was baked to obtain a color filter.

[Film thickness measurement] The film thickness FT (μm) of the obtained color filter was measured using a film thickness measuring apparatus (DEKTAK3; manufactured by Nippon Vacuum Technology Co., Ltd.).

[chromaticity measurement] The obtained color filter was measured for spectrometry using a colorimeter (OSP-SP-200; manufactured by Olympus Co., Ltd.), and measured in the XYZ color system of CIE using the characteristic function of the C light source. The xy chromaticity coordinates (x, y) of . The xy chromaticity coordinates of the coloring composition layer after prebaking and the color filter after postbaking were measured, and Δx and Δy were calculated from the following equations. When Δx and Δy were obtained, the film thicknesses of Example 1 and Comparative Example 1 were the same. Δx = (x value of color filter after post-baking) - (x value of coloring composition layer after pre-baking) Δy=(y value of color filter after post-baking)-(y value of coloring composition layer after pre-baking) For example, in the green area, the larger the absolute values of Δx and Δy, the higher the dark color effect from the pre-baking to the post-baking can be said. [Industrial Availability]

The colored curable resin composition of the present invention can be suitably used for the manufacture of color filters, display devices, and solid-state imaging elements.

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Claims (8)

A colored curable resin composition, characterized in that it comprises a colorant (A), a resin (B), a polymerizable compound (C) and a polymerization initiator (D), As the resin (B), a polymer containing a tertiary carbon-containing (meth)acrylate unit (a1) and an acid group-containing unsaturated monomer unit (b1) as a constituent unit is contained. The colored curable resin composition according to claim 1, wherein the (b1) unsaturated monomer having an acid group is at least one selected from acrylic acid and methacrylic acid. The colored curable resin composition according to claim 1 or claim 2, wherein the resin (B) has an acid value exceeding 80 mgKOH/g and a weight average molecular weight of 9000 or less. The colorable curable resin composition according to any one of Claims 1 to 3, wherein the colorant (A) contains at least a green colorant. The colored curable resin composition according to claim 4, wherein the green colorant is at least one selected from the group consisting of C.I. Pigment Green 58 and C.I. Pigment Green 59. The colored curable resin composition according to any one of claim 1 to claim 5, wherein the colorant (A) further comprises a yellow colorant selected from the group consisting of C.I. Pigment Yellow 138, C.I. Pigment At least one of Yellow 139, C.I. Pigment Yellow 150, and C.I. Pigment Yellow 185. A color filter formed of the coloring curable resin composition according to any one of Claims 1 to 6. A display device comprising the color filter as claimed in claim 7.