JP2011116803A - Coloring composition for color filters and color filter using the same, and display device - Google Patents

Abstract

（式中、Ｒ¹、Ｒ²、Ｒ³、Ｒ⁴、Ｒ⁵及びＲ⁶は、各々独立に水素原子、置換基を有していてもよいアルキル基又は置換基を有していてもよいアリール基のいずれかを示す。）
【選択図】なしThe present invention provides a color composition for color filters, a color filter, and a display device, which have high heat resistance and light resistance, high exposure sensitivity and excellent development solubility.
A color composition for a color filter comprising a binder resin, a crosslinkable monomer, a photopolymerization initiator, a colorant and a solvent, wherein the colorant is a triarylmethane dye represented by the following general formula (I): object.

(In the formula, R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ may each independently have a hydrogen atom, an alkyl group which may have a substituent, or a substituent. Indicates any of aryl groups.)
[Selection figure] None

Description

  The present invention relates to a coloring composition for a color filter, a color filter using the same, and a display device, and in particular, a coloring composition for a color filter having high heat resistance and light resistance and high adhesion of a colored layer to a substrate. The present invention relates to a color filter and a display device using the same.

A color filter may be used for a liquid crystal or an electroluminescence (EL) display device. The color filter has a structure in which a colored layer is laminated on a substrate, and the colored layer is required to have heat resistance and light resistance.
As a material used for the colored layer, an example using a triarylmethane dye and an aromatic sulfonic acid as a counter anion of the triarylmethane dye in order to improve durability to heat and light is known (for example, Patent Literatures 1 to 3).

Among them, in Patent Document 1, durability is improved by introducing a photopolymerizable functional group into an aromatic ring of an aromatic sulfonic acid and forming a chemical bond between the photopolymerizable resin and the crosslinkable monomer contained therein.
However, triarylmethane dyes with aromatic sulfonic acid as the counter anion have a uniform ink composition due to poor solubility in ester solvents such as propylene glycol monomethyl ether acetate (PGMEA), acrylic acid resin and crosslinkable monomers. Even if it can be made into a solution, the dye precipitates in the coating film, which causes problems such as loss of the high permeability that is characteristic of the dye, and the specifications as a colorant for color filters are sufficient. Since it does not satisfy, it has not yet reached practical use.
Patent Document 2 describes a composition containing a colorant having a triarylmethane dye having a specific structure and an aromatic sulfonate ion as a counter anion, but has sufficient adhesion and light resistance to the substrate. It wasn't.

On the other hand, as a means for improving the durability of a cationic dye such as triarylmethane, Patent Document 3 discloses that an imido acid ion is used as a counter anion. The triarylmethane dye using imide acid as the counter anion exhibits high solubility in ester solvents such as PGMEA, acrylic acid resin and crosslinkable monomer, and gives a uniform coating film. In addition, the dye itself is superior in durability compared to a triarylmethane dye having an aromatic sulfonate ion as a counter anion, and is promising as a coloring dye for a color filter.
However, a composition in which an acrylic acid resin, a crosslinkable monomer, a photopolymerizable initiator and a solvent are mixed with a triarylmethane dye using imide acid has low exposure sensitivity and poor solubility during development. There was a problem.

Japanese Patent No. 4266627 JP 2008-304766 A JP 2007-503477 A

As described above, with a colored composition using a conventional triarylmethane dye, although heat resistance can be secured to some extent, light resistance is not sufficient, and the exposure sensitivity is low during the plate-making process, resulting in poor curing. There was a problem that development solubility was low.
The present invention has been made in order to solve the above-mentioned problems, and has a color composition for a color filter having high heat resistance and light resistance, high exposure sensitivity during exposure / development process, and excellent development solubility. An object is to provide a color filter and a display device used.

As a result of intensive studies to solve the above problems, the present inventors have determined that the counter anion in the triarylmethane dye is an oxazolidinone sulfonylimide acid ion, thereby maintaining solubility and light resistance in an organic solvent while maintaining heat resistance. The present invention has been completed by finding that it is possible to perform patterning without compromising exposure sensitivity and development solubility without compromising exposure performance.
That is, the present invention
(1) includes a binder resin, a crosslinkable monomer, a photopolymerization initiator, a colorant and a solvent,
A coloring composition for a color filter, wherein the colorant is a triarylmethane dye represented by the following general formula (I):

(In the formula, R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ may each independently have a hydrogen atom, an alkyl group which may have a substituent, or a substituent. Any one of aryl groups, and at least one of R ¹ and R ² , R ³ and R ⁴ , and R ⁵ and R ⁶ may be bonded to form a part of a ring structure or a heterocyclic structure; X in the formula represents a heterocycle having a nitrogen atom and a carbonyl group in the skeleton, which may have a substituent, and Y represents that at least a part of hydrogen atoms may be substituted with fluorine atoms. An alkyl group),

(2) The triarylmethane dye according to (1), wherein X in the general formula (I) is a heterocyclic ring represented by the following general formula (II):

(3) The coloring composition for a color filter according to the above (1) or (2), wherein Y in the general formula (I) is a perfluoroalkyl group,
(4) In the general formula (I), R ⁵ is a hydrogen atom, and R ¹ , R ² , R ³ , R ⁴ , and R ⁶ are each independently an alkyl group having 1 to 20 carbon atoms (1 ) To (3), a coloring composition for a color filter,
(5) The coloring composition for a color filter according to the above (4), wherein R ¹ , R ² , R ³ , R ⁴ and R ⁶ are all the same.
(6) A color filter comprising at least a colored layer on the substrate, wherein the colored layer is formed using the colored composition for color filter according to any one of (1) to (5) above, and (7) A display device comprising the color filter according to (6) above,
It is.

  According to the present invention, there are provided a coloring composition for a color filter having high heat resistance and light resistance, high exposure sensitivity during exposure / development process and excellent development solubility, and a color filter and a display device using the same. be able to.

Embodiments of the present invention will be described in detail below, but the present invention is not limited to the following embodiments, and various modifications can be made within the scope of the gist of the present invention.
<Coloring composition for color filter>
The coloring composition for a color filter of this embodiment includes a binder resin, a crosslinkable monomer, a photopolymerization initiator, a coloring agent, and a solvent, and the coloring agent is represented by the following general formula (I). It is characterized by being.

In the above formula, R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ may each independently have a hydrogen atom, an alkyl group which may have a substituent, or a substituent. Any one of aryl groups, and at least one of R ¹ and R ² , R ³ and R ⁴ , and R ⁵ and R ⁶ may be bonded to form a part of a ring structure or a heterocyclic structure; Good. X in the formula represents a heterocycle having a nitrogen atom and a carbonyl group in the skeleton, which may have a substituent, and Y represents an alkyl group in which at least part of the hydrogen atoms may be substituted with fluorine atoms It is.

  Conventionally, when a triarylmethane dye is used as a colorant to form a resist, there has been a problem that exposure sensitivity during the exposure / development process is greatly reduced. On the other hand, as a result of investigations by the present inventors, it was found that the exposure sensitivity is greatly improved while maintaining heat resistance by using oxazolidinone sulfonylimide acid ion as the counter anion in the triarylmethane dye. .

(Coloring agent)
First, the colorant in the present embodiment will be described.
The colorant in the present embodiment is a triarylmethane dye represented by the general formula (I), and examples of the alkyl group in the R ^{1 to} R ⁶ of the general formula (I) include a saturated alkyl group and an unsaturated alkyl group. And cycloalkyl groups, and these include substituents such as aryl groups, alkyloxy groups, aryloxy groups, acyloxy groups, halogen atoms, acylamino groups, alkyloxycarbonyl groups, aminocarbonyl groups, hydroxy groups, and cyano groups. You may have.
More specifically, the alkyl group may be a linear, branched or cyclic alkyl group, such as a methyl group, an ethyl group, an n-propyl group, an n-butyl group, an n-amyl group, an n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, n-undecyl group, n-dodecyl group, n-tridecyl group, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecyl group, n-nonadecyl group, n-eicosanyl group, i-propyl group, sec-butyl group, i-butyl group, t-butyl group, 1-methylbutyl group, 1-ethylpropyl group 2-methylbutyl group, i-amyl group, neopentyl group, 1,2-dimethylpropyl group, 1,1-dimethylpropyl group, t-amyl group, 1,3-dimethylbutyl group, , 3-dimethylbutyl group, 2-ethylbutyl group, 2-ethyl-2-methylpropyl group, linear or branched heptyl group, 1-methylheptyl group, 2-ethylhexyl group, 1,5-dimethylhexyl group, t -Octyl group, branched nonyl group, branched decyl group, branched undecyl group, branched dodecyl group, branched tridecyl group, branched tetradecyl group, branched pentadecyl group, branched hexadecyl group, branched heptadecyl group, branched Octadecyl group, linear or branched nonadecyl group, linear or branched eicosanyl group, cyclopropyl group, cyclopropylmethyl group, cyclobutyl group, cyclobutylmethyl group, cyclopentyl group, cyclohexyl group, cyclohexylmethyl group, cycloheptyl group , Cyclooctyl group, cyclohexyl Propyl group, cyclododecyl group, norbornyl group, bornyl group, cis-miltanyl group, isopinocanphenyl group, noradamantyl group, adamantyl group, adamantylmethyl group, 1- (1-adamantyl) ethyl group, 3,5-dimethyl Preferred examples include an adamantyl group, a quinuclidinyl group, a cyclopentylethyl group, and a bicyclooctyl group.

Examples of the aryl group in R ^{1 to} R ⁶ include a phenyl group, a naphthyl group, a biphenylenyl group, an acenaphthenyl group, a fluorenyl group, an anthracenyl group, an anthraquinonyl group, a pyrenyl group, and a heterocyclic group. , Alkyloxy group, aryloxy group, halogen atom, nitro group, cyano group, hydroxy group, substituted carbamoyl group, substituted sulfamoyl group, substituted amino group, substituted oxycarbonyl group, substituted oxysulfonyl group, alkylthio group, arylsulfonyl group, And may have a substituent such as a phenyl group.

More specifically, for example, the substituted phenyl group includes an o-, m- or p-methylphenyl group, an o-, m- or p-ethylphenyl group, an o-, m- or p-propylphenyl group. , O-, m- or p-isopropylphenyl group, o-, m- or p-tert-butylphenyl group, o-, m- or p-aminophenyl group, o-, m- or p- (N, N-dimethylamino) phenyl group, o-, m- or p-nitrophenyl group, o-, m- or p-hydroxyphenyl group, o-, m- or p-methoxyphenyl group, o-, m- or p-ethoxyphenyl group, o-, m-, p- (trifluoromethyl) phenyl group, o-, m-, p- (trifluoromethoxy) phenyl, o-, m-, p- (trifluoro) Romethylsulfanyl) phenyl, o-, m- or p-fluorophenyl, o-, m- or p-chlorophenyl, o-, m- or p-bromophenyl, o-, m- or p-iodo Examples include phenyl group, 3,4- or 3,5-dimethoxyphenyl, 5-fluoro-2-methylphenyl, 3,4,5-trimethoxyphenyl, 2,4,5-trimethylphenyl, and the like.
Further, for example, as an aryl group having an alkyl group as a substituent, a benzyl group, 4-methoxyphenylethyl group, 3-methoxyphenylethyl group, 2-methoxybenzyl group, 3-methoxybenzyl group, 4-methoxybenzyl group, 2-ethoxybenzyl group, 2-methylbenzyl group, 3-methylbenzyl group, 4-tert-butylbenzyl group, 2- (trifluoromethyl) benzyl group, 3- (trifluoromethyl) benzyl group, 4-fluorobenzyl Group, 3-iodobenzyl group, 4- (trifluoromethoxy) benzyl group, 3- (trifluoromethoxy) benzyl group and 4- (trifluoromethylsulfanyl) benzyl group.

Further, in the general formula (I), any ^one of R ¹ and R ² , R ³ and R ⁴ , and R ⁵ and R ⁶ is bonded to form a part of a ring structure or a heterocyclic structure. Examples of the ring include piperidine, morpholine, pyrrolidine, piperazine, hexamethyleneimine and the like. Examples of the substituent represented by R ₁ R ₂ N—, R ₃ R ₄ N—, and R ₅ R ₆ N— include, for example, a pyrrolidino group, a piperazino group, a morpholino group, an N-ethylpiperazino group, Dimethylamino group, diethylamino group, dipropylamino group, dibutylamino group, N-ethyl-N-isobutylamino group, N-ethyl-benzylamino group, diamylamino group, dihexylamino group, dioctylamino group, N-ethyl-N -Tetrafurfurylamino group, dibenzylamino group, etc. are mentioned. Among these, a 5-membered ring and a 6-membered ring are preferable.

Among these, R ⁵ is a hydrogen atom, and R ¹ , R ² , R ³ , R ⁴ and R ⁶ are preferably each independently an alkyl group from the viewpoint of ease of dye production. Preferably has 1 to 20 carbon atoms, more preferably 1 to 10 carbon atoms, and particularly preferably an ethyl group and a methyl group.
Further, as described above, R ¹ , R ² , R ³ , R ⁴ and R ⁶ may be different or the same, but are preferably the same from the viewpoint of the dye structure.

On the other hand, in the oxazolidinone sulfonylimide acid ion which is a counter anion, as described above, X represents a heterocycle having a nitrogen atom and a carbonyl group in the skeleton, which may have a substituent.
The heterocyclic ring is not particularly limited as long as it has a nitrogen atom and a carbonyl group in the skeleton, and examples thereof include those having the structures described below.

  In the above formulas, all Z's may be the same or different. Specific examples include hydrogen atom; halogen atom such as fluorine atom, chlorine atom and bromine atom; formyl group; hydroxyl group; carboxyl group; cyano group; Group: amino group; methyl group, trifluoromethyl group, ethyl group, pentafluoroethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, n-pentyl group, n -Hexyl group, cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, 1,2,2-trimethylbutyl group, 1,1,2-trimethylbutyl group, 1-ethyl-2-methylpropyl group, cyclohexyl group, n-heptyl group, 2-methylhexyl group, 3-methylhexyl group, 4-methylhexyl group, 5-methylhexyl group, , 4-dimethylpentyl group, n-octyl group, 2-ethylhexyl group, 2,5-dimethylhexyl group, 2,5,5-triethylpentyl group, 2,4-dimethylhexyl group, 2,2,4-trimethyl An alkyl group having 1 to 8 carbon atoms such as pentyl group; methoxy group, ethoxy group, n-propoxy group, isopropoxy group, n-butoxy group, tert-butoxy group, sec-butoxy group, n-pentyloxy group, iso An alkoxy group having 1 to 8 carbon atoms such as -pentyloxy group, n-hexyloxy group, n-octyloxy group, methoxymethoxy group, ethoxyethoxy group, 3- (iso-propyloxy) propyloxy group; acetyl group, Propiol group, butyryl group, isobutyryl group, valeryl group, isovaleryl group, pivaloyl group, hexanoyl group, heptanoyl group, etc. C2-C7 acyl group; vinyl group, propenyl group, butenyl group, pentenyl group, hexenyl group, cyclopentenyl group, cyclohexenyl group and the like alkenyl group having 2 to 6 carbon atoms; hydroxymethyl group, hydroxyethyl group, etc. A methoxycarbonyl group, an ethoxycarbonyl group, an n-propoxycarbonyl group, an isopropoxycarbonyl group, an n-butoxycarbonyl group, a tert-butoxycarbonyl group, a sec-butoxycarbonyl group, an n- C2-C7 alkoxycarbonyl groups such as pentyloxycarbonyl group and n-hexyloxycarbonyl group; C1-C6 such as methylamino group, ethylamino group, n-propylamino group and n-butylamino group Alkylamino group; dimethylamino group, diethylamino A dialkylamino group having 2 to 8 carbon atoms such as di-n-propylamino group and di-n-butylamino group; methoxycarbonylmethyl group, ethoxycarbonylmethyl group, n-propoxycarbonylmethyl group, isopropoxycarbonyl C3-C7 alkoxycarbonylalkyl groups such as ethyl group and phenoxycarbonyl group; methylthio group, ethylthio group, n-propylthio group, tert-butylthio group, sec-butylthio group, n-pentylthio group, n-hexylthio group, etc. An alkylthio group having 1 to 6 carbon atoms of: methylsulfonyl group, trifluoromethylsulfonyl group, ethylsulfonyl group, pentafluoroethylsulfonyl group, n-propylsulfonyl group, isopropylsulfonyl group, n-butylsulfonyl group, tert-butylsulfonyl Group, C1-C6 alkylsulfonyl groups such as ec-butylsulfonyl group, n-pentylsulfonyl group, n-hexylsulfonyl group; methylcarbonylamino group, ethylcarbonylamino group, n-propylcarbonylamino group, isopropylcarbonylamino group And an alkylcarbonylamino group having 2 to 6 carbon atoms such as an n-butylcarbonylamino group, a tert-butylcarbonylamino group, a sec-butylcarbonylamino group, and an n-pentylcarbonylamino group.

  Among these, those having a five-membered ring structure containing nitrogen and oxygen are preferable, and a heterocyclic ring represented by the following general formula (II) is particularly preferable.

Examples of the alkyl group constituting Y include the same alkyl groups as those described above for R ^{1 to} R ^6, and a part of hydrogen atoms may be substituted with fluorine atoms. Particularly preferred is a fluorinated alkyl group having 1 to 3 carbon atoms and having some or all of the hydrogen atoms substituted with fluorine atoms. Specifically, for example, trifluoromethyl group, difluoromethyl group, fluoromethyl group, pentafluoroethyl group, 2,2,2-trifluoroethyl group, 2-fluoroethyl group, 3,3,3-trifluoro A propyl group, a 3-fluoropropyl group, etc. can be mentioned.

  Examples of the triarylmethane dye represented by the general formula (I) include compounds represented by the following exemplified compounds (1) to (3).

Like the exemplary compounds (1) to (3), exemplary compounds in which R ⁵ in the general formula (I) is a hydrogen atom, and R ¹ , R ² , R ³ , R ^4, and R ⁶ are alkyl groups. The exemplified compound (1) in which R ¹ , R ² , R ³ , R ⁴ and R ⁶ are all the same is particularly preferable.

The triarylmethane dye represented by the general formula (I) can be synthesized by a known method. As a synthesis method, for example, the method described in “Review Review Synthetic Dyes” (Horiguchi Hiroshi, Sankyo Publishing, 1968) is useful.
Counter anion, a dye represented by the following formula, for example counter anion Cl ^- to the dye represented by the corresponding oxazolidinone imide acid was added, can be synthesized by a salt exchange.

Specifically, the counter anion is Cl ^- to dissolve the dye represented by the reaction solvent, the corresponding oxazolidinone imide acid was added and, after stirring, the precipitate can be synthesized by removing by filtration. The amount of oxazolidinone sulfonylimide acid added is, for example, about 1 to 3 equivalents. Examples of the reaction solvent include water; alcohol solvents such as methanol, ethanol and 2-propanol; or a mixed solvent thereof. The reaction temperature is preferably, for example, 0 ° C. to 40 ° C.

(Binder resin)
The binder resin used in the present embodiment is not particularly limited, but is preferably selected from the viewpoints of heat resistance, developability, availability, and the like. Moreover, it is preferable that it is alkali-soluble.
The alkali-soluble binder resin is preferably a linear organic polymer, soluble in an organic solvent, and developable with a weak alkaline aqueous solution. Examples of such a linear organic high molecular polymer include polymers having a carboxylic acid in the side chain, such as JP-A-59-44615, JP-B-54-34327, JP-B-58-12777, and JP-B. Methacrylic acid copolymer, acrylic acid copolymer, itaconic acid copolymer, crotonic acid as described in Japanese Patent Application Laid-Open No. 54-25957, Japanese Patent Application Laid-Open No. 59-53836, Japanese Patent Application Laid-Open No. 59-71048 There are a copolymer, a maleic acid copolymer, a partially esterified maleic acid copolymer, and the like, and an acidic cellulose derivative having a carboxylic acid in the side chain is also useful. In addition to this, an acid anhydride added to a polymer having a hydroxyl group, polyhydroxystyrene resin, polysiloxane resin, poly (2-hydroxyethyl (meth) acrylate), polyvinylpyrrolidone, polyethylene oxide, polyvinyl alcohol Etc. are also useful.

The alkali-soluble binder resin may be one obtained by copolymerizing a hydrophilic monomer, and examples thereof include alkoxyalkyl (meth) acrylate, hydroxyalkyl (meth) acrylate, and glycerol (meth) acrylate. (Meth) acrylamide, N-methylol acrylamide, secondary and tertiary alkyl acrylamide, dialkylaminoalkyl (meth) acrylate, morpholine (meth) acrylate, N-vinylpyrrolidone, N-vinylcaprolactam, vinylimidazole, vinyltriazole, Methyl (meth) acrylate, ethyl (meth) acrylate, branched or linear propyl (meth) acrylate, branched or linear butyl (meth) acrylate, phenoxyhydroxypropyl (meth) ) Acrylate, and the like.
Other hydrophilic monomers include tetrahydrofurfuryl group, phosphoric acid, phosphate ester, quaternary ammonium salt, ethyleneoxy chain, propyleneoxy chain, sulfonic acid and its salts, and monomers containing morpholinoethyl group. is there.

In order to improve the crosslinking efficiency, a polymerizable group may be included in the side chain, and a polymer containing an allyl group, a (meth) acryl group, an allyloxyalkyl group or the like in the side chain is also useful. Although the example of the polymer containing these polymeric groups is shown below, if alkali-soluble groups, such as a COOH group, OH group, an ammonium group, and a carbon-carbon unsaturated bond are contained, it will not be limited to these.
Reactive with OH groups in copolymers of OH groups such as 2-hydroxyethyl acrylate, COOH groups such as methacrylic acid and monomers such as acrylic or vinyl compounds copolymerizable therewith A compound obtained by reacting a compound having an epoxy ring with a carbon-carbon unsaturated bond group, for example, a compound such as glycidyl acrylate, can be used. In the reaction with the OH group, a compound having an acid anhydride, an isocyanate group and an acryloyl group in addition to the epoxy ring can be used. Further, a compound obtained by reacting an unsaturated carboxylic acid such as acrylic acid with a compound having an epoxy ring disclosed in JP-A-6-102669 and JP-A-6-1938, is saturated or unsaturated polybasic. A reaction product obtained by reacting an acid anhydride can also be used.

  Examples of the compound having both an alkali-solubilizing group such as a COOH group and a carbon-carbon unsaturated group include, for example, Dynar NR series (manufactured by Mitsubishi Rayon Co., Ltd.), Photomer 6173 (COOH group-containing Polyethane acryloligomer, Diamond Shamrock Co., Ltd.). Ltd.,) Biscote R-264, KS resist 106 (all manufactured by Osaka Organic Chemical Industry Co., Ltd.), Cyclomer P series, Plaxel CF200 series (all manufactured by Daicel Chemical Industries, Ltd.), Ebecryl 3800 (Daicel) UCB Co., Ltd.).

Moreover, as the binder resin used in the present embodiment, an alkali-soluble phenol resin can also be used. The alkali-soluble phenol resin can be suitably used when the color composition for color filter of the present embodiment is a positive composition. Examples of the alkali-soluble phenol resin include novolak resins and vinyl polymers.
Examples of the novolak resin include those obtained by condensing phenols and aldehydes in the presence of an acid catalyst. Examples of the phenols include phenol, cresol, ethylphenol, butylphenol, xylenol, phenylphenol, catechol, resorcinol, pyrogallol, naphthol, and bisphenol A. The above phenols can be used alone or in combination of two or more. Examples of the aldehydes include formaldehyde, paraformaldehyde, acetaldehyde, propionaldehyde, benzaldehyde, and the like.
Specific examples of the novolak resin include, for example, a condensation product of metacresol, paracresol, or a mixture thereof and formalin. The novolak resin may be adjusted in molecular weight distribution by means of fractionation or the like. Moreover, you may mix the low molecular weight component which has phenolic hydroxyl groups, such as bisphenol C and bisphenol A, in the said novolak resin.

Among these various binder resins, the binder resin used in the present embodiment is, from the viewpoint of heat resistance, polyhydroxystyrene resin; polysiloxane resin; (meth) acrylic resin, acrylamide resin, acrylic / acrylamide. Acrylic resins such as copolymer resins are preferred. In addition, acrylic resins such as (meth) acrylic resins, acrylamide resins, and acrylic / acrylamide copolymer resins are preferable from the viewpoint of improving adhesion to a substrate and developing properties described later.
The (meth) acrylic resin includes a copolymer composed of monomers selected from benzyl (meth) acrylate, (meth) acrylic acid, hydroxyethyl (meth) acrylate, (meth) acrylamide, and the like, and a polymerizable side chain. (Meth) acrylic resins having, for example, Cyclomer P series, Plaxel CF200 series (all manufactured by Daicel Chemical Industries, Ltd.), Ebecryl 3800 (manufactured by Daicel UC Corporation), dial NR series (Mitsubishi Rayon ( Co., Ltd.), Biscote R264, KS resist 106 (both manufactured by Osaka Organic Chemical Industry Co., Ltd.) and the like are preferable.

The binder resin may developability, from the viewpoint of liquid viscosity, weight average molecular weight is preferably a polymer of 1000-2 × 10 ⁵ (polystyrene equivalent value measured by GPC), the weight of from 2000 to 1 × 10 ⁵ A coalescence is further preferred, and a polymer of 3000 to 5 × 10 ⁴ is particularly preferred.
Moreover, the usage-amount of binder resin has the preferable range of 10-90 mass% with respect to the total solid in the coloring composition for color filters of this embodiment from viewpoints of developability etc., and 20-80 mass%. The range is more preferable, and the range of 30 to 70% by mass is particularly preferable.

(Crosslinkable monomer)
Any crosslinkable monomer can be used as long as it is photopolymerizable in this embodiment, but it has at least one addition polymerizable ethylene group and has a boiling point of 100 ° C. or higher under normal pressure. Compounds with saturated groups are preferred. Specific examples thereof include monofunctional acrylates and methacrylates such as ethylene glycol mono (meth) acrylate, propylene glycol mono (meth) acrylate, and phenoxyethyl (meth) acrylate; ethylene glycol di (meth) acrylate, trimethylolethanetri (Meth) acrylate, neopentyl glycol di (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, hexanediol (Meth) acrylate, trimethylolpropane tri (acryloyloxypropyl) ether, tri (acryloyloxyethyl) isocyanurate And (meth) acrylate obtained by adding ethylene oxide or propylene oxide to polyfunctional alcohols such as glycerin and trimethylolethane; JP-B-48-41708, JP-B-50-6034, JP-A-51 Urethane acrylates as described in JP-B-37193; polyester acrylates described in JP-A-48-64183, JP-B-49-43191 and JP-B-52-30490; epoxy resin And polyfunctional acrylates and methacrylates such as epoxy acrylates which are reaction products of (meth) acrylic acid; and mixtures thereof. Furthermore, Japan Adhesion Association Vol. 20, no. 7, pages 300 to 308 are introduced as photocurable monomers and oligomers.

As the crosslinkable monomer, a (meth) acrylic ester monomer is preferable, and a tetrafunctional or higher (meth) acrylic ester monomer is particularly preferable.
The content of the crosslinkable monomer in the composition is preferably from 0.1 to 90% by mass, more preferably from 1.0 to 80% by mass, based on the total solid content, from the viewpoint of curability and the like. The range of 2.0-70 mass% is especially preferable.

(Photopolymerization initiator)
The photopolymerization initiator in the present embodiment is not particularly limited as long as it can polymerize the above-described polymerizable monomer, but may be selected from the viewpoints of characteristics, initiation efficiency, absorption wavelength, availability, cost, and the like. preferable.
Examples of the photopolymerization initiator include trihalomethyltriazine compounds, benzyldimethyl ketal compounds, α-hydroxyketone compounds, α-aminoketone compounds, phosphine oxide compounds, metallocene compounds, oxime compounds, triarylimidazole dimers, benzoates. Thiazole compounds, benzophenone compounds, acetophenone compounds and derivatives thereof, cyclopentadiene-benzene-iron complexes and salts thereof, halomethyloxadiazole compounds, 3-aryl-substituted coumarin compounds, etc., α-aminoketone compounds, phosphine It is preferable to include at least one compound selected from the group consisting of oxide compounds, metallocene compounds, oxime compounds, and triarylimidazole dimers.
The photopolymerization initiator is preferably a compound that does not generate an acid by decomposition.

  Examples of the active halogen compounds such as the halomethyloxadiazole compounds include 2-halomethyl-5-vinyl-1,3,4-oxadiazole compounds described in JP-B-57-6096, 2-trichloromethyl, and the like. -5-styryl-1,3,4-oxadiazole, 2-trichloromethyl-5- (p-cyanostyryl) -1,3,4-oxadiazole, 2-trichloromethyl-5- (p-methoxy) Styryl) -1,3,4-oxadiazole and the like.

  As photopolymerization initiators for trihalomethyl-s-triazine compounds, vinyl-halomethyl-s-triazine compounds described in JP-B-59-1281 and 2- (naphtho compounds described in JP-A-53-133428) can be used. -1-yl) -4,6-bis-halomethyl-s-triazine compounds and 4- (p-aminophenyl) -2,6-di-halomethyl-s-triazine compounds.

  Examples of the α-aminoketone compound include Irgacure series (Irgacure 907, Irgacure 369) manufactured by Ciba Specialty Chemicals, 2-methyl-1-phenyl-2-morpholinopropan-1-one, 2- And methyl-1- [4- (hexyl) phenyl] -2-morpholinopropan-1-one, 2-ethyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1, and the like.

  The oxime compound is not particularly limited, but 2- (O-benzoyloxime) -1- [4- (phenylthio) phenyl] -1,2-octanedione, 1- (4-methylsulfanyl-phenyl)- Butane-1,2-butane-2-oxime-O-acetate, 1- (4-methylsulfanyl-phenyl) -butan-1-one oxime-O-acetate, hydroxyimino- (4-methylsulfanyl-phenyl) -acetic acid Examples include ethyl ester-O-acetate, hydroxyimino- (4-methylsulfanyl-phenyl) -acetic acid ethyl ester-O-benzoate, and the like.

These photopolymerization initiators can be used in combination with a sensitizer and a light stabilizer.
Specific examples thereof include benzoin, benzoin methyl ether, 9-fluorenone, 2-chloro-9-fluorenone, 2-methyl-9-fluorenone, 9-anthrone, 2-bromo-9-anthrone, and 2-ethyl-9-. Anthrone, 9,10-anthraquinone, 2-ethyl-9,10-anthraquinone, 2-t-butyl-9,10-anthraquinone, 2,6-dichloro-9,10-anthraquinone, xanthone, 2-methylxanthone, 2 -Methoxyxanthone, 2-methoxyxanthone, thioxanthone, 2,4-diethylthioxanthone, acridone, 10-butyl-2-chloroacridone, benzyl, dibenzalacetone, p- (dimethylamino) phenylstyryl ketone, p- ( Dimethylamino) phenyl-p-methylstyryl keto Benzophenone, p- (dimethylamino) benzophenone (or Michler's ketone), p- (diethylamino) benzophenone, benzoanthrone, and the like, benzothiazole compounds described in Japanese Patent Publication No. 51-48516, and tinuvin 1130 and 400 Can be mentioned.

In addition to the above photopolymerization initiators, other known photopolymerization initiators can be used for the color filter coloring composition of the present embodiment.
Specifically, the vicinal polyketol aldonyl compound disclosed in US Pat. No. 2,367,660, US Pat. Nos. 2,367,661 and 2,367,670 are disclosed. Α-carbonyl compounds disclosed in US Pat. No. 2,448,828, acyloin ethers disclosed in US Pat. No. 2,448,828, α-carbonization disclosed in US Pat. No. 2,722,512 Aromatic acyloin compounds substituted with hydrogen, polynuclear quinone compounds disclosed in US Pat. Nos. 3,046,127 and 2,951,758, US Pat. No. 3,549,367 Triarylimidazole dimer / p-aminophenyl ketone combination disclosed in Japanese Patent No. 51-48516 Compound / trihalomethyl-s-triazine compound and the like.

  The amount of the photopolymerization initiator used is preferably 0.01% by mass to 50% by mass, more preferably 1% by mass to 30% by mass, and more preferably 1% by mass to 20% by mass with respect to the solid content of the crosslinkable monomer. % Range is particularly preferred. When the usage-amount of a photoinitiator exists in the range of 0.01 mass%-50 mass%, it can prevent that molecular weight becomes low too much and film | membrane intensity | strength becomes weak.

(solvent)
The solvent used in the present embodiment is basically not particularly limited as long as the solubility and applicability of the composition are satisfied. In particular, the solvent should be selected in consideration of the solubility, applicability, and safety of the dye and binder resin. Is preferred.
Suitable solvents include esters such as ethyl acetate, n-butyl acetate, isobutyl acetate, amyl formate, isoamyl acetate, isobutyl acetate, butyl propionate, isopropyl butyrate, ethyl butyrate, butyl butyrate, alkyl esters, methyl lactate , Ethyl lactate, methyl oxyacetate, ethyl oxyacetate, butyl oxyacetate, methyl methoxyacetate, ethyl methoxyacetate, butyl methoxyacetate, methyl ethoxyacetate, ethyl ethoxyacetate, methyl 3-oxypropionate, ethyl 3-oxypropionate, etc. Of 3-oxypropionic acid alkyl esters (for example, methyl 3-methoxypropionate, ethyl 3-methoxypropionate, methyl 3-ethoxypropionate, ethyl 3-ethoxypropionate);

2-oxypropionic acid alkyl esters such as methyl 2-oxypropionate, ethyl 2-oxypropionate, propyl 2-oxypropionate (for example, methyl 2-methoxypropionate, ethyl 2-methoxypropionate, 2-methoxy Propyl propionate, methyl 2-ethoxypropionate, ethyl 2-ethoxypropionate, methyl 2-oxy-2-methylpropionate, ethyl 2-oxy-2-methylpropionate, methyl 2-methoxy-2-methylpropionate Ethyl 2-ethoxy-2-methylpropionate); methyl pyruvate, ethyl pyruvate, propyl pyruvate, methyl acetoacetate, ethyl acetoacetate, methyl 2-oxobutanoate, ethyl 2-oxobutanoate, etc .;

Ethers such as diethylene glycol dimethyl ether, tetrahydrofuran, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, methyl cellosolve acetate, ethyl cellosolve acetate, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, propylene glycol methyl ether, propylene glycol methyl ether Acetates, propylene glycol ethyl ether acetate, propylene glycol propyl ether acetate and the like; ketones such as methyl ethyl ketone, cyclohexanone, 2-heptanone and 3-heptanone; aromatic hydrocarbons such as toluene and xylene are preferred.

  Among these, the solvent used in this embodiment includes methyl 3-ethoxypropionate, ethyl 3-ethoxypropionate, ethyl cellosolve acetate, ethyl lactate, diethylene glycol dimethyl ether, butyl acetate, methyl 3-methoxypropionate, 2- More preferred are heptanone, cyclohexanone, ethyl carbitol acetate, butyl carbitol acetate, propylene glycol methyl ether, propylene glycol methyl ether acetate and the like.

In the coloring composition for color filter of the present embodiment, various additives, for example, fillers, polymer compounds other than the above, surfactants, adhesion promoters, antioxidants, ultraviolet absorbers, anti-agglomeration as required. An agent or the like can be added.
Specific examples of these additives include fillers such as glass and alumina; polymer compounds other than binder resins such as polyvinyl alcohol, polyacrylic acid, polyethylene glycol monoalkyl ether, and polyfluoroalkyl acrylate; nonionic, cationic And anionic surfactants: vinyltrimethoxysilane, vinyltriethoxysilane, vinyltris (2-methoxyethoxy) silane, N- (2-aminoethyl) -3-aminopropylmethyldimethoxysilane, N- (2 -Aminoethyl) -3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 2- (3,4-epoxycyclohexyl) ) Ethyltrimetoki Adhesion promoters such as silane, 3-chloropropylmethyldimethoxysilane, 3-chloropropyltrimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane; 2,2-thiobis (4-methyl- 6-t-butylphenol), 2,6-di-t-butylphenol and other antioxidants: 2- (3-t-butyl-5-methyl-2-hydroxyphenyl) -5-chlorobenzotriazole, alkoxybenzophenone, etc. And an anti-aggregation agent such as sodium polyacrylate.

  Further, in the case where the alkali solubility of the region to be developed and removed is promoted and the developability is further improved, the coloring composition for color filter of the present embodiment has an organic carboxylic acid, preferably having a molecular weight of 1000 or less. Addition of a low molecular weight organic carboxylic acid can be performed. Specifically, aliphatic monocarboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid, valeric acid, pivalic acid, caproic acid, diethyl acetic acid, enanthic acid, caprylic acid; oxalic acid, malonic acid, succinic acid, glutar Aliphatic dicarboxylic acids such as acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, brassic acid, methylmalonic acid, ethylmalonic acid, dimethylmalonic acid, methylsuccinic acid, tetramethylsuccinic acid, citraconic acid; Aliphatic tricarboxylic acids such as carbaryl acid, aconitic acid, and camphoronic acid; aromatic monocarboxylic acids such as benzoic acid, toluic acid, cumic acid, hemelitic acid, and mesitylene acid; phthalic acid, isophthalic acid, terephthalic acid, trimellitic acid, trimesin Aromatic polycarboxylic acids such as acid, merophanic acid, pyromellitic acid; phenylacetic acid, Doroatoropa acid, hydrocinnamic acid, mandelic acid, phenyl succinic acid, atropic acid, cinnamic acid, methyl cinnamate, benzyl cinnamate, cinnamylidene acetic acid, coumaric acid, other carboxylic acids such as umbellic acid.

<Color filters and display devices>
The color filter of the present embodiment includes at least a colored layer on a substrate, and the colored layer is formed using the colored composition for a color filter of the present embodiment.
In the color filter of this embodiment, the colored composition for a color filter is applied onto a substrate by a coating method such as spin coating, casting coating, roll coating, and the like to form a colored layer, which is exposed through a predetermined mask pattern. And it can manufacture by forming a negative or positive colored pattern by developing with a developing solution. The color filter manufacturing method may include a step of curing the resist pattern by heating and / or exposure, if necessary.
As the radiation used at this time, ultraviolet rays such as g-line, h-line and i-line are particularly preferably used.

Examples of the substrate include soda glass, Pyrex (registered trademark) glass, and quartz glass used for liquid crystal display elements, and those obtained by attaching a transparent conductive film to these, and photoelectric conversion element substrates used for imaging elements, for example, A silicon substrate, a complementary metal oxide semiconductor (CMOS), etc. are mentioned. These substrates may be formed with black stripes that optically isolate each pixel.
If necessary, an undercoat layer may be provided on these substrates in order to improve adhesion with the upper layer, prevent diffusion of substances, or planarize the substrate surface.

As the developer used in the production of the color filter of the present embodiment, any developer can be used as long as it dissolves the color filter coloring composition of the present embodiment and does not dissolve the radiation irradiated portion. . Specifically, a combination of various organic solvents or an alkaline aqueous solution can be used.
As said organic solvent, the above-mentioned solvent used when preparing the composition of this embodiment is mentioned.

  Examples of the alkaline aqueous solution include sodium hydroxide, potassium hydroxide, sodium carbonate, sodium oxalate, sodium metasuccinate, aqueous ammonia, ethylamine, diethylamine, dimethylethanolamine, tetramethylammonium hydroxide, tetraethylammonium hydroxide, Concentration of an alkaline compound such as choline, pyrrole, piperidine, 1,8-diazabicyclo- [5.4.0] -7-undecene is 0.001 to 10% by mass, preferably 0.01 to 1% by mass. An alkaline aqueous solution dissolved in this manner is used. When a developer composed of such an alkaline aqueous solution is used, it is generally washed with water after development.

The color filter of the present embodiment can be used for a solid-state imaging device such as an organic or inorganic EL element, a liquid crystal display element, or a CCD, and the display device of the present embodiment includes this color filter.
For example, when the obtained color filter (display side substrate) and the TFT array substrate (liquid crystal drive side substrate) are opposed to each other, and the inner peripheral side peripheral portions of both the substrates are bonded with a sealant, the both substrates have a cell gap of a predetermined distance. It is pasted together while holding it. An active matrix color liquid crystal display device belonging to a liquid crystal panel can be obtained by filling the liquid crystal in the gap between the substrates and sealing the liquid crystal. In the case of an organic EL element, for example, it can be used by being laminated on a light emitting layer.

  Hereinafter, the present invention will be described more specifically with reference to examples and comparative examples, but the present invention is not limited to these examples.

Example 1
(Synthesis of (oxazolidinonesulfonyl) (trifluoromethanesulfonylimidic acid) triethylamine salt)
Chlorosulfonyl isocyanate 8.00 g (56.5 mmol) manufactured by Tokyo Chemical Industry Co., Ltd. was dissolved in methylene chloride and cooled to 5 ° C. or lower. To this, 7.42 g (59.4 mmol) of 2-bromoethanol manufactured by Tokyo Chemical Industry Co., Ltd. was added dropwise at 5 ° C. or less, and stirred at 10 ° C. or less for 1 hour after completion of the addition. The product thus prepared is hereinafter referred to as “reaction solution A”.
Next, 8.43 g (56.5 mmol) of trifluoromethanesulfonamide manufactured by Tokyo Chemical Industry Co., Ltd. was dissolved in 20 mL of methylene chloride, and the internal temperature was cooled to 5 ° C. or lower. 14.30 g (141.4 mmol) of Wako Pure Chemical Industries, Ltd. (triethylamine) was added dropwise so that the internal temperature did not exceed 10 ° C. After completion of the addition, (Prepared Reaction Solution A) was added dropwise at 10 ° C. or less. . Then, it stirred at 10 degrees C or less for 1 hour, and then stirred at room temperature for 10 hours.
The reaction solution was extracted by adding 100 mL of water. The separated organic layer was washed with water, dehydrated with magnesium sulfate, and then the organic layer was concentrated under reduced pressure with an evaporator. (Yield 47%) was obtained.
About the following structural formula (5), it confirmed that it was the target compound from the following analysis result.
MS (ESI) (m / z): 102 (+), 297 (-)
Elemental analysis values: CHN measured values (30.22%, 4.94%, 10.38%); theoretical values (30.07%, 5.05%, 10.52%)

(Synthesis of dyes)
5 g (9.73 mmol) of Basic Blue 7 (CI-42595) manufactured by Tokyo Chemical Industry Co., Ltd. represented by the following structural formula (4) is dissolved in 30 mL of methanol, and is represented by the following structural formula (5) (oxazolidinonesulfonyl) While stirring (trifluoromethanesulfonylimidic acid) triethylamine salt, 3.88 g (9.73 mmol) was added, and the mixture was further stirred at room temperature for 1 hour. Methanol in the solution was concentrated with an evaporator, 100 mL of water was added, and the precipitate was collected by filtration and washed with water. The cake was dried under reduced pressure to obtain 6.72 g (yield 89%) of dye A represented by the exemplified compound (1).

About the said dye A, it confirmed that it was the target compound from the following analysis result.
MS (ESI) (m / z): 478 (+), 297 (-)
Elemental analysis values: CHN measured values (57.48%, 5.88%, 8.83%); theoretical values (57.27%, 5.72%, 9.03%)

(Preparation of coloring composition for color filter)
First, a photosensitive transparent resin composition having the following composition was prepared.
PGMEA solution of acrylic acid resin (active ingredient 42% by mass, resin (benzyl methacrylate / methacrylic acid = 62/38 (mass ratio)), acid value: 70 mgKOH / g, weight average molecular weight: 9000, PGMEA = propylene glycol monomethyl ether Acetate): 18 parts by mass. Multifunctional acrylate monomer (SR399E, Sakai Chemical): 8 parts by mass. Photopolymerization initiator (2-methyl-1 [4- (methylthio) phenyl] -2-morpholinopropane-1- On (trade name: Irgacure 907, manufactured by Ciba Specialty Chemicals): 2 parts by mass / photosensitizer (4,4′-dimethylaminobenzophenone): 0.2 parts by mass

Next, the following components were mixed and stirred to prepare a colored resin composition (colored composition for color filter) having a non-volatile component of 30% by mass.
-PGMEA solution of 10% by weight of dye A: 10 parts by mass-Photosensitive transparent resin composition: 20 parts by mass-Fluorine-based additive (Megafac R-08MH (manufactured by DIC Corporation)): 0.02 parts by mass・ PGMEA: 2 parts by mass

(Evaluation)
Using the above colored resin composition as a coating liquid, this is applied onto a glass substrate by spin coating, dried at 80 ° C., and exposed to 100 mJ / m ^{2 of} ultraviolet light with a high-pressure mercury lamp from the coating film side and cured. A coating film for evaluation was prepared. Using this coating film, exposure sensitivity, light resistance and heat resistance were evaluated by the following methods. The evaluation results are shown in Table 1.

-Exposure sensitivity-
The entire surface of the coating film on the produced glass substrate was exposed with a high-pressure mercury lamp, and the irradiation amount was changed. When the finger is brought into contact with the surface of the coating film, the fingerprint is not attached, and it is cured by applying a scratch of about 1 cm with a spatula, and it is confirmed by visual observation and resistance when the scratch occurs. The exposure amount was determined and used as the exposure sensitivity. In the case of poor curing, there was no resistance at the time of scratching with a spatula, and resistance was felt if curing had progressed sufficiently, and the difference could be discriminated when scratching 1 cm.

-Development solubility-
In the same manner as in the heat resistance evaluation, the coating film on the produced glass substrate was shower-developed with an alkaline developer (0.05 mass% potassium hydroxide aqueous solution) for 60 seconds, and further washed with ultrapure water for 60 seconds. Thus, it was visually determined whether or not the coating film was completely dissolved, and the development solubility was evaluated according to the following criteria. The film thickness was measured with a stylus type surface shape measuring instrument Dektak 150 manufactured by ULVAC, Inc. before and after development.
<Development solubility evaluation criteria>
(Circle): The film thickness after image development was 60% or less compared with the film thickness before image development.
X: The film thickness after development was 70% or more compared to the film thickness before development.

-Heat resistance-
The glass substrate on which the coating film has been prepared is placed on a hot plate so that the substrate surface is in contact with the glass substrate, and is allowed to stand under the following three conditions (Left + exposure), before and after being left with the transmittance peak value. The chromaticity change in the coating film, that is, the ΔEab value, was measured using a microspectroscope OSP-SP200 manufactured by Olympus Corporation. The higher the transmittance and the smaller the ΔEab value, the better the heat resistance.
Condition (a): After standing at 80 ° C. for 3 minutes, exposure was performed with a high-pressure mercury lamp at 100 mJ / m ² .
Condition (b): left at 170 ° C. for 30 minutes.
Condition (c): left at 230 ° C. for 30 minutes.

-Light resistance-
A sample of the light resistance test was prepared by laminating a glass substrate coated with an adhesive to a coating film on a glass substrate produced in the same manner as in the heat resistance evaluation. Using a xenon lamp (Cirrus weather meter manufactured by Atlas Co., CIRA as the inner filter, and soda lime as the outer filter: cut at a wavelength of 300 nm or less) for this sample, the illuminance at a wavelength of 420 nm is 1.2 mW / m ² After irradiation for 70 hours (equivalent to 300 kJ / m ² ), the transmittance and ΔEab value were measured in the same manner as in the heat resistance evaluation.

Comparative Example 1
In the preparation of the coloring composition for the color filter in Example 1, instead of Dye A, Basic Blue 7 (CI-42595, the structural formula (4)) manufactured by Tokyo Chemical Industry Co., Ltd. was used. In the same manner as in Example 1, a colored composition for a color filter was produced. Evaluation similar to Example 1 was performed using this. The evaluation results are shown in Table 1.

Comparative Example 2
In Example 1, evaluation was performed in the same manner as in Example 1 except that the compound represented by the following structural formula (6) was used instead of Dye A. The compound represented by the following structural formula (6) was the same as in Example 1 except that equimolar amounts of p-toluenesulfonic acid were used in place of potassium perfluorooctylsulfonate in the synthesis of the dye in Example 1. And synthesized. The evaluation results are shown in Table 1.

Comparative Example 3
In Example 1, evaluation was performed in the same manner as in Example 1 except that the compound represented by the following structural formula (7) was used instead of the dye A. The compound represented by the following structural formula (7) was the same as in Example 1 except that, in the synthesis of the dye in Example 1, equimolar amount of bistrifluoromethanesulfonylimide was used instead of potassium perfluorooctylsulfonate. And synthesized.

Comparative Example 4
In Example 1, evaluation was performed in the same manner as in Example 1 except that the compound represented by the following structural formula (8) was used instead of Dye A. The compound represented by the following structural formula (8) was the same as in Example 1 except that, in the synthesis of the dye in Example 1, equimolar amount of 2-naphthalenesulfonic acid was used instead of sodium perfluorooctylsulfonate. And synthesized.

  As shown in the results of Table 1, in the coloring composition for a color filter using a triarylmethane dye having an oxazolidinone sulfonylimide acid ion as a counter anion of Examples, not only is excellent in heat resistance and light resistance, Not only the exposure sensitivity in blending with the photosensitive resin was good, but also the development solubility in an alkaline aqueous solution was good. On the other hand, in the comparative example using a triarylmethane dye different from the present invention, although heat resistance and exposure sensitivity are satisfactory to some extent, it is not suitable for patterning by mask exposure-development because of poor development solubility in an alkaline aqueous solution. I know that there is.

When a colored layer is formed using the colored composition for a color filter of the present invention, a color filter having high heat resistance and light resistance and high adhesion of the colored layer to the substrate can be obtained.
For this reason, the color filter of this invention is suitable for color filters, such as an organic or inorganic EL element, a liquid crystal display element, and CCD.

Claims (7)

A coloring composition for a color filter comprising a binder resin, a crosslinkable monomer, a photopolymerization initiator, a colorant and a solvent, wherein the colorant is a triarylmethane dye represented by the following general formula (I).

(In the formula, R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ may each independently have a hydrogen atom, an alkyl group which may have a substituent, or a substituent. Any one of aryl groups, and at least one of R ¹ and R ² , R ³ and R ⁴ , and R ⁵ and R ⁶ may be bonded to form a part of a ring structure or a heterocyclic structure; X in the formula represents a heterocycle having a nitrogen atom and a carbonyl group in the skeleton, which may have a substituent, and Y represents that at least a part of hydrogen atoms may be substituted with fluorine atoms. An alkyl group.) The triarylmethane dye according to claim 1, wherein X in the general formula (I) is a heterocyclic ring represented by the following general formula (II).

  The coloring composition for a color filter according to claim 1 or 2, wherein Y in the general formula (I) is a perfluoroalkyl group. R ⁵ in the general formula (I) is a hydrogen atom, and R ¹ , R ² , R ³ , R ⁴ , and R ⁶ are each independently an alkyl group having 1 to 20 carbon atoms. The coloring composition for color filters in any one. The coloring composition for a color filter according to claim ⁴ , wherein R ¹ , R ² , R ³ , R ⁴ , and R ⁶ are all the same.   A color filter comprising at least a colored layer on a substrate, wherein the colored layer is formed using the colored composition for a color filter according to any one of claims 1 to 5.   A display device comprising the color filter according to claim 6.