WO2023176882A1 - 着色樹脂組成物、硬化物、カラーフィルタ及び画像表示装置 - Google Patents

着色樹脂組成物、硬化物、カラーフィルタ及び画像表示装置 Download PDF

Info

Publication number
WO2023176882A1
WO2023176882A1 PCT/JP2023/010072 JP2023010072W WO2023176882A1 WO 2023176882 A1 WO2023176882 A1 WO 2023176882A1 JP 2023010072 W JP2023010072 W JP 2023010072W WO 2023176882 A1 WO2023176882 A1 WO 2023176882A1
Authority
WO
WIPO (PCT)
Prior art keywords
group
mass
resin composition
colored resin
formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2023/010072
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
紫陽 平岡
宏明 石井
幸治 福岡
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Chemical Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Chemical Corp filed Critical Mitsubishi Chemical Corp
Priority to KR1020247029184A priority Critical patent/KR20240163067A/ko
Priority to JP2024508220A priority patent/JPWO2023176882A1/ja
Priority to CN202380026537.2A priority patent/CN118843831A/zh
Publication of WO2023176882A1 publication Critical patent/WO2023176882A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00—Processes of polymerisation
    • C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00—Processes of polymerisation
    • C08F2/46—Polymerisation initiated by wave energy or particle radiation
    • C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
    • C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00—Other synthetic dyes of known constitution
    • C09B57/10—Metal complexes of organic compounds not being dyes in uncomplexed form
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/60—Additives non-macromolecular
    • C09D7/63—Additives non-macromolecular organic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/65—Additives macromolecular
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/20—Filters
    • G—PHYSICS
    • G02—OPTICS
    • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333—Constructional arrangements; Manufacturing methods
    • G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G02F1/133509—Filters, e.g. light shielding masks
    • G02F1/133514—Colour filters
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
    • G03F7/0007—Filters, e.g. additive colour filters; Components for display devices
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
    • G03F7/105—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having substances, e.g. indicators, for forming visible images
    • G—PHYSICS
    • G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
    • G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
    • G09F9/00—Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements
    • G09F9/30—Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements

Definitions

  • the present invention relates to a colored resin composition, a cured product, a color filter, and an image display device.
  • This application claims priority based on Japanese Patent Application No. 2022-040964 filed in Japan on March 16, 2022, the contents of which are incorporated herein.
  • pigment dispersion methods dyeing methods, electrodeposition methods, and printing methods are known as methods for manufacturing color filters used in liquid crystal display devices and the like.
  • the pigment dispersion method which has excellent properties on average in terms of spectral properties, durability, pattern shape, accuracy, etc., is most widely adopted.
  • color filters are required to have higher brightness, higher contrast, and a wider color gamut.
  • Pigments are generally used as coloring materials to determine the color of color filters from the viewpoint of heat resistance, light resistance, etc.
  • pigments are no longer able to meet market demands, especially for high brightness, and color
  • the use of dyes instead of pigments as materials is being actively investigated. For example, studies have been made to use phthalocyanine dyes for green pixel applications (see, for example, Patent Document 1).
  • the present inventors conducted a study and found that in the colored resin composition described in Patent Document 1, the solubility in the developer greatly changes depending on the content ratio of the phthalocyanine dye in the colorant, and the phthalocyanine dye It has been found that when the content ratio of the dye is low, the rate of dissolution into the developer becomes slow. It has also been found that this tendency is particularly pronounced when the pre-bake temperature is relatively low. Furthermore, in the colored resin composition described in Patent Document 1, depending on the content ratio of the phthalocyanine dye in the colorant, there is a possibility that a residue may be generated after development, and the contrast of the obtained green pixels may be reduced. It was also found that there is a risk of the product being inferior.
  • an object of the present invention is to provide a colored resin composition that has a high dissolution rate in a developer and has high production efficiency even when the prebaking temperature is relatively low.
  • Another object of the present invention is to provide a colored resin composition in which the generation of residue is suppressed and the resulting green pixels have excellent contrast.
  • the present inventors have found that the above problem can be solved by setting the content ratio of a specific phthalocyanine compound in the colorant to a specific ratio or more, and have arrived at the present invention. That is, the present invention has the following configuration.
  • a colored resin composition containing (A) a colorant, (B) a solvent, (C) an alkali-soluble resin, (D) a photopolymerization initiator, and (E) a photopolymerizable monomer,
  • the colorant (A) contains a phthalocyanine compound having a chemical structure represented by the following general formula (1) and a yellow colorant,
  • a colored resin composition wherein the content of the phthalocyanine compound in the colorant (A) is 65% by mass or more and 90% by mass or less.
  • a 1 to A 16 each independently represent a hydrogen atom, a halogen atom, or a group represented by the following general formula (2). However, one or more of A 1 to A 16 represents a fluorine atom, and one or more of A 1 to A 16 represents a group represented by the following general formula (2).
  • X represents a divalent linking group.
  • the benzene ring in formula (2) may have any substituent. * represents a bond.
  • [2] The colored resin composition of [1], wherein the content of the phthalocyanine compound in the colorant (A) is 70% by mass or more and 90% by mass or less.
  • [3] The colored resin composition of [1] or [2], wherein the halogen atoms in A 1 to A 16 in formula (1) are fluorine atoms.
  • one or more of A 1 to A 4 is a fluorine atom
  • one or more of A 5 to A 8 is a fluorine atom
  • one of A 9 to A 12 is a fluorine atom.
  • one or more of A 1 to A 4 is a group represented by the formula (2)
  • one or more of A 5 to A 8 is a group represented by the formula (2).
  • the yellow coloring material is C.I. I. Pigment Yellow 138, C. I.
  • a color filter comprising pixels made using the colored resin composition according to any one of [1] to [10].
  • the present invention it is possible to provide a colored resin composition that has a high dissolution rate in a developer and has high production efficiency even when the pre-bake temperature is relatively low. Further, according to the present invention, it is possible to provide a colored resin composition in which the generation of residue is suppressed and the resulting green pixels have excellent contrast.
  • FIG. 1 is a schematic cross-sectional view showing an example of an organic EL element having a color filter according to the present invention.
  • the term "weight average molecular weight” refers to the weight average molecular weight (Mw) in terms of polystyrene measured by GPC (gel permeation chromatography).
  • total solid content shall mean all components other than the solvent in the colored resin composition. Even if components other than the solvent are liquid at room temperature, they are not included in the solvent but included in the total solid content.
  • the "amine value” refers to the amine value in terms of effective solid content unless otherwise specified, and is a value expressed by the amount of base and the mass of KOH equivalent to 1 g of solid content of the dispersant.
  • C.I means color index.
  • the colored resin composition of the present invention comprises (A) a colorant, (B) a solvent, (C) an alkali-soluble resin, (D) a photoinitiator, and (E) a photopolymerizable monomer. Contains. Furthermore, if necessary, other additives other than the above-mentioned components may be blended.
  • (A) Colorant The (A) colorant contained in the colored resin composition of the present invention is a phthalocyanine compound (hereinafter referred to as "phthalocyanine compound") having a chemical structure represented by the following general formula (1). 1)) and yellow colorants.
  • phthalocyanine compound a phthalocyanine compound having a chemical structure represented by the following general formula (1).
  • the content of the phthalocyanine compound (1) in the colorant is 65% by mass or more and 90% by mass or less.
  • a 1 to A 16 each independently represent a hydrogen atom, a halogen atom, or a group represented by the following general formula (2). However, one or more of A 1 to A 16 represents a fluorine atom, and one or more of A 1 to A 16 represents a group represented by the following general formula (2).
  • X represents a divalent linking group.
  • the benzene ring in formula (2) may have any substituent.
  • * represents a bond.
  • the colorant (A) contained in the colored resin composition of the present invention contains a phthalocyanine compound (1), and the content of the phthalocyanine compound (1) in the colorant (A) is 65% by mass or more and 90% by mass or less.
  • Phthalocyanine compound (1) has one or more hydrogen atoms constituting the phthalocyanine skeleton substituted with a fluorine atom with a small atomic radius, and has a structure that does not easily inhibit association between phthalocyanine compounds (1).
  • the alkali-soluble resin (C) contained in the colored resin composition of the present invention is wrapped around the aggregate to form a complex, and the phthalocyanine It is thought that the dissolution rate is faster than when compound (1) is used alone. At this time, if the prebaking temperature is low, association between the phthalocyanine compounds (1) is difficult to occur.
  • the content of the phthalocyanine compound (1) is 65% by mass or more, the association between the phthalocyanine compounds (1) is less likely to be inhibited by other colorants, and even when the pre-bake temperature is low, the phthalocyanine compound (1) )
  • the phthalocyanine compound (1) As the formation of regular aggregates progresses, local aggregation becomes less likely to occur, improving transmittance and contrast, and as the molecular weight increases as aggregates, alkali-soluble resin is formed around them. It is thought that this makes it easier for the particles to wrap around each other, increasing the dissolution rate and suppressing the generation of residue during development.
  • a 1 to A 16 each independently represent a hydrogen atom, a halogen atom, or a group represented by the following general formula (2). However, one or more of A 1 to A 16 represents a fluorine atom, and one or more of A 1 to A 16 represents a group represented by the following general formula (2).
  • X represents a divalent linking group.
  • the benzene ring in formula (2) may have any substituent.
  • * represents a bond.
  • Examples of the halogen atom in A 1 to A 16 include a fluorine atom, a chlorine atom, and a bromine atom. Fluorine atoms are preferred from the viewpoint of high brightness. Further, it is preferable that one or more of A 1 to A 16 is a fluorine atom, more preferably 6 or more fluorine atoms, further preferably 7 or more, particularly preferably 8 or more, and fluorine atoms is 15 or less, preferably 12 or less, and more preferably 10 or less. Setting the value above the lower limit tends to improve the stability of the phthalocyanine compound (1), and setting the value below the upper limit improves the affinity with the dispersant and solvent in the colored resin composition. Tend. The above upper and lower limits can be arbitrarily combined. For example, the number of substituents representing fluorine atoms among A 1 to A 16 is 1 to 15, preferably 6 to 12, more preferably 7 to 12, and even more preferably 8 to 10.
  • X in formula (2) represents a divalent linking group.
  • the divalent linking group is not particularly limited, but includes, for example, an oxygen atom, a sulfur atom, a -N(R a1 )- group (R a1 represents a hydrogen atom or an aliphatic hydrocarbon group having 1 to 6 carbon atoms). ). From the viewpoint of stability during firing, an oxygen atom or a sulfur atom is preferred, and an oxygen atom is more preferred.
  • the benzene ring in formula (2) may have any substituent.
  • Substituents are not particularly limited, but include, for example, a halogen atom, an alkyl group (-R A group), an alkoxy group (-OR A group (however, R A represents an alkyl group)), an alkoxycarbonyl group (-COOR A group (however, R A represents an alkyl group)), aryl group (-R B group), aryloxy group (-OR B group (however, R B represents an aryl group)), aryloxycarbonyl group (-COOR B group (wherein R B represents an aryl group)). From the viewpoint of development solubility and brightness, an alkoxycarbonyl group is preferred.
  • the alkyl group (R A ) contained in these groups may be linear, branched, or cyclic, but is preferably a linear alkyl group from the viewpoint of affinity with organic solvents.
  • the number of carbon atoms in the alkyl group (R A ) is not particularly limited, but is preferably 1 or more, more preferably 2 or more, and preferably 6 or less, more preferably 5 or less, and even more preferably 4 or less. Setting the amount above the lower limit tends to suppress aggregation and suppressing foreign substances, and setting it below the upper limit tends to improve solvent affinity and stability over time. The above upper and lower limits can be arbitrarily combined.
  • the alkyl group preferably has 1 to 6 carbon atoms, more preferably 1 to 5 carbon atoms, and even more preferably 2 to 4 carbon atoms.
  • the alkyl group (R A ) include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, and a hexyl group. From the viewpoint of inhibiting aggregation, a methyl group or an ethyl group is preferable, and an ethyl group is more preferable. preferable.
  • the aryl group (R B ) contained in these groups may be an aromatic hydrocarbon ring group or an aromatic heterocyclic group.
  • the number of carbon atoms in the aryl group (R B ) is not particularly limited, but is preferably 4 or more, more preferably 6 or more, preferably 12 or less, more preferably 10 or less, and even more preferably 8 or less. Setting the amount above the lower limit tends to suppress aggregation due to steric repulsion, and setting the amount below the upper limit tends to improve solvent affinity and stability over time.
  • the above upper and lower limits can be arbitrarily combined; for example, the number of carbon atoms in the aryl group is preferably 4 to 12, more preferably 4 to 10, and even more preferably 6 to 8.
  • the aromatic hydrocarbon ring in the aromatic hydrocarbon ring group may be a single ring or a condensed ring.
  • Examples of the aromatic hydrocarbon ring group include a benzene ring, a naphthalene ring, a pentalene ring, an indene ring, an azulene ring, and a heptalene ring, each having one free valence.
  • the aromatic heterocycle in the aromatic heterocyclic group may be a single ring or a condensed ring.
  • aromatic heterocyclic groups include furan rings, thiophene rings, pyrrole rings, 2H-pyran rings, 4H-thiopyran rings, pyridine rings, 1,3-oxazole rings, and isoxazole rings, each having one free valence.
  • the number of substituents is not particularly limited, but the dye molecules stack with each other, improving heat resistance and suppressing a decrease in brightness due to decomposition of the dye. In view of this, it is preferable that the number of substitutions per benzene ring is 1.
  • the substitution position may be o-position, m-position, or p-position, but stacking in a close-packed structure is possible. From this point of view, p-position is preferred.
  • One or more of A 1 to A 16 represents a fluorine atom.
  • one or more of A 1 to A 4 is a fluorine atom
  • one or more of A 5 to A 8 is a fluorine atom.
  • one or more of A 9 to A 12 is a fluorine atom
  • one or more of A 13 to A 16 is a fluorine atom
  • two or more of A 1 to A 4 are is a fluorine atom
  • two or more of A 5 to A 8 are fluorine atoms
  • two or more of A 9 to A 12 are fluorine atoms
  • two or more of A 13 to A 16 are fluorine atoms. More preferably, it is a fluorine atom.
  • one or more of A 1 to A 16 represents a group represented by formula (2).
  • one or more of A 1 to A 4 is a group represented by formula (2)
  • one or more of A 5 to A 8 is a group represented by formula (2).
  • a group represented by formula (2), one or more of A 9 to A 12 is a group represented by formula (2), and one or more of A 13 to A 16 is a group represented by formula (2).
  • Two or more of A 1 to A 4 are preferably groups represented by formula (2), and two or more of A 5 to A 8 are preferably groups represented by formula (2).
  • a group in which two or more of A 9 to A 12 are groups represented by formula (2), and two or more of A 13 to A 16 are groups represented by formula (2).
  • a 2 , A 3 , A 6 , A 7 , A 10 , A 11 , A 14 , and A 15 are groups represented by formula (2). and A 1 , A 4 , A 5 , A 8 , A 9 , A 12 , A 13 , and A 16 are preferably halogen atoms; A 2 , A 3 , A 6 , A 7 , A 10 , A 11 , A 14 , and A 15 are groups represented by formula (2), and A 1 , A 4 , A 5 , A 8 , A 9 , A 12 , A 13 , and A It is particularly preferred that 16 is a fluorine atom.
  • Examples of the phthalocyanine compound (1) include the following compounds.
  • Et represents an ethyl group.
  • a known method can be adopted, for example, the method described in Japanese Patent Application Laid-Open No. 05-345861 can be adopted.
  • the content of the phthalocyanine compound (1) in the colorant (A) in the colored resin composition of the present invention is 65% by mass or more, preferably 70% by mass or more in the total solid content of the colorant (A), and , 90% by mass or less, preferably 85% by mass or less, more preferably 80% by mass or less.
  • the temperature is equal to or higher than the lower limit, the dissolution rate tends to be faster even when the pre-bake temperature is low, and the adhesion to the substrate tends to be better. Furthermore, contrast tends to be high and residues tend to be suppressed. Furthermore, by setting the chromaticity below the upper limit value, there is a tendency that the chromaticity required for a color filter can be ensured.
  • the content of the phthalocyanine compound (1) in the (A) colorant in the colored resin composition is 65 to 90% by mass, preferably 70 to 90% by mass, based on the total solid content of the (A) colorant. , more preferably 70 to 85% by mass, and even more preferably 70 to 80% by mass.
  • Coloring agent contains a yellow coloring material in addition to the phthalocyanine compound (1).
  • the colorant contains a yellow coloring material in addition to the phthalocyanine compound (1), there is a tendency that the color reproducibility required for green pixels can be achieved.
  • the yellow coloring material include yellow pigments and yellow dyes.
  • yellow pigments examples include C.I. I. Pigment Yellow 1, 1:1, 2, 3, 4, 5, 6, 9, 10, 12, 13, 14, 16, 17, 20, 24, 31, 32, 34, 35, 35: 1, 36, 36:1, 37, 37:1, 40, 41, 42, 43, 48, 53, 55, 61, 62, 62:1, 63, 65, 73, 74, 75, 81, 83, 86, 87, 93, 94, 95, 97, 100, 101, 104, 105, 108, 109, 110, 111, 116, 117, 119, 120, 125, 126, 127, 127:1, 128, 129, 133, 134, 136, 137, 138, 139, 142, 147, 148, 150, 151, 153, 154, 155, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 172, 173, 174, 175, 176, 180
  • C. From the viewpoint of high brightness and high color gamut, C. I. Pigment Yellow 83, 117, 129, 138, 139, 154, 155, 180, 185, nickel azo complexes represented by formula (i) are preferred; I. Pigment Yellow 83, 138, 139, 180, 185 and the nickel azo complex represented by formula (i) are more preferred.
  • Examples of the yellow dye include barbituric acid azo dyes, pyridone azo dyes, pyrazolone azo dyes, quinophthalone dyes, and cyanine dyes. Specific examples thereof include specific compounds described in Japanese Patent Application Publication No. 2010-168531.
  • Examples of solvent dyes include C.I. I.
  • Examples include Solvent Yellow 4, 14, 15, 23, 24, 38, 62, 63, 68, 79, 82, 94, 98, 99, 162, and 163.
  • Examples of acid dyes include C.I. I. Acid Green 1, 3, 5, 9, 16, 25, 27, 50, 58, 63, 65, 80, 104, 105, 106, 109, C.
  • a direct dye for example, C.I. I. Direct Yellow 2, 33, 34, 35, 38, 39, 43, 47, 50, 54, 58, 68, 69, 70, 71, 86, 93, 94, 95, 98, 102, 108, 109, 129 , 136, 138, and 141 dyes.
  • a mordant dye for example, C.I. I. Examples include Mordant Yellow 5, 8, 10, 16, 20, 26, 30, 31, 33, 42, 43, 45, 56, 61, 62, 65 dyes.
  • the colorant (A) may contain other colorants in addition to the phthalocyanine compound (1) and the yellow colorant.
  • Other colorants include pigments and dyes.
  • a green coloring material such as a green pigment or a green dye, for example.
  • green pigments include C.I. I. Pigment Green 7, 36, 58, 59, 62, and 63, and C. I. Pigment Green 58 is preferred.
  • solvent dyes include C.I. I. Examples include Solvent Green 1, 3, 4, 5, 7, 28, 29, 32, 33, 34, and 35.
  • acid dyes include C.I. I.
  • Examples include Mordant Green 1, 3, 4, 5, 10, 15, 19, 26, 29, 33, 34, 35, 41, 43, and 53. From the viewpoint of suppressing dye decomposition during thermal firing, C.I. I. Solvent Green 1, 3, 4, 5, 7, 28, 29, 32, 33, 34, and 35 are preferred.
  • the average primary particle diameter of the pigment is preferably 0.2 ⁇ m or less, more preferably 0.1 ⁇ m or less, particularly preferably 0.04 ⁇ m or less.
  • a solvent salt milling method is suitably used.
  • the content ratio of the colorant (A) in the colored resin composition of the present invention is not particularly limited, but is preferably 10% by mass or more, more preferably 15% by mass or more, and 20% by mass in the total solid content of the colored resin composition.
  • the above is more preferable, even more preferably 25% by mass or more, particularly preferably 30% by mass or more, and preferably 80% by mass or less, more preferably 60% by mass or less, even more preferably 50% by mass or less, and 40% by mass.
  • the following are particularly preferred. Setting the value above the lower limit value tends to make it possible to reproduce a wide range of hues, and setting the value below the upper limit value tends to ensure stability over time.
  • the above upper and lower limits can be arbitrarily combined.
  • the content of the colorant (A) in the colored resin composition is preferably 10 to 80% by mass, more preferably 15 to 80% by mass, and further preferably 20 to 60% by mass in the total solid content of the colored resin composition. It is preferably 25 to 50% by weight, even more preferably 30 to 40% by weight.
  • the content of the phthalocyanine compound (1) in the colored resin composition of the present invention is not particularly limited, but is preferably 1% by mass or more, more preferably 3% by mass or more, and 5% by mass in the total solid content of the colored resin composition.
  • the above is more preferable, even more preferably 10% by mass or more, particularly preferably 15% by mass or more, also preferably 50% by mass or less, more preferably 40% by mass or less, even more preferably 30% by mass or less, and 20% by mass.
  • the following are particularly preferred. Setting the value above the lower limit value tends to improve brightness, and setting the value below the upper limit value tends to ensure stability over time.
  • the above upper and lower limits can be arbitrarily combined.
  • the content of the phthalocyanine compound (1) in the colored resin composition is more preferably 3 to 50% by mass, even more preferably 5 to 50% by mass, and 10 to 40% by mass in the total solid content of the colored resin composition. is even more preferred, and 15 to 30% by mass is particularly preferred.
  • the yellow colorant in the total solid content of the colored resin composition of the present invention is preferably 2% by mass or more, more preferably 4% by mass or more, even more preferably 6% by mass or more, and preferably 25% by mass or less, and 20% by mass or more. It is more preferably at most 10% by mass, even more preferably at most 10% by mass. Setting the value above the lower limit value tends to reproduce the color required for green pixels, and setting the value below the upper limit value tends to increase the dissolution rate and further increase the contrast. The above upper and lower limits can be arbitrarily combined.
  • the content of the yellow colorant is preferably 2 to 25% by mass, and 4 to 20% by mass in the total solid content of the colored resin composition. is more preferable, and even more preferably 6 to 10% by mass.
  • the content ratio of the yellow coloring material in the (A) colorant is preferably 5% by mass or more, more preferably 10% by mass or more, even more preferably 15% by mass or more, and 20% by mass or more. Even more preferred. Further, it is preferably 35% by mass or less, more preferably 30% by mass or less. Setting the value above the lower limit value tends to reproduce the color required for green pixels, and setting the value below the upper limit value tends to increase the dissolution rate and further increase the contrast. The above upper and lower limits can be arbitrarily combined. For example, when the colorant (A) contains a yellow colorant, the content of the yellow colorant in the colorant (A) is preferably 5 to 35% by mass, and preferably 10 to 35% by mass. is more preferable, and even more preferably 15 to 30% by mass.
  • the mass-based content ratio of the phthalocyanine compound (1) and the yellow colorant is preferably 1.8 or more, more preferably 2 or more, and even more preferably 2.3 or more. Further, it is preferably 9 or less, more preferably 7 or less, and even more preferably 6 or less. Setting the amount above the lower limit value tends to increase the dissolution rate, and setting it below the upper limit value tends to make it possible to reproduce the color required for a green pixel. The above upper and lower limits can be arbitrarily combined.
  • the content ratio of the phthalocyanine compound (1) and the yellow colorant on a mass basis is 1.8 to 9. It is preferably from 1.8 to 7, even more preferably from 1.8 to 6, even more preferably from 2 to 6.
  • the content thereof is not particularly limited, but is preferably 1% by mass or more, more preferably 3% by mass or more in the total solid content of the colored resin composition.
  • the content is more preferably 5% by mass or more, even more preferably 7% by mass or more, particularly preferably 10% by mass or more, and preferably 30% by mass or less, more preferably 25% by mass or less, and even more preferably 20% by mass or less. Setting the value above the lower limit value tends to make it possible to reproduce a wide range of hues, and setting the value below the upper limit value tends to ensure stability over time.
  • the above upper and lower limits can be arbitrarily combined.
  • the content of the other colorants is preferably 1 to 30% by mass, more preferably 3 to 30% by mass in the total solid content of the colored resin composition. , more preferably 5 to 25% by weight, even more preferably 7 to 25% by weight, particularly preferably 10 to 20% by weight.
  • Examples of the solvent include ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, propylene glycol mono-n-butyl ether, Propylene glycol-t-butyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol mono-n-butyl ether, methoxymethylpentanol, propylene glycol monoethyl ether, dipropylene glycol monoethyl ether, dipropylene glycol monomethyl ether, 3-methyl - Glycol monoalkyl ethers such as 3-methoxybutanol, triethylene glycol monomethyl ether, triethylene glycol monoethyl ether, tripropylene glycol methyl ether;
  • Glycol dialkyl ethers such as ethylene glycol dimethyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol dipropyl ether, diethylene glycol dibutyl ether, dipropylene glycol dimethyl ether; Ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, ethylene glycol mono-n-butyl ether acetate, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, propylene glycol monopropyl ether acetate, propylene glycol monobutyl ether acetate, methoxybutyl Acetate, 3-methoxybutyl acetate, methoxypentyl acetate, diethylene glycol monomethyl ether acetate, diethylene glycol monoethyl ether acetate, diethylene glycol mono-n
  • Glycol diacetates such as ethylene glycol diacetate, 1,3-butylene glycol diacetate, 1,6-hexanol diacetate; Alkyl acetates such as cyclohexanol acetate; Ethers such as amyl ether, propyl ether, diethyl ether, dipropyl ether, diisopropyl ether, butyl ether, diamyl ether, ethyl isobutyl ether, dihexyl ether; Such as acetone, methyl ethyl ketone, methyl amyl ketone, methyl isopropyl ketone, methyl isoamyl ketone, diisopropyl ketone, diisobutyl ketone, methyl isobutyl ketone, cyclohexanone, ethyl amyl ketone, methyl butyl ketone, methyl hexyl ketone
  • Aromatic hydrocarbons such as benzene, toluene, xylene, and cumene; Amyl formate, ethyl formate, ethyl acetate, butyl acetate, propyl acetate, amyl acetate, methyl isobutyrate, ethylene glycol acetate, ethyl propionate, propyl propionate, butyl butyrate, isobutyl butyrate, methyl isobutyrate, ethyl Caprylate, butyl stearate, ethyl benzoate, methyl 3-ethoxypropionate, ethyl 3-ethoxypropionate, methyl 3-methoxypropionate, ethyl 3-methoxypropionate, propyl 3-methoxypropionate, 3-methoxypropionate linear or cyclic esters such as butyl, ⁇ -butyrolactone; Alkoxycarboxylic acids such as 3-methoxyprop
  • solvents include, for example, Mineral Spirit, Valsol #2, Apco #18 Solvent, Apco Thinner, Socal Solvent No. 1 and no. 2.
  • Solvesso #150 Shell TS28 Solvent, carbitol, ethyl carbitol, butyl carbitol, methyl cellosolve, ethyl cellosolve, ethyl cellosolve acetate, methyl cellosolve acetate, diglyme (all trade names).
  • solvents may be used alone or in combination of two or more.
  • the solvent (B) is preferably a solvent with a boiling point of 100 to 200°C (under a pressure of 1013.25 [hPa]. Hereinafter, all boiling points are the same). . More preferred is a solvent with a boiling point of 120 to 170°C. Glycol alkyl ether acetates are preferred from the viewpoint of good balance in coating properties, surface tension, etc., and relatively high solubility of constituent components in the composition.
  • Glycol alkyl ether acetates may be used alone or in combination with other solvents. Particularly preferred solvents used in combination are glycol monoalkyl ethers. Propylene glycol monomethyl ether is preferred from the viewpoint of solubility of the constituent components in the composition. Glycol monoalkyl ethers have high polarity, and if the amount added is too large, the pigment tends to aggregate, which tends to reduce the storage stability such as increasing the viscosity of the colored resin composition obtained later. When alkyl ethers are used in combination, the proportion of glycol monoalkyl ethers in the solvent (B) is preferably 5 to 30% by mass, more preferably 5 to 20% by mass.
  • a solvent having a boiling point of 150° C. or higher can be used in combination.
  • the colored resin composition becomes difficult to dry, but it has the effect of making it difficult to destroy the mutual relationships among the constituent components in the pigment dispersion due to rapid drying.
  • the content of the solvent with a boiling point of 150°C or higher in the solvent (B) is preferably 3 to 50% by mass, more preferably 5 to 40% by mass, Particularly preferred is 5 to 30% by weight.
  • the solvent with a boiling point of 150° C. or higher may be a glycol alkyl ether acetate or a glycol alkyl ether, and in this case, there is no need to separately contain a solvent with a boiling point of 150° C. or higher.
  • diethylene glycol mono-n-butyl ether acetate diethylene glycol monoethyl ether acetate, dipropylene glycol methyl ether acetate, 1,3-butylene glycol diacetate, and 1,6-hexanol diacetate.
  • triacetin triacetin.
  • suitable solvents (B) When forming pixels of a color filter by an inkjet method, suitable solvents (B) have a boiling point of preferably 130°C or more and 300°C or less, more preferably 150°C or more and 280°C or less. By setting it to the lower limit or more, the uniformity of the resulting coating film tends to be better, and by setting it to the upper limit or less, it tends to easily reduce the amount of residual solvent during firing.
  • the vapor pressure of the solvent used is preferably 10 mmHg or less, more preferably 5 mmHg or less, still more preferably 1 mmHg or less, from the viewpoint of uniformity of the resulting coating film.
  • the ink emitted from the nozzle is very fine, ranging from several to several tens of pL, so the solvent evaporates and the ink condenses and dries before it lands around the nozzle opening or within the pixel bank. It tends to harden.
  • the solvent (B) contains a solvent with a high boiling point, and specifically, it is preferable that the solvent (B) contains a solvent with a boiling point of 180° C. or higher. It is more preferable to include a solvent with a boiling point of 200°C or higher, and it is particularly preferable to include a solvent with a boiling point of 220°C or higher.
  • the content ratio of the solvent with a boiling point of 180°C or higher in the solvent (B) is preferably 50% by mass or more, more preferably 70% by mass or more, and 90% by mass or more. is most preferred. By setting it to the above lower limit or more, the effect of preventing evaporation of the solvent from the droplets tends to be sufficiently exhibited.
  • solvents with a boiling point of 180°C or higher examples include diethylene glycol mono-n-butyl ether acetate, diethylene glycol monoethyl ether acetate, dipropylene glycol methyl ether acetate, 1,3-butylene glycol diacetate, 1,6-hexanol diacetate, and triacetin. .
  • a solvent having a boiling point lower than 180° C. may be included in order to adjust the viscosity of the colored resin composition and the solubility of the solid content.
  • a solvent having low viscosity, high solubility, and low surface tension is preferable, and for example, ethers, esters, and ketones are preferable.
  • cyclohexanone, dipropylene glycol dimethyl ether, and cyclohexanol acetate are preferred.
  • the ejection stability in the inkjet method may deteriorate.
  • the content of alcohol in the solvent (B) is preferably 20% by mass or less, more preferably 10% by mass or less, and particularly preferably 5% by mass or less.
  • the content ratio of the solvent (B) in the colored resin composition of the present invention is not particularly limited, but its upper limit is preferably 99% by mass or less, more preferably 90% by mass or less, and even more preferably 85% by mass or less. . When the amount is below the upper limit, it tends to be easier to form a coating film.
  • the lower limit of the solvent content is preferably 70% by mass or more, more preferably 75% by mass or more, and even more preferably 80% by mass or more, taking into account the viscosity suitable for coating.
  • the above upper and lower limits can be arbitrarily combined.
  • the content of the solvent in the colored resin composition is preferably 70 to 99% by mass, more preferably 75 to 90% by mass, and even more preferably 80 to 85% by mass.
  • (C) Alkali-soluble resin The colored resin composition of the present invention contains (C) an alkali-soluble resin.
  • C alkali-soluble resin
  • Alkali-soluble resins include, for example, Japanese Unexamined Patent Application No. 7-207211, Japanese Unexamined Patent Application No. 8-259876, Japanese Unexamined Patent Application No. 10-300922, and Japanese Unexamined Patent Application No. 11-140144.
  • Japanese Patent Application Publication No. 11-174224, Japanese Publication No. 2000-56118, and Japanese Publication No. 2003-233179 can be used.
  • Preferred are the following resins (C-1) to (C-5).
  • (C-1) An unsaturated monobasic acid is added to at least a portion of the epoxy groups in the copolymer of an epoxy group-containing (meth)acrylate and another radically polymerizable monomer. or an alkali-soluble resin obtained by adding a polybasic acid anhydride to at least a portion of the hydroxyl groups generated by the addition reaction (hereinafter sometimes referred to as "resin (C-1)").
  • (C-2) Linear alkali-soluble resin containing a carboxyl group in the main chain (hereinafter sometimes referred to as "resin (C-2)").
  • (C-3) A resin in which an epoxy group-containing unsaturated compound is added to the carboxyl group portion of the resin (C-2) (hereinafter sometimes referred to as “resin (C-3)”).
  • (C-4) (meth)acrylic resin (hereinafter sometimes referred to as “resin (C-4)")
  • (C-5) Epoxy (meth)acrylate resin having a carboxyl group (hereinafter sometimes referred to as “resin (C-5)”). Particularly preferred is resin (C-1).
  • Resins (C-2) to (C-5) may be any resin as long as it has solubility to the extent that it can be dissolved in an alkaline developer and the desired development process can be carried out, and each resin is disclosed in Japanese Patent Application Publication No. 2009
  • the resins described in the same item in Japanese Patent No. 025813 can be preferably employed.
  • (C-1) A copolymer of an epoxy group-containing (meth)acrylate and another radically polymerizable monomer, in which an unsaturated monobasic acid is added to at least a portion of the epoxy groups in the copolymer.
  • Examples include resins obtained by adding a monobasic acid, or alkali-soluble resins obtained by adding a polybasic acid anhydride to 10 to 100 mol% of the hydroxyl groups generated by the addition reaction.
  • epoxy group-containing (meth)acrylates examples include glycidyl (meth)acrylate, 3,4-epoxybutyl (meth)acrylate, (3,4-epoxycyclohexyl)methyl (meth)acrylate, and 4-hydroxybutyl (meth)acrylate.
  • An example is acrylate glycidyl ether. Among them, glycidyl (meth)acrylate is preferred.
  • These epoxy group-containing (meth)acrylates may be used alone or in combination of two or more.
  • the other radically polymerizable monomer to be copolymerized with the epoxy group-containing (meth)acrylate is preferably a mono(meth)acrylate having a structure represented by the following general formula (V).
  • R 91 to R 98 each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms. Note that R 96 and R 98 or R 95 and R 97 may be linked to each other to form a ring.
  • the ring formed by connecting R 96 and R 98 or R 95 and R 97 is preferably an aliphatic ring, and may be either saturated or unsaturated, and Preferably, the number is 5-6.
  • a structure represented by the following general formula (Va), (Vb), or (Vc) is preferable.
  • the mono(meth)acrylates having the structure represented by formula (V) may be used alone or in combination of two or more.
  • mono(meth)acrylate having the structure represented by the formula (V) various known mono(meth)acrylates can be used as long as they have the structure represented by the formula (V), but in particular, the following general formula ( Mono(meth)acrylates represented by VI) are preferred.
  • R 89 represents a hydrogen atom or a methyl group
  • R 90 represents a structure represented by formula (V).
  • a repeating unit derived from a mono(meth)acrylate represented by formula (VI) is contained in a copolymer of an epoxy group-containing (meth)acrylate and another radically polymerizable monomer, the formula (VI)
  • the content of the repeating units derived from the mono(meth)acrylate expressed is preferably 5 to 90 mol%, more preferably 10 to 70 mol%, among the repeating units derived from other radically polymerizable monomers. Particularly preferred is 15 to 50 mol%.
  • Radically polymerizable monomers other than the mono(meth)acrylate represented by formula (VI) are not particularly limited, but include, for example, styrene, styrene ⁇ -, o-, m-, Vinyl aromatics such as p-alkyl, nitro, cyano, amide, and ester derivatives; dienes such as butadiene, 2,3-dimethylbutadiene, isoprene, and chloroprene; methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, n-butyl (meth)acrylate, sec-butyl (meth)acrylate, tert-butyl (meth)acrylate, (meth) Pentyl acrylate, neopentyl (meth)acrylate, isoamyl (meth)acrylate, hexyl (meth)acryl
  • (Meth)acrylic acid esters ; (meth)acrylic acid amide, (meth)acrylic acid N,N-dimethylamide, (meth)acrylic acid N,N-diethylamide, (meth)acrylic acid N,N-dipropylamide , (meth)acrylic acid amides such as (meth)acrylic acid N,N-di-isopropylamide, (meth)acrylic acid anthracenylamide; (meth)acrylic acid anilide, (meth)acryloylnitrile, acrolein, vinyl chloride , vinyl compounds such as vinylidene chloride, vinyl fluoride, vinylidene fluoride, N-vinylpyrrolidone, vinylpyridine, vinyl acetate; unsaturated dicarboxylic acid diesters such as diethyl citraconate, diethyl maleate, diethyl fumarate, diethyl itaconate, etc.
  • monomaleimides such as N-phenylmaleimide, N-cyclohexylmaleimide, N-laurylmaleimide, and N-(4-hydroxyphenyl)maleimide; and N-(meth)acryloyl phthalimide.
  • styrene, benzyl (meth)acrylate, and monomaleimide are preferred from the viewpoint of imparting excellent heat resistance and strength to the colored resin composition.
  • the copolymer of epoxy group-containing (meth)acrylate and other radically polymerizable monomer contains any repeating unit derived from styrene, benzyl (meth)acrylate, or monomaleimide, other radical polymerization
  • the repeating units derived from the monomer the total content of the repeating units derived from styrene, the repeating units derived from benzyl (meth)acrylate, and the repeating units derived from monomaleimide is 1 to 70 mol%. Preferably, 3 to 50 mol% is more preferable.
  • a known solution polymerization method can be applied to the copolymerization reaction of the epoxy group-containing (meth)acrylate and other radically polymerizable monomers.
  • the solvent used is not particularly limited as long as it is inert to radical polymerization, and commonly used organic solvents can be used.
  • solvents used in the solution polymerization method include ethylene glycol monoalkyl ether acetates such as ethyl acetate, isopropyl acetate, cellosolve acetate, and butyl cellosolve acetate; diethylene glycol monoalkyl ether acetates such as diethylene glycol monomethyl ether acetate, carbitol acetate, and butyl carbitol acetate; Alkyl ether acetates; Propylene glycol monoalkyl ether acetates; Acetate esters such as dipropylene glycol monoalkyl ether acetates; Ethylene glycol dialkyl ethers; Diethylene glycol dialkyl ethers such as methyl carbitol, ethyl carbitol, butyl carbitol ; Triethylene glycol dialkyl ethers; Propylene glycol dialkyl ethers; Dipropylene glycol dialkyl ethers; Ethers such
  • the amount of the solvent used in the solution polymerization method is preferably 30 to 1000 parts by weight, more preferably 50 to 800 parts by weight, based on 100 parts by weight of the resulting copolymer. By controlling the amount of solvent used within the above range, it tends to become easier to control the molecular weight of the copolymer.
  • the radical polymerization initiator used in the copolymerization reaction is not particularly limited as long as it can initiate radical polymerization, and commonly used organic peroxide catalysts and azo compound catalysts can be used. .
  • the organic peroxide catalyst include catalysts classified as known ketone peroxides, peroxyketals, hydroperoxides, diallyl peroxides, diacyl peroxides, peroxy esters, and peroxydicarbonates.
  • radical polymerization initiator used in the copolymerization reaction examples include benzoyl peroxide, dicumyl peroxide, diisopropyl peroxide, di-t-butyl peroxide, t-butyl peroxybenzoate, and t-hexyl peroxybenzoate.
  • the azo compound catalyst examples include azobisisobutyronitrile and azobiscarbonamide.
  • one or more radical polymerization initiators having an appropriate half-life are used depending on the polymerization temperature.
  • the amount of the radical polymerization initiator used is usually 0.5 to 20 parts by weight, preferably 1 to 10 parts by weight, based on 100 parts by weight of the monomers used in the copolymerization reaction.
  • the copolymerization reaction may be carried out by dissolving the monomers and radical polymerization initiator used in the copolymerization reaction in a solvent and raising the temperature while stirring, or by dissolving the monomers and radical polymerization initiator used in the copolymerization reaction in a solvent and raising the temperature while stirring.
  • the monomer may be added dropwise into a heated and stirred solvent, or a radical polymerization initiator may be added to the solvent and the monomer may be added dropwise into the heated solvent. Reaction conditions can be set depending on the target molecular weight.
  • the copolymer of epoxy group-containing (meth)acrylate and other radically polymerizable monomers includes 5 to 90 mol% of repeating units derived from epoxy group-containing (meth)acrylate and other radically polymerizable monomers. It is preferable that the repeating unit consists of 10 to 95 mol% of the repeating unit derived from the epoxy group-containing (meth)acrylate and 20 to 80 mol% of the repeating unit originating from the epoxy group-containing (meth)acrylate and another radically polymerizable monomer.
  • unsaturated monobasic acids can be used, such as unsaturated carboxylic acids having an ethylenically unsaturated double bond.
  • unsaturated monobasic acids to be added to epoxy groups include (meth)acrylic acid; crotonic acid; o-, m-, p-vinylbenzoic acid; or monocarboxylic acids such as (meth)acrylic acid substituted with a cyano group, etc., with (meth)acrylic acid being preferred.
  • One type of unsaturated monobasic acid may be used alone, or two or more types may be used in combination.
  • an unsaturated monobasic acid By adding an unsaturated monobasic acid to an epoxy group, polymerizability can be imparted to the resin (C-1).
  • the unsaturated monobasic acid is added to, for example, 10 to 100 mol%, preferably 30 to 100 mol%, more preferably 50 to 100 mol% of the epoxy groups possessed by the copolymer. By setting it as the above-mentioned lower limit or more, there is a tendency for the stability of the colored resin composition to improve over time.
  • a known method can be used to add an unsaturated monobasic acid to the epoxy group of the copolymer.
  • polybasic acid anhydride to be added to the hydroxyl group generated when an unsaturated monobasic acid is added to the epoxy group of the copolymer
  • a known polybasic acid anhydride can be used.
  • polybasic acid anhydrides include dibasic acid anhydrides such as maleic anhydride, succinic anhydride, itaconic anhydride, phthalic anhydride, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, and chlorendic anhydride; trimellitic anhydride;
  • examples include anhydrides of acids having three or more bases, such as pyromellitic anhydride, benzophenonetetracarboxylic anhydride, and biphenyltetracarboxylic anhydride. Among these, tetrahydrophthalic anhydride and succinic anhydride are preferred.
  • These polybasic acid anhydrides may be used alone or in combination of two or more.
  • Alkali solubility can be imparted to the resin (C-1) by adding a polybasic acid anhydride to the hydroxyl group generated when an unsaturated monobasic acid is added to the epoxy group of the copolymer.
  • the polybasic acid anhydride contains, for example, 10 to 100 mol%, preferably 20 to 90 mol%, more preferably 30 to 30 mol% of the hydroxyl groups produced by adding an unsaturated monobasic acid to the epoxy group of the copolymer. It is added to 80 mol%.
  • a method for adding a polybasic acid anhydride to a hydroxyl group generated by adding an unsaturated monobasic acid to an epoxy group possessed by the copolymer a known method can be employed.
  • glycidyl (meth)acrylate or a glycidyl ether compound having a polymerizable unsaturated group may be added to some of the generated carboxyl groups. good.
  • a glycidyl ether compound having no polymerizable unsaturated group may be added to a portion of the generated carboxy groups.
  • both a glycidyl ether compound having a polymerizable unsaturated group and a glycidyl ether compound not having a polymerizable unsaturated group may be added.
  • the glycidyl ether compound having no polymerizable unsaturated group include glycidyl ether compounds having a phenyl group or an alkyl group.
  • Commercially available glycidyl ether compounds having no polymerizable unsaturated groups include, for example, Nagase ChemteX's product names "Denacol EX-111", “Denacol EX-121", “Denacol EX-141", and "Denacol EX-141". Denacol EX-145,”"DenacolEX-146,”"DenacolEX-171,” and "Denacol EX-192.”
  • the structure of the resin (C-1) is described in, for example, Japanese Patent Application Publication No. 8-297366 and Japanese Patent Application Publication No. 2001-89533.
  • the weight average molecular weight of the resin (C-1) measured by GPC in terms of polystyrene is not particularly limited, but is preferably from 3,000 to 100,000, particularly preferably from 5,000 to 50,000.
  • the ratio of the weight average molecular weight (Mw) to the number average molecular weight (Mw/Mn) of the resin (C-1) is preferably 2.0 to 5.0.
  • an acrylic copolymer resin having an ethylenically unsaturated group in the side chain is preferable.
  • the partial structure containing the side chain having an ethylenically unsaturated group in the acrylic copolymer resin having an ethylenically unsaturated group in the side chain is not particularly limited, but the coating film curability upon exposure to ultraviolet rays and alkaline development From the viewpoint of achieving both alkali solubility and alkali solubility, it is preferable to have, for example, a partial structure represented by the following general formula (CI).
  • R 1 and R 2 each independently represent a hydrogen atom or a methyl group. * represents a bond.
  • the partial structure represented by the formula (CI) from the viewpoint of sensitivity and alkali developability, the partial structure represented by the following general formula (CI') is preferable.
  • R 1 and R 2 each independently represent a hydrogen atom or a methyl group.
  • R x represents a hydrogen atom or a polybasic acid residue.
  • the polybasic acid residue means a monovalent group obtained by removing one OH group from a polybasic acid or its anhydride.
  • polybasic acids include maleic acid, succinic acid, itaconic acid, phthalic acid, tetrahydrophthalic acid, hexahydrophthalic acid, pyromellitic acid, trimellitic acid, benzophenonetetracarboxylic acid, methylhexahydrophthalic acid, and endomethylene.
  • examples include tetrahydrophthalic acid, chlorendic acid, methyltetrahydrophthalic acid, and biphenyltetracarboxylic acid.
  • maleic acid, succinic acid, itaconic acid, phthalic acid, tetrahydrophthalic acid, hexahydrophthalic acid, pyromellitic acid, trimellitic acid, and biphenyltetracarboxylic acid are preferred; is more preferable.
  • These polybasic acids may be used alone or in combination of two or more.
  • (c1) When the acrylic copolymer resin having an ethylenically unsaturated group in the side chain has a partial structure represented by formula (CI), (c1) In the acrylic copolymer resin having an ethylenically unsaturated group in the side chain,
  • the content ratio of the partial structure represented by formula (CI) is not particularly limited, but is preferably 10 mol% or more, more preferably 20 mol% or more, even more preferably 30 mol% or more, even more preferably 40 mol% or more.
  • the coating film curability during exposure to ultraviolet rays is particularly preferred, and when setting it below the above upper limit, the alkali solubility during alkali development tends to improve.
  • the above upper and lower limits can be arbitrarily combined.
  • the content of the partial structure represented by formula (CI) in the acrylic copolymer resin having an ethylenically unsaturated group in the side chain (c1) is preferably 10 to 95 mol%, more preferably 20 to 90 mol%. It is preferably 30 to 85 mol%, even more preferably 40 to 80 mol%, particularly preferably 50 to 75 mol%, and most preferably 65 to 70 mol%.
  • (c1) When the acrylic copolymer resin having an ethylenically unsaturated group in the side chain has a partial structure represented by formula (CI'), (c1) the acrylic copolymer resin having an ethylenically unsaturated group in the side chain
  • the content ratio of the partial structure represented by formula (CI') in is not particularly limited, but is preferably 10 mol% or more, more preferably 20 mol% or more, even more preferably 30 mol% or more, and 40 mol% or more.
  • the content of the partial structure represented by formula (CI) in the acrylic copolymer resin having an ethylenically unsaturated group in the side chain (c1) is preferably 10 to 95 mol%, more preferably 20 to 90 mol%. It is preferably 30 to 85 mol%, even more preferably 40 to 80 mol%, particularly preferably 50 to 75 mol%, and most preferably 65 to 70 mol%.
  • R 3 represents a hydrogen atom or a methyl group
  • R 4 represents an alkyl group which may have a substituent, an aromatic ring group which may have a substituent, or a substituent. Represents an optional alkenyl group.
  • R 4 represents an alkyl group that may have a substituent, an aromatic ring group that may have a substituent, or an alkenyl group that may have a substituent.
  • alkyl group for R 4 include linear, branched or cyclic alkyl groups.
  • the number of carbon atoms is preferably 1 or more, more preferably 3 or more, further preferably 5 or more, particularly preferably 8 or more, and preferably 20 or less, more preferably 18 or less, further preferably 16 or less, and 14 or less. It is even more preferable, and 12 or less is particularly preferable.
  • the alkyl group preferably has 1 to 20 carbon atoms, more preferably 1 to 18 carbon atoms, even more preferably 3 to 16 carbon atoms, even more preferably 5 to 14 carbon atoms, and particularly preferably 8 to 12 carbon atoms.
  • Examples of the alkyl group include a methyl group, an ethyl group, a cyclohexyl group, a dicyclopentanyl group, and a dodecanyl group. From the viewpoint of developability, a dicyclopentanyl group and a dodecanyl group are preferred, and a dicyclopentanyl group is more preferred.
  • substituents that the alkyl group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group. , acryloyl group, and methacryloyl group. From the viewpoint of developability, hydroxy groups and oligoethylene glycol groups are preferred.
  • Examples of the aromatic ring group for R 4 include a monovalent aromatic hydrocarbon ring group and a monovalent aromatic heterocyclic group.
  • the number of carbon atoms is preferably 6 or more, preferably 24 or less, more preferably 22 or less, even more preferably 20 or less, and particularly preferably 18 or less. Setting the value above the lower limit tends to improve lipophilicity and improving solubility in solvents, while setting the value below the upper limit tends to improve hydrophilicity and improve alkali solubility. be.
  • the above upper and lower limits can be arbitrarily combined.
  • the aromatic ring group preferably has 6 to 24 carbon atoms, more preferably 6 to 22 carbon atoms, even more preferably 6 to 20 carbon atoms, and particularly preferably 6 to 18 carbon atoms.
  • the aromatic hydrocarbon ring in the aromatic hydrocarbon ring group may be a single ring or a condensed ring, such as a benzene ring, a naphthalene ring, an anthracene ring, a phenanthrene ring, a perylene ring, a tetracene ring, and a pyrene ring.
  • the aromatic heterocycle in the aromatic heterocyclic group may be a single ring or a condensed ring, such as a furan ring, a benzofuran ring, a thiophene ring, a benzothiophene ring, a pyrrole ring, a pyrazole ring, and an imidazole ring.
  • oxadiazole ring indole ring, carbazole ring, pyrroloimidazole ring, pyrrolopyrazole ring, pyrrolopyrrole ring, thienopyrrole ring, thienothiophene ring, furopyrrole ring, furofuran ring, thienofuran ring, benzisoxazole ring, benzisothiazole ring, Examples include benzimidazole ring, pyridine ring, pyrazine ring, pyridazine ring, pyrimidine ring, triazine ring, quinoline ring, isoquinoline ring, shinoline ring, quinoxaline ring, phenanthridine ring, perimidine ring, quinazoline ring, quinazolinone ring, and azulene ring.
  • a benzene ring group and a naphthalene ring group are preferable, and a benzene ring group is more preferable.
  • substituents that the aromatic ring group may have include methyl group, ethyl group, propyl group, methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, and epoxy group.
  • oligoethylene glycol group, phenyl group, and carboxy group From the viewpoint of developability, hydroxy groups and oligoethylene glycol groups are preferred.
  • alkenyl group for R 4 examples include linear, branched or cyclic alkenyl groups.
  • the number of carbon atoms is preferably 2 or more, preferably 22 or less, more preferably 20 or less, even more preferably 18 or less, even more preferably 16 or less, and particularly preferably 14 or less. Setting the value above the lower limit tends to improve lipophilicity and improving solubility in solvents, while setting the value below the upper limit tends to improve hydrophilicity and improve alkali solubility. be.
  • the above upper and lower limits can be arbitrarily combined.
  • the alkenyl group preferably has 2 to 22 carbon atoms, more preferably 2 to 20 carbon atoms, even more preferably 2 to 18 carbon atoms, even more preferably 2 to 16 carbon atoms, and particularly preferably 2 to 14 carbon atoms.
  • alkenyl group examples include vinyl group, allyl group, 2-propen-2-yl group, 2-buten-1-yl group, 3-buten-1-yl group, 2-penten-1-yl group, 3 -penten-2-yl group, hexenyl group, cyclobutenyl group, cyclopentenyl group, and cyclohexenyl group. From the viewpoint of developability, a vinyl group and an allyl group are preferred, and a vinyl group is more preferred.
  • alkenyl group may have examples include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group.
  • substituents that the alkenyl group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group.
  • substituents that the alkenyl group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group.
  • hydroxy groups and oligoethylene glycol groups are preferred.
  • R 4 represents an alkyl group that may have a substituent, an aromatic ring group that may have a substituent, or an alkenyl group that may have a substituent, and has an effect on developability and film strength. From this point of view, an alkyl group or an alkenyl group is preferable, and an alkyl group is more preferable.
  • (c1) When the acrylic copolymer resin having an ethylenically unsaturated group in the side chain has a partial structure represented by formula (CII), (c1) In the acrylic copolymer resin having an ethylenically unsaturated group in the side chain,
  • the content of the partial structure represented by formula (CII) is not particularly limited, but is preferably 1 mol% or more, more preferably 5 mol% or more, even more preferably 10 mol% or more, particularly preferably 20 mol% or more, Moreover, it is preferably 70 mol% or less, more preferably 60 mol% or less, even more preferably 50 mol% or less, and particularly preferably 40 mol% or less.
  • the content of the partial structure represented by formula (CII) in the acrylic copolymer resin having an ethylenically unsaturated group in the side chain (c1) is preferably 1 to 70 mol%, more preferably 5 to 60 mol%. , more preferably 10 to 50 mol%, particularly preferably 20 to 40 mol%.
  • the acrylic copolymer resin contains a partial structure represented by formula (CI)
  • the other partial structure included is represented by the following general formula (CIII) from the viewpoint of suppressing brightness reduction by improving heat resistance.
  • a partial structure is included.
  • R 5 represents a hydrogen atom or a methyl group
  • R 6 represents an alkyl group that may have a substituent, an alkenyl group that may have a substituent, or an alkenyl group that may have a substituent.
  • t represents an integer from 0 to 5.
  • R 6 is an alkyl group that may have a substituent, an alkenyl group that may have a substituent, an alkynyl group that may have a substituent, a hydroxy group, a carboxy group, Represents a halogen atom, an alkoxy group that may have a substituent, a thiol group, or an alkyl sulfide group that may have a substituent.
  • alkyl group for R 6 include linear, branched, or cyclic alkyl groups.
  • the number of carbon atoms is preferably 1 or more, more preferably 3 or more, further preferably 5 or more, and preferably 20 or less, more preferably 18 or less, further preferably 16 or less, even more preferably 14 or less, and even more preferably 12 or less. is particularly preferred. Setting the value above the lower limit tends to improve lipophilicity and improving solubility in solvents, while setting the value below the upper limit tends to improve hydrophilicity and improve alkali solubility. be. The above upper and lower limits can be arbitrarily combined.
  • the alkyl group preferably has 1 to 20 carbon atoms, more preferably 1 to 18 carbon atoms, even more preferably 3 to 16 carbon atoms, even more preferably 3 to 14 carbon atoms, and particularly preferably 5 to 12 carbon atoms.
  • Examples of the alkyl group include a methyl group, an ethyl group, a cyclohexyl group, a dicyclopentanyl group, and a dodecanyl group. From the viewpoint of heat resistance, a dicyclopentanyl group and a dodecanyl group are preferred, and a dicyclopentanyl group is more preferred.
  • substituents that the alkyl group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group. , acryloyl group, and methacryloyl group. From the viewpoint of developability, hydroxy groups and oligoethylene glycol groups are preferred.
  • alkenyl group for R 6 examples include linear, branched, or cyclic alkenyl groups.
  • the number of carbon atoms is preferably 2 or more, preferably 22 or less, more preferably 20 or less, even more preferably 18 or less, even more preferably 16 or less, and particularly preferably 14 or less. Setting the value above the lower limit tends to improve lipophilicity and improving solubility in solvents, while setting the value below the upper limit tends to improve hydrophilicity and improve alkali solubility. be.
  • the above upper and lower limits can be arbitrarily combined.
  • the alkenyl group preferably has 2 to 22 carbon atoms, more preferably 2 to 20 carbon atoms, even more preferably 2 to 18 carbon atoms, even more preferably 2 to 16 carbon atoms, and particularly preferably 2 to 14 carbon atoms.
  • alkenyl group examples include vinyl group, allyl group, 2-propen-2-yl group, 2-buten-1-yl group, 3-buten-1-yl group, 2-penten-1-yl group, 3 -penten-2-yl group, hexenyl group, cyclobutenyl group, cyclopentenyl group, and cyclohexenyl group. From the viewpoint of exposure sensitivity during UV exposure, vinyl groups and allyl groups are preferred, and vinyl groups are more preferred.
  • alkenyl group may have examples include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group.
  • substituents that the alkenyl group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group.
  • substituents that the alkenyl group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group.
  • hydroxy groups and oligoethylene glycol groups are preferred.
  • alkynyl group for R 6 examples include linear, branched or cyclic alkynyl groups.
  • the number of carbon atoms is preferably 2 or more, preferably 22 or less, more preferably 20 or less, even more preferably 18 or less, even more preferably 16 or less, and particularly preferably 14 or less. Setting the value above the lower limit tends to improve lipophilicity and improving solubility in solvents, while setting the value below the upper limit tends to improve hydrophilicity and improve alkali solubility. be.
  • the above upper and lower limits can be arbitrarily combined.
  • the alkynyl group preferably has 2 to 22 carbon atoms, more preferably 2 to 20 carbon atoms, even more preferably 2 to 18 carbon atoms, even more preferably 2 to 16 carbon atoms, and particularly preferably 2 to 14 carbon atoms.
  • alkynyl group examples include 1-propyn-3-yl group, 1-butyn-4-yl group, 1-pentyn-5-yl group, 2-methyl-3-butyn-2-yl group, 1,4 -pentadiyn-3-yl group, 1,3-pentadiyn-5-yl group, and 1-hexyn-6-yl group.
  • alkynyl group may have examples include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group.
  • substituents that the alkynyl group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group.
  • substituents that the alkynyl group may have examples of substituents that the alkynyl group may have examples of substituents that the alkynyl group may have examples of substituents that the alkynyl group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group.
  • halogen atom for R 6 examples include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
  • a fluorine atom is preferred from the viewpoint of storage stability of the acrylic copolymer resin.
  • Examples of the alkoxy group for R 6 include linear, branched, or cyclic alkoxy groups.
  • the number of carbon atoms is preferably 1 or more, preferably 20 or less, more preferably 18 or less, even more preferably 16 or less, even more preferably 14 or less, and particularly preferably 12 or less. Setting the value above the lower limit tends to improve lipophilicity and improving solubility in solvents, while setting the value below the upper limit tends to improve hydrophilicity and improve alkali solubility. be.
  • the above upper and lower limits can be arbitrarily combined.
  • the alkoxy group preferably has 1 to 20 carbon atoms, more preferably 1 to 18 carbon atoms, even more preferably 1 to 16 carbon atoms, even more preferably 1 to 14 carbon atoms, and particularly preferably 1 to 12 carbon atoms.
  • alkoxy group examples include methoxy group, ethoxy group, propoxy group, isopropoxy group, butoxy group, and isobutoxy group.
  • substituents that the alkoxy group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, phenyl group, and carboxy group. , acryloyl group, and methacryloyl group. From the viewpoint of developability, hydroxy groups and oligoethylene glycol groups are preferred.
  • alkyl sulfide group for R 6 examples include linear, branched or cyclic alkyl sulfide groups.
  • the number of carbon atoms is preferably 1 or more, preferably 20 or less, more preferably 18 or less, even more preferably 16 or less, even more preferably 14 or less, and particularly preferably 12 or less. Setting the value above the lower limit tends to improve lipophilicity and improving solubility in solvents, while setting the value below the upper limit tends to improve hydrophilicity and improve alkali solubility. be.
  • the above upper and lower limits can be arbitrarily combined.
  • the number of carbon atoms in the alkyl sulfide group is preferably 1 to 20, more preferably 1 to 18, even more preferably 1 to 16, even more preferably 1 to 14, and particularly preferably 1 to 12.
  • alkyl sulfide group examples include a methyl sulfide group, an ethyl sulfide group, a propyl sulfide group, and a butyl sulfide group. From the viewpoint of developability, methyl sulfide groups and ethyl sulfide groups are preferred.
  • substituents that the alkyl group in the alkyl sulfide group may have include methoxy group, ethoxy group, chloro group, bromo group, fluoro group, hydroxy group, amino group, epoxy group, oligoethylene glycol group, and phenyl group. group, carboxy group, acryloyl group, and methacryloyl group. From the viewpoint of developability, hydroxy groups and oligoethylene glycol groups are preferred.
  • R 6 is an alkyl group that may have a substituent, an alkenyl group that may have a substituent, an alkynyl group that may have a substituent, a hydroxy group, a carboxy group, a halogen atom, an alkoxy group , represents a hydroxyalkyl group, a thiol group, or an alkyl sulfide group that may have a substituent, and from the viewpoint of developability, a hydroxy group or a carboxy group is preferable, and a carboxy group is more preferable.
  • t represents an integer from 0 to 5. From the viewpoint of ease of manufacture, t is preferably 0.
  • the content ratio of the partial structure represented by formula (CIII) is not particularly limited, but is preferably 1 mol% or more, more preferably 2 mol% or more, even more preferably 5 mol% or more, particularly preferably 8 mol% or more, Further, it is preferably 50 mol% or less, more preferably 40 mol% or less, even more preferably 30 mol% or less, and particularly preferably 20 mol% or less.
  • the value above the lower limit tends to improve heat resistance and suppressing a decrease in brightness
  • setting the value below the upper limit increases the content of other partial structures and tends to improve alkali solubility.
  • the above upper and lower limits can be arbitrarily combined.
  • the content of the partial structure represented by formula (CIII) in the acrylic copolymer resin having an ethylenically unsaturated group in the side chain (c1) is preferably 1 to 50 mol%, more preferably 2 to 40 mol%. , 5 to 30 mol% is more preferable, and 8 to 20 mol% is particularly preferable.
  • R 7 represents a hydrogen atom or a methyl group.
  • (c1) When containing a partial structure represented by formula (CIV) in an acrylic copolymer resin having an ethylenically unsaturated group in its side chain, (c1) an acrylic copolymer resin having an ethylenically unsaturated group in its side chain
  • the content ratio of the partial structure represented by formula (CIV) in is not particularly limited, but is preferably 5 mol% or more, more preferably 10 mol% or more, even more preferably 20 mol% or more, and 80 mol% or less. It is preferably 70% by mole or less, more preferably 60% by mole or less.
  • the content ratio of the partial structure represented by formula (CIV) in the acrylic copolymer resin having an ethylenically unsaturated group in the side chain (c1) is preferably 5 to 80 mol%, and more preferably 10 to 70 mol%, More preferably 20 to 60% mole.
  • the acid value of the alkali-soluble resin is not particularly limited, but is preferably 10 mgKOH/g or more, more preferably 30 mgKOH/g or more, even more preferably 40 mgKOH/g or more, even more preferably 50 mgKOH/g or more, and even more preferably 60 mgKOH/g.
  • the above is particularly preferable, and also preferably 300 mgKOH/g or less, more preferably 250 mgKOH/g or less, even more preferably 200 mgKOH/g or less, even more preferably 150 mgKOH/g or less, and particularly preferably 100 mgKOH/g or less.
  • the alkali solubility tends to improve
  • the content is equal to or less than the upper limit
  • the storage stability and substrate adhesion of the colored resin composition tend to improve.
  • the above upper and lower limits can be arbitrarily combined.
  • the acid value of the alkali-soluble resin (C) is preferably 10 to 300 mgKOH/g, more preferably 30 to 300 mgKOH/g, even more preferably 40 to 250 mgKOH/g, even more preferably 50 to 200 mgKOH/g, and even more preferably 60 to 300 mgKOH/g. 150 mgKOH/g is particularly preferred.
  • the weight average molecular weight of the alkali-soluble resin (C) is not particularly limited, but is preferably 1,000 or more, more preferably 2,000 or more, even more preferably 4,000 or more, even more preferably 6,000 or more, even more preferably 7,000 or more, particularly preferably 8,000 or more, and preferably 30,000 or less, more preferably 20,000 or less, still more preferably 15,000 or less, particularly preferably 10,000 or less.
  • the content is equal to or more than the lower limit, heat resistance and coating film curability tend to improve, and when the content is equal to or less than the upper limit, alkali solubility tends to improve.
  • the above upper and lower limits can be arbitrarily combined.
  • the weight average molecular weight of the alkali-soluble resin (C) is preferably from 1,000 to 30,000, more preferably from 2,000 to 30,000, even more preferably from 4,000 to 20,000, even more preferably from 6,000 to 20,000, even more preferably from 7,000 to 15,000, and even more preferably from 8,000 to 15,000. 10,000 is particularly preferred.
  • the content ratio of the alkali-soluble resin (C) in the colored resin composition of the present invention is not particularly limited, but is preferably 5% by mass or more, more preferably 10% by mass or more, and 20% by mass in the total solid content of the colored resin composition. % or more, even more preferably 30% by mass or more, particularly preferably 40% by mass or more, and preferably 80% by mass or less, more preferably 70% by mass or less, even more preferably 60% by mass or less, and 50% by mass or less. % or less is particularly preferable. Setting the amount at or above the lower limit tends to improve the coating film curability upon exposure to ultraviolet rays, and setting the amount at or below the upper limit tends to improve solubility in the developer and suppress residues.
  • the content of the alkali-soluble resin (C) in the colored resin composition is preferably 5 to 80% by mass, more preferably 10 to 80% by mass, and more preferably 20 to 70% by mass in the total solid content of the colored resin composition. %, even more preferably 30 to 60% by weight, particularly preferably 40 to 50% by weight.
  • the colored resin composition of the present invention contains (D) a photopolymerization initiator.
  • a photopolymerization initiator By containing a photopolymerization initiator, film curability can be imparted by photopolymerization.
  • the photopolymerization initiator can also be used as a mixture (photopolymerization initiation system) with an accelerator (chain transfer agent) and an optionally added additive such as a sensitizing dye.
  • the photopolymerization initiation system is a component that has the function of directly absorbing light or being photosensitized to cause a decomposition reaction or a hydrogen abstraction reaction to generate polymerization-active radicals.
  • photopolymerization initiator examples include metallocene compounds containing titanocene compounds described in Japanese Patent Application Laid-open Nos. 59-152396 and 61-151197, and Japanese Patent Applications 10-39503. Hexaarylbiimidazole derivatives, halomethyl-s-triazine derivatives, N-aryl- ⁇ -amino acids such as N-phenylglycine, N-aryl- ⁇ -amino acid salts, N-aryl- ⁇ -amino acid esters described in publications Examples include radical activators such as, ⁇ -aminoalkylphenone compounds, and oxime ester initiators described in Japanese Patent Application Publication No. 2000-80068.
  • Photopolymerization initiators that can be used in the present invention are listed below. 2-(4-methoxyphenyl)-4,6-bis(trichloromethyl)-s-triazine, 2-(4-methoxynaphthyl)-4,6-bis(trichloromethyl)-s-triazine, 2-(4 Halomethylated triazine derivatives such as -ethoxynaphthyl)-4,6-bis(trichloromethyl)-s-triazine and 2-(4-ethoxycarbonylnaphthyl)-4,6-bis(trichloromethyl)-s-triazine;
  • Benzophenone derivatives such as benzophenone, Michler's ketone, 2-methylbenzophenone, 3-methylbenzophenone, 4-methylbenzophenone, 2-chlorobenzophenone, 4-bromobenzophenone, 2-carboxybenzophenone; 2,2-dimethoxy-2-phenylacetophenone, 2,2-diethoxyacetophenone, 1-hydroxycyclohexylphenyl ketone, ⁇ -hydroxy-2-methylphenylpropanone, 1-hydroxy-1-methylethyl-(p -isopropylphenyl)ketone, 1-hydroxy-1-(p-dodecylphenyl)ketone, 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one, 1,1,1 -Acetophenone derivatives such as trichloromethyl-(p-butylphenyl)ketone; Thioxanthone derivatives such as thioxanthone, 2-ethyl
  • Benzoic acid ester derivatives such as ethyl p-dimethylaminobenzoate and ethyl P-diethylaminobenzoate; Acridine derivatives such as 9-phenylacridine and 9-(p-methoxyphenyl)acridine; Phenazine derivatives such as 9,10-dimethylbenzphenazine; Anthrone derivatives such as benzanthrone; dicyclopentadienyl-Ti-dichloride, dicyclopentadienyl-Ti-bis-phenyl, dicyclopentadienyl-Ti-bis-2,3,4,5,6-pentafluorophenyl-1-yl, dicyclopentadienyl-Ti-bis-2,3,5,6-tetrafluorophenyl-1-yl, dicyclopentadienyl-Ti-bis-2,4,6-trifluorophenyl-1-yl, Dicyclopen
  • Oxime ester compounds have a structure that absorbs ultraviolet rays, a structure that transmits light energy, and a structure that generates radicals, so they are highly sensitive even in small amounts and are stable against thermal reactions. Therefore, it is possible to design a highly sensitive colored resin composition in a small amount.
  • oxime ester compounds having a carbazole ring which may have a substituent are preferred.
  • oxime ester compounds examples include compounds represented by the following general formula (I-1).
  • R 21a represents a hydrogen atom, an alkyl group that may have a substituent, or an aromatic ring group that may have a substituent.
  • R 21b represents any substituent containing an aromatic ring or a heteroaromatic ring.
  • R 22a represents an alkanoyl group which may have a substituent or an aryloyl group which may have a substituent.
  • the number of carbon atoms in the alkyl group in R 21a is not particularly limited, but from the viewpoint of solubility in solvents and sensitivity to exposure, it is preferably 1 or more, more preferably 2 or more, and preferably 20 or less, more preferably 15 or less. , more preferably 10 or less, particularly preferably 5 or less.
  • the above upper and lower limits can be arbitrarily combined.
  • the alkyl group preferably has 1 to 20 carbon atoms, more preferably 1 to 15 carbon atoms, even more preferably 1 to 10 carbon atoms, even more preferably 1 to 5 carbon atoms, and particularly preferably 2 to 5 carbon atoms.
  • alkyl group examples include a methyl group, an ethyl group, a propyl group, a cyclopentylethyl group, and a propyl group.
  • substituents that the alkyl group may have include aromatic ring groups, hydroxyl groups, carboxy groups, halogen atoms, amino groups, amide groups, 4-(2-methoxy-1-methyl)ethoxy-2- Examples include methylphenyl group and N-acetyl-N-acetoxyamino group. From the viewpoint of ease of synthesis, it is preferable that it is unsubstituted.
  • Examples of the aromatic ring group for R 21a include aromatic hydrocarbon ring groups and aromatic heterocyclic groups.
  • the number of carbon atoms in the aromatic ring group is not particularly limited, but is preferably 5 or more from the viewpoint of solubility in the colored resin composition. Further, from the viewpoint of developability, it is preferably 30 or less, more preferably 20 or less, even more preferably 12 or less, and particularly preferably 8 or less. The above upper and lower limits can be arbitrarily combined.
  • the number of carbon atoms in the aromatic ring group is preferably 5 to 30, more preferably 5 to 20, even more preferably 5 to 12, particularly preferably 5 to 8.
  • Examples of the aromatic ring group include a phenyl group, a naphthyl group, a pyridyl group, a furyl group, and a fluorenyl group. From the viewpoint of developability, a phenyl group, a naphthyl group, and a fluorenyl group are preferable, and a phenyl group and a fluorenyl group are more preferable.
  • substituents that the aromatic ring group may have include a hydroxyl group, an alkyl group that may have a substituent, an alkoxy group that may have a substituent, a carboxy group, a halogen atom, Examples include an amino group, an amide group, and an alkyl group.
  • R 21a is preferably an alkyl group that may have a substituent, more preferably an unsubstituted alkyl group, and even more preferably a methyl group.
  • R 21b is any substituent containing an aromatic ring or a heteroaromatic ring.
  • a carbazolyl group that may have a substituent a thioxanthonyl group that may have a substituent, a diphenyl sulfide group that may have a substituent, or A fluorenyl group which may have a substituent, and a group in which these groups are connected to a carbonyl group are preferred.
  • a carbazolyl group that may have a substituent or a group in which a carbazolyl group that may have a substituent and a carbonyl group are preferred.
  • substituents that the carbazolyl group may have include alkyl groups having 1 to 10 carbon atoms such as methyl group and ethyl group; alkoxy groups having 1 to 10 carbon atoms such as methoxy group and ethoxy group; F, Halogen atoms such as Cl, Br, I; acyl groups having 1 to 10 carbon atoms; alkyl ester groups having 1 to 10 carbon atoms; alkoxycarbonyl groups having 1 to 10 carbon atoms; halogenated alkyl groups having 1 to 10 carbon atoms; Aromatic ring group having 4 to 10 carbon atoms; Amino group; Aminoalkyl group having 1 to 10 carbon atoms; Hydroxyl group; Nitro group; CN group; Arylyl group which may have a substituent; a heteroaryloyl group which may have a substituent; and a thenoyl group which may have a substituent.
  • the number of carbon atoms in the alkanoyl group in R22a is not particularly limited, but from the viewpoint of solubility in solvents and sensitivity, it is preferably 2 or more, more preferably 3 or more, and preferably 20 or less, more preferably 15 or less, and It is preferably 10 or less, particularly preferably 5 or less.
  • the above upper and lower limits can be arbitrarily combined.
  • the alkanoyl group preferably has 2 to 20 carbon atoms, more preferably 2 to 15 carbon atoms, even more preferably 2 to 10 carbon atoms, even more preferably 2 to 5 carbon atoms, and particularly preferably 3 to 5 carbon atoms.
  • alkanoyl group examples include an acetyl group, an ethyl group, a propanoyl group, and a butanoyl group.
  • substituents that the alkanoyl group may have include aromatic ring groups, hydroxyl groups, carboxy groups, halogen atoms, amino groups, and amide groups, and from the viewpoint of ease of synthesis, unsubstituted It is preferable.
  • the number of carbon atoms in the aryloyl group in R22a is not particularly limited, but from the viewpoint of solubility in solvents and sensitivity, it is preferably 7 or more, more preferably 8 or more, and preferably 20 or less, more preferably 15 or less, and Preferably it is 10 or less.
  • the above upper and lower limits can be arbitrarily combined.
  • the aryloyl group preferably has 7 to 20 carbon atoms, more preferably 7 to 15 carbon atoms, even more preferably 7 to 10 carbon atoms, and particularly preferably 8 to 10 carbon atoms.
  • Examples of the aryloyl group include a benzoyl group and a naphthoyl group.
  • substituents that the aryloyl group may have include a hydroxyl group, a carboxy group, a halogen atom, an amino group, an amide group, and an alkyl group.From the viewpoint of ease of synthesis, unsubstituted groups are preferable. preferable.
  • Examples of the compound represented by the formula (I-1) include compounds represented by the following general formula (I-2) or (I-3) from the viewpoint of light absorption to the i-line (365 nm) of the exposure light source. It will be done.
  • R 21a and R 22a have the same meanings as in formula (I-1).
  • R 23a represents an alkyl group which may have a substituent.
  • R 24a represents an alkyl group that may have a substituent, an aryloyl group that may have a substituent, a heteroaryloyl group that may have a substituent, or a nitro group.
  • the benzene ring constituting the carbazole ring may be further fused with an aromatic ring to form a polycyclic aromatic ring.
  • the number of carbon atoms in the alkyl group in R 23a is not particularly limited, but from the viewpoint of solubility in solvents, it is preferably 1 or more, more preferably 2 or more, and preferably 20 or less, more preferably 15 or less, and even more preferably It is 10 or less, particularly preferably 5 or less.
  • the above upper and lower limits can be arbitrarily combined.
  • the alkyl group preferably has 1 to 20 carbon atoms, more preferably 1 to 15 carbon atoms, even more preferably 1 to 10 carbon atoms, even more preferably 1 to 5 carbon atoms, and particularly preferably 2 to 5 carbon atoms.
  • alkyl group examples include methyl group, ethyl group, propyl group, butyl group, and cyclohexyl group.
  • substituents that the alkyl group may have include a carbonyl group, a carboxy group, a hydroxy group, a phenyl group, a benzyl group, a cyclohexyl group, and a nitro group. From the viewpoint of ease of synthesis, it is preferable that it is unsubstituted. From the viewpoint of solubility in solvents and ease of synthesis, R 23a is more preferably an ethyl group.
  • the number of carbon atoms in the alkyl group in R24a is not particularly limited, but from the viewpoint of solubility in solvents, it is preferably 1 or more, more preferably 2 or more, and preferably 20 or less, more preferably 15 or less, and even more preferably It is 10 or less, particularly preferably 5 or less.
  • the above upper and lower limits can be arbitrarily combined.
  • the alkyl group preferably has 1 to 20 carbon atoms, more preferably 1 to 15 carbon atoms, even more preferably 1 to 10 carbon atoms, even more preferably 1 to 5 carbon atoms, and particularly preferably 2 to 5 carbon atoms.
  • alkyl group examples include methyl group, ethyl group, propyl group, butyl group, and cyclohexyl group.
  • substituents that the alkyl group may have include a carbonyl group, a carboxy group, a hydroxy group, a phenyl group, a benzyl group, a cyclohexyl group, and a nitro group. From the viewpoint of ease of synthesis, it is preferable that it is unsubstituted.
  • the number of carbon atoms in the aryloyl group in R24a is not particularly limited, but from the viewpoint of solubility in solvents, it is preferably 7 or more, more preferably 8 or more, even more preferably 9 or more, and preferably 20 or less, more preferably It is 15 or less, more preferably 10 or less, particularly preferably 9 or less.
  • the above upper and lower limits can be arbitrarily combined.
  • the aryloyl group preferably has 7 to 20 carbon atoms, more preferably 8 to 15 carbon atoms, even more preferably 9 to 10 carbon atoms, and particularly preferably 9 carbon atoms.
  • Examples of the aryloyl group include a benzoyl group and a naphthoyl group.
  • Examples of the substituent that the aryloyl group may have include a carbonyl group, a carboxy group, a hydroxy group, a phenyl group, a benzyl group, a cyclohexyl group, and a nitro group. From the viewpoint of ease of synthesis, an ethyl group is preferred.
  • the number of carbon atoms in the heteroaryloyl group in R24a is not particularly limited, but from the viewpoint of solubility in solvents, it is preferably 7 or more, more preferably 8 or more, even more preferably 9 or more, and preferably 20 or less, more It is preferably 15 or less, more preferably 10 or less, particularly preferably 9 or less.
  • the above upper and lower limits can be arbitrarily combined.
  • the heteroaryloyl group preferably has 7 to 20 carbon atoms, more preferably 8 to 15 carbon atoms, even more preferably 9 to 10 carbon atoms, and particularly preferably 9 carbon atoms.
  • heteroaryl group examples include a benzoyl group, a fluorobenzoyl group, a chlorobenzoyl group, a bromobenzoyl group, a fluoronaphthoyl group, a chloronaphthoyl group, and a bromonaphthoyl group.
  • substituents that the heteroaryloyl group may have include a carbonyl group, a carboxy group, a hydroxy group, a phenyl group, a benzyl group, a cyclohexyl group, and a nitro group. From the viewpoint of ease of synthesis, it is preferable that it is unsubstituted. From the viewpoint of sensitivity, R 24a is preferably an aryloyl group which may have a substituent, and more preferably a benzoyl group.
  • the benzene ring constituting the carbazole ring may be further fused with an aromatic ring to form a polycyclic aromatic ring.
  • oxime ester compounds examples include OXE-02 and OXE-03 manufactured by BASF, TR-PBG-304 and TR-PBG-314 manufactured by Changzhou Strong Electronics New Materials, and N-1919 manufactured by ADEKA. , NCI-930, and NCI-831.
  • oxime ester compounds include the following compounds.
  • photopolymerization initiators may be used alone or in combination of two or more.
  • a chain transfer agent is a compound that has the function of receiving generated radicals and transferring the received radicals to other compounds.
  • various chain transfer agents can be used as long as they are compounds having the above functions, but examples include compounds containing a mercapto group and carbon tetrachloride, which tend to have a high chain transfer effect. It is more preferable to use a mercapto group-containing compound from the following. This is thought to be because bond cleavage is likely to occur due to the small S--H bond energy, and hydrogen abstraction reactions and chain transfer reactions are likely to occur. Effective for improving sensitivity and surface hardening.
  • Examples of mercapto group-containing compounds include 2-mercaptobenzothiazole, 2-mercaptobenzimidazole, 2-mercaptobenzoxazole, 3-mercapto-1,2,4-triazole, 2-mercapto-4(3H)-quinazoline, Mercapto group-containing compounds with aromatic rings such as ⁇ -mercaptonaphthalene and 1,4-dimethylmercaptobenzene; hexanedithiol, decanedithiol, butanediol bis(3-mercaptopropionate), butanediol bisthioglycolate, Ethylene glycol bis(3-mercaptopropionate), ethylene glycol bisthioglycolate, trimethylolpropane tris(3-mercaptopropionate), trimethylolpropane tristhioglycolate, trishydroxyethyl tristhiopropionate, penta Erythritol tetrakis (3-mer
  • 2-mercaptobenzothiazole and 2-mercaptobenzimidazole are preferable, and as the aliphatic mercapto group-containing compound, trimethylolpropane tris (3-mercaptopropionate), Pentaerythritol Tetrakis (3-Mercaptopropionate), Pentaerythritol Tris (3-Mercaptopropionate), Trimethylolpropane Tris (3-Mercaptobutyrate), Pentaerythritol Tetrakis (3-Mercaptobutyrate), Pentaerythritol Tris (3-mercaptobutyrate), 1,3,5-tris(3-mercaptobutyloxyethyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione are preferred.
  • aliphatic mercapto group-containing compounds are preferred, such as trimethylolpropane tris (3-mercaptopropionate), pentaerythritol tetrakis (3-mercaptopropionate), and pentaerythritol tris (3-mercaptopropionate).
  • chain transfer agents may be used alone or in combination of two or more.
  • the content ratio of the photopolymerization initiator (D) is not particularly limited, but is preferably 0.5% by mass or more, and 0.8% by mass or more in the total solid content of the colored resin composition. is more preferable, 1% by mass or more is even more preferable, 1.2% by weight or more is particularly preferable, 10% by weight or less is more preferable, more preferably 8% by weight or less, even more preferably 6% by weight or less, 4% by weight.
  • the following are particularly preferred. Setting the amount above the lower limit value tends to improve the curability of the coating film, and setting it below the upper limit value tends to improve the brightness by reducing visible light absorption. The above upper and lower limits can be arbitrarily combined.
  • the content ratio of the photopolymerization initiator (D) is preferably 0.5 to 10% by mass, more preferably 0.8 to 8% by mass in the total solid content of the colored resin composition. , more preferably 1 to 6% by weight, particularly preferably 1.2 to 4% by weight.
  • the colored resin composition of the present invention contains a chain transfer agent
  • its content is not particularly limited, but it is preferably 0.1% by mass or more, and 0.2% by mass or more in the total solid content of the colored resin composition. is more preferable, more preferably 0.3% by mass or more, particularly preferably 0.4% by mass or more, and preferably 3% by mass or less, more preferably 2.5% by mass or less, even more preferably 2% by mass or less. , 1.5% by mass or less is particularly preferred.
  • the content is equal to or more than the lower limit, solvent resistance tends to be improved, and when the content is equal to or less than the upper limit, storage stability tends to be improved.
  • the above upper and lower limits can be arbitrarily combined.
  • the content thereof is preferably 0.1 to 3% by mass, and 0.2 to 2.5% by mass in the total solid content of the colored resin composition. It is more preferably 0.3 to 2% by mass, even more preferably 0.4 to 1.5% by mass.
  • the colored resin composition of the present invention contains (E) a photopolymerizable monomer.
  • the photopolymerizable monomer is not particularly limited as long as it is a polymerizable low-molecular compound, but it is an addition-polymerizable compound having at least one ethylenic double bond (hereinafter referred to as "ethylenic compound"). ) is preferred.
  • the ethylenic compound is a compound having an ethylenic double bond that undergoes addition polymerization and hardening due to the action of a photopolymerization initiator when the colored resin composition of the present invention is irradiated with actinic rays.
  • the monomer in the present invention means a concept opposite to a so-called polymer substance, and means a concept that includes dimers, trimers, and oligomers in addition to monomers in a narrow sense.
  • the photopolymerizable monomer it is particularly desirable to use a polyfunctional ethylenic monomer having two or more ethylenic double bonds in one molecule.
  • the number of ethylenic double bonds that the polyfunctional ethylenic monomer has is not particularly limited, but is preferably 2 or more, more preferably 4 or more, still more preferably 5 or more, and Preferably it is 8 or less, more preferably 7 or less.
  • the value above the lower limit value tends to result in high sensitivity, and setting the value below the upper limit value tends to improve the solubility in a solvent.
  • the above upper and lower limits can be arbitrarily combined.
  • the number of ethylenic double bonds that the polyfunctional ethylenic monomer has is preferably 2 to 8, more preferably 2 to 7, even more preferably 4 to 7, and particularly preferably 5 to 7.
  • ethylenic compounds include unsaturated carboxylic acids, esters of unsaturated carboxylic acids and monohydroxy compounds, esters of aliphatic polyhydroxy compounds and unsaturated carboxylic acids, and aromatic polyhydroxy compounds and unsaturated carboxylic acids.
  • esters obtained by the esterification reaction between unsaturated carboxylic acids and polyhydric carboxylic acids and polyhydric hydroxy compounds such as the aforementioned aliphatic polyhydroxy compounds and aromatic polyhydroxy compounds, polyisocyanate compounds and (meth)acryloyl
  • Examples include ethylenic compounds having a urethane skeleton that are reacted with a containing hydroxy compound.
  • esters of aliphatic polyhydroxy compounds and unsaturated carboxylic acids include ethylene glycol diacrylate, triethylene glycol diacrylate, trimethylolpropane triacrylate, trimethylolethane triacrylate, pentaerythritol diacrylate, and pentaerythritol triacrylate. , pentaerythritol tetraacrylate, dipentaerythritol tetraacrylate, dipentaerythritol pentaacrylate, dipentaerythritol hexaacrylate, and glycerol acrylate.
  • acrylic acid part of these acrylates can be replaced with methacrylic acid ester, itaconic acid ester, which is replaced with itaconic acid part, crotonic acid ester, which is replaced with crotonic acid part, or maleic acid, which is replaced with maleic acid part.
  • esters include esters.
  • esters of aromatic polyhydroxy compounds and unsaturated carboxylic acids include hydroquinone diacrylate, hydroquinone dimethacrylate, resorcin diacrylate, resorcin dimethacrylate, and pyrogallol triacrylate.
  • the ester obtained by the esterification reaction of an unsaturated carboxylic acid, a polyhydric carboxylic acid, and a polyhydric hydroxy compound is not necessarily a single substance, but may be a mixture.
  • condensates of acrylic acid, phthalic acid and ethylene glycol condensates of acrylic acid, maleic acid and diethylene glycol, condensates of methacrylic acid, terephthalic acid and pentaerythritol, condensates of acrylic acid, adipic acid, butanediol and glycerin.
  • condensates of acrylic acid, phthalic acid and ethylene glycol condensates of acrylic acid, maleic acid and diethylene glycol
  • condensates of methacrylic acid, terephthalic acid and pentaerythritol condensates of acrylic acid, adipic acid, butanediol and glycerin.
  • Examples of the ethylenic compound having a urethane skeleton obtained by reacting a polyisocyanate compound with a (meth)acryloyl group-containing hydroxy compound include aliphatic diisocyanates such as hexamethylene diisocyanate and trimethylhexamethylene diisocyanate; cyclohexane diisocyanate, isophorone diisocyanate, etc.
  • Alicyclic diisocyanates aromatic diisocyanates such as tolylene diisocyanate and diphenylmethane diisocyanate, and 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 3-hydroxy(1,1,1-triacryloyloxymethyl)propane, 3- Examples include reactants with (meth)acryloyl group-containing hydroxy compounds such as hydroxy(1,1,1-trimethacryloyloxymethyl)propane.
  • ethylenic compounds used in the present invention include, for example, acrylamides such as ethylenebisacrylamide; allyl esters such as diallyl phthalate; and vinyl group-containing compounds such as divinyl phthalate.
  • the ethylenic compound may be a monomer having an acid value.
  • the monomer having an acid value is an ester of an aliphatic polyhydroxy compound and an unsaturated carboxylic acid, and the unreacted hydroxy group of the aliphatic polyhydroxy compound is reacted with a non-aromatic carboxylic acid anhydride to form an acid group.
  • Preferred are polyfunctional monomers in which the aliphatic polyhydroxy compound is pentaerythritol and/or dipentaerythritol.
  • One type of these monomers may be used alone, but since it is difficult to use a single compound in production, two or more types may be used in combination. Further, if necessary, a polyfunctional monomer having no acid group and a polyfunctional monomer having an acid group may be used in combination as monomers.
  • the preferred acid value of the polyfunctional monomer having an acid group is 0.1 to 40 mgKOH/g, particularly preferably 5 to 30 mgKOH/g. Setting the value above the lower limit tends to improve development and dissolution characteristics, and setting the value below the upper limit allows for better manufacturing and handling, resulting in improved photopolymerization performance, pixel surface smoothness, etc. It tends to improve curing properties. Therefore, when using two or more types of polyfunctional monomers with different acid groups, or when using polyfunctional monomers that do not have acid groups together, the acid groups as a whole of the polyfunctional monomers should be adjusted so that they fall within the above range. is preferred.
  • more preferable polyfunctional monomers having acid groups include dipentaerythritol hexaacrylate, dipentaerythritol pentaacrylate, and dipentaerythritol pentaacrylate succinate ester commercially available as TO1382 manufactured by Toagosei Co., Ltd. as main components. It is a mixture of This polyfunctional monomer and other polyfunctional monomers can also be used in combination. Furthermore, polyfunctional monomers described in paragraphs [0056] and [0057] of Japanese Patent Application Publication No. 2013-140346 can also be used.
  • the polymerizable monomer described in Japanese Patent Application Publication No. 2013-195971 from the viewpoint of improving the chemical resistance of pixels and the linearity of the edges of pixels, it is preferable to use the polymerizable monomer described in Japanese Patent Application Publication No. 2013-195971. From the viewpoint of achieving both the sensitivity of the coating film and the shortening of the development time, it is preferable to use the polymerizable monomer described in Japanese Patent Application Publication No. 2013-195974.
  • the content of the photopolymerizable monomer (E) is not particularly limited, but is preferably more than 0% by mass, more preferably 5% by mass or more in the total solid content of the colored resin composition. , more preferably 10% by mass or more, even more preferably 15% by mass or more, particularly preferably 20% by mass or more, and preferably 70% by mass or less, more preferably 60% by mass or less, even more preferably 50% by mass. % or less, even more preferably 40% by mass or less, particularly preferably 30% by mass or less.
  • the content ratio of the photopolymerizable monomer (E) in the colored resin composition is preferably more than 0% by mass and 70% by mass or less, more preferably 5 to 60% by mass, and 10% by mass or less, more preferably 5 to 60% by mass, based on the total solid content of the colored resin composition. It is more preferably from 15 to 40% by weight, even more preferably from 15 to 40% by weight, particularly preferably from 20 to 30% by weight.
  • the colored resin composition of the present invention may further contain solid contents other than the above-mentioned components, if necessary.
  • solid contents include dispersants, dispersion aids, surfactants, and adhesion improvers.
  • Dispersant dispersion aid
  • the colored resin composition of the present invention contains a pigment as the colorant (A)
  • it preferably contains a dispersant for the purpose of stably dispersing the pigment.
  • a dispersant it is preferable to use a polymer dispersant because it has excellent dispersion stability over time.
  • polymeric dispersants include urethane dispersants, polyethyleneimine dispersants, polyoxyethylene alkyl ether dispersants, polyoxyethylene glycol diester dispersants, sorbitan aliphatic ester dispersants, and aliphatic modified polyesters. Examples include system dispersants.
  • polymer dispersants examples include trade names such as EFKA (registered trademark, manufactured by BASF), DisperBYK (registered trademark, manufactured by BYK Chemie), DISPARON (registered trademark, manufactured by Kusumoto Kasei Co., Ltd.), and SOLSPERSE (registered trademark, manufactured by Lubricant Chemicals). (manufactured by Sol Co., Ltd.), KP (manufactured by Shin-Etsu Chemical Co., Ltd.), Polyflow (manufactured by Kyoeisha Chemical Co., Ltd.), and the dispersant described in Japanese Patent Application Publication No. 2013-119568.
  • EFKA registered trademark, manufactured by BASF
  • DisperBYK registered trademark, manufactured by BYK Chemie
  • DISPARON registered trademark, manufactured by Kusumoto Kasei Co., Ltd.
  • SOLSPERSE registered trademark, manufactured by Lubricant Chemicals
  • a block copolymer having a functional group containing a nitrogen atom is preferable, and an acrylic block copolymer having a functional group containing a nitrogen atom is more preferable.
  • the block copolymer having a functional group containing a nitrogen atom consists of an A block having a quaternary ammonium base and/or an amino group in the side chain, and a B block having no quaternary ammonium base and amino group.
  • AB block copolymers and BAB block copolymers are preferred.
  • Examples of functional groups containing a nitrogen atom include primary to tertiary amino groups and quaternary ammonium bases. From the viewpoint of dispersibility and storage stability, primary to tertiary amino groups are preferred, and tertiary amino groups are more preferred.
  • the structure of the repeating unit having a tertiary amino group in the block copolymer is not particularly limited, it is preferably a repeating unit represented by the following general formula (d1) from the viewpoint of dispersibility and storage stability.
  • R 1 and R 2 each independently have a hydrogen atom, an alkyl group that may have a substituent, an aryl group that may have a substituent, or a substituent. R 1 and R 2 may be bonded to each other to form a cyclic structure.
  • R 3 is a hydrogen atom or a methyl group.
  • X is a divalent linking group.
  • the number of carbon atoms in the optionally substituted alkyl group in R 1 and R 2 of formula (d1) is not particularly limited, but is preferably 1 or more, and preferably 10 or less, and 6 It is more preferably at most 4, and even more preferably at most 4.
  • the number is preferably 1 to 10, more preferably 1 to 6, and even more preferably 1 to 4.
  • the alkyl group include methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, and octyl group.
  • a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, and a hexyl group are preferable, and a methyl group, an ethyl group, a propyl group, and a butyl group are more preferable.
  • the alkyl group may be linear or branched.
  • the alkyl group may include a cyclic structure such as a cyclohexyl group or a cyclohexylmethyl group.
  • the number of carbon atoms in the optionally substituted aryl group in R 1 and R 2 of formula (d1) is not particularly limited, but is usually 6 or more, preferably 16 or less, and 12 or less. More preferably, it is 8 or less. For example, the number is preferably 6 to 16, more preferably 6 to 12, and even more preferably 6 to 8.
  • aryl group examples include phenyl group, methylphenyl group, ethylphenyl group, dimethylphenyl group, diethylphenyl group, naphthyl group, and anthracenyl group; phenyl group, methylphenyl group, ethylphenyl group, dimethylphenyl group, A diethylphenyl group is preferable, and a phenyl group, a methylphenyl group, and an ethylphenyl group are more preferable.
  • the number of carbon atoms in the optionally substituted aralkyl group in R 1 and R 2 of formula (d1) is not particularly limited, but is preferably 7 or more, and preferably 16 or less, and 12 It is more preferably at most 9, even more preferably at most 9.
  • the number is preferably 7 to 16, more preferably 7 to 12, and even more preferably 7 to 9.
  • the aralkyl group include phenylmethylene group, phenylethylene group, phenylpropylene group, phenylbutylene group, and phenylisopropylene group.
  • a phenylmethylene group, a phenylethylene group, a phenylpropylene group, and a phenylbutylene group are preferred, and a phenylmethylene group and a phenylethylene group are more preferred.
  • R 1 and R 2 are each preferably an alkyl group that may independently have a substituent, and more preferably a methyl group or an ethyl group. .
  • Examples of the substituents that the alkyl group, aralkyl group, and aryl group in formula (d1) may have include a halogen atom, an alkoxy group, a benzoyl group, and a hydroxyl group. From the viewpoint of ease of synthesis, it is preferable that it is unsubstituted.
  • the cyclic structure formed by bonding R 1 and R 2 to each other includes, for example, a 5- to 7-membered nitrogen-containing monocyclic ring or a condensed ring formed by condensing two of these.
  • the nitrogen-containing heterocycle is preferably non-aromatic, and more preferably a saturated ring.
  • the following cyclic structure (IV) can be mentioned, for example.
  • These cyclic structures may further have a substituent.
  • the divalent linking group X is, for example, an alkylene group having 1 to 10 carbon atoms, an arylene group having 6 to 12 carbon atoms, a -CONH-R 13 - group, a -COOR 14 - group , R 13 and R 14 are a single bond, an alkylene group having 1 to 10 carbon atoms, or an ether group (alkyloxyalkyl group) having 2 to 10 carbon atoms, preferably a -COO-R 14 - group. It is.
  • the content ratio of the repeating unit represented by formula (d1) in all repeating units of the block copolymer is preferably 1 mol% or more, more preferably 5 mol% or more, even more preferably 10 mol% or more, and 15 mol%. % or more, even more preferably 20 mol% or more, particularly preferably 25 mol% or more, and preferably 90 mol% or less, more preferably 70 mol% or less, even more preferably 50 mol% or less, and 40 mol% or less. % or less is particularly preferable.
  • the above upper and lower limits can be arbitrarily combined.
  • the content of the repeating unit represented by formula (d1) in all repeating units of the block copolymer is preferably 1 to 90 mol%, more preferably 5 to 90 mol%, and 10 to 70 mol%. It is more preferably 15 to 70 mol%, even more preferably 20 to 50 mol%, and particularly preferably 25 to 40 mol%.
  • the block copolymer preferably has a repeating unit represented by the following general formula (d2) from the viewpoint of increasing the compatibility of the dispersant with a binder component such as a solvent and improving dispersion stability.
  • R 10 is an ethylene group or a propylene group
  • R 11 is an alkyl group which may have a substituent
  • R 12 is a hydrogen atom or a methyl group.
  • n is an integer from 1 to 20.
  • the number of carbon atoms in the optionally substituted alkyl group in R 11 of formula (d2) is not particularly limited, but is preferably 1 or more, more preferably 2 or more, and preferably 10 or less, and 6 or less. More preferably, 4 or less is even more preferable.
  • the above upper and lower limits can be arbitrarily combined.
  • the alkyl group preferably has 1 to 10 carbon atoms, more preferably 1 to 6 carbon atoms, even more preferably 1 to 4 carbon atoms, and particularly preferably 2 to 4 carbon atoms.
  • alkyl group examples include methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, and octyl group.
  • a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, and a hexyl group are preferable, and a methyl group, an ethyl group, a propyl group, and a butyl group are more preferable.
  • the alkyl group may be linear or branched.
  • the alkyl group may include a cyclic structure such as a cyclohexyl group or a cyclohexylmethyl group.
  • alkyl group may have include a halogen atom, an alkoxy group, a benzoyl group, and a hydroxyl group. From the viewpoint of ease of synthesis, it is preferable that it is unsubstituted.
  • n in formula (d2) is preferably 1 or more, more preferably 2 or more, and is preferably 20 or less, more preferably 10 or less, and even more preferably 5 or less. .
  • the above upper and lower limits can be arbitrarily combined.
  • n is preferably 1 to 10, more preferably 2 to 5.
  • the content ratio of the repeating unit represented by formula (d2) in all repeating units of the block copolymer is preferably 1 mol% or more, more preferably 2 mol% or more, even more preferably 4 mol% or more, and The content is preferably 30 mol% or less, more preferably 20 mol% or less, and even more preferably 10 mol% or less.
  • the content of the repeating unit represented by formula (d2) in all repeating units of the block copolymer is preferably 1 to 30 mol%, more preferably 2 to 20 mol%, and 4 to 10 mol%. More preferred.
  • the block copolymer preferably has a repeating unit represented by the following general formula (d3) from the viewpoint of increasing the compatibility of the dispersant with a binder component such as a solvent and improving dispersion stability.
  • R 8 is an alkyl group that may have a substituent, an aryl group that may have a substituent, or an aralkyl group that may have a substituent.
  • R 9 is a hydrogen atom or a methyl group.
  • the number of carbon atoms in the optionally substituted alkyl group in R 8 of formula (d3) is not particularly limited, but is preferably 1 or more, preferably 10 or less, and more preferably 6 or less.
  • 1 to 10 is preferable, and 1 to 6 is more preferable.
  • alkyl group include methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, and octyl group.
  • a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, and a hexyl group are preferable, and a methyl group, an ethyl group, a propyl group, and a butyl group are more preferable.
  • the alkyl group may be linear or branched.
  • the alkyl group may include a cyclic structure such as a cyclohexyl group or a cyclohexylmethyl group.
  • the number of carbon atoms in the optionally substituted aryl group in R 8 of formula (d3) is not particularly limited, but is preferably 6 or more, preferably 16 or less, and more preferably 12 or less.
  • 6 to 16 is preferable, and 6 to 12 is more preferable.
  • the aryl group include phenyl group, methylphenyl group, ethylphenyl group, dimethylphenyl group, diethylphenyl group, naphthyl group, and anthracenyl group.
  • a phenyl group, a methylphenyl group, an ethylphenyl group, a dimethylphenyl group, and a diethylphenyl group are preferable, and a phenyl group, a methylphenyl group, and an ethylphenyl group are more preferable.
  • the number of carbon atoms in the optionally substituted aralkyl group in R 8 of formula (d3) is not particularly limited, but is preferably 7 or more, preferably 16 or less, and more preferably 12 or less.
  • 7 to 16 is preferable, and 7 to 12 is more preferable.
  • the aralkyl group include phenylmethylene group, phenylethylene group, phenylpropylene group, phenylbutylene group, and phenylisopropylene group.
  • a phenylmethylene group, a phenylethylene group, a phenylpropylene group, and a phenylbutylene group are preferred, and a phenylmethylene group and a phenylethylene group are more preferred.
  • R 8 is preferably an alkyl group or an aralkyl group, and more preferably a methyl group, an ethyl group, or a phenylmethylene group.
  • substituents that the alkyl group in R 8 may have include a halogen atom and an alkoxy group.
  • substituents that the aryl group or aralkyl group may have include a chain alkyl group, a halogen atom, and an alkoxy group.
  • the chain alkyl group represented by R 8 includes both straight chain and branched chain alkyl groups.
  • the content of the repeating unit represented by formula (d3) in all repeating units of the block copolymer is preferably 30 mol% or more, more preferably 40 mol% or more, even more preferably 50 mol% or more, and It is preferably 80 mol% or less, more preferably 70 mol% or less. Within the above range, it tends to be possible to achieve both dispersion stability and high brightness. The above upper and lower limits can be arbitrarily combined.
  • the content of the repeating unit represented by formula (d3) in all repeating units of the block copolymer is preferably 30 to 80 mol%, more preferably 40 to 80 mol%, and 50 to 70 mol%. More preferred.
  • the block copolymer may have repeating units other than the repeating unit represented by formula (d1), the repeating unit represented by formula (d2), and the repeating unit represented by formula (d3).
  • repeating units include styrene monomers such as styrene and ⁇ -methylstyrene; (meth)acrylate monomers such as (meth)acrylic acid chloride; (meth)acrylamide, N- Examples include repeating units derived from (meth)acrylamide monomers such as methylol acrylamide; vinyl acetate; acrylonitrile; allyl glycidyl ether, crotonic acid glycidyl ether; and N-methacryloylmorpholine.
  • block copolymer having an A block having a repeating unit represented by formula (d1) and a B block not having a repeating unit represented by formula (d1). It is preferable.
  • the block copolymer is preferably an AB block copolymer or a BAB block copolymer. It is more preferable that the B block has a repeating unit represented by formula (d2) and/or a repeating unit represented by formula (d3).
  • Repeating units other than the repeating unit represented by formula (d1) may be contained in the A block.
  • Examples of such repeating units include the above-mentioned repeating units derived from (meth)acrylic acid esters.
  • the content of repeating units other than the repeating unit represented by formula (d1) in the A block is preferably 0 to 50 mol%, more preferably 0 to 20 mol%, and even more preferably 0 mol%.
  • Repeating units other than the repeating unit represented by formula (d2) and the repeating unit represented by formula (d3) may be contained in the B block.
  • Examples of such repeating units include styrene monomers such as styrene and ⁇ -methylstyrene; (meth)acrylate monomers such as (meth)acrylic acid chloride; (meth)acrylamide, N- Examples include repeating units derived from (meth)acrylamide monomers such as methylol acrylamide; vinyl acetate; acrylonitrile; allyl glycidyl ether, crotonic acid glycidyl ether; and N-methacryloylmorpholine.
  • the content of repeating units other than the repeating unit represented by formula (d2) and the repeating unit represented by formula (d3) in block B is preferably 0 to 50 mol%, more preferably 0 to 20 mol%. , more preferably 0 mol %.
  • the acid value of the block copolymer is preferably lower from the viewpoint of dispersibility, particularly preferably 0 mgKOH/g.
  • the acid value represents the number of mg of KOH required to neutralize 1 g of solid content of the dispersant.
  • the amine value of the block copolymer is preferably 30 mgKOH/g or more, more preferably 50 mgKOH/g or more, even more preferably 70 mgKOH/g or more, even more preferably 90 mgKOH/g or more, from the viewpoint of dispersibility and developability. It is particularly preferably 100 mgKOH/g or more, particularly preferably 105 mgKOH/g or more, and preferably 150 mgKOH/g or less, more preferably 130 mgKOH/g or less. The above upper and lower limits can be arbitrarily combined.
  • the amine value herein refers to the amine value in terms of effective solid content, and is a value expressed by the base amount and the equivalent mass of KOH per 1 g of solid content of the dispersant.
  • the weight average molecular weight of the block copolymer is preferably 1,000 to 30,000. When it is within the above range, the dispersion stability becomes good and there is a tendency that dry foreign matter is less likely to be generated during coating by a slit nozzle method.
  • Block copolymers can be produced by known methods. For example, it can be produced by living polymerization of monomers into which each of the repeating units described above is introduced.
  • living polymerization method for example, Japanese Unexamined Patent Publication No. 9-62002, Japanese Unexamined Patent Publication No. 2002-31713, and P. Lutz, P. Masson et al, Polym. Bull. 12, 79 (1984), B. C. Anderson, G. D. Andrews et al, Macromolecules, 14, 1601 (1981), K. Hatada, K. Ute, et al, Polym. J. 17,977 (1985), K. Hatada, K. Ute, et al, Polym. J.
  • the content of the dispersant is not particularly limited, but is preferably 0.001% by mass or more, and 0.01% by mass in the total solid content of the colored resin composition.
  • the above is more preferable, 0.1% by mass or more is still more preferable, 1% by weight or more is even more preferable, 2% by weight or more is especially preferable, 25% by weight or less is preferable, 20% by weight or less is more preferable, 15 It is more preferably at most 10% by mass, particularly preferably at most 10% by mass.
  • the content of the dispersant is preferably 0.001 to 25% by mass, more preferably 0.01 to 25% by mass in the total solid content of the colored resin composition. , more preferably 0.1 to 20% by weight, even more preferably 1 to 15% by weight, particularly preferably 2 to 10% by weight.
  • the content ratio of the dispersant to the pigment is not particularly limited, but is preferably 0.5 parts by mass or more based on 100 parts by mass of the pigment. More preferably 5 parts by mass or more, still more preferably 10 parts by mass or more, even more preferably 15 parts by mass or more, particularly preferably 20 parts by mass or more, and preferably 70 parts by mass or less, more preferably 50 parts by mass.
  • the amount is preferably 40 parts by mass or less, particularly preferably 30 parts by mass or less.
  • the content of the dispersant is preferably 0.5 to 70 parts by mass, more preferably 5 to 70 parts by mass, and 10 to 100 parts by mass. It is more preferably from 15 to 40 parts by weight, even more preferably from 15 to 40 parts by weight, and particularly preferably from 20 to 30 parts by weight.
  • the colored resin composition of the present invention may contain, for example, a pigment derivative as a dispersion aid in order to improve the dispersibility and dispersion stability of the pigment.
  • a pigment derivative include azo, phthalocyanine, quinacridone, benzimidazolone, quinophthalone, isoindolinone, isoindoline, dioxazine, anthraquinone, indanthrene, and perylene.
  • examples include derivatives of perinone, diketopyrrolopyrrole, and dioxazine pigments.
  • Substituents for pigment derivatives include, for example, sulfonic acid groups, sulfonamide groups and quaternary salts thereof, phthalimidomethyl groups, dialkylaminoalkyl groups, hydroxyl groups, carboxy groups, and amide groups directly on the pigment skeleton, or alkyl groups and aryl groups. , a heterocyclic group, etc., preferably a sulfonamide group, a quaternary salt thereof, or a sulfonic acid group, more preferably a sulfonic acid group. Furthermore, a plurality of these substituents may be substituted on one pigment skeleton, or a mixture of compounds having different numbers of substitutions may be used.
  • pigment derivatives include sulfonic acid derivatives of azo pigments, sulfonic acid derivatives of phthalocyanine pigments, sulfonic acid derivatives of quinophthalone pigments, sulfonic acid derivatives of isoindoline pigments, sulfonic acid derivatives of anthraquinone pigments, sulfonic acid derivatives of quinacridone pigments, Examples include sulfonic acid derivatives of diketopyrrolopyrrole pigments and sulfonic acid derivatives of dioxazine pigments.
  • the colored resin composition of the present invention may contain a surfactant, and examples of the surfactant include anionic, cationic, nonionic, amphoteric surfactants, etc. Although various surfactants can be used, nonionic surfactants are preferred since they are less likely to adversely affect various properties.
  • the content of the surfactant is not particularly limited, but is preferably 0.001% by mass or more, more preferably 0.001% by mass or more in the total solid content of the colored resin composition.
  • the content of the surfactant is preferably 0.001 to 10% by mass, more preferably 0.01 to 1% by mass, and more preferably 0.05 to 0.5% by mass based on the total solid content of the colored resin composition. is more preferred, and 0.1 to 0.3% by mass is particularly preferred.
  • the colored resin composition of the present invention may contain an adhesion improver in order to improve the adhesion to the substrate.
  • adhesion improvers include silane coupling agents and titanium coupling agents. Silane coupling agents are preferred. Examples of the silane coupling agent include KBM-402, KBM-403, KBM-502, KBM-5103, KBE-9007, X-12-1048, X-12-1050 (manufactured by Shin-Etsu Silicone Co., Ltd.), and Z-6040. , Z-6043, and Z-6062 (manufactured by Dow Corning Toray Industries). One type of silane coupling agent may be used alone, or two or more types may be used in combination in any combination and ratio.
  • the colored resin composition of the present invention may contain an adhesion improver other than the silane coupling agent. Examples include phosphoric acid adhesion improvers and other adhesion improvers.
  • (meth)acryloyloxy group-containing phosphates are preferred.
  • Phosphoric acid-based adhesion improvers represented by the following general formulas (g1), (g2), and (g3) are preferred.
  • R 51 each independently represents a hydrogen atom or a methyl group.
  • l and l' each independently represent an integer of 1 to 10, and m each independently represents 1, 2 or 3.
  • Other adhesion improvers include, for example, TEGO (registered trademark) Add Bond LTH (manufactured by Evonik). These phosphoric acid-based adhesion improvers and other adhesives may be used alone or in combination of two or more.
  • the colored resin composition of the present invention contains an adhesion improver
  • its content is not particularly limited, but it is preferably 0.1% by mass or more, and 0.2% by mass or more in the total solid content of the colored resin composition. is more preferably 0.3% by mass or more, further preferably 0.4% by mass or more, further preferably 3% by mass or less, more preferably 2% by mass or less, even more preferably 1.5% by mass or less. , 1% by mass or less is particularly preferred.
  • the content is equal to or more than the lower limit, patterning properties tend to be improved and pattern adhesion under high humidity conditions tends to be improved, and when the content is equal to or less than the upper limit, the generation of residue tends to be suppressed.
  • the above upper and lower limits can be arbitrarily combined.
  • the content thereof is preferably 0.1 to 3% by mass, more preferably 0.2 to 2% by mass, and 0.3 to 2% by mass based on the total solid content. More preferably 1.5% by weight, particularly preferably 0.4 to 1% by weight.
  • (A) When preparing a colorant containing a pigment, first weigh the pigment, solvent, and dispersant in predetermined amounts, and in a dispersion treatment step, disperse the colorant containing the pigment to prepare a pigment dispersion. .
  • a paint conditioner, sand grinder, ball mill, roll mill, stone mill, jet mill, homogenizer, etc. can be used. By performing this dispersion treatment, the colorant is made into fine particles, so that the coating properties of the colored resin composition are improved, and the transmittance of pixels on the color filter substrate of the product is improved.
  • a dispersion aid or the like When dispersing the pigment, as mentioned above, it is preferable to use a dispersion aid or the like as appropriate.
  • a dispersion aid or the like When performing the dispersion treatment using a sand grinder, it is preferable to use glass beads or zirconia beads with a diameter of 0.1 to several mm.
  • the temperature during the dispersion treatment is preferably set in a range of 0°C or higher, more preferably room temperature or higher, and preferably 100°C or lower, more preferably 80°C or lower. Note that the dispersion time may be adjusted as appropriate, since the appropriate time varies depending on the composition of the pigment dispersion liquid, the size of the sand grinder, and the like.
  • a solvent, an alkali-soluble resin, a photopolymerization initiator, a photopolymerizable monomer, and if necessary, components other than those mentioned above are mixed into the pigment dispersion obtained by the above dispersion treatment to form a uniform dispersion solution.
  • fine dust may be mixed in, so it is preferable to filter the obtained pigment dispersion liquid using a filter or the like.
  • the cured product of the present invention is obtained by curing the colored resin composition of the present invention.
  • the color filter of the present invention includes pixels created using the colored resin composition of the present invention. An example of a method for manufacturing a color filter will be described below.
  • Substrate (support) The substrate to which the colored resin composition of the present invention is applied is preferably a transparent substrate, and its material is not particularly limited as long as it is transparent and has appropriate strength.
  • Materials include, for example, polyester resins such as polyethylene terephthalate, polyolefin resins such as polypropylene and polyethylene, thermoplastic resin sheets such as polycarbonate, polymethyl methacrylate, and polysulfone, epoxy resins, unsaturated polyester resins, and poly(meth)acrylics.
  • thermosetting resin sheets such as resin based resins, and various types of glasses. Among these, glass or heat-resistant resin is preferred from the viewpoint of heat resistance.
  • the substrate to which the colored resin composition is applied and the substrate provided with the black matrix described below may be treated with corona discharge treatment, ozone treatment, a silane coupling agent, or a urethane-based
  • a thin film formation process using various resins such as resin may also be performed.
  • the thickness of the substrate is preferably 0.05 mm or more, more preferably 0.1 mm or more, and preferably 10 mm or less, more preferably 7 mm or less. For example, it is preferably 0.05 to 10 mm, more preferably 0.1 to 7 mm.
  • the film thickness is preferably 0.01 ⁇ m or more, more preferably 0.05 ⁇ m or more, and preferably 10 ⁇ m or less, more preferably 5 ⁇ m or less.
  • it is preferably 0.01 to 10 ⁇ m, more preferably 0.05 to 5 ⁇ m.
  • the color filter of the present invention can be manufactured by providing a black matrix on a transparent substrate and further forming usually red, green, and blue pixel images.
  • the colored resin composition of the present invention is preferably used as a coating liquid for forming green pixels (resist pattern) among red, green, and blue pixels.
  • a green pixel (resist pattern) forming coating liquid on a resin black matrix forming surface formed on a transparent substrate, or on a metal black matrix forming surface formed using a chromium compound or other light-shielding metal material, A pixel image is formed by performing coating, heating drying, image exposure, development, and baking.
  • the black matrix is formed on a substrate using a light-shielding metal thin film or a colored resin composition for black matrix.
  • a light-shielding metal material for example, metal chromium, chromium compounds such as chromium oxide and chromium nitride, and nickel and tungsten alloys are used, and a plurality of layers of these may be used.
  • a metal light-shielding film is generally formed by a sputtering method. After forming a desired film pattern using a positive photoresist, for chromium, a mixture of ceric ammonium nitrate and perchloric acid and/or nitric acid is used. Other materials are etched using an etching solution appropriate for the material, and finally the positive photoresist is removed using a special remover to form a black matrix. can.
  • a thin film of these metals or metal/metal oxides is formed on a transparent substrate by vapor deposition or sputtering.
  • the coating film is exposed and developed using a photomask having a repeating pattern such as a stripe, mosaic, or triangle to form a resist image.
  • this coating film can be subjected to an etching process to form a black matrix.
  • a colored resin composition containing a black colorant is used to form a black matrix.
  • black colorants such as carbon black, graphite, iron black, aniline black, cyanine black, titanium black, etc., or red, green, blue, etc. appropriately selected from inorganic or organic pigments and dyes.
  • a black matrix can be formed using a colored resin composition containing a mixed black coloring material in a manner similar to the method for forming red, green, and blue pixels described below.
  • the pixel forming step of forming a pixel includes a coating step of coating the colored resin composition on the substrate and a prebaking step of prebaking the coating film obtained in the coating step.
  • a coating process of coating a colored resin composition of one color among red, green, and blue on a substrate provided with a black matrix for example, a coating process of coating a colored resin composition of one color among red, green, and blue on a substrate provided with a black matrix, a pre-baking process of drying (pre-baking) the obtained coating film, and a coating process.
  • a photomask is placed on the film, and pixels are formed by thermal curing or photocuring as required, through an exposure step of image exposure through this photomask, and a development step.
  • a color filter image can be formed by performing these steps for each of the three colored resin compositions of red, green, and blue.
  • the colored resin composition of the present invention is preferably used as a composition for forming a green or blue pixel (resist pattern) among red, green, and blue pixels, and can be used as a composition for forming a green pixel. More preferred. For example, on a resin black matrix forming surface formed on a substrate using a green or blue pixel (resist pattern) forming composition, or on a metal black matrix forming surface formed using a chromium compound or other light-shielding metal material. Pixels are formed thereon by performing coating, drying (pre-baking), image exposure, development, and thermosetting or photocuring.
  • the colored resin composition can be applied onto the substrate by, for example, a spinner method, a wire bar method, a flow coating method, a die coating method, a roll coating method, or a spray coating method.
  • the die coating method significantly reduces the amount of colored resin composition used, has no influence from the mist that adheres when using the spin coating method, and furthermore suppresses the generation of foreign matter. , is preferable from a comprehensive viewpoint.
  • the thickness of the coating film after drying is preferably 0.2 ⁇ m or more, more preferably 0.5 ⁇ m or more, even more preferably 0.8 ⁇ m or more, and preferably 20 ⁇ m or less, more preferably 10 ⁇ m.
  • the thickness is more preferably 5 ⁇ m or less.
  • the thickness is preferably 0.2 to 20 ⁇ m, more preferably 0.5 to 10 ⁇ m, and even more preferably 0.8 to 5 ⁇ m.
  • Pre-bake step The coating film obtained in the coating step is preferably dried (pre-bake) by a drying method using a hot plate, an IR oven, or a convection oven. After pre-drying, it is preferable to heat again and pre-bake.
  • the pre-drying conditions can be appropriately selected depending on the type of the solvent component, the performance of the dryer used, and the like.
  • the drying temperature and drying time are selected depending on the type of solvent component, the performance of the dryer used, etc., but specifically, the drying temperature is preferably 40°C or higher, more preferably 50°C or higher, and The temperature is preferably 80° C. or lower, more preferably 70° C. or lower, and the drying time is preferably 15 seconds or more, more preferably 30 seconds or more, and preferably 5 minutes or less, more preferably 3 minutes or less.
  • the temperature conditions for pre-baking are preferably higher than the pre-drying temperature.
  • the temperature is 80°C or higher, preferably 90°C or higher, particularly preferably 100°C or higher, and preferably 200°C or lower, more preferably 160°C or lower, particularly preferably 130°C or lower.
  • Setting the amount above the lower limit tends to increase the dissolution rate, while setting it below the upper limit tends to cause the binder resin to decompose, induce thermal polymerization, and cause poor development.
  • the above upper and lower limits can be arbitrarily combined; for example, the prebaking temperature is preferably 80 to 200°C, more preferably 90 to 130°C, particularly preferably 100 to 130°C.
  • the drying time for pre-bake depends on the heating temperature, but is preferably 10 seconds or more, more preferably 15 seconds or more, and preferably 10 minutes or less, more preferably 5 minutes or less.
  • Exposure Step In the pixel formation step, it is preferable to have an exposure step after the pre-baking step.
  • the exposure step is performed by overlaying a negative matrix pattern on the coating film obtained through the pre-baking step and irradiating it with an ultraviolet or visible light source through this mask pattern.
  • exposure may be performed after forming an oxygen barrier layer such as a polyvinyl alcohol layer on the photopolymerizable layer.
  • the light source used for the above exposure is not particularly limited.
  • Examples of light sources include lamp light sources such as xenon lamps, halogen lamps, tungsten lamps, high-pressure mercury lamps, ultra-high-pressure mercury lamps, metal halide lamps, medium-pressure mercury lamps, low-pressure mercury lamps, carbon arcs, fluorescent lamps, argon ion lasers, YAG lasers, etc.
  • Laser light sources include excimer lasers, nitrogen lasers, helium cadmium lasers, and semiconductor lasers.
  • An optical filter can also be used when irradiating light with a specific wavelength.
  • Developing Step In the pixel forming step, it is preferable to include a developing step after the exposure step. After the coating film using the colored resin composition of the present invention is exposed to light in the above exposure step, it is subjected to a development step in which development is performed using an aqueous solution containing a surfactant and an alkaline compound. can be manufactured by forming an image on it.
  • This aqueous solution may further contain an organic solvent, a buffer, a complexing agent, a dye or a pigment.
  • alkaline compounds include sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, sodium silicate, potassium silicate, sodium metasilicate, sodium phosphate, and phosphorus.
  • Inorganic alkaline compounds such as acid potassium, sodium hydrogen phosphate, potassium hydrogen phosphate, sodium dihydrogen phosphate, potassium dihydrogen phosphate, ammonium hydroxide, mono-, di- or triethanolamine, mono-, di- or trimethylamine, mono-, di- or triethylamine, mono- or di-isopropylamine, n-butylamine, mono-, di- or triisopropanolamine, ethyleneimine, ethylenediimine, tetramethylammonium hydroxide (TMAH), choline, etc.
  • Examples include organic alkaline compounds. These alkaline compounds may be used alone or in combination of two or more.
  • surfactants include nonionic surfactants such as polyoxyethylene alkyl ethers, polyoxyethylene alkylaryl ethers, polyoxyethylene alkyl esters, sorbitan alkyl esters, and monoglyceride alkyl esters, and alkylbenzene sulfonic acids.
  • nonionic surfactants such as polyoxyethylene alkyl ethers, polyoxyethylene alkylaryl ethers, polyoxyethylene alkyl esters, sorbitan alkyl esters, and monoglyceride alkyl esters, and alkylbenzene sulfonic acids.
  • anionic surfactants such as salts, alkylnaphthalene sulfonates, alkyl sulfates, alkyl sulfonates, and sulfosuccinic acid ester salts
  • amphoteric surfactants such as alkyl betaines and amino acids.
  • organic solvent examples include isopropyl alcohol, benzyl alcohol, ethyl cellosolve, butyl cellosolve, phenyl cellosolve, propylene glycol, and diacetone alcohol.
  • Organic solvents can be used in combination with aqueous solutions.
  • the development temperature is preferably 10°C or higher, more preferably 15°C or higher, even more preferably 20°C or higher, and preferably 50°C or lower, more preferably 45°C or lower, More preferably, the temperature is 40°C or lower.
  • the temperature is preferably 10 to 50°C, more preferably 15 to 45°C, and even more preferably 20 to 40°C.
  • the developing method can be any method such as an immersion developing method, a spray developing method, a brush developing method, an ultrasonic developing method, or the like.
  • thermosetting Process In the pixel forming process, it is also preferable to include a thermosetting process after the development process.
  • the heat curing conditions in the heat curing process are such that the temperature is preferably 100°C or higher, more preferably 150°C or higher, and preferably 280°C or lower, more preferably 250°C or lower, and the time is preferably 5 minutes. The duration is preferably 60 minutes or less.
  • the formation of one color patterning pixel is completed.
  • a color filter can be manufactured. Note that the order of patterning the four colors is not limited to the above order.
  • the color filter of the present invention can be used as a part of parts of color displays, liquid crystal display devices, etc. by forming transparent electrodes such as ITO on the image as it is.
  • transparent electrodes such as ITO
  • a top coat layer of polyamide, polyimide, or the like may be provided on the image, if necessary.
  • IPS mode planar alignment drive system
  • a transparent electrode may not be formed.
  • Image display device panel
  • the image display device according to the present invention has a color filter manufactured by the manufacturing method according to the present invention.
  • a liquid crystal display device and an organic EL display device will be described in detail as image display devices.
  • [4-1] Liquid Crystal Display Device A method for manufacturing a liquid crystal display device of the present invention will be described.
  • an alignment film is usually formed on the color filter produced by the manufacturing method of the present invention, and after spacers are sprinkled on the alignment film, the liquid crystal display device is bonded to a counter substrate to form a liquid crystal cell. , Inject liquid crystal into the formed liquid crystal cell and connect it to the counter electrode to complete the process.
  • the alignment film is preferably a resin film such as polyimide. Gravure printing and/or flexographic printing are usually used to form the alignment film, and the thickness of the alignment film is several tens of nanometers. After the alignment film is hardened by thermal baking, the surface is treated by irradiation with ultraviolet rays or treatment with a rubbing cloth to obtain a surface condition that allows adjustment of the tilt of the liquid crystal.
  • the size of the spacer is determined according to the gap between the spacer and the opposing substrate, and a size of 2 to 8 ⁇ m is usually suitable. It is also possible to form a photo spacer (PS) of a transparent resin film on the color filter substrate by photolithography and use this instead of the spacer.
  • PS photo spacer
  • As the counter substrate an array substrate is usually used, and a TFT (thin film transistor) substrate is particularly suitable.
  • the bonding gap with the counter substrate varies depending on the use of the liquid crystal display device, but is preferably selected in the range of 2 ⁇ m or more and 8 ⁇ m or less.
  • a sealing material such as epoxy resin.
  • the sealing material is cured by UV irradiation and/or heating, and the periphery of the liquid crystal cell is sealed.
  • the liquid crystal cell whose periphery is sealed is cut into panel units, the pressure is reduced in a vacuum chamber, the liquid crystal injection port is immersed in the liquid crystal, and the liquid crystal is injected into the liquid crystal cell by leaking the inside of the chamber. .
  • the degree of reduced pressure in the liquid crystal cell is preferably 1 x 10 -2 Pa or less, more preferably 1 x 10 -3 or less, and preferably 1 x 10 -7 Pa or more, more preferably 1 x 10 -6 Pa or more. is within the range of For example, it is preferably 1 ⁇ 10 -7 to 1 ⁇ 10 -2 Pa, more preferably 1 ⁇ 10 -6 to 1 ⁇ 10 -3 Pa. Further, it is preferable to heat the liquid crystal cell when the pressure is reduced, and the heating temperature is preferably 30°C or higher, more preferably 50°C or higher, and preferably 100°C or lower, more preferably 90°C or lower. For example, the temperature is preferably 30 to 100°C, more preferably 50 to 90°C.
  • the temperature is preferably kept at a reduced pressure for at least 10 minutes and at most 60 minutes, and then immersed in the liquid crystal.
  • a liquid crystal display device (panel) is completed by curing the liquid crystal injection port of the liquid crystal cell into which the liquid crystal is injected and sealing it with a UV curing resin.
  • the type of liquid crystal is not particularly limited, and may be any conventionally known liquid crystal such as aromatic, aliphatic, polycyclic compounds, lyotropic liquid crystal, thermotropic liquid crystal, etc. Nematic liquid crystals, smectic liquid crystals, cholesteric liquid crystals, and the like are known as thermotropic liquid crystals, but any of them may be used.
  • Organic EL display device When producing an organic EL display device having a color filter produced by the manufacturing method of the present invention, for example, as shown in FIG. A multicolor organic EL device is manufactured by laminating an organic light emitter 500 via an organic protective layer 30 and an inorganic oxide film 40 on a blue color filter in which pixels 20 are formed using the composition.
  • the organic light emitter 500 can be laminated by sequentially forming a transparent anode 50, a hole injection layer 51, a hole transport layer 52, a light emitting layer 53, an electron injection layer 54, and a cathode 55 on the upper surface of the color filter. , a method of bonding an organic light emitter 500 formed on a separate substrate onto the inorganic oxide film 40, and the like.
  • the organic EL element 100 manufactured in this manner is applicable to both passive drive type organic EL display devices and active drive type organic EL display devices.
  • ⁇ Phthalocyanine compound A> A phthalocyanine compound A having the following chemical structure, which was synthesized based on Example 30 of Japanese Patent Publication No. 05-345861, was used.
  • Et in the formula represents ethyl
  • the amine value is 120 mgKOH/g and the acid value is less than 1 mgKOH/g.
  • the content of repeating units represented by the following formulas (1a), (2a), (3a), (4a), and (5a) in all repeating units is less than 1 mol%, 34.5 mol%, and 6 mol%, respectively. .9 mol%, 13.8 mol%, and 6.9 mol%.
  • F-513M tricyclodecane skeleton
  • the inside of the reaction vessel was replaced with air, and 0.7 parts by mass of trisdimethylaminomethylphenol and 0.12 parts by mass of hydroquinone were added to 67 parts by mass of acrylic acid, and the reaction was continued at 120° C. for 6 hours. Thereafter, 15 parts by mass of tetrahydrophthalic anhydride (THPA) and 0.7 parts by mass of triethylamine were added, and the mixture was reacted at 120° C. for 3.5 hours.
  • THPA tetrahydrophthalic anhydride
  • the weight average molecular weight Mw of the thus obtained alkali-soluble resin B measured by GPC in terms of polystyrene was about 9000, the acid value was 24 mgKOH/g, and the double bond equivalent was 260 g/mol.
  • F-513M tricyclodecane skeleton
  • alkali-soluble resin C which has an acid value of 89 mgKOH/g, has the highest solubility.
  • alkali-soluble resin A and alkali-soluble resin B which have low and comparable acid values, alkali-soluble resin B, which contains more glycidyl methacrylate with high hydrophilicity, has higher solubility.
  • ⁇ Alkali-soluble resin D> Prepare a separable flask equipped with a cooling tube as a reaction tank, charge it with 400 parts by mass of propylene glycol monomethyl ether acetate, replace it with nitrogen, and heat it in an oil bath while stirring to raise the temperature of the reaction tank to 90°C. did.
  • an alkali-soluble resin D having a polystyrene-equivalent weight average molecular weight Mw of 9000, an acid value of 101 mgKOH/g, and a double bond equivalent of 550 g/mol as measured by GPC was obtained.
  • Green dye dispersion B was prepared in the same manner as green dye dispersion A, except that phthalocyanine compound A was changed to phthalocyanine compound B and each raw material was blended as shown in Table 1.
  • Me in the formula represents methyl.
  • Colored resin compositions 1 to 8 were prepared by mixing the components listed in Table 2 at the solid content ratios listed.
  • colored resin compositions 1 to 8 propylene glycol monomethyl ether acetate (PGMEA) and propylene glycol monomethyl ether (PGME) were used as solvents so that the total solid content of the colored resin composition was 15% by mass.
  • the mixing ratio (mass ratio) of PGMEA/PGME in the colored resin composition obtained was 90/10.
  • the obtained colored resin composition was spin-coated onto a 50 mm square, 0.7 mm thick glass substrate (manufactured by AGC, AN100) so that the film thickness after thermosetting (baking) was 2.0 ⁇ m. After coating and drying under reduced pressure, it was prebaked on a hot plate at the temperature listed in Table 3 for 90 seconds to produce a colored substrate. Further, after drying under reduced pressure in the same manner, instead of pre-baking, heat curing treatment was performed at 230° C. for 20 minutes in a clean oven to create a colored substrate after baking.
  • the spectral transmission spectrum was measured every 1 nm from wavelength 380 nm to 780 nm using a spectrophotometer U-3310 manufactured by Hitachi, Ltd., and was converted into an absorption spectrum.
  • the value of absorbance at wavelength n is defined as A n
  • the similar value of the colored substrate after firing is defined as A 0 n .
  • the degree of spectral change was defined by the following formula as an index of how much the absorption spectrum of the colored substrate differs from that of the colored substrate after firing. Table 3 shows the calculated degree of spectral change. The smaller the degree of spectral change in the following formula, the more the phthalocyanine compound (1) forms aggregates during pre-baking and is closer to the state after firing to completely form aggregates.
  • the obtained colored resin composition was spin-coated onto a 50 mm square, 0.7 mm thick glass substrate (manufactured by AGC, AN100) so that the film thickness after thermosetting (baking) was 2.0 ⁇ m. and prebaked at 100°C for 90 seconds.
  • exposure treatment was performed using a 2 kW high-pressure mercury lamp at an exposure amount of 40 mJ/cm 2 and an illuminance of 30 mW/cm 2 through an exposure mask having a plurality of linear openings with a width of 1 to 50 ⁇ m.
  • a development process was performed using a 0.04% by mass aqueous potassium hydroxide solution at a developer temperature of 23° C. for 60 seconds.
  • the obtained colored resin composition was spin-coated onto a 50 mm square, 0.7 mm thick glass substrate (manufactured by AGC, AN100) so that the film thickness after thermosetting (baking) was 2.0 ⁇ m. and prebaked at 100°C for 90 seconds.
  • an exposure treatment was performed using a 2kW high-pressure mercury lamp at an exposure amount of 40 mJ/cm 2 and an illuminance of 30 mW/cm 2 , and a heat curing treatment was performed at 230° C. for 20 minutes to prepare a substrate for contrast evaluation.
  • ⁇ Residue evaluation> A patterned substrate was prepared in the same manner as in the adhesion evaluation, and a pattern corresponding to a linear opening with a width of 50 ⁇ m was observed using an optical microscope. If no residue was observed inside the opening, the rating was A. If some residue was observed in the opening but there was no practical problem, it was rated B. If any residue was observed in the opening, it was rated C. The evaluation results are shown in Table 4.
  • the colorant contains a colorant other than the phthalocyanine compound (1), which inhibits the association between the phthalocyanine compounds (1) due to ⁇ - ⁇ stacking with the aromatic ring contained in its structure.
  • the dissolution rate also showed a similar tendency, and as the content ratio of the phthalocyanine compound (1) in the colorant (A) increased, the dissolution rate remained constant when the pre-bake temperature was gradually raised from 80°C. The pre-bake temperature becomes lower. This is because the phthalocyanine compound (1) forms an aggregate, and the alkali-soluble resin (C) contained in the colored resin composition forms a complex around it, and the phthalocyanine compound (1) forms an aggregate.
  • the dissolution rate was faster than when it was used alone.
  • the development time can be shortened.
  • the dissolution rate can be increased with a lower pre-bake temperature, which can contribute to improving the production efficiency of color filters and the like.
  • the solubility of the alkali-soluble resin (C) can be made relatively low, so it is thought that the pattern is less likely to peel off during development and the adhesion is improved.

Landscapes

  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Optics & Photonics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Materials Engineering (AREA)
  • Nonlinear Science (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Structural Engineering (AREA)
  • Architecture (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Mathematical Physics (AREA)
  • Theoretical Computer Science (AREA)
  • Optical Filters (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polymerisation Methods In General (AREA)
PCT/JP2023/010072 2022-03-16 2023-03-15 着色樹脂組成物、硬化物、カラーフィルタ及び画像表示装置 Ceased WO2023176882A1 (ja)

Priority Applications (3)

Application Number Priority Date Filing Date Title
KR1020247029184A KR20240163067A (ko) 2022-03-16 2023-03-15 착색 수지 조성물, 경화물, 컬러 필터 및 화상 표시 장치
JP2024508220A JPWO2023176882A1 (https=) 2022-03-16 2023-03-15
CN202380026537.2A CN118843831A (zh) 2022-03-16 2023-03-15 着色树脂组合物、固化物、滤色器和图像显示装置

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2022-040964 2022-03-16
JP2022040964 2022-03-16

Publications (1)

Publication Number Publication Date
WO2023176882A1 true WO2023176882A1 (ja) 2023-09-21

Family

ID=88023913

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2023/010072 Ceased WO2023176882A1 (ja) 2022-03-16 2023-03-15 着色樹脂組成物、硬化物、カラーフィルタ及び画像表示装置

Country Status (5)

Country Link
JP (1) JPWO2023176882A1 (https=)
KR (1) KR20240163067A (https=)
CN (1) CN118843831A (https=)
TW (1) TW202402820A (https=)
WO (1) WO2023176882A1 (https=)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020046655A (ja) * 2018-09-14 2020-03-26 Jsr株式会社 感光性着色組成物、カラーフィルタ及び表示素子

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113272346B (zh) * 2019-02-21 2025-04-15 三菱化学株式会社 着色树脂组合物、滤色片、以及图像显示装置

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020046655A (ja) * 2018-09-14 2020-03-26 Jsr株式会社 感光性着色組成物、カラーフィルタ及び表示素子

Also Published As

Publication number Publication date
TW202402820A (zh) 2024-01-16
CN118843831A (zh) 2024-10-25
KR20240163067A (ko) 2024-11-18
JPWO2023176882A1 (https=) 2023-09-21

Similar Documents

Publication Publication Date Title
CN102719148A (zh) 颜料分散液、滤色片用着色组合物、滤色片、液晶显示装置及有机el显示器
JP7451906B2 (ja) 着色樹脂組成物、カラーフィルタ、及び画像表示装置
JP2019113732A (ja) 着色樹脂組成物、カラーフィルタ、及び画像表示装置
JP7833289B2 (ja) 着色樹脂組成物、カラーフィルタ、及び画像表示装置
JP2025137571A (ja) 着色樹脂組成物、カラーフィルタ、画像表示装置、及び着色剤分散液
JP7207173B2 (ja) 着色樹脂組成物、カラーフィルタ、及び画像表示装置
KR102879164B1 (ko) 착색 수지 조성물, 컬러 필터 및 화상 표시 장치
JP7848683B2 (ja) 着色樹脂組成物、カラーフィルタ、及び画像表示装置
JP7180545B2 (ja) カラーフィルタ用着色組成物、及び感光性着色樹脂組成物
WO2023176888A1 (ja) カラーフィルタの製造方法、及び画像表示装置の製造方法
JP2024040909A (ja) 着色樹脂組成物、カラーフィルタ、及び画像表示装置
JP7447397B2 (ja) 感光性着色樹脂組成物、カラーフィルタ、及び画像表示装置
WO2023095828A1 (ja) 着色樹脂組成物、着色樹脂組成物セット、及びカラーフィルタ
WO2023176882A1 (ja) 着色樹脂組成物、硬化物、カラーフィルタ及び画像表示装置
JP7159948B2 (ja) 着色樹脂組成物、カラーフィルタ、及び画像表示装置
WO2024075837A1 (ja) 着色剤含有液、着色樹脂組成物、カラーフィルタ、画像表示装置、及び着色樹脂組成物の製造方法
WO2023063336A1 (ja) 着色樹脂組成物、カラーフィルタ及び画像表示装置
JP7395986B2 (ja) 着色樹脂組成物、カラーフィルタ、及び画像表示装置

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 23770835

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2024508220

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 202380026537.2

Country of ref document: CN

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 23770835

Country of ref document: EP

Kind code of ref document: A1