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Compound or its tautomer, metal complex compound, colored photosensitive curing composition, color filter, and production

a technology of metal complex compound and pigment, applied in the field of compound or its tautomer, metal complex compound, colored photosensitive curing composition, color filter, etc., can solve the problems of dyes generally being less light stability and heat resistance than pigments, and difficulty in further improving resolution

Inactive Publication Date: 2012-06-07
FUJIFILM CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides a compound or its tautommer, a metal complex compound, a colored photosensitive curing composition, a color filter used the composition, and its production. The metal complex compound is obtained from a metal or metal compound and a dipyrromethene-based compound. The compound has a specific formula and can be used as a colorant in the photosensitive curing composition. The composition can be used to produce a color filter with improved color accuracy and stability. The invention also provides a method for producing the metal complex compound.

Problems solved by technology

Recently, in the color filter for solid state image sensing devices, even higher resolution has become desirable, but the conventional pigment dispersions have difficulties in further improving the resolution.
Because of problems such as the generation of color irregularities due to coarse particles of the pigment, it is not suitable for uses which require fine patterns such as solid state image sensing devices.
(1) Dyes are generally lower in light stability and heat resistance than pigments.
(2) It is difficult to obtain a liquid curing composition having a desired spectrum with a common colorant, because such a colorant is less soluble in aqueous alkaline solution or organic solvent (hereinafter, suitably referred to as solvent).
(3) It is difficult to control the solubility (printing efficiency) of the cured area and the uncured area, because the dye used often interacts with other components in the curing composition.
(4) When the molar absorption coefficient (ε) of the dye used is low, the dye needs to be added in a larger amount and thus, the amounts of the other components in the curing composition such as polymerizable compound (monomer), binder, and photopolymerization initiator must be reduced, which leads to deterioration in the curing efficiency of the composition, the heat resistance after curing, and the developing efficiency of the (non) cured area.
Due to these problems, it has been difficult to form colored patterns that are detailed and have a thin film in high-resolution color filters.
It is thus necessary to add a colorant to the curing composition in a larger amount for obtaining a desired absorption, leading to the problems described above.

Method used

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  • Compound or its tautomer, metal complex compound, colored photosensitive curing composition, color filter, and production
  • Compound or its tautomer, metal complex compound, colored photosensitive curing composition, color filter, and production
  • Compound or its tautomer, metal complex compound, colored photosensitive curing composition, color filter, and production

Examples

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synthesis example

[0191]Hereinafter, methods of synthesizing the colorant represented by the Formula (A) or (B) will be described in detail along the following scheme D, by taking the exemplary compound CI-29 above as an example.

[0192](Synthesis of Intermediate A)

[0193]Sodium carbonate (16.5 g, 0.156 mol) was added to a mixture of 3-nitrophthalonitrile (25 g, 0.144 mol), DMSO (200 ml), and sodium 3-mercaptopropanesulfonate salt (32 g, 0.18 mol), and the mixture was stirred as heated to 60° C. for 3 hours. The reaction mixture was poured into 10% sodium chloride water (300 g), and the precipitated solid was collected by filtration and washed with a mixed liquid of isopropanol / water (3 / 1). Water (200 ml), acetic acid (3 ml) and Na2WO4 (2 g) were added to the solid; 31% hydrogen peroxide solution (50 ml) was added thereto; and the mixture was stirred while heated at 60° C. After stirring fro 4 hours, the reaction mixture was poured into isopropanol (500 ml), and the precipitated solid was collected by f...

example 1

[0312]Intermediates 4, 5, and 11 (compounds represented by Formula (IV)), and exemplary compounds shown below were synthesized along the reaction scheme A to C described above according to the synthesis method described above. The molar absorption coefficient of each synthesized exemplary compound was determined in ethyl acetate solution (by using a spectrophotometer UV-2400PC (manufactured by Shimadzu Corporation)), and the maximum absorption wavelength (λmax) and the molar absorption coefficient (ε) are summarized in the following Table 4. The absorbance (Abs) of each colorant at 450 nm was evaluated, as normalized with respect to 1.0 of the absorbance at the measurement maximum absorption wavelength (λmax). Results are summarized in Table 4.

TABLE 4Abs. at 450 nm,Exemplarynormalized to Abs. =compoundλmaxε1.0 at λmaxIII-1533.11300000.0125III-45546.71283000.0068III-70540.01260000.0068III-80540.01230000.0100II-5514.6807000.1300I-1558.31290000.0096I-2578.31225000.0041I-4540.01190000.0...

example 2

[0314]1) Preparation of Resist Solution

[0315]Propylene glycol monomethylether acetate (PGMEA) 19.20 parts

[0316]Ethyl lactate 36.67 parts

[0317]Binder (benzyl methacrylate / methacrylic acid / 2-hydroxyethyl methacrylate) copolymer (molar ratio: 60:20:20) 41% EL solution 30.51 parts

[0318]Dipentaerythritol hexaacrylate 12.20 parts

[0319]Polymerization inhibitor (p-methoxyphenol) 0.0061 parts

[0320]Fluorochemical surfactant 0.83 parts

[0321]Photopolymerization initiator TAZ-107 (manufactured by Midori Kagaku Co., Ltd.) 0.586 parts

[0322]These components were blended and solubilized, to give a resist solution.

[0323]2) Preparation of Glass Substrate Having an Undercoat Layer

[0324]A glass substrate (Corning 1737) was ultrasonicated in 0.5% aqueous NaOH solution, dehydrated, and baked (200° C. / 20 minutes).

[0325]The resist solution 1) above was then applied on a clean glass substrate to a film thickness of 2.0 μm by a spin coater, and the plate was dried under heat at 220° C. for 1 hour, to give a c...

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Abstract

Provided is a colored photosensitive curing composition useful for color filters in primary colors, including blue, green, and red, having a high molar absorption coefficient and allowing a reduction in film thickness and superior color purity and fastness. A colored photosensitive curing composition, comprising, as its colorant, a dipyrromethene-based metal complex compound obtained from a metal or metal compound and a dipyrromethene-based compound represented by the following Formula (I):wherein in Formula (I), R1 to R6 each independently represent a hydrogen atom or a substituent group; and R7 represents a hydrogen or halogen atom, or an alkyl, aryl or heterocyclic group.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This application is a Continuation of U.S. application Ser. No. 11 / 905,028 filed Sep. 27, 2007, which claims priority under 35 USC 119 from Japanese Patent Application No. 2006-263580 and No. 2007-117651. The contents of the prior applications are incorporated by reference in their entirety.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]The invention relates to a compound or its tautomer, a metal complex compound, and a colored photosensitive curing composition that are used favorably in production of a color filter for use in liquid crystal display elements and solid-state image sensing devices, a color filter, and a method for producing the same.[0004]2. Description of the Related Art[0005]A pigment dispersion method has been used as one of the methods for producing color filters for use in liquid crystal display elements and solid-state image sensing devices. The pigment dispersion method is a method of producing a colo...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): G02B5/23C07D207/44C07D401/14C07D519/00C07F1/08C07F3/06C07F15/06C09B23/00C09B47/24G02B5/20G02B5/22G03F7/004
CPCC07D207/335C09B23/0008C09B23/04C09B47/0671C09B47/0673C09B47/0675C09B47/0676C09B47/0678C09B55/003C09B63/005C09B67/0033G03C1/735G03F7/0007G03F7/027
Inventor MIZUKAWA, YUKIGOTO, RYOJITAKAKUWA, HIDEKIOGIYAMA, MASASHIFUJIMORI, TORU
Owner FUJIFILM CORP
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