CN102952122A - Compound used in color composition - Google Patents

Compound used in color composition Download PDF

Info

Publication number
CN102952122A
CN102952122A CN2012102813873A CN201210281387A CN102952122A CN 102952122 A CN102952122 A CN 102952122A CN 2012102813873 A CN2012102813873 A CN 2012102813873A CN 201210281387 A CN201210281387 A CN 201210281387A CN 102952122 A CN102952122 A CN 102952122A
Authority
CN
China
Prior art keywords
compound
formula
expression
carbonatoms
methyl
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.)
Pending
Application number
CN2012102813873A
Other languages
Chinese (zh)
Inventor
辰巳泰基
芦田徹
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Publication of CN102952122A publication Critical patent/CN102952122A/en
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/78—Ring systems having three or more relevant rings
    • C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
    • C07D311/82—Xanthenes
    • 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
    • C09B57/14—Benzoxanthene dyes; Benzothioxanthene dyes

Abstract

The invention provides a compound represented by formula(I). In the formula(I), R1 and R2 represent hydrogen atoms or alkyl groups respectively and independently, R3 represents -SO3, -SO3-M+, -CO2H or -CO2-M+. M+ represents (R11)4N+,Na+ or K+, R11 represents hydrogen atom, alkyl group or aralkyl, m represent an integer between 0 and 2, n and p represent integers between 0 and 2 respectively and independently.

Description

The coloured composition compound
Technical field
The present invention relates to the compound for dyestuff.
Background technology
Dyestuff is used for utilizing reflected light or transmitted light Show Color in fields such as filamentary material, liquid crystal indicator, ink-jet.As such dyestuff, be widely known by the people just like having the rhodamine B xanthene skeleton, following formula (a) expression (the 1st edition the 274th page of thin Tian Fengzhu " reactive monoazo dyestuffs chemistry ", in May, 1973 (strain) skill newspaper hall).
Figure BDA00001990923300011
Conventionally known above-claimed cpd differs and fully satisfies surely solvability in organic solvent.
Summary of the invention
The present invention includes the invention of following [1] ~ [9] record.
[1] the coloured composition compound shown in the formula (I).
Formula (I):
Figure BDA00001990923300012
[in the formula (I),
R 1And R 2The alkyl that represents independently of one another hydrogen atom or carbonatoms 1 ~ 6.
R 3Expression-SO 3H ,-SO 3 -M +,-CO 2H or-CO 2 -M +
M +Expression (R 11) 4N +, Na +Or K +R 11Expression hydrogen atom, the alkyl of carbonatoms 1 ~ 20 or the aralkyl of carbonatoms 7 ~ 10,4 R 11Be same to each other or different to each other.
M represents 0 ~ 2 integer.M is 2 o'clock, 2 R 3Be same to each other or different to each other.
N and p represent 0 ~ 2 integer independently of one another.]
[2] the coloured composition compound of formula (I ') expression.
Formula (I '):
Figure BDA00001990923300021
[formula (I ') in, R 1, R 2, R 3, m, n and p represent the meaning same as described above separately.]
[3] such as [1] or [2] described coloured composition compound, wherein, R 1And R 2Be hydrogen atom or methyl independently of one another.
[4] such as each described coloured composition compounds of [1] ~ [3], wherein, R 3For-SO 3H or-SO 3 -M +
[5] such as each described coloured composition compound of [1] ~ [4], wherein, m is 0 or 1.
[6] such as each described coloured composition compound of [1] ~ [5], wherein, n is 1.
[7] such as each described coloured composition compound of [1] ~ [6], wherein, p is 1.
[8] coloured composition of formula (I ') expression is with the manufacture method of compound,
Comprise the operation that the compound of the compound that makes formula (II) expression and formula (III) expression reacts,
Figure BDA00001990923300022
[in the formula (II), R 1, R 2, R 3And m represents the meaning same as described above separately.]
Figure BDA00001990923300031
[in the formula (III), n and p represent the meaning same as described above separately.]
Figure BDA00001990923300032
[formula (I ') in, R 1, R 2, R 3, m, n and p represent the meaning same as described above separately.]
[9] such as [8] described manufacture method, wherein, the compound that the compound that makes formula (II) expression and formula (III) represent does not substantially exist under the condition of solvent and reacts.
Coloured composition of the present invention is excellent with the solvability of compound in organic solvent.
Embodiment
Compound of the present invention is the represented compound of formula (I) (below be sometimes referred to as " compound (I) ").Compound of the present invention also comprises its tautomer and salt thereof.This salt for example can be enumerated, an alkali metal salts such as lithium salts, sylvite, sodium salt etc.
Formula (I):
Figure BDA00001990923300033
[in the formula (I), R 1, R 2, R 3, m, n and p represent the meaning same as described above separately.]
R 1And R 2Be the alkyl of hydrogen atom or carbonatoms 1 ~ 6 independently respectively, consider from the facile aspect of the appearance of raw material, preferred hydrogen atom or methyl, more preferably hydrogen atom.The alkyl of carbonatoms 1 ~ 6 there can be exemplified, methyl, ethyl, propyl group, sec.-propyl, butyl, isobutyl-, amyl group, isopentyl, neo-pentyl, hexyl etc.
R 3For-SO 3H ,-SO 3 -M +,-CO 2H or-CO 2 -M +Herein, M +For +N(R 11) 4, Na +Or K +, preferred +N(R 11) 4R 11Be the alkyl of hydrogen atom, carbonatoms 1 ~ 20 or the aralkyl of carbonatoms 7 ~ 10, +N(R 11) 44 R 11In, preferably at least 2 is the alkyl of carbonatoms 5 ~ 20.
R 11In the alkyl of carbonatoms 1 ~ 20 can enumerate methyl, ethyl, propyl group, sec.-propyl, butyl, isobutyl-, amyl group, isopentyl, neo-pentyl, hexyl, heptyl, octyl group, 2-ethylhexyl, nonyl, decyl, dodecyl, hexadecyl, eicosyl etc.
R 11In the aralkyl of carbonatoms 7 ~ 10 can enumerate benzyl, styroyl, phenyl butyl etc.
M represents 0 ~ 2 integer.Wherein, consider from the viewpoint in one's hands of raw material that preferred m is 0 or 1, more preferably 0.
N represents 0 ~ 2 integer.Wherein, consider from the viewpoint in one's hands of raw material that preferred n is 1.
P represents 0 ~ 2 integer.Wherein, consider from the viewpoint in one's hands of raw material that preferred p is 1.
Among the compound (I), from angle easy to manufacture, the compound of preferred formula (I ') expression (below be sometimes referred to as " compound (I ') ".）。
Figure BDA00001990923300041
[formula (I ') in, R 1, R 2, R 3, m, n and p represent the meaning same as described above separately.]
Compound (I ') can be enumerated respectively compound shown in formula (I-1) ~ formula (I-16) etc.The compound of preferred formula (I-1), formula (I-3), formula (I-5) or formula (I-7) expression, the more preferably compound of formula (I-1) expression.
Figure BDA00001990923300051
Figure BDA00001990923300061
Then, the manufacture method of the compound in the compound (I) (I ') described.
Manufacture method as compound (I '), can enumerate the manufacture method of the operation of the compound that comprises the compound that makes formula (II) expression (below be sometimes referred to as " compound (II) ") and formula (III) expression (below be sometimes referred to as " compound (III) ") reaction
[in the formula (II), R 1, R 2, R 3And m represents the meaning same as described above separately.]
Figure BDA00001990923300072
[in the formula (III), n and p represent the meaning same as described above separately.]
This reaction also can be implemented in the presence of solvent, but from the angle of yield, does not preferably use in fact solvent, does not namely substantially exist under the condition of solvent to implement.Reaction by compound (II) is mixed with compound (III), is implemented the under agitation slaking of mixture that obtains usually." not using in fact solvent " herein refers to, not using is enough to make compound (II) and compound (III) to dissolve simultaneously the solvent of the abundant amount that reacting field can be provided, " do not exist under the condition of solvent in fact " and refer to, not existing is enough to make compound (II) and compound (III) to dissolve simultaneously the solvent of the abundant amount that reacting field can be provided, typically refer to the total usage quantity with respect to compound (II) and compound (III), less than 1 quality %, the amount of preferred less than 0.1 quality %.
As above-mentioned solvent, can enumerate: the hydrocarbon solvents such as toluene, dimethylbenzene; The halogenated hydrocarbon solvents such as chlorobenzene, dichlorobenzene, chloroform; The alcoholic solvents such as methyl alcohol, ethanol, butanols; The nitro-hydrocarbon solvents such as oil of mirbane; The ketone solvents such as mibk; The amide solvents such as 1-Methyl-2-Pyrrolidone etc.
Preferred 30 ℃ ~ 180 ℃ of temperature of reaction, more preferably 80 ℃ ~ 130 ℃.Preferred 1 hour ~ 12 hours of reaction times, more preferably 3 hours ~ 8 hours.
The usage quantity of compound (III) is with respect to 1 mole compound (II), and is preferred more than 2 moles below 16 moles, more preferably more than 2 moles below 10 moles.
The method of obtaining compound as target compound (I ') from reaction mixture is not particularly limited, and can adopt various known methods.For example, reaction mixture and acid (such as acetic acid etc.) can be mixed together, filter and collect the crystal of separating out.For aforementioned acid, preferably prepare in advance aqueous acid, again reaction mixture is added in the above-mentioned aqueous solution.Temperature when adding reaction mixture is preferred more than 10 ℃ below 50 ℃, more preferably more than 20 ℃ below 50 ℃, further preferably more than 20 ℃ below 30 ℃.In addition, add to reaction mixture in the aqueous acid after, preferably in synthermal lower stirring about 0.5 ~ 2 hour.Preferably with the washings such as crystal water of leaching, then carry out drying.In addition, as required, can also be further purified by known methods such as recrystallizations.
The compound of the present invention that obtains accordingly is useful as dyestuff.In addition, the solvability of compound of the present invention in organic solvent is high, and be therefore especially useful as the dyestuff that uses in the colored filter of the display unit such as liquid crystal indicator.
Applicable dyestuff is the dyestuff take compound of the present invention (I) as effective constituent among the present invention.
Applicable coloured composition among the present invention contains dyestuff take compound of the present invention (I) as effective constituent as tinting material (below be sometimes referred to as " tinting material (A) "), preferably further also contains resin (B).This coloured composition more preferably further contains polymerizable compound (C), polymerization starter (D) and solvent (E).
Tinting material (A) is except containing take compound of the present invention (I) as the dyestuff of effective constituent, also can further contain pigment and/or from take compound of the present invention (I) as the different dyestuff of the dyestuff of effective constituent.
Can exemplify in Colour Index (Colour Index) (the The Society of Dyers and Colourists of association of Britain dyeing man publishes) from the dyestuff different take compound of the present invention (I) as the dyestuff of effective constituent and to be classified as solvent dye (Solvent), matching stain (Acid), basic dyestuff (Basic), chemically-reactive dyes (Reactive), substantive dyestuff (Direct), dispersed dye (Disperse), or the dyestuff of vat dyes (Vat) etc.More specifically, can exemplify the dyestuff of following Colour Index (C.I.) numbering, but be not limited to this.
C.I. solvent yellow 25,79,81,82,83,89;
C.I. turmeric yellow 7,23,25,42,65,76;
C.I. reactivity yellow 2,76,116;
C.I. directly yellow 4,28,44,86,132;
C.I. DISPERSE YELLOW 54,76;
C.I. solvent orange 41,54,56,99;
C.I. von Muller's indicator 56,74,95,108,149,162;
C.I. the reactivity orange 16;
C.I. direct orange 26;
C.I. solvent red 24,49,90,91,118,119,122,124,125,127,130,132,160,218;
C.I. Xylene Red 73,91,92,97,138,151,211,274,289;
C.I. acid violet 102;
C.I. solvent green 1,5;
C.I. acid green 3,5,9,25,28;
C.I. alkali green 1;
C.I. Vat green 1 etc.
Pigment can exemplify pigment dyestuff or mineral dye commonly used in the colo(u)rant dispersion resist.Mineral dye can exemplify metal oxide or the such metallic compound of metallic complex salt, particularly, can exemplify oxide compound or the complex metal oxides of the metals such as iron, cobalt, aluminium, cadmium, lead, copper, titanium, magnesium, chromium, zinc, antimony.In addition, pigment dyestuff and mineral dye specifically can exemplify, and are classified as the compound of pigment (Pigment) according to Colour Index (Colour Index) (the The Society of Dyers and Colourists of association of Britain dyeing man publishes).More specifically, can exemplify the pigment of following Colour Index (C.I.) numbering, but be not limited to this.
C.I. Pigment Yellow 73 20,24,31,53,83,86,93,94,109,110,117,125,137,138,139,147,148,150,153,154,166,173 and 180;
C.I. pigment Orange 13,31,36,38,40,42,43,51,55,59,61,64,65 and 71;
C.I. Pigment Red 9,97,105,122,123,144,149,166,168,176,177,180,192,215,216,224,242,254,255 and 264;
C.I. pigment violet 14,19,23,29,32,33,36,37 and 38;
C.I. pigment Green 7,10,15,25,36,47 and 58 etc.
The content of tinting material (A), with respect to the solids component in the coloured composition, preferred 5 ~ 60 quality %.Here, solids component refers to, the total of the composition in the coloured composition after the desolventizing.
Contained preferred 3 ~ 100 quality % take compound of the present invention (I) as the content of the dyestuff of effective constituent in the tinting material (A).
Can distinguish alone or in combination from the dye well pigment different take compound of the present invention (I) as the dyestuff of effective constituent and to use with the dyestuff take compound of the present invention (I) as effective constituent more than 2 kinds.
Resin (B) is not particularly limited, and uses which type of resin all can.
Resin (B) preferred bases soluble resin more preferably contains the resin by the structural unit of (methyl) vinylformic acid derivation.Here, (methyl) vinylformic acid represents vinylformic acid and/or methacrylic acid.
Resin (B) specifically can exemplified by methyl vinylformic acid/methacrylic acid benzyl ester multipolymer, methacrylic acid/methacrylic acid benzyl ester/styrol copolymer, methacrylic acid/methacrylic acid benzyl ester/isobornyl methacrylate multipolymer, methacrylic acid/styrene/methacrylic acid benzyl ester/N-phenylmaleimide multipolymer, methacrylic acid/styrene/methacrylic acid glycidyl ester copolymer etc.
The polystyrene conversion weight-average molecular weight of resin (B) is preferred 5,000 ~ 35,000, and more preferably 6,000 ~ 30,000.
Preferred 50 ~ the 150mgKOH/g of acid number of resin (B), more preferably 60 ~ 135mgKOH/g.
The content of resin (B), with respect to the solids component of coloured composition, preferred 7 ~ 65 quality %, more preferably 13 ~ 60 quality %.
Polymerizable compound (C) so long as the living radical that produces by polymerization starter (D), acid etc. can polymerization compound just be not particularly limited.For example can exemplify, have the compound etc. of the ethene unsaturated link(age) of polymerizability.
Described polymerizable compound (C) preferably has the optical polymerism compound of 3 above polymerizable groups.Optical polymerism compound with 3 above polymerizable groups can exemplify, pentaerythritol tetracrylate, pentaerythritol tetramethacrylate, five vinylformic acid dipentaerythritol ester, pentamethyl-vinylformic acid dipentaerythritol ester, six vinylformic acid dipentaerythritol ester, hexamethyl vinylformic acid dipentaerythritol ester etc.Above-mentioned polymerizable compound (C) can be used alone or in combination of two or more kinds.
The content of polymerizable compound (C), with respect to the solids component of coloured composition, preferred 5 ~ 65 quality %, more preferably 10 ~ 60 quality %.
Described polymerization starter (D) can exemplify living radical and produce agent, acidogenic agent etc.Living radical produces agent by the effect generation living radical of heat or light.Above-mentioned living radical produces agent can exemplified by alkyl groups phenyl ketone compound, thioxanthone compound, triaizine compounds, oxime compound etc.
Described alkyl phenyl ketone compound can exemplify, 2-methyl-2-morpholino-1-(4-methylthio group phenyl)-1-acetone, 2-hydroxy-2-methyl-1-phenyl-1-acetone, benzyl dimethyl ketal, 2-hydroxy-2-methyl-1-(4-(2-hydroxyl-oxethyl) phenyl)-1-acetone, 1-hydroxy-cyclohexyl phenyl ketone etc.
Described thioxanthone compound can exemplify ITX, ITX, 2,4-diethyl thioxanthone, 2,4-two clopenthixal ketones, 1-chloro-4-propoxy-thioxanthone etc.
Described triaizine compounds can exemplify, 2,4-two (trichloromethyl)-6-(4-p-methoxy-phenyl)-1,3, the 5-triazine, 2,4-two (trichloromethyl)-6-(4-methoxyl group naphthyl)-1,3,5-triazines, 2,4-two (trichloromethyl)-6-(4-methoxyl-styrene)-1,3,5-triazine, 2,4-two (trichloromethyl)-6-(2-(5-methyl furan-2-yl) vinyl)-1,3, the 5-triazine, 2,4-two (trichloromethyl)-6-(2-(furans-2-yl) vinyl)-1,3, the 5-triazine, 2,4-two (trichloromethyl)-6-(2-(4-diethylamino-2-aminomethyl phenyl) vinyl)-1,3,5-triazines, 2,4-two (trichloromethyl)-6-(2-(3, the 4-Dimethoxyphenyl) vinyl)-1,3,5-triazines etc.
Described oxime compound can exemplify O-acyl group oxime compound; its concrete example has; N-benzoyloxy-1-(4-thiophenyl phenyl)-1-butanone-2-imines, N-benzoyloxy-1-(4-thiophenyl phenyl)-1-octanone-2-imines, N-acetoxyl group-1-[9-ethyl-6-(2-methyl benzoyl)-9H-carbazole-3-yl] ethane-1-imines, N-acetoxyl group-1-[9-ethyl-6-{ 2-methyl-4-(3; 3-dimethyl-2,4-dioxane amyl group methoxyl group) benzoyl }-9H-carbazole-3-yl] ethane-1-imines etc.
In addition; living radical produces agent and also for example can use; 2,4,6-trimethylbenzoyl diphenyl phosphine oxide, 2; 2 '-two (Chloro-O-Phenyl)-4; 4 ', 5,5 '-tetraphenyl-1; 2 '-diimidazole, 10-butyl-2-chloro-acridine ketone, 2-ethyl-anthraquinone, benzil (benzil), 9,10-phenanthrenequione, camphorquinone, phenyl oxoethanoic acid methyl ester, two cyclopentadiene titanium compounds etc.
Described acidogenic agent can exemplify as, salt, tosic acid p-Nitrobenzyl class, the tosic acid benzoin ester classes etc. such as 4-hydroxy phenyl dimethyl sulfonium tosilate, 4-hydroxy phenyl dimethyl sulfonium hexafluoro antimonate, 4-acetoxyl group phenyl dimethyl sulfonium tosilate, 4-acetoxyl group phenyl methyl benzyl sulfonium hexafluoro antimonate, triphenylsulfonium tosilate, triphenylsulfonium hexafluoro antimonate, phenylbenzene iodine tosilate, phenylbenzene iodine hexafluoro antimonate.
These polymerization starters (D) can use separately also and can be used in combination more than 2 kinds.
The content of polymerization starter (D), with respect to total amount 100 mass parts of resin (B) and polymerizable compound (C), preferred 0.1 ~ 30 mass parts, more preferably 1 ~ 20 mass parts.The content of polymerization starter can high-sensitivity in above-mentioned scope, and the time shutter shortens, and productivity improves, and is therefore comparatively desirable.
Solvent (E) can exemplify, ether solvents, aromatic hydrocarbon solvents, ketone solvent, alcoholic solvent, ester solvent, amide solvent etc.
Described ether solvents can exemplify, tetrahydrofuran (THF), tetrahydropyrans, Isosorbide-5-Nitrae-dioxane, the glycol monomethyl methyl ether, ethylene glycol monomethyl ether, the glycol monomethyl propyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, TC, the Diethylene Glycol single-butyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol methyl ethyl ether, the Diethylene Glycol dipropyl ether, the Diethylene Glycol dibutyl ether, propylene glycol monomethyl ether, propylene glycol list ethyl ether acetic ester, propylene glycol list propyl ether acetic ester, the ethylene glycol monomethyl ether acetate, ethylene glycol monomethyl ether acetate, the TC acetic ester, Diethylene Glycol single-butyl ether acetic ester etc.
Above-mentioned aromatic hydrocarbon solvents can exemplify, benzene,toluene,xylene, sym-trimethylbenzene etc.
Above-mentioned ketone solvent can exemplify, acetone, 2-butanone, 2-heptanone, 3-heptanone, dipropyl ketone, 4-methyl-2 pentanone, 4-hydroxy-4-methyl-2-pentanone, cyclopentanone, pimelinketone etc.
Above-mentioned alcoholic solvent can exemplify, methyl alcohol, ethanol, propyl alcohol, butanols, hexanol, hexalin, ethylene glycol, glycerol etc.
Above-mentioned ester solvent can exemplify, vinyl acetic monomer, n-butyl acetate, isobutyl acetate, pentyl formate, isoamyl acetate, isobutyl acetate, butyl propionate, isopropyl butyrate, ethyl butyrate, butyl butyrate, alkyl esters, methyl lactate, ethyl lactate, n-Butyl lactate, Methoxy Methyl Acetate, the Methoxy acetic acid ethyl ester, the Methoxy acetic acid butyl ester, the oxyethyl group ritalin, the oxyethyl group vinyl acetic monomer, the 3-methoxy methyl propionate, 3-methoxy propyl acetoacetic ester, 3-ethoxy-propionic acid methyl esters, the 3-ethoxyl ethyl propionate, the 2-methoxy methyl propionate, 2-methoxy propyl acetoacetic ester, 2-methoxy propyl propyl propionate, 2-ethoxy-propionic acid methyl esters, the 2-ethoxyl ethyl propionate, 2-methoxyl group-2 Methylpropionic acid methyl esters, 2-oxyethyl group-2 Methylpropionic acid ethyl ester, Pyruvic Acid Methyl ester, Pyruvic Acid Ethyl ester, Propyl pyruvate, methyl acetoacetate, ethyl 3-oxobutanoate, 3-methoxyl group butylacetic acid ester, 3-methyl-3-methoxyl group butylacetic acid ester, gamma-butyrolactone etc.
Above-mentioned amide solvent can exemplify, DMF, N,N-dimethylacetamide, N-Methyl pyrrolidone etc.
These solvents can use separately also and can be used in combination more than 2 kinds.
The content of solvent in the coloured composition (E), with respect to coloured composition, preferred 70 ~ 95 quality %, more preferably 75 ~ 90 quality %.
Coloured composition can also contain the various additives such as tensio-active agent, weighting agent, other macromolecular compounds, adhesive accelerant, antioxidant, UV light absorber, photostabilizer, chain-transfer agent as required.
(I) is useful as dyestuff for compound of the present invention.Because molar absorptivity is high, and shows high solvability in organic solvent, so the dyestuff that especially uses in the colored filter as display unit such as liquid crystal indicators is useful.
In addition, the coloured composition that contains the compounds of this invention (I) can be applied to have colored filter in known manner as various machines relevant with rendered image such as the display unit (for example, known liquid crystal indicator, organic El device etc.) of the part of its component parts, solid-state imagers.
Embodiment
Then enumerate embodiment, the present invention is described more specifically.In an embodiment, if do not specify, the % of expression content or usage quantity and part are all take quality as benchmark.
In following examples, the structure of compound is determined by mass spectroscopy (LC:Agilent system 1200 types, MASS:Agilent LC/MSD type processed).
(embodiment 1)
With 75.0 parts of 15.0 parts of compounds, METHYLPYRROLIDONEs and 25.8 parts of mixing of decahydroquinoline (Tokyo changes into industry (strain) system) of following formula (II-1) expression, the mixture that obtains was stirred 24 hours under 110 ℃.After above-mentioned reaction solution is cooled to room temperature, add in the mixed solution of 600 parts in water, 100 parts of 35% hydrochloric acid, stirred 1 hour in the room temperature.After the crystal of separating out collected as the residue of suction strainer, carry out drying, obtain 19.5 parts of the compounds of formula (I-1) expression.Yield is 86%.
Figure BDA00001990923300131
The evaluation of the compound shown in the formula (I-1)
(mass spectroscopy) ionization mode=ESI+:m/z=[M+H] +611.4
Accurate mass: 610.3
＜mensuration of solubleness 〉
Try to achieve by the following method the compound and the solubleness of rhodamine B (Tokyo changes into industry (strain) system) in propylene glycol monomethyl ether (hereinafter to be referred as PGME), ethyl lactate (hereinafter to be referred as EL) that obtain among the embodiment 1.
In the 50ml sample hose, with compound and above-mentioned solvent, then, the jam-pack sample hose is 30 ℃ of lower ultra-sonic oscillation machine vibration 3 minutes of using in following ratio.Then, place after 30 minutes suction strainer, its residue of visual observations under the room temperature.When not finding insolubles is arranged, namely be judged to be favorable solubility, enter zero in table 1 acceptance of the bid; When discovery has insolubles, namely be judged to be poorly solublely, enter in table 1 acceptance of the bid *.
2% compound 0.02g, solvent 1g
[table 1]
Figure BDA00001990923300132
Compound (a) is rhodamine B (Tokyo changes into industry (strain) system).
(embodiment 2)
(preparation of coloured composition)
(A) tinting material: compound (I-1): 20 parts of the compounds that obtains among the embodiment 1
(B-1) resin: methacrylic acid/benzyl methacrylate multipolymer (mol ratio: 30/70; Weight-average molecular weight 10700, acid number 70mgKOH/g) 70 parts
(C-1) polymerizable compound: 30 parts of six vinylformic acid dipentaerythritol ester (Japanese chemical drug society system)
(D-1) Photoepolymerizationinitiater initiater: benzyl dimethyl ketal (イ Le ガ キ ュ ア (registered trademark) 651; The production of BASFJapan company) 15 parts
(E-1) solvent: 680 parts of dimethyl formamides
Mix above-mentioned substance, obtain coloured composition.
(making of colored filter)
With spin-coating method coloured composition obtained above is coated on glassly, makes volatile component volatilization.After the cooling, use the figuratum silica glass of tool photomask processed and exposure machine to carry out rayed.
After the rayed, develop with potassium hydroxide aqueous solution, be heated to 200 ℃ with stove, obtain colored filter.
According to the above results as can be known, compound of the present invention demonstrates high-dissolvability to organic solvent.In addition, use when containing the coloured composition of this compound, the generation of foreign matter is few, can make high-quality colored filter.
The solvability of compound of the present invention in organic solvent is excellent.

Claims (9)

1. the compound shown in the formula (I),
Formula (I):
Figure FDA00001990923200011
In the formula (I),
R 1And R 2The alkyl that represents independently of one another hydrogen atom or carbonatoms 1 ~ 6;
R 3Expression-SO 3H ,-SO 3 -M +,-CO 2H or-CO 2 -M +
M +Expression (R 11) 4N +, Na +Or K +, R 11Expression hydrogen atom, the alkyl of carbonatoms 1 ~ 20 or the aralkyl of carbonatoms 7 ~ 10,4 R 11Be same to each other or different to each other;
M represents 0 ~ 2 integer, and m is 2 o'clock, 2 R 3Be same to each other or different to each other;
N and p represent 0 ~ 2 integer independently of one another.
2. the compound of formula (I ') expression,
Formula (I '):
Formula (I ') in,
R 1And R 2The alkyl that represents independently of one another hydrogen atom or carbonatoms 1 ~ 6;
R 3Expression-SO 3H ,-SO 3 -M +,-CO 2H or-CO 2 -M +
M +Expression (R 11) 4N +, Na +Or K +, R 11Expression hydrogen atom, the alkyl of carbonatoms 1 ~ 20 or the aralkyl of carbonatoms 7 ~ 10,4 R 11Be same to each other or different to each other;
M represents 0 ~ 2 integer, and m is 2 o'clock, 2 R 3Be same to each other or different to each other;
N and p represent 0 ~ 2 integer independently of one another.
3. compound as claimed in claim 1 or 2, wherein, R 1And R 2Be hydrogen atom or methyl independently of one another.
4. such as each described compound of claim 1 ~ 3, wherein, R 3For-SO 3H or-SO 3 -M +
5. such as each described compound of claim 1 ~ 4, wherein, m is 0 or 1.
6. such as each described compound of claim 1 ~ 5, wherein, n is 1.
7. such as each described compound of claim 1 ~ 6, wherein, p is 1.
8. the manufacture method of the compound of formula (I ') expression,
Comprise the operation that the compound of the compound that makes formula (II) expression and formula (III) expression reacts,
In the formula (II),
R 1And R 2The alkyl that represents independently of one another hydrogen atom or carbonatoms 1 ~ 6;
R 3Expression-S O3H ,-SO 3 -M +,-CO 2H or-CO 2 -M +
M +Expression (R 11) 4N +, Na +Or K +, R 11Expression hydrogen atom, the alkyl of carbonatoms 1 ~ 20 or the aralkyl of carbonatoms 7 ~ 10,4 R 11Be same to each other or different to each other;
M represents 0 ~ 2 integer, and m is 2 o'clock, 2 R 3Be same to each other or different to each other;
Figure FDA00001990923200031
In the formula (III), n and p represent 0 ~ 2 integer independently of one another;
Figure FDA00001990923200032
Formula (I ') in, R 1, R 2, R 3, m, n and p represent the meaning same as described above separately.
9. manufacture method as claimed in claim 8, wherein, the compound that the compound that makes formula (II) expression and formula (III) represent does not substantially exist under the condition of solvent and reacts.
CN2012102813873A 2011-08-11 2012-08-09 Compound used in color composition Pending CN102952122A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2011175675A JP2013036006A (en) 2011-08-11 2011-08-11 Compound
JP2011-175675 2011-08-11

Publications (1)

Publication Number Publication Date
CN102952122A true CN102952122A (en) 2013-03-06

Family

ID=47761561

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2012102813873A Pending CN102952122A (en) 2011-08-11 2012-08-09 Compound used in color composition

Country Status (4)

Country Link
JP (1) JP2013036006A (en)
KR (1) KR20130018160A (en)
CN (1) CN102952122A (en)
TW (1) TW201311829A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI644905B (en) * 2013-05-31 2018-12-21 南韓商東友精細化工有限公司 Compound and coloring curable resin composition

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5897044A (en) * 1981-12-04 1983-06-09 Konishiroku Photo Ind Co Ltd Formation of color image
US4405788A (en) * 1979-12-26 1983-09-20 Polaroid Corporation Bicyclo nitrogenheterocyclic substituted sulfofluoresceins, fluoresceins and xanthenes
WO2000064988A1 (en) * 1999-04-23 2000-11-02 Molecular Probes, Inc. Xanthene dyes and their application as luminescence quenching compounds
US6323337B1 (en) * 2000-05-12 2001-11-27 Molecular Probes, Inc. Quenching oligonucleotides
CN102914942A (en) * 2011-08-05 2013-02-06 住友化学株式会社 Colored curable resin composition

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4267251A (en) * 1979-12-26 1981-05-12 Polaroid Corporation Novel image dye-providing materials, photographic products and processes
WO2009046165A1 (en) * 2007-10-03 2009-04-09 Epoch Biosciences, Inc. Amide-substituted xanthene dyes
JP6094050B2 (en) * 2011-04-15 2017-03-15 住友化学株式会社 Colored photosensitive resin composition
JP6028326B2 (en) * 2011-08-04 2016-11-16 住友化学株式会社 Colored curable resin composition
JP5923960B2 (en) * 2011-08-05 2016-05-25 住友化学株式会社 Colored curable resin composition
JP2013053099A (en) * 2011-08-11 2013-03-21 Sumitomo Chemical Co Ltd Compound

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4405788A (en) * 1979-12-26 1983-09-20 Polaroid Corporation Bicyclo nitrogenheterocyclic substituted sulfofluoresceins, fluoresceins and xanthenes
JPS5897044A (en) * 1981-12-04 1983-06-09 Konishiroku Photo Ind Co Ltd Formation of color image
WO2000064988A1 (en) * 1999-04-23 2000-11-02 Molecular Probes, Inc. Xanthene dyes and their application as luminescence quenching compounds
US6323337B1 (en) * 2000-05-12 2001-11-27 Molecular Probes, Inc. Quenching oligonucleotides
CN102914942A (en) * 2011-08-05 2013-02-06 住友化学株式会社 Colored curable resin composition

Also Published As

Publication number Publication date
KR20130018160A (en) 2013-02-20
JP2013036006A (en) 2013-02-21
TW201311829A (en) 2013-03-16

Similar Documents

Publication Publication Date Title
CN102757668B (en) Salt for dye
CN102618085B (en) Salt and dyestuff
CN104861691A (en) Dye and colored curable resin composition
CN103571233A (en) Salt for dye
CN104559323A (en) Dye compound and colored curable resin composition
CN101870673B (en) Dye compound
CN102604429B (en) Salt for dye
CN105315722A (en) Salified dye and coloring curable resin composition
CN102952122A (en) Compound used in color composition
CN102952109A (en) Compound used in color composition
CN104860979A (en) Compound And Colored Curable Resin Composition
CN105198831A (en) Compound and coloring curable resin composition
KR20120116340A (en) Compound
KR20120031128A (en) Compounds and colored photosensitive resin compositions containing the same
TW201313701A (en) Compound
JP5831135B2 (en) Compound
JP2013036001A (en) Compound
JP5772505B2 (en) Compound
CN102134262A (en) Pyridine ketone complex
JP2013032458A (en) Compound
JP2013043966A (en) Compound
JP2012224664A (en) Compound
JP2013032467A (en) Compound
JP2013091723A (en) Compound
JP2013032322A (en) Compound

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20130306