ES2401458T3 - Filtros de color azul con contraste mejorado - Google Patents
Filtros de color azul con contraste mejorado Download PDFInfo
- Publication number
- ES2401458T3 ES2401458T3 ES07712161T ES07712161T ES2401458T3 ES 2401458 T3 ES2401458 T3 ES 2401458T3 ES 07712161 T ES07712161 T ES 07712161T ES 07712161 T ES07712161 T ES 07712161T ES 2401458 T3 ES2401458 T3 ES 2401458T3
- Authority
- ES
- Spain
- Prior art keywords
- phthalocyanine
- copper
- meth
- copper phthalocyanine
- independently
- 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.)
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- 238000000034 method Methods 0.000 claims abstract description 55
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims abstract description 51
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 claims abstract description 42
- 239000001000 anthraquinone dye Substances 0.000 claims abstract description 35
- FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 claims abstract description 30
- 229910052802 copper Inorganic materials 0.000 claims abstract description 22
- 239000010949 copper Substances 0.000 claims abstract description 22
- 239000007788 liquid Substances 0.000 claims abstract description 22
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims abstract description 22
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000006185 dispersion Substances 0.000 claims abstract description 20
- 239000000725 suspension Substances 0.000 claims abstract description 19
- 239000000758 substrate Substances 0.000 claims abstract description 18
- VVOLVFOSOPJKED-UHFFFAOYSA-N copper phthalocyanine Chemical compound [Cu].N=1C2=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC=1C1=CC=CC=C12 VVOLVFOSOPJKED-UHFFFAOYSA-N 0.000 claims abstract description 15
- 238000010521 absorption reaction Methods 0.000 claims abstract description 11
- 238000001429 visible spectrum Methods 0.000 claims abstract description 10
- 238000001035 drying Methods 0.000 claims abstract description 9
- -1 hydroxy, amino Chemical group 0.000 claims description 117
- 239000000203 mixture Substances 0.000 claims description 77
- 150000001875 compounds Chemical class 0.000 claims description 56
- 239000000975 dye Substances 0.000 claims description 54
- 229910052736 halogen Inorganic materials 0.000 claims description 39
- 150000002367 halogens Chemical class 0.000 claims description 39
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 38
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 35
- 239000011230 binding agent Substances 0.000 claims description 31
- 239000000049 pigment Substances 0.000 claims description 21
- 125000001424 substituent group Chemical group 0.000 claims description 17
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 125000001931 aliphatic group Chemical group 0.000 claims description 8
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 4
- 125000004043 oxo group Chemical group O=* 0.000 claims description 3
- 101100240517 Caenorhabditis elegans nhr-11 gene Chemical group 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- KCNKJCHARANTIP-SNAWJCMRSA-N allyl-{4-[3-(4-bromo-phenyl)-benzofuran-6-yloxy]-but-2-enyl}-methyl-amine Chemical group C=1OC2=CC(OC/C=C/CN(CC=C)C)=CC=C2C=1C1=CC=C(Br)C=C1 KCNKJCHARANTIP-SNAWJCMRSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- LRMDXTVKVHKWEK-UHFFFAOYSA-N 1,2-diaminoanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=C(N)C(N)=CC=C3C(=O)C2=C1 LRMDXTVKVHKWEK-UHFFFAOYSA-N 0.000 abstract description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 218
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 68
- 229920001577 copolymer Polymers 0.000 description 35
- 238000009472 formulation Methods 0.000 description 31
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 30
- 229920002554 vinyl polymer Polymers 0.000 description 30
- 239000011521 glass Substances 0.000 description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 29
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 28
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 25
- 239000011541 reaction mixture Substances 0.000 description 25
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 24
- 101000977048 Streptomyces cinnamonensis Uncharacterized protein in mutB 3'region Proteins 0.000 description 22
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 22
- 238000003756 stirring Methods 0.000 description 17
- 239000004925 Acrylic resin Substances 0.000 description 16
- 125000000217 alkyl group Chemical group 0.000 description 16
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 16
- 229910052739 hydrogen Inorganic materials 0.000 description 16
- 239000001257 hydrogen Substances 0.000 description 16
- 239000000243 solution Substances 0.000 description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 14
- 239000002253 acid Substances 0.000 description 14
- 229920000642 polymer Polymers 0.000 description 13
- 238000007639 printing Methods 0.000 description 13
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 12
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 12
- 150000002431 hydrogen Chemical class 0.000 description 11
- 239000000843 powder Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
- 239000001055 blue pigment Substances 0.000 description 10
- 238000000576 coating method Methods 0.000 description 10
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 10
- 238000001914 filtration Methods 0.000 description 10
- 239000000976 ink Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 229920002120 photoresistant polymer Polymers 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 10
- 238000004128 high performance liquid chromatography Methods 0.000 description 9
- 125000001624 naphthyl group Chemical group 0.000 description 9
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 8
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 description 8
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 8
- 238000010411 cooking Methods 0.000 description 8
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 8
- 238000011161 development Methods 0.000 description 8
- 239000002270 dispersing agent Substances 0.000 description 8
- 238000001704 evaporation Methods 0.000 description 8
- 230000008020 evaporation Effects 0.000 description 8
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 8
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 8
- QRHHZFRCJDAUNA-UHFFFAOYSA-N 2-(4-methoxyphenyl)-4,6-bis(trichloromethyl)-1,3,5-triazine Chemical compound C1=CC(OC)=CC=C1C1=NC(C(Cl)(Cl)Cl)=NC(C(Cl)(Cl)Cl)=N1 QRHHZFRCJDAUNA-UHFFFAOYSA-N 0.000 description 7
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 7
- 239000004305 biphenyl Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 7
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 7
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 description 6
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 6
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- GLLRIXZGBQOFLM-UHFFFAOYSA-N Xanthorin Natural products C1=C(C)C=C2C(=O)C3=C(O)C(OC)=CC(O)=C3C(=O)C2=C1O GLLRIXZGBQOFLM-UHFFFAOYSA-N 0.000 description 6
- 150000004056 anthraquinones Chemical class 0.000 description 6
- 235000010290 biphenyl Nutrition 0.000 description 6
- 238000000113 differential scanning calorimetry Methods 0.000 description 6
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 6
- 229920002223 polystyrene Polymers 0.000 description 6
- 239000000741 silica gel Substances 0.000 description 6
- 229910002027 silica gel Inorganic materials 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 5
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 239000002202 Polyethylene glycol Substances 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
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- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 5
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 4
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 description 4
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 4
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 4
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- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 3
- CGLVZFOCZLHKOH-UHFFFAOYSA-N 8,18-dichloro-5,15-diethyl-5,15-dihydrodiindolo(3,2-b:3',2'-m)triphenodioxazine Chemical compound CCN1C2=CC=CC=C2C2=C1C=C1OC3=C(Cl)C4=NC(C=C5C6=CC=CC=C6N(C5=C5)CC)=C5OC4=C(Cl)C3=NC1=C2 CGLVZFOCZLHKOH-UHFFFAOYSA-N 0.000 description 3
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- 230000002378 acidificating effect Effects 0.000 description 3
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 3
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- 125000003710 aryl alkyl group Chemical group 0.000 description 3
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- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 125000004149 thio group Chemical group *S* 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 238000000411 transmission spectrum Methods 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
- C09B1/54—Amino-hydroxy-anthraquinones; Ethers and esters thereof etherified
- C09B1/542—Anthraquinones with aliphatic, cycloaliphatic, araliphatic or aromatic ether groups
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
-
- 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
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
- G02B5/223—Absorbing filters containing organic substances, e.g. dyes, inks or pigments
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0041—Optical brightening agents, organic pigments
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Optics & Photonics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Optical Filters (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06110105 | 2006-02-17 | ||
| EP06110105 | 2006-02-17 | ||
| EP06110553 | 2006-03-01 | ||
| EP06110553 | 2006-03-01 | ||
| PCT/EP2007/051154 WO2007093536A2 (en) | 2006-02-17 | 2007-02-07 | Blue colour filters with enhanced contrast |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2401458T3 true ES2401458T3 (es) | 2013-04-19 |
Family
ID=38440262
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07712161T Active ES2401458T3 (es) | 2006-02-17 | 2007-02-07 | Filtros de color azul con contraste mejorado |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8148358B2 (enExample) |
| EP (1) | EP1984457B1 (enExample) |
| JP (1) | JP5335442B2 (enExample) |
| KR (1) | KR101455122B1 (enExample) |
| CN (1) | CN101384672B (enExample) |
| ES (1) | ES2401458T3 (enExample) |
| TW (1) | TWI415906B (enExample) |
| WO (1) | WO2007093536A2 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4575967B2 (ja) * | 2008-03-12 | 2010-11-04 | 住友ゴム工業株式会社 | カラーフィルタの製造方法 |
| TWI466964B (zh) * | 2008-10-28 | 2015-01-01 | Sumitomo Chemical Co | 著色組成物之製造方法 |
| US8669026B2 (en) | 2009-01-19 | 2014-03-11 | Basf Se | Black matrix for colour filters |
| JP2011221515A (ja) | 2010-03-23 | 2011-11-04 | Fujifilm Corp | カラーフィルタ及び電子表示装置 |
| CN102620243B (zh) * | 2011-02-01 | 2014-04-09 | 光宝电子(广州)有限公司 | 照明装置与其介质层的调色剂颜色选择方法 |
| JP5962388B2 (ja) * | 2011-10-07 | 2016-08-03 | 住友化学株式会社 | 着色硬化性樹脂組成物 |
| JP5932435B2 (ja) * | 2012-03-29 | 2016-06-08 | サカタインクス株式会社 | カラーフィルター用青色顔料分散組成物及びそれを含有するカラーフィルター用青色顔料分散レジスト組成物 |
| TWI624452B (zh) * | 2017-05-10 | 2018-05-21 | 財團法人工業技術研究院 | 蒽醌化合物以及其作為染料之用途 |
| JP7263709B2 (ja) * | 2018-07-20 | 2023-04-25 | 東洋インキＳｃホールディングス株式会社 | カラーフィルタ用着色組成物およびカラーフィルタ |
Family Cites Families (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1981424A (en) * | 1934-06-27 | 1934-11-20 | Excel Auto Radiator Company | Heat exchange device |
| GB623593A (en) * | 1946-03-07 | 1949-05-19 | American Cyanamid Co | Green pigment compositions |
| CH430911A (de) * | 1958-04-23 | 1967-02-28 | Geigy Ag J R | Verfahren zur Herstellung von sulfonierten Farbstoffen |
| CH636893A5 (de) * | 1977-05-26 | 1983-06-30 | Ciba Geigy Ag | Wasserloesliche anthrachinonfarbstoffe. |
| LU78509A1 (de) * | 1977-11-14 | 1979-06-13 | Ciba Geigy Ag | Verfahren zur herstellung neuer anthrachinonverbindungen |
| US4244691A (en) * | 1978-11-24 | 1981-01-13 | Ciba-Geigy Corporation | Novel water-soluble anthraquinone dyes |
| US4465491A (en) * | 1982-01-18 | 1984-08-14 | Ciba-Geigy Corporation | Solid dye preparation of water soluble dyes with aliphatic aminocarboxylic acid |
| JPS60192903A (ja) * | 1984-03-14 | 1985-10-01 | Canon Inc | カラ−フイルタ− |
| JPS61165704A (ja) * | 1984-12-28 | 1986-07-26 | Canon Inc | カラ−フイルタ− |
| US4793692A (en) * | 1984-12-14 | 1988-12-27 | Canon Kabushiki Kaisha | Color filter |
| DE3783128D1 (de) * | 1986-12-29 | 1993-01-28 | Ciba Geigy Ag | Neue stoffzusammensetzungen auf der basis von c.i. pigment rot 177. |
| GB9107651D0 (en) * | 1991-04-11 | 1991-05-29 | Ciba Geigy Ag | Pigment compositions |
| JP3229642B2 (ja) * | 1992-03-11 | 2001-11-19 | 三井化学株式会社 | カラーフィルター用青色色素 |
| DE69421122T2 (de) * | 1993-07-09 | 2000-01-20 | Mitsui Chemicals, Inc. | Neue Farbstoffe und ihre Verwendung |
| JP3655328B2 (ja) * | 1993-07-09 | 2005-06-02 | 三井化学株式会社 | 新規色素およびその用途 |
| JPH0829771A (ja) * | 1994-07-15 | 1996-02-02 | Canon Inc | カラーフィルタ、その製造方法、及びカラーフィルタを備えた液晶パネル |
| JPH08100122A (ja) * | 1994-08-02 | 1996-04-16 | Mitsui Toatsu Chem Inc | 光学フィルター用ポリイミド樹脂組成物 |
| KR100200199B1 (ko) * | 1994-08-02 | 1999-06-15 | 사또 아끼오 | 광학필터용 폴리이미드수지조성물 |
| JPH08295820A (ja) * | 1995-04-25 | 1996-11-12 | Mitsubishi Chem Corp | カラーフィルター用顔料分散液 |
| JP3126665B2 (ja) * | 1996-09-30 | 2001-01-22 | 株式会社日本触媒 | 色素組成物およびこれを用いてなるカラーフィルター |
| KR100256392B1 (ko) * | 1996-09-30 | 2000-05-15 | 겐지 아이다 | 칼라필터용 감광성 수지 착색 조성물 및 이로부터 형성된 칼라필터 및 그 제조방법 |
| US5834122A (en) * | 1996-11-25 | 1998-11-10 | Hoechst Celanese Corp. | Spectrally tuned multiple bandpass filters for video displays |
| JP2000047016A (ja) * | 1998-07-27 | 2000-02-18 | Toppan Printing Co Ltd | カラーフィルター及びその製造方法 |
| JP2000044822A (ja) * | 1998-08-03 | 2000-02-15 | Toppan Printing Co Ltd | 着色組成物及びそれを用いたカラーフィルター並びにその製造方法 |
| JP3736221B2 (ja) * | 1998-08-28 | 2006-01-18 | 凸版印刷株式会社 | カラーフィルターおよびこれを備えた液晶表示装置 |
| JP2001066421A (ja) * | 1999-08-31 | 2001-03-16 | Mitsubishi Chemicals Corp | 光線透過フィルター |
| JP2001108815A (ja) * | 1999-10-07 | 2001-04-20 | Toppan Printing Co Ltd | カラーフィルター及びその製造方法 |
| JP3389561B2 (ja) * | 1999-11-19 | 2003-03-24 | 山陽色素株式会社 | 光選択吸収性フィルター及び該フィルターを備えたカラー表示装置 |
| EP1130065B1 (en) * | 2000-02-04 | 2006-03-08 | Dainichiseika Color & Chemicals Mfg. Co. Ltd. | Pigment compositions, production process thereof; colorants; and colored articles |
| CN100480336C (zh) * | 2000-07-07 | 2009-04-22 | 西巴特殊化学品控股有限公司 | 颜料酞菁铜固溶体以及包含它的透明分散体 |
| JP2002322380A (ja) * | 2001-04-25 | 2002-11-08 | Fuji Photo Film Co Ltd | ビス型アントラキノン化合物、これを含む着色樹脂組成物及び着色感光性組成物、並びにカラーフィルタ |
| ATE545681T1 (de) * | 2002-03-22 | 2012-03-15 | Huntsman Adv Mat Switzerland | Anthrachinonfarbstoffe |
| JP4552377B2 (ja) * | 2003-01-15 | 2010-09-29 | コニカミノルタホールディングス株式会社 | アントラピリジン化合物及びその製造方法 |
| JP2004307632A (ja) * | 2003-04-07 | 2004-11-04 | Konica Minolta Holdings Inc | インクジェット用インク、インクジェット記録方法 |
| JP4378163B2 (ja) * | 2003-12-16 | 2009-12-02 | 東洋インキ製造株式会社 | カラーフィルタ用青色着色組成物およびカラーフィルタ |
| JP2005196018A (ja) * | 2004-01-09 | 2005-07-21 | Konica Minolta Holdings Inc | カラートナー、光記録媒体、感熱転写記録材料、及びカラーフィルター |
| EP2078978A3 (en) * | 2004-04-26 | 2009-07-22 | Mitsubishi Chemical Corporation | LCD backlight containing a LED with adapted light emission and suitable colour filters |
| JP2006010910A (ja) * | 2004-06-24 | 2006-01-12 | Sumitomo Chemical Co Ltd | 着色感光性組成物 |
| TW200613452A (en) * | 2004-06-25 | 2006-05-01 | Clariant Int Ltd | Bridged bisanthraquinone dye derivatives |
| WO2006024617A1 (en) * | 2004-09-03 | 2006-03-09 | Huntsman Advanced Materials (Switzerland) Gmbh | Compositions containing anthraquinone dyes |
-
2007
- 2007-02-07 KR KR1020087022714A patent/KR101455122B1/ko not_active Expired - Fee Related
- 2007-02-07 WO PCT/EP2007/051154 patent/WO2007093536A2/en not_active Ceased
- 2007-02-07 US US12/223,140 patent/US8148358B2/en not_active Expired - Fee Related
- 2007-02-07 JP JP2008554735A patent/JP5335442B2/ja not_active Expired - Fee Related
- 2007-02-07 ES ES07712161T patent/ES2401458T3/es active Active
- 2007-02-07 CN CN2007800057027A patent/CN101384672B/zh not_active Expired - Fee Related
- 2007-02-07 EP EP07712161A patent/EP1984457B1/en not_active Not-in-force
- 2007-02-16 TW TW096106167A patent/TWI415906B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CN101384672A (zh) | 2009-03-11 |
| EP1984457A2 (en) | 2008-10-29 |
| JP5335442B2 (ja) | 2013-11-06 |
| KR20080105085A (ko) | 2008-12-03 |
| JP2009527014A (ja) | 2009-07-23 |
| TWI415906B (zh) | 2013-11-21 |
| KR101455122B1 (ko) | 2014-10-28 |
| WO2007093536A2 (en) | 2007-08-23 |
| EP1984457B1 (en) | 2013-01-09 |
| CN101384672B (zh) | 2012-08-08 |
| WO2007093536A3 (en) | 2008-02-28 |
| US20100227199A1 (en) | 2010-09-09 |
| US8148358B2 (en) | 2012-04-03 |
| TW200736348A (en) | 2007-10-01 |
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