JP5251329B2

JP5251329B2 - カラーフィルタ用青色着色組成物、カラーフィルタおよびカラー表示装置

カラーフィルタ用青色着色組成物、カラーフィルタおよびカラー表示装置 Download PDF

Info

Publication number: JP5251329B2
Authority: JP; Japan
Prior art keywords: pigment; blue; color filter; color; red
Prior art date: 2008-07-22
Legal status : Active

Application number

JP2008189131A

Other languages

English (en)

Japanese (ja)

Other versions

JP2010026334A (ja

JP2010026334A5 (zh

Inventor

充志西田

高士中村

英雄高橋

美智子玉野

Current Assignee

Toyo Ink SC Holdings Co Ltd

Original Assignee

Toyo Ink SC Holdings Co Ltd

Priority date

2008-07-22

Filing date

2008-07-22

Publication date

2013-07-31

2008-07-22 Application filed by Toyo Ink SC Holdings Co Ltd filed Critical Toyo Ink SC Holdings Co Ltd

2008-07-22 Priority to JP2008189131A priority Critical patent/JP5251329B2/ja

2009-07-09 Priority to TW098123277A priority patent/TWI454754B/zh

2009-07-21 Priority to KR1020090066433A priority patent/KR20100010490A/ko

2009-07-22 Priority to CN200910161608.1A priority patent/CN101634725B/zh

2010-02-04 Publication of JP2010026334A publication Critical patent/JP2010026334A/ja

2011-04-14 Publication of JP2010026334A5 publication Critical patent/JP2010026334A5/ja

2013-07-31 Application granted granted Critical

2013-07-31 Publication of JP5251329B2 publication Critical patent/JP5251329B2/ja

Status Active legal-status Critical Current

2028-07-22 Anticipated expiration legal-status Critical

Links

239000000203 mixture Substances 0.000 title claims description 134
238000004040 coloring Methods 0.000 title claims description 74
239000000049 pigment Substances 0.000 claims description 179
229920005989 resin Polymers 0.000 claims description 53
239000011347 resin Substances 0.000 claims description 53
229910052751 metal Inorganic materials 0.000 claims description 48
239000002184 metal Substances 0.000 claims description 48
XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 claims description 47
239000001055 blue pigment Substances 0.000 claims description 42
239000001018 xanthene dye Substances 0.000 claims description 39
239000003086 colorant Substances 0.000 claims description 36
239000000178 monomer Substances 0.000 claims description 19
239000003505 polymerization initiator Substances 0.000 claims description 16
239000001022 rhodamine dye Substances 0.000 claims description 6
239000010410 layer Substances 0.000 description 94
238000000034 method Methods 0.000 description 60
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239000006185 dispersion Substances 0.000 description 44
239000000463 material Substances 0.000 description 39
238000002347 injection Methods 0.000 description 36
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NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 21
239000003999 initiator Substances 0.000 description 21
238000002834 transmittance Methods 0.000 description 21
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239000002253 acid Substances 0.000 description 18
239000000975 dye Substances 0.000 description 17
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239000001052 yellow pigment Substances 0.000 description 15
239000011521 glass Substances 0.000 description 13
239000000243 solution Substances 0.000 description 13
239000004925 Acrylic resin Substances 0.000 description 12
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238000006243 chemical reaction Methods 0.000 description 10
239000001054 red pigment Substances 0.000 description 10
238000004519 manufacturing process Methods 0.000 description 9
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238000000295 emission spectrum Methods 0.000 description 8
239000001056 green pigment Substances 0.000 description 8
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238000001035 drying Methods 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000001914 filtration Methods 0.000 description 4
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 description 4
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
229910052725 zinc Inorganic materials 0.000 description 4
IYZMXHQDXZKNCY-UHFFFAOYSA-N 1-n,1-n-diphenyl-4-n,4-n-bis[4-(n-phenylanilino)phenyl]benzene-1,4-diamine Chemical compound C1=CC=CC=C1N(C=1C=CC(=CC=1)N(C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 IYZMXHQDXZKNCY-UHFFFAOYSA-N 0.000 description 3
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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 3
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125000003277 amino group Chemical group 0.000 description 3
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239000012965 benzophenone Substances 0.000 description 3
UFVXQDWNSAGPHN-UHFFFAOYSA-K bis[(2-methylquinolin-8-yl)oxy]-(4-phenylphenoxy)alumane Chemical compound [Al+3].C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC([O-])=CC=C1C1=CC=CC=C1 UFVXQDWNSAGPHN-UHFFFAOYSA-K 0.000 description 3
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229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
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125000005504 styryl group Chemical group 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
238000012719 thermal polymerization Methods 0.000 description 3
TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 3
238000007740 vapor deposition Methods 0.000 description 3
CFXQEHVMCRXUSD-UHFFFAOYSA-N 1,2,3-Trichloropropane Chemical compound ClCC(Cl)CCl CFXQEHVMCRXUSD-UHFFFAOYSA-N 0.000 description 2
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VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical class NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 2
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UHXOHPVVEHBKKT-UHFFFAOYSA-N 1-(2,2-diphenylethenyl)-4-[4-(2,2-diphenylethenyl)phenyl]benzene Chemical group C=1C=C(C=2C=CC(C=C(C=3C=CC=CC=3)C=3C=CC=CC=3)=CC=2)C=CC=1C=C(C=1C=CC=CC=1)C1=CC=CC=C1 UHXOHPVVEHBKKT-UHFFFAOYSA-N 0.000 description 2
SPDPTFAJSFKAMT-UHFFFAOYSA-N 1-n-[4-[4-(n-[4-(3-methyl-n-(3-methylphenyl)anilino)phenyl]anilino)phenyl]phenyl]-4-n,4-n-bis(3-methylphenyl)-1-n-phenylbenzene-1,4-diamine Chemical compound CC1=CC=CC(N(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=CC(=CC=2)C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=CC(=CC=2)N(C=2C=C(C)C=CC=2)C=2C=C(C)C=CC=2)C=2C=C(C)C=CC=2)=C1 SPDPTFAJSFKAMT-UHFFFAOYSA-N 0.000 description 2
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UOCMXZLNHQBBOS-UHFFFAOYSA-N 2-(1,3-benzoxazol-2-yl)phenol zinc Chemical compound [Zn].Oc1ccccc1-c1nc2ccccc2o1.Oc1ccccc1-c1nc2ccccc2o1 UOCMXZLNHQBBOS-UHFFFAOYSA-N 0.000 description 2
FQJQNLKWTRGIEB-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-5-[3-[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]phenyl]-1,3,4-oxadiazole Chemical compound C1=CC(C(C)(C)C)=CC=C1C1=NN=C(C=2C=C(C=CC=2)C=2OC(=NN=2)C=2C=CC(=CC=2)C(C)(C)C)O1 FQJQNLKWTRGIEB-UHFFFAOYSA-N 0.000 description 2
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125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 2
FGTYTUFKXYPTML-UHFFFAOYSA-N 2-benzoylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 FGTYTUFKXYPTML-UHFFFAOYSA-N 0.000 description 2
POSWICCRDBKBMH-UHFFFAOYSA-N 3,3,5-trimethylcyclohexan-1-one Chemical compound CC1CC(=O)CC(C)(C)C1 POSWICCRDBKBMH-UHFFFAOYSA-N 0.000 description 2
SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 2
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HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
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UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
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