KR20060047458A

KR20060047458A - 착색층 형성용 감방사선성 조성물, 칼라 필터 및 액정 표시패널

착색층 형성용 감방사선성 조성물, 칼라 필터 및 액정 표시패널 Download PDF

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Publication number: KR20060047458A
Authority: KR; South Korea
Prior art keywords: group; acid; weight; meth; pigment
Prior art date: 2004-04-27
Legal status : Ceased

Application number

KR1020050034446A

Other languages

English (en)

Korean (ko)

Inventor

사또꼬 아비꼬

시게루 아베

도미오 나가쯔까

Original Assignee

제이에스알 가부시끼가이샤

Priority date

2004-04-27

Filing date

2005-04-26

Publication date

2006-05-18

2005-04-26 Application filed by 제이에스알 가부시끼가이샤 filed Critical 제이에스알 가부시끼가이샤

2006-05-18 Publication of KR20060047458A publication Critical patent/KR20060047458A/ko

Status Ceased legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 129
230000005855 radiation Effects 0.000 title claims abstract description 90
239000004973 liquid crystal related substance Substances 0.000 title claims description 15
239000000178 monomer Substances 0.000 claims abstract description 45
229920005989 resin Polymers 0.000 claims abstract description 43
239000011347 resin Substances 0.000 claims abstract description 43
150000001875 compounds Chemical class 0.000 claims abstract description 32
230000015572 biosynthetic process Effects 0.000 claims abstract description 20
239000003086 colorant Substances 0.000 claims abstract description 20
239000011342 resin composition Substances 0.000 claims abstract description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 21
125000003545 alkoxy group Chemical group 0.000 claims description 19
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 15
125000006165 cyclic alkyl group Chemical group 0.000 claims description 14
125000001424 substituent group Chemical group 0.000 claims description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 5
239000007788 liquid Substances 0.000 abstract description 64
239000003505 polymerization initiator Substances 0.000 abstract description 46
238000011109 contamination Methods 0.000 abstract description 13
PUBNJSZGANKUGX-UHFFFAOYSA-N 2-(dimethylamino)-2-[(4-methylphenyl)methyl]-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=C(C)C=C1 PUBNJSZGANKUGX-UHFFFAOYSA-N 0.000 abstract description 9
238000000859 sublimation Methods 0.000 abstract description 7
230000008022 sublimation Effects 0.000 abstract description 7
239000003513 alkali Substances 0.000 abstract description 5
239000000463 material Substances 0.000 abstract description 2
239000000049 pigment Substances 0.000 description 197
-1 zincated Chemical compound 0.000 description 76
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 58
239000000758 substrate Substances 0.000 description 56
239000010408 film Substances 0.000 description 43
239000000852 hydrogen donor Substances 0.000 description 35
238000000576 coating method Methods 0.000 description 25
239000011248 coating agent Substances 0.000 description 23
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125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 22
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 21
239000000243 solution Substances 0.000 description 21
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 20
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 20
239000002904 solvent Substances 0.000 description 20
150000001412 amines Chemical class 0.000 description 19
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 19
238000000034 method Methods 0.000 description 17
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical class SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 13
VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 12
VYHBFRJRBHMIQZ-UHFFFAOYSA-N bis[4-(diethylamino)phenyl]methanone Chemical compound C1=CC(N(CC)CC)=CC=C1C(=O)C1=CC=C(N(CC)CC)C=C1 VYHBFRJRBHMIQZ-UHFFFAOYSA-N 0.000 description 12
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238000006243 chemical reaction Methods 0.000 description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 11
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LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
239000011159 matrix material Substances 0.000 description 9
WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 8
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 8
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239000012860 organic pigment Substances 0.000 description 8
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125000003277 amino group Chemical group 0.000 description 7
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OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
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230000000996 additive effect Effects 0.000 description 6
239000006229 carbon black Substances 0.000 description 6
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125000000623 heterocyclic group Chemical group 0.000 description 6
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150000007524 organic acids Chemical class 0.000 description 6
150000004027 organic amino compounds Chemical class 0.000 description 6
239000007787 solid Substances 0.000 description 6
239000004094 surface-active agent Substances 0.000 description 6
HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 5
FLFWJIBUZQARMD-UHFFFAOYSA-N 2-mercapto-1,3-benzoxazole Chemical compound C1=CC=C2OC(S)=NC2=C1 FLFWJIBUZQARMD-UHFFFAOYSA-N 0.000 description 5
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150000008062 acetophenones Chemical class 0.000 description 5
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230000008901 benefit Effects 0.000 description 5
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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 description 5
238000010304 firing Methods 0.000 description 5
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238000004528 spin coating Methods 0.000 description 5
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PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 4
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125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 4
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FZYCEURIEDTWNS-UHFFFAOYSA-N prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1.CC(=C)C1=CC=CC=C1 FZYCEURIEDTWNS-UHFFFAOYSA-N 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
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125000006606 n-butoxy group Chemical group 0.000 description 3
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