JP2008268854A - ブラックマトリックス用感光性樹脂組成物、それを用いた硬化物及びカラーフィルター - Google Patents
ブラックマトリックス用感光性樹脂組成物、それを用いた硬化物及びカラーフィルター Download PDFInfo
- Publication number
- JP2008268854A JP2008268854A JP2007298420A JP2007298420A JP2008268854A JP 2008268854 A JP2008268854 A JP 2008268854A JP 2007298420 A JP2007298420 A JP 2007298420A JP 2007298420 A JP2007298420 A JP 2007298420A JP 2008268854 A JP2008268854 A JP 2008268854A
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- Prior art keywords
- acid
- resin composition
- alkali
- general formula
- photosensitive resin
- 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.)
- Granted
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- 239000011342 resin composition Substances 0.000 title claims abstract description 44
- 239000011159 matrix material Substances 0.000 title claims abstract description 31
- 229920005989 resin Polymers 0.000 claims abstract description 74
- 239000011347 resin Substances 0.000 claims abstract description 74
- 239000000049 pigment Substances 0.000 claims abstract description 16
- 239000003999 initiator Substances 0.000 claims abstract description 15
- 239000000178 monomer Substances 0.000 claims abstract description 14
- 150000001732 carboxylic acid derivatives Chemical group 0.000 claims abstract description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 abstract description 24
- 239000003513 alkali Substances 0.000 abstract description 14
- 239000002253 acid Substances 0.000 description 65
- -1 dihydroxypropyl acrylate compound Chemical class 0.000 description 55
- 150000001875 compounds Chemical class 0.000 description 41
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 31
- 239000004593 Epoxy Substances 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 24
- 239000007787 solid Substances 0.000 description 23
- 238000003786 synthesis reaction Methods 0.000 description 22
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 20
- 238000011161 development Methods 0.000 description 17
- 230000018109 developmental process Effects 0.000 description 17
- 239000010408 film Substances 0.000 description 17
- 239000002904 solvent Substances 0.000 description 15
- 239000007795 chemical reaction product Substances 0.000 description 14
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 14
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- 239000000243 solution Substances 0.000 description 13
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 12
- 150000008065 acid anhydrides Chemical class 0.000 description 12
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 10
- 238000000576 coating method Methods 0.000 description 10
- 239000004973 liquid crystal related substance Substances 0.000 description 10
- 238000005227 gel permeation chromatography Methods 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000000758 substrate Substances 0.000 description 8
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 8
- KMOUUZVZFBCRAM-UHFFFAOYSA-N 1,2,3,6-tetrahydrophthalic anhydride Chemical compound C1C=CCC2C(=O)OC(=O)C21 KMOUUZVZFBCRAM-UHFFFAOYSA-N 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 6
- 229930185605 Bisphenol Natural products 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 238000001723 curing Methods 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- 230000035945 sensitivity Effects 0.000 description 6
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 5
- WKDNYTOXBCRNPV-UHFFFAOYSA-N bpda Chemical compound C1=C2C(=O)OC(=O)C2=CC(C=2C=C3C(=O)OC(C3=CC=2)=O)=C1 WKDNYTOXBCRNPV-UHFFFAOYSA-N 0.000 description 5
- 238000010894 electron beam technology Methods 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 4
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical group C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000012860 organic pigment Substances 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 230000002194 synthesizing effect Effects 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 3
- JVERADGGGBYHNP-UHFFFAOYSA-N 5-phenylbenzene-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C1=C(C(O)=O)C(C(=O)O)=CC(C=2C=CC=CC=2)=C1C(O)=O JVERADGGGBYHNP-UHFFFAOYSA-N 0.000 description 3
- YWFPGFJLYRKYJZ-UHFFFAOYSA-N 9,9-bis(4-hydroxyphenyl)fluorene Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 YWFPGFJLYRKYJZ-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000012965 benzophenone Substances 0.000 description 3
- ZCILODAAHLISPY-UHFFFAOYSA-N biphenyl ether Natural products C1=C(CC=C)C(O)=CC(OC=2C(=CC(CC=C)=CC=2)O)=C1 ZCILODAAHLISPY-UHFFFAOYSA-N 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- 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 2
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 2
- UITKHKNFVCYWNG-UHFFFAOYSA-N 4-(3,4-dicarboxybenzoyl)phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1C(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 UITKHKNFVCYWNG-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
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- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- 238000000016 photochemical curing Methods 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- UOHMMEJUHBCKEE-UHFFFAOYSA-N prehnitene Chemical compound CC1=CC=C(C)C(C)=C1C UOHMMEJUHBCKEE-UHFFFAOYSA-N 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
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- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000012719 thermal polymerization Methods 0.000 description 2
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- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- DJKGDNKYTKCJKD-BPOCMEKLSA-N (1s,4r,5s,6r)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene-5,6-dicarboxylic acid Chemical compound ClC1=C(Cl)[C@]2(Cl)[C@H](C(=O)O)[C@H](C(O)=O)[C@@]1(Cl)C2(Cl)Cl DJKGDNKYTKCJKD-BPOCMEKLSA-N 0.000 description 1
- VMHYWKBKHMYRNF-UHFFFAOYSA-N (2-chlorophenyl)-phenylmethanone Chemical compound ClC1=CC=CC=C1C(=O)C1=CC=CC=C1 VMHYWKBKHMYRNF-UHFFFAOYSA-N 0.000 description 1
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
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Landscapes
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Abstract
【解決手段】(i)1分子内にカルボン酸残基及び重合性不飽和基を有するアルカリ可溶性樹脂、(ii)少なくとも1個以上のエチレン性不飽和結合を有する光重合性モノマー、(iii)光重合開始剤、及び(iv)遮光性顔料を必須の成分として含有することを特徴とするブラックマトリックス用感光性樹脂組成物である。
【選択図】なし
Description
(ii)少なくとも1個以上のエチレン性不飽和結合を有する光重合性モノマー、
(iii)光重合開始剤、及び
(iv)遮光性顔料
を必須の成分として含有することを特徴とするブラックマトリックス用感光性樹脂組成物である。
本発明の感光性樹脂組成物は、一般式(1)で表されるアルカリ可溶性樹脂を主成分として含有するアルカリ現像型感光性樹脂組成物としての性質を有する樹脂組成物である。一般式(1)で表されるアルカリ可溶性樹脂は、(メタ)アクリル酸を有するジオール化合物に由来する光重合性不飽和基を有するためにラジカル重合性を有するほか、ジカルボン酸又はその酸一無水物及びテトラカルボン酸又はその酸二無水物に由来する酸性基を含有するためアルカリ可溶性を有する。
先ず、9,9-ビス(4-ヒドロキシフェニル)フルオレンとエピクロロヒドリンとを反応させて下記一般式(10)で表されるビスフェノールフルオレン型エポキシ化合物を合成し、このビスフェノールフルオレン型エポキシ化合物とCH2=CHR5-COOH(R5は前記と同じ)で表される(メタ)アクリル酸とを反応させて下記一般式(11)で表されるビスフェノールフルオレン型エポキシ(メタ)アクリレート樹脂を合成する。次いで、このビスフェノールフルオレン型エポキシ(メタ)アクリレート樹脂をプロピレングリコールモノメチルエーテルアセテート等の溶剤中で加熱下、酸二無水物(B)、オキシラン化合物(C)、酸一無水物(D)と順次反応させて、上記一般式(1)のアルカリ可溶性樹脂を得る。
合成例(及び比較合成例)中で得られた樹脂溶液(反応生成物やアルカリ可溶性樹脂の場合を含む)1gをガラスフィルター〔重量:W0(g)〕に含浸させて秤量し〔W1(g)〕、160℃にて2hr加熱した後の重量〔W2(g)〕から次式より求めた。
固形分濃度(重量%)=100×(W2―W0)/(W1―W0)
樹脂溶液をジオキサンに溶解させ、フェノールフタレインを指示薬として1/10N−KOH水溶液で滴定して求めた。
テトラヒドロフランを展開溶媒として、ゲルパーミュエーションクロマトグラフィー(GPC)にて標準ポリスチレン換算値として重量平均分子量(Mw)を求めた値である。
FHPA:ビスフェノールフルオレン型エポキシ樹脂とアクリル酸との等当量反応物(新日鐵化学社製、ASF-400溶液:固形分濃度50wt%、固形分換算の酸価1.28mgKOH/g)
FHPPA:ビス(フェニルフェノール)フルオレン型エポキシ樹脂とアクリル酸との等当量反応物(50wt%PGMEA溶液、固形分換算の酸価7.51mgKOH/g)
BisA-GEA:ビスフェノールAジグリシジルエーテルとアクリル酸との当量反応物(50wt%PGMEA溶液、固形分換算の酸価1.72mgKOH/g)
BPDA:3,3',4,4'-ビフェニルテトラカルボン酸二無水物
BTDA:3,3',4,4'-ベンゾフェノンテトラカルボン酸二無水物
ODPA:3,3',4,4'-オキシジフェニルテトラカルボン酸二無水物
CHDA:3,3',4,4'-オキシジフェニルテトラカルボン酸二無水物
THPA:1,2,3,6-テトラヒドロフタル酸無水物
HHPA:ヘキサヒドロフタル酸無水物
GMA:グリシジルメタクリレート
HBAGE:4-ヒドロキシブチルアクリレートグリシジルエーテル
TEAB:臭化テトラエチルアンモニウム
TPP:トリフェニルホスフィン
PGMEA:プロピレングリコールモノメチルエーテルアセテート
還留冷却器付き1000ml四つ口フラスコ中にFHPA〔(A)成分〕の50%PGMEA溶液を600.00g(0.49mol)、BPDA〔(B)成分〕を72.75g(0.247mol)、PGMEAを39.56g、及びTPPを1.30g仕込み、120〜125℃で加熱下に2hr撹拌し、更に70〜75℃にて6hrの加熱撹拌を行い、反応生成物(a)を得た。得られた反応生成物(a)の固形分濃度は52.4wt%、樹脂の酸価(固形分換算)は78.0mgKOH/g、及びGPC分析による重量平均分子量(Mw)は3400であった。
上記合成例1におけるTHPA〔(D)成分〕の仕込み量を118.68g(0.78mol)に変えた以外は、合成例1と同様にして反応を行い、アルカリ可溶性樹脂(i)-2を得た。
還留冷却器付き1000ml四つ口フラスコ中にFHPA(A)の50%PGMEA溶液を600.00g(0.49mol)、BPDA〔(B)成分〕を96.02g(0.33mol)、PGMEAを4.36g、及びTEABを1.02g仕込み、120〜125℃で加熱下に2hr撹拌し、更に60〜65℃にて8hrの加熱撹拌を行い、反応生成物(b)を得た。得られた反応生成物(b)の固形分濃度は57.8wt%、酸価(固形分換算)は91.6mgKOH/g、GPC分析によるMwは8800であった。
還留冷却器付き500ml四つ口フラスコ中にFHPAの50%PGMEA溶液を206.26g(0.17mol)、BPDAを0.085mol、THPAを0.085mol、PGMEAを26.0g及びTPPを0.45g仕込み、120〜125℃で加熱下に6hr撹拌し、樹脂(i)-4を得た。得られた樹脂溶液の固形分濃度は55.6wt%、酸価(固形分換算)は103.0mgKOH/g、GPC分析によるMwは2600であった。
還留冷却器付き1000ml四つ口フラスコ中にFHPAの50%PGMEA溶液を600.00g(0.49mol)、BPDAを96.02g(0.33mol)、PGMEAを4.36g、及びTEABを1.02g仕込み、120〜125℃で加熱下に2hr撹拌し、更に60〜65℃にて8hrの加熱撹拌を行い、樹脂(i)-5を得た。得られた樹脂溶液の固形分濃度は58.5wt%、酸価(固形分換算)は91.0mgKOH/g、GPC分析によるMwは8600であった。
(i)-2成分:上記合成例2で得られたアルカリ可溶性樹脂
(i)-3成分:上記合成例3で得られたアルカリ可溶性樹脂
(i)-4成分:上記比較合成例1で得られたアルカリ可溶性樹脂
(i)-5成分:上記比較合成例2で得られたアルカリ可溶性樹脂
(ii)-1 成分:ジペンタエリスリトールヘキサアクリレート
(ii)-2 成分:トリメチロールプロパントリアクリレート
(iii)-1成分:オキシムエステル系光重合開始剤(チバスペシャリティケミカルズ製、イルガキュアOXE02)
(iii)-2成分:ベンゾフェノン系光重合開始剤(チバスペシャリティケミカルズ製、イルガキュア 369)
(iv)-1成分:顔料濃度20.0%、総固形分24%のカーボン分散体(平均粒径100〜130nm)
(iv)-2成分:顔料濃度20.0%、総固形分29%のカーボン分散体(平均粒径100〜150nm)
溶剤-1:プロピレングリコールモノメチルエーテルアセテート
溶剤-2:シクロヘキサノン
添加剤-1:シランカップリング剤(東レダウコーニング製SH-6040)
表2に示したブラックレジスト用感光性樹脂組成物を、スピンコーターを用いて125mm×125mmのガラス基板上にポストベーク後の膜厚が0.9〜1.0μmとなるように塗布し、80℃で1分間プリベークして塗布板を作成した。その後、500W/cm2の高圧水銀ランプで波長365nmの照度100mJ/cm2の紫外線を照射し感光部分の光硬化反応を行った。次に、この露光済み塗板を0.04wt%水酸化カリウム水溶液または0.5wt%炭酸ナトリウム水溶液中、24℃のシャワー現像にてパターンが現像されてからさらに30秒の現像を行い、さらにスプレー水洗を行い、塗膜の未露光部を除去した。その後、熱風乾燥機を用いて230℃、30分間加熱乾燥処理を行って、実施例1〜6、及び比較例1〜4に係るブラックマトリックスを得た。
触針式段差形状測定装置(ケーエルエー・テンコール(株)製 商品名P-10)を用いて測定した。
アルカリ現像時、全てのパターンが見えるのに要した時間を記録し、現像時間が120秒を超えてもパターンが見えない場合は×とした。
10μmパターンマスクで露光した部分を現像した際に、パターンが見えてからパターン部が10±1μmを維持している時間を記録した。パターン部の線幅は測長顕微鏡((株)ニコン製 商品名XD-20)を用いて測定した。
現像後のパターンを、走査型電子顕微鏡((株)KEYENCE製 商品名VE-780)を用いて観察し、パターンの断面形状が順テーパーを維持している場合は○、逆テーパーや剥がれが生じた場合は×とした。
現像後の10μm線について上記測長顕微鏡でパターン部の直線性やフリンジなどの有無を評価した。そこで、直線性がよく、フリンジなどが発生していないものに関しては○<良好>とし、フリンジなどが発生し、直線性の悪いものを×<不良>と評価した。各項目とも非常に良好な場合に限り◎と評価した。
光学濃度計(大塚電子株式会社製)を用いて測定した。
Claims (3)
- (i)下記一般式(1)で表されて、1分子内にカルボン酸残基及び重合性不飽和基を有するアルカリ可溶性樹脂、
(ii)少なくとも1個以上のエチレン性不飽和結合を有する光重合性モノマー、
(iii)光重合開始剤、及び
(iv)遮光性顔料
を必須の成分として含有することを特徴とするブラックマトリックス用感光性樹脂組成物。 - 請求項1に記載のブラックマトリックス用感光性樹脂組成物を硬化させて得た硬化物。
- 請求項1に記載のブラックマトリックス用感光性樹脂組成物を塗布し、硬化させて得られる硬化物によって形成されたカラーフィルター。
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Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101943863A (zh) * | 2009-03-03 | 2011-01-12 | 新日铁化学株式会社 | 黑抗蚀剂用感光性树脂组合物及滤色器遮光膜 |
CN104062848A (zh) * | 2013-03-19 | 2014-09-24 | 奇美实业股份有限公司 | 感光性树脂组成物、黑色矩阵、彩色滤光片及液晶显示元件 |
JP2014201710A (ja) * | 2013-04-09 | 2014-10-27 | ナガセケムテックス株式会社 | 感光性アルカリ可溶性樹脂 |
JP2014206727A (ja) * | 2013-03-21 | 2014-10-30 | 新日鉄住金化学株式会社 | 絶縁膜用感光性樹脂組成物及び硬化物 |
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Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5315106B2 (ja) | 2009-03-25 | 2013-10-16 | 新日鉄住金化学株式会社 | アルカリ可溶性樹脂及びその製造方法、並びにアルカリ可溶性樹脂を用いた感光性樹脂組成物 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003176343A (ja) * | 2001-12-11 | 2003-06-24 | Nagase Chemtex Corp | 光重合性不飽和樹脂、その製造方法及びそれを用いたアルカリ可溶型感放射線性樹脂組成物 |
JP2004069754A (ja) * | 2002-08-01 | 2004-03-04 | Tokyo Ohka Kogyo Co Ltd | 光重合性黒色組成物及び黒色パターンの形成方法 |
JP2005258254A (ja) * | 2004-03-15 | 2005-09-22 | Sumitomo Chemical Co Ltd | 黒色感光性樹脂組成物 |
JP2006003860A (ja) * | 2003-11-26 | 2006-01-05 | Nippon Steel Chem Co Ltd | 感光性樹脂組成物及びそれを用いたカラーフィルター |
JP2006276421A (ja) * | 2005-03-29 | 2006-10-12 | Nippon Steel Chem Co Ltd | 感光性樹脂組成物及びそれを用いたカラーフィルター |
-
2007
- 2007-11-16 JP JP2007298420A patent/JP5133658B2/ja active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003176343A (ja) * | 2001-12-11 | 2003-06-24 | Nagase Chemtex Corp | 光重合性不飽和樹脂、その製造方法及びそれを用いたアルカリ可溶型感放射線性樹脂組成物 |
JP2004069754A (ja) * | 2002-08-01 | 2004-03-04 | Tokyo Ohka Kogyo Co Ltd | 光重合性黒色組成物及び黒色パターンの形成方法 |
JP2006003860A (ja) * | 2003-11-26 | 2006-01-05 | Nippon Steel Chem Co Ltd | 感光性樹脂組成物及びそれを用いたカラーフィルター |
JP2005258254A (ja) * | 2004-03-15 | 2005-09-22 | Sumitomo Chemical Co Ltd | 黒色感光性樹脂組成物 |
JP2006276421A (ja) * | 2005-03-29 | 2006-10-12 | Nippon Steel Chem Co Ltd | 感光性樹脂組成物及びそれを用いたカラーフィルター |
Cited By (10)
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US9063422B2 (en) | 2011-11-25 | 2015-06-23 | Chi Mei Corporation | Photosensitive resin composition and application of the same |
US9791773B2 (en) | 2012-12-20 | 2017-10-17 | Chi Mei Corporation | Photosensitive resin composition, color filter and liquid crystal display device |
CN104062848A (zh) * | 2013-03-19 | 2014-09-24 | 奇美实业股份有限公司 | 感光性树脂组成物、黑色矩阵、彩色滤光片及液晶显示元件 |
JP2014206727A (ja) * | 2013-03-21 | 2014-10-30 | 新日鉄住金化学株式会社 | 絶縁膜用感光性樹脂組成物及び硬化物 |
JP2014201710A (ja) * | 2013-04-09 | 2014-10-27 | ナガセケムテックス株式会社 | 感光性アルカリ可溶性樹脂 |
US9557443B2 (en) | 2013-06-20 | 2017-01-31 | Chi Mei Corporation | Photosensitive resin composition, black matrix, color filter, and liquid crystal display device |
JP2015111264A (ja) * | 2013-12-03 | 2015-06-18 | 奇美實業股▲分▼有限公司 | 感光性樹脂組成物、カラーフィルターおよびその製造方法、ならびに液晶表示装置 |
US10591816B2 (en) | 2014-10-15 | 2020-03-17 | Chi Mei Corporation | Photosensitive resin composition, color filter, and liquid crystal display element thereof |
KR20220131162A (ko) | 2021-03-19 | 2022-09-27 | 닛테츠 케미컬 앤드 머티리얼 가부시키가이샤 | 감광성 수지, 그것을 사용한 감광성 수지 조성물, 그 경화물 및 컬러 필터 |
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