TWI326296B - Colored photosensitive resin composition - Google Patents
Colored photosensitive resin composition Download PDFInfo
- Publication number
- TWI326296B TWI326296B TW092130729A TW92130729A TWI326296B TW I326296 B TWI326296 B TW I326296B TW 092130729 A TW092130729 A TW 092130729A TW 92130729 A TW92130729 A TW 92130729A TW I326296 B TWI326296 B TW I326296B
- Authority
- TW
- Taiwan
- Prior art keywords
- acid
- mass
- pigment
- resin composition
- photosensitive resin
- Prior art date
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- 239000011342 resin composition Substances 0.000 title claims description 64
- 150000001875 compounds Chemical class 0.000 claims description 39
- 239000000758 substrate Substances 0.000 claims description 26
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 25
- 239000002904 solvent Substances 0.000 claims description 24
- 229920000642 polymer Polymers 0.000 claims description 17
- 239000003086 colorant Substances 0.000 claims description 13
- 239000003999 initiator Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 4
- 239000004973 liquid crystal related substance Substances 0.000 claims description 4
- 229930003658 monoterpene Natural products 0.000 claims description 3
- 150000002773 monoterpene derivatives Chemical class 0.000 claims description 3
- 235000002577 monoterpenes Nutrition 0.000 claims description 3
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 claims 5
- 239000000049 pigment Substances 0.000 description 114
- -1 4-hydroxy-4-methyl-2-pentanyl Chemical group 0.000 description 77
- 239000002253 acid Substances 0.000 description 39
- 238000004040 coloring Methods 0.000 description 32
- 239000000052 vinegar Substances 0.000 description 27
- 235000021419 vinegar Nutrition 0.000 description 27
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 23
- 229920001577 copolymer Polymers 0.000 description 18
- 239000003795 chemical substances by application Substances 0.000 description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 13
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 13
- 239000004094 surface-active agent Substances 0.000 description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000003822 epoxy resin Substances 0.000 description 12
- 229920000647 polyepoxide Polymers 0.000 description 12
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 239000010408 film Substances 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 9
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 8
- 230000007774 longterm Effects 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 8
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- 239000002270 dispersing agent Substances 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 6
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 150000002576 ketones Chemical class 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 6
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 5
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 230000000977 initiatory effect Effects 0.000 description 5
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 229920002125 Sokalan® Polymers 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 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 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000004584 polyacrylic acid Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 3
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 3
- DAWJJMYZJQJLPZ-UHFFFAOYSA-N 2-sulfanylprop-2-enoic acid Chemical compound OC(=O)C(S)=C DAWJJMYZJQJLPZ-UHFFFAOYSA-N 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- NUPSHWCALHZGOV-UHFFFAOYSA-N Decyl acetate Chemical compound CCCCCCCCCCOC(C)=O NUPSHWCALHZGOV-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229930182558 Sterol Natural products 0.000 description 3
- 244000028419 Styrax benzoin Species 0.000 description 3
- 235000000126 Styrax benzoin Nutrition 0.000 description 3
- 235000008411 Sumatra benzointree Nutrition 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
- REUQOSNMSWLNPD-UHFFFAOYSA-N [2-(diethylamino)phenyl]-phenylmethanone Chemical compound CCN(CC)C1=CC=CC=C1C(=O)C1=CC=CC=C1 REUQOSNMSWLNPD-UHFFFAOYSA-N 0.000 description 3
- 125000002723 alicyclic group Chemical group 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229960002130 benzoin Drugs 0.000 description 3
- 239000001273 butane Substances 0.000 description 3
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 3
- 229940018557 citraconic acid Drugs 0.000 description 3
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 3
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 3
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000001530 fumaric acid Substances 0.000 description 3
- 235000019382 gum benzoic Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 3
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 3
- AGVKXDPPPSLISR-UHFFFAOYSA-N n-ethylcyclohexanamine Chemical compound CCNC1CCCCC1 AGVKXDPPPSLISR-UHFFFAOYSA-N 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 235000003702 sterols Nutrition 0.000 description 3
- 239000001384 succinic acid Substances 0.000 description 3
- 238000005496 tempering Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- GOVVHAHLSILYMB-UHFFFAOYSA-N 1-propoxythioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C=CC=C2OCCC GOVVHAHLSILYMB-UHFFFAOYSA-N 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-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
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-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
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 2
- WXUAQHNMJWJLTG-UHFFFAOYSA-N 2-methylbutanedioic acid Chemical compound OC(=O)C(C)CC(O)=O WXUAQHNMJWJLTG-UHFFFAOYSA-N 0.000 description 2
- OQEBBZSWEGYTPG-UHFFFAOYSA-N 3-aminobutanoic acid Chemical compound CC(N)CC(O)=O OQEBBZSWEGYTPG-UHFFFAOYSA-N 0.000 description 2
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
- 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 2
- HRXZRAXKKNUKRF-UHFFFAOYSA-N 4-ethylaniline Chemical compound CCC1=CC=C(N)C=C1 HRXZRAXKKNUKRF-UHFFFAOYSA-N 0.000 description 2
- JJMDCOVWQOJGCB-UHFFFAOYSA-N 5-aminopentanoic acid Chemical compound [NH3+]CCCCC([O-])=O JJMDCOVWQOJGCB-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 240000006927 Foeniculum vulgare Species 0.000 description 2
- 235000004204 Foeniculum vulgare Nutrition 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- FFOPEPMHKILNIT-UHFFFAOYSA-N Isopropyl butyrate Chemical compound CCCC(=O)OC(C)C FFOPEPMHKILNIT-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- NLAYKKCTVQAUDJ-UHFFFAOYSA-N [3-propanoyloxy-2-[[3-propanoyloxy-2,2-bis(propanoyloxymethyl)propoxy]methyl]-2-(propanoyloxymethyl)propyl] propanoate Chemical compound CCC(=O)OCC(COC(=O)CC)(COC(=O)CC)COCC(COC(=O)CC)(COC(=O)CC)COC(=O)CC NLAYKKCTVQAUDJ-UHFFFAOYSA-N 0.000 description 2
- IDLJKTNBZKSHIY-UHFFFAOYSA-N [4-(diethylamino)phenyl]-phenylmethanone Chemical compound C1=CC(N(CC)CC)=CC=C1C(=O)C1=CC=CC=C1 IDLJKTNBZKSHIY-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002318 adhesion promoter Substances 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 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
- 239000012965 benzophenone Substances 0.000 description 2
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
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- SATVIFGJTRRDQU-UHFFFAOYSA-N potassium hypochlorite Chemical compound [K+].Cl[O-] SATVIFGJTRRDQU-UHFFFAOYSA-N 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- KLGDFPXJKLQRRN-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C.CC(C)OC(=O)C(C)=C KLGDFPXJKLQRRN-UHFFFAOYSA-N 0.000 description 1
- WHMQHKUIPUYTKP-UHFFFAOYSA-N propane-1,2,3-triol;propanoic acid Chemical compound CCC(O)=O.OCC(O)CO WHMQHKUIPUYTKP-UHFFFAOYSA-N 0.000 description 1
- HJSRRUNWOFLQRG-UHFFFAOYSA-N propanedioic acid Chemical compound OC(=O)CC(O)=O.OC(=O)CC(O)=O HJSRRUNWOFLQRG-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- CYIRLFJPTCUCJB-UHFFFAOYSA-N propyl 2-methoxypropanoate Chemical compound CCCOC(=O)C(C)OC CYIRLFJPTCUCJB-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- ILPVOWZUBFRIAX-UHFFFAOYSA-N propyl 2-oxopropanoate Chemical compound CCCOC(=O)C(C)=O ILPVOWZUBFRIAX-UHFFFAOYSA-N 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000001057 purple pigment Substances 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000002730 succinyl group Chemical group C(CCC(=O)*)(=O)* 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- LPVTUVQARHJGJL-UHFFFAOYSA-N tert-butyl 2-sulfanylpropanoate Chemical compound CC(S)C(=O)OC(C)(C)C LPVTUVQARHJGJL-UHFFFAOYSA-N 0.000 description 1
- FQFILJKFZCVHNH-UHFFFAOYSA-N tert-butyl n-[3-[(5-bromo-2-chloropyrimidin-4-yl)amino]propyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCCNC1=NC(Cl)=NC=C1Br FQFILJKFZCVHNH-UHFFFAOYSA-N 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
Classifications
-
- 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
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
-
- 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
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/10—Amino derivatives of triarylmethanes
- C09B11/24—Phthaleins containing amino groups ; Phthalanes; Fluoranes; Phthalides; Rhodamine dyes; Phthaleins having heterocyclic aryl rings; Lactone or lactame forms of triarylmethane dyes
-
- 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
-
- 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
- G03F7/004—Photosensitive materials
-
- 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
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
-
- 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
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/032—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders
- G03F7/033—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders the binders being polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
-
- 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
- G03F7/004—Photosensitive materials
- G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Materials For Photolithography (AREA)
Description
1326296 玖、發明說明 【發明所屬之技術領域】 本發明係關於著色光敏性樹脂組成物。 【先前技術】 著色光敏性樹脂組成物係含有著色劑的光敏性樹脂組 成物’乃供以形成構成彩色濾光片之著色圖案用的有效材 料。在此所謂「彩色濾光片」係指供使用於將液晶顯示裝 置的顯示圖像彩色化、或供將利用固體攝影元件所拍攝到 的圖像予以彩色化之用的光學元件。所謂「著色圖案」係 指如红、綠、藍等的顏色圖像、黑矩陣等,有線狀、或馬 賽克狀。 近年來,隨著彩色濾光片生產量的增加,在製造時所 採用的著色光敏性樹脂組成物的生產亦將隨之增加❶但 是,若著色光敏性樹脂組成物大量生產的話,等到實際使 用時距離彩色渡以從製造相庫存期間很長,此時便發 生著色光敏性樹脂組成物之著色劑成分沉澱等現象,若在 此㈣下使用於彩色渡光片之製造的#,將造成良率降低 的問題。在此,便有提案藉由將顏料利用月旨肪族醇或脂肪 族胺施行處理’而改善顏料的分散性,俾改善彩色濾光片 形成材料之長期安定性(保存安定性)的方法(參照㈣文 獻1 ),但是難謂長期安定性屬於良好者。 專利文獻1 曰本專利特開平9-178923號公報 【發明内容】 315191 5 1326296 本發明之目的在於提供一種長期安定性良好的著色光 敏性樹脂組成物。 本發明者乃為獲得可解決上述問題的著色光敏性樹脂 組成物,經深入鑽研結果發現藉由使用含丙二醇單甲醚醋 S“曰與4_羥基_4_曱基_2_戊酮的溶劑以作為著色光敏性樹 月:組成物溶劑,便可改善著色光敏性樹脂组成物之長期安 疋性’遂完成本發明。 ^即,本發明所提供的著色光敏性樹脂組成物,係含有 者色劑(A)、黏結劑聚合物(B)、光聚合性化合物卜光聚 T起始劑(D)、及溶劑(E);其中,溶劑(E)係含有:丙二醇 單甲醚醋酸酯與4·羥基_4-甲基-2-戊酮。 再者,本發明所提供的圖案之形成方法,係將上述組 j物塗布於基板上,經去除揮發成分而形成著色層,並隔 著光罩對該著色層進行曝光並顯影。 【實施方式】 本發月之著色光敏性樹脂組成物,係含有著色劑(A)、 黏結劑聚合物(B)、光聚合性化合物(c)、光聚合起始劑 (D)、及溶劑(E);而溶劑(E)係含有:丙二醇單曱醚醋酸酯 與4_羥基-4-甲基-2-戊鲷。 本毛明中所採用的著色劑(A)最好為顏料,而顏料可舉 例如:有機顏料、無機顏料。 顏料具體而言可舉例如:在色彩指南(丁heS〇ciety 〇f
Dyers and c〇1〇urists公司發行)中被歸類為顏料(Hgment) 的化。物。具體而1•’可舉例如:c]顏料黃! ' C丄顏料
3I519I 6 1326296 黃3、C.I.顏料黃12、C.I.顏料黃13、C.I·顏料黃14、C.I. 顏料黃15、C.I.顏料黃16、C.I.顏料黃17、C.I.顏料黃20 ' C.I.顏料黃24、C.I·顏料黃31、C.I.顏料黃53、C.I.顏料黃 83、C.I.顏料黃 86、C.I.顏料黃 93、C.I.顏料黃 94、C.I. 顏料黃109、C.I.顏料黃110、C.I.顏料黃117、C.I.顏料黃 125、C.I.顏料黃 128、C.I.顏料黃 137、C.I.顏料黃 138、 C.I.顏料黃139、C.I.顏料黃147、C.I.顏料黃148、C.I.顏 料黃150、C.I.顏料黃153、C.I.顏料黃154、C.I.顏料黃166、 C.I.顏料黃173、C.I.顏料黃194、C.I.顏料黃214等黃色顏 料; C.I.顏料橙13、C.I·顏料橙31、C.I.顏料橙36、C.I. 顏料橙38、C.I.顏料橙40、C.I.顏料橙42、C.I.顏料橙43、 C.I.顏料橙51、C.I.顏料橙55、C.I.顏料橙59、C.I.顏料橙 61、C.I.顏料橙 64、C.I.顏料橙 65、C.I.顏料橙 71、C.I. 顏料橙73等橙色顏料; C.I.顏料紅9、C.I.顏料紅97、C.I.顏料紅105、C.I. 顏料紅1 22、C ·I ·顏料紅1 23、C ·I·顏料紅1 44、C. I ·顏料紅 149、C.I.顏料紅 166、C.I.顏料紅 168、C.I.顏料紅 176、 C.I.顏料紅177、C.I.顏料紅180、C.I.顏料紅192、C.I.顏 料紅209、C.I.顏料紅215、C.I.顏料紅216、C.I.顏料紅224、 C.I.顏料紅242、C.I.顏料紅254 ' C.I.顏料紅255、C.I.顏 料紅264、C.I.顏料紅' C.I.顏料紅265等紅色顏料; C.I.顏料藍15、C.I.顏料藍15 : 3、C.I.顏料藍15 : 4、 C.I.顏料藍]5 : 6、C.I.顏料藍60等藍色顏料; 7 315191 C.I.顏料紫i、(:丄顏料紫19 ,紫〜丄顏料紫32、CJ,料紫36顏料紫m顏 1色顏料; ’、 C.1.顏料紫38等 :::綠7、。.顏料綠36等綠. 丄顏料棕23、C丄顏料棕 , C·1·顏料黑!、C丄顏…广色顏料; ρ γ . ”、7痒黑色顏制·望; m 攸C·1.顏料黃!38、C丄顏料黃 切。最好含有 顏料紅177、CJm 2〇9 ••顏料黃H C.I. 23、C.I.顏料藍15 : 6、及 · ·,員料紅254、CU.顏料紫 種顏料者。 ...顏料綠36中至少選擇其中叉 該等有機顏料與無機顏料可 使用2種以上。 早獨使用,亦可混合 s如在形成紅色圖像時,最好 丄顏料黃139 ;而在 ·.顏料紅209與 顏料綠36、(^顏料〜 圖像時,最好含有從 種之顏料;在开藍^ 〇、CJ.顏料黃138中至少選擇} 6。 冢時最好含有C.I.顏料藍】5 : •亥等之中,就從耐熱性、 好採用有機顏料。 …生優越的硯點而言’最 上述顏料中,古桃± 理、採用經導入酸性美1 需要亦可施行如:松香處 理、利用5八早 I或驗性基之顏料衍生物等的表面處 硫酸微粒二I:對顏料表面施行接枝處理 '利用 溶劑或水等施行 飞』用供去除雜貝用之有機 ’處理、利用離子性雜質的離子交換法 315191 8 1326296 等施行去除處理等處理。 著色光敏性樹脂組成物固形份中的著色劑(A)含量,最 好在25質量°/〇以上、60質量%以下,尤以27質量%以上、 55質量%以下為佳,更以30質量%以上、50質量以下為 佳。 若著色劑(A)含量在25質量%以上、6〇質量%以下的 話’在當作彩色遽光片使用時的顏色濃度將充足,且因為 在組成物中可含有需要量之黏結劑聚合物,因此可形成機 械強度足夠的圖案,所以屬於較佳狀況。 在此所明「著色光敏性樹脂組成物固形分」係指從著 色光敏性樹脂組成物中去除(E)後的殘餘部分。 著色劑⑷最好粒徑均勻。當著色劑⑷屬於顏料的情 況時,利用含有顏料分散劑並施行分散處理, 料在溶液中呈均句分散狀態的顏料分散液。 顏 離子分散劑可舉例如:陽離子系、陰離子系、非 使用Ϊ…、“旨類、聚胺系等界面活性劑等,可單獨 使用或組合使用2種以上。 干词 顏料分散劑的传用旦批—Α 在…八 對者色劑⑷平均1質量份,最好 在1貝置份以下,尤以柄曰 取好 ... ·〇5貝置份以上,0.5質量份以 為佳。若上述顏料分散劑 伤从下 在1質量份以下的話,便且=者色劑平均1質量份 傾向,因而屬較佳狀況。獲得均句分散狀態顏料的 士發明中所採用的點結劑聚合物⑻,可使用如八, 基之單體、及能與該單體 3羧 八水合之其他單體的共聚物等丙 315191 9 1326296 烯酸系共聚物等。 含缓基之單體可舉例如:不飽和單羧酸、不飽和二羧 酸、不飽和二羧酸等不飽和多元羧酸等之分子中至少具有 1個叛基的不飽和叛酸。 在此,不飽和單羧酸可舉例如:丙烯酸、曱基丙烯酸、 巴豆油酸、α -氣丙烯酸 '肉桂酸等。不飽和二羧酸可舉例 如.順丁烯一酸、反丁烯二酸、衣康酸、檸康酸、中康酸 等。 不飽和多元羧酸係可為如:順丁烯二酸酐、衣康酸酐、 檸康酸if等酸if。此外,殘和多元㈣可為其單(2_甲基 丙烯酿氧基烧基)醋,譬如:琥辑酸單(2_丙烯酿氧基乙基) 醋、琥拍酸單(2-曱基丙烯醯氧基乙基)醋、鄰苯二甲酸單(2_ 丙稀酿氧基乙基㈣、鄰苯二甲酸單(2_甲基丙稀酸氧基乙 基)醋等。不飽和多元羧酸亦可為二末端為二羧基聚合物的 早(甲基)丙稀酸酿,可舉例如:ω,基聚己内醋單丙烯酸 L叛基聚己内醋單甲基丙歸酸醋等。該等含缓基的單 體可單獨使用或混合使用2種以上。 上述能與含竣基之單體共聚合的其他單體,可舉例 如·‘笨乙烯U基苯乙稀、鄰乙稀基甲苯間乙稀基^ 苯、對乙烯基甲苯、對氣苯乙稀、鄰甲氧基笨乙稀、間甲 乳基f乙婦、對甲氧基苯乙婦、鄰乙烯基T基甲趟、間乙 細基节基甲驗'對乙烯基T基甲越、鄰乙稀基节基縮水甘 4二間乙烯基节基縮水甘油驗、對乙稀基节基縮水甘油 _、印等芳香族乙烯化合物; 31519) 10 1326296 丙稀酸甲酿、曱基丙浠酸甲酯 '丙晞酸乙酯、甲基丙 烯酸乙酯、丙烯酸正丙酯、曱基丙烯酸正丙酯、丙烯酸異 丙酯 '曱基丙烯酸異丙酯、丙烯酸正丁酯、甲基丙稀酸正 丁酯、丙烯酸異丁酯、甲基丙烯酸異丁酯、丙稀酸第二丁 酯、甲基丙烯酸第二丁酯、丙稀酸第三丁酯、曱基丙稀酸 第三丁酯、丙烯酸2 -經乙酯、甲基丙稀酸2 -經乙酯、丙烯 酸2-羥丙酯、甲基丙烯酸2-羥丙酯、丙稀酸3-羥丙酯、曱 基丙稀酸3-經丙酯、丙稀酸2-經丁酯、甲基丙烯酸2 -經丁 酯、丙烯酸3 -經丁酯、甲基丙烯酸3 -經丁酯、丙稀酸4 -羥丁酯、甲基丙烯酸4-羥丁酯、丙烯酸烯丙酯、甲基丙烯 酸烯丙酯、丙烯酸苄酯、甲基丙烯酸苄酯、丙烯酸環己酯、 甲基丙烯酸環己酯、丙烯酸苯酯、甲基丙烯酸苯酯、丙烯 酸2-曱氧基乙酯 '甲基丙烯酸2-曱氧基乙酯、丙烯酸2-笨氧基乙酯、曱基丙烯酸2-苯氧基乙酯、丙烯酸曱氧基二 乙二醇酯、甲基丙稀酸甲氧基二乙二醇酯、丙烯酸甲氧基 三乙二醇酯 '曱基丙烯酸甲氧基三乙二醇酯、丙烯酸曱氧 基丙二醇酯、甲基丙烯酸曱氧基丙二醇酯、丙烯酸曱氧基 二丙二醇酯、甲基丙稀酸甲氧基二丙二醇酯、丙稀酸異冰 片酯、甲基丙烯酸異冰片酯、丙烯酸二環戍二稀酯、曱基 丙烯酸二環戊二稀酯、丙烯酸2 -羥基-3-苯氧基丙酿、甲基 两稀酸2 -輕基-3-苯氧基丙酷、丙三醇单丙細酸S旨、丙二醇 單甲基丙烯酸酯等不飽和羧酸酯類; 丙烯酸2-胺基乙酯、甲基丙烯酸2-胺基乙酯、丙烯酸 2 -二甲胺基乙酯、甲基丙烯酸2 -二甲胺基乙酯、丙烯酸2_ π 315191 1326296 胺基丙酯、曱基丙烯酸2_胺基丙酯、丙烯酸2-二甲胺基丙 酯、甲基丙烯酸2-二甲胺基丙酯、丙烯酸3-胺基丙酯、甲 基丙烯酸3-胺基丙酯、丙烯酸3-二甲胺基丙酯、甲基丙烯 酸3 ·二甲胺基丙酯等不飽和羧酸胺烷基酯類; 丙稀酸縮水甘油酷、曱基丙炸酸縮水甘油醋等不飽和 緩酸縮水甘油醋類; 醋酸乙烯酯、丙酸乙稀酯、丁酸乙烯酯 '苯曱酸乙歸 酯等羧酸乙烯酯類; 乙烯甲醚、乙烯乙醚、烯丙縮水甘油醚等不飽和醚類; 丙烯腈、甲基丙烯腈、α -氣丙烯腈、氰化亞乙烯等氰 化乙烯化合物; 丙烯醯胺、甲基丙烯醯胺、α-氣丙烯醯胺、Ν_2_羥乙 基丙烯醯胺、Ν-2-羥乙基曱基丙烯醯胺等不飽和醯胺類; 順丁烯二醯亞胺、N—苯基順丁烯二醯亞胺、Ν_環己基 順丁烯一醯亞胺等不飽和醯亞胺類; 1,3 -丁一烯、異戊二烯、氣丁二烯等脂肪族共軛二烯 類; 聚苯乙稀、聚丙烯酸曱酷、聚甲基丙稀酸甲酷、聚丙 稀酸正丁 S旨、$甲基丙烯酸正丁醋、聚石夕氧垸之聚合物分 子鍵末端具有I丙稀醯基或單甲基丙稀酿基的巨單體類 等0 該等單體可單獨使用或混合使用2種以 量,最好為10 更以25至40質 50質量%,尤以15至40質量%』 315191 12 1326296 量%為更佳。上述含羧基單體單位含量若為1〇至5〇質量 %的話,則對顯影液的溶解性較佳,在顯影時具有正確地 形成圖案的傾向’因而屬較佳狀況。 上述丙烯酸酯系聚合物可舉例如:(甲基)丙烯酸/(甲基) 丙婦酸曱酿共聚物、(甲基)丙歸酸/(甲基)丙稀酸卞醋共聚 物、(甲基)丙烯酸/(甲基)丙烯酸2_羥乙醋/(甲基)丙烯酸苄 西曰共聚物、(甲基)丙烯酸/(甲基)丙烯酸曱酯/聚苯乙烯巨單 體,、聚物、(甲基)丙烯酸/(甲基)丙烯酸甲酯/聚(甲基)丙烯 酸甲醋巨單體共聚物、(甲基)丙稀酸/(甲基)丙稀酸节醋/聚 笨乙稀巨單體共聚物、(甲基)丙稀酸/(甲基)丙稀酸节醋/聚 (甲基)丙烯酸甲醋巨單體共聚物、(甲基)丙烯酸/(甲基)丙 烯酸2-羥乙酯/(甲基)丙烯酸苄酯/聚苯乙烯巨單體共聚 物、(甲基)丙烯酸/(甲基)丙稀酸2_經乙醋/(甲基)丙稀酸〒 醋/聚(甲基)丙稀酸甲酿巨單體共聚物、(甲基)丙烤酸/苯乙 稀/(甲基)丙烯酉文卞醋/Ν_苯基順丁稀二醒亞胺共聚物、(甲 基)丙料/琥站酸單(2·丙稀酿氧基乙基)醋/苯乙稀/(甲基) 丙稀酸〒醋/Ν -装其丨丨IS -Τ 丘-杜π 土頃丁烯一醯亞胺共聚物、(甲基)丙稀酸 /琥拍酸單(2-丙烯酿氧基乙基)醋/苯乙稀/(甲基)丙烯酸稀 a NJ基项丁烯一醯亞胺共聚物、(曱基)丙烯酸/(曱基) 丙稀酸〒"酿/N - ϋ其丨丨is τ· P 长 本暴順丁烯二醯亞胺/笨乙烯/丙三醇單(曱 基)丙稀酸醋共聚物望 „ .. _ 象物專。另外’所謂「(甲基)丙烯酸酯」係 指丙烯酸酯、或甲基丙烯酸酯。 ’、中最好使用如:(甲基)丙烯酸/(甲基)丙烯酸T s旨 …κ物(曱基)丙稀酸/(甲基)丙稀酸节酿/苯乙稀共聚物、 315191 1326296 (甲基)丙稀酸/(曱基)丙稀酸曱酿共聚物、(曱基)丙稀酸/(曱 基)丙烯酸甲酯/苯乙烯共聚物等。 上述丙烯酸系聚合物的聚笨乙烯換算重量平均分子 量,以3,〇〇〇至400,000為佳,以5,〇〇〇至1()(),_為更佳, 又以W 40,00(^最佳。若分子量為3 〇〇〇至彻,〇〇〇 的話’便具有塗膜硬度提高,殘膜率亦較高,未曝光部分 對顯影液的溶解性佳,且解像度提昇的傾向,因而屬較佳 狀況。 再者,上述丙烯酸系共聚物的酸值以3〇至25〇 , 尤以60至18〇為更佳,又 至16〇為最佳。若上述酸 值在30至25〇的話,則對顯影液的溶解性將提昇,使未曝 光。Ρ刀易於洛解,此外在高感度化顯影時將有殘留曝光部 圖案並提昇殘膜率的傾向,因而屬於較佳狀況。在此酸值 係對丙烯酸系共聚物lg進行尸 的測量值,通常可採用Mu k 氧化鉀量(mg) 蒂了彳木用虱氧化鉀水溶液進行滴定而求取。 者色光敏性樹脂組成物固形份中的黏結劑聚合物⑻ …以5質量%以上、9〇質量%以下為佳尤以質量 %以上、8 0質景〇/丨v 丁达系 ° 為更佳,又以20質量%以上'70質 量%以下為最佳。若含詈.ς使曰。/ 的話,在質里上、90質量%以下 好的傾向,而且切現象’具有密接性趨於良 較m ,、有提昇解像度與殘膜率的傾向,因而屬
本發明中戶斤起;A 射,並利用從先=性化合物(C)’係藉由光的照 尤^合起始劑(D)所產生的活性自由基、酸 315I91 14 1326296 等,而可進行聚合的化合物,可舉例如:具聚合性碳碳不 飽和鍵的化合物等。 上述光聚合性化合物(c)最好為3官能基以上之多官 能基光聚合性化合4勿。3冑能基以上之多官能基光聚合性 化合物可舉例> :季戊四醇四丙烯酸酯、季戊四醇四甲基 丙烯酸酯、二季戊四醇五丙烯酸酯、二季戊四醇五甲基= 烯酸酯、二季戊四醇六丙烯酸酯、二季戊四醇六甲基=烯 酸酯等。上述光聚合性化合物(c)可單獨使用亦可纽人 用2種以上。 口 t f色光敏性樹脂組成物固形份中之光聚合性化合物(c 之含量’以在5質量%以上、9〇質量%以下為佳以 量%以上、8〇質量%以下為更佳,又以20質量%以上、7〇 :量%以下為最佳。若上述光聚合性化合物(c)含量在5所 量%以上、90質量%以下的話’將引起充分的硬化且殘膜貝 率將提昇,圖案不易發生底切現象而呈現密接性佳的傾、 向,因而屬較佳狀況。 本發明中所採用的光聚合起始劑(D),最好至少含 種苯乙酮系化合物。 苯乙酮系化合物可舉例如:二乙氧基苯乙酮、 冬嗎啉代小(4·甲基苯硫基)丙炫·ι酮、2_經基_2 土 苯基丙烷· 1_酮、苄其_ A · 卞基一 f基酮縮醇、2_羥基_2_甲基 (2-羥基乙氧其)贫| 軋基)本基]丙烷-1·酮、]-羥基環己基苯酮、2_羥 基-2-甲基小[4-〇甲基乙烯基)苯基]丙烷_ι·酮之 等,最好為2_甲其9 L 、物 f基嗎啉代-1-(4·甲基苯基硫)丙院 315191 15 1326296 乙酮系及其他光聚合起始 劑,可舉例如:藉由光之 由基產生劑、酸產生劑 等。此外,亦可組合使用複數苯 劑。苯乙酮系以外的光聚合起始 照射而產生活性自由基的活性自 等。 苯 苯 活性自由基產生劑可舉例如:苯偶因系化合物、 甲,系化合物、噻嘲_系化合物、三嗪系化合物等。 苯偶因系化合物可舉例如:苯偶因、苯偶因甲_ 偶因乙醚 '苯偶因丙醚、苯偶因異丁醚等。 二t甲'系化合物可舉例如:二苯甲酮、鄰苯醯基苯 甲酸甲醋、4-苯基二苯甲酮、4_苯甲醯_4,_甲基二苯基硫 謎、3,3’,4,4,-四-(第三丁基過氧化幾基)二苯曱酮、2^ 三甲基二苯甲酮等。 ’’ 2-異丙基噻噸酮' 4_異丙 2,4- 一乳嚷°镇綱、丨—氣-心 噻噸_系化合物可舉例如 基噻噸銅、2,4-二乙基噻噸綱 丙氧基噻噸酮等。 广秦系化合物可舉例如:2,心雙(三氣甲基)邻甲氧 基本基)1,3,5 一秦、2,4-雙(三氣甲基)_6_(4_甲氧基蔡基)_ 1,3,5-三嗪、2,4-雙(二翕 φ (一乳甲基)-6-(4-曱氧基苯乙烯基)_ 1,3,5-三嗪、2,4-雙(三氣甲基 土)6-[2-(5 -甲基咲喃_2·基)乙嫌 基]-1,3,5-三嗪' 2,4-雙(二氣田Ar + 鄉 艾乳甲基)-6-[2-(呋喃-2-基)乙烯 基]-1,3,5-三嗪、2,4-雙畜田甘、 又(一虱甲基)-6-[2-(4-二乙胺基_2_甲 基苯基)乙稀基]-1,3,5_三唪、 产 奈 2,4-雙(二氣甲基)-6-|"2-(3 4- 二甲氧基苯基)乙烯基]_丨,3,5三嗪等。 活性自由基產生劑可掂 Η木用如_2,4,6-三甲基苯甲醯基二 315191 16 1326296 苯基膦氧化物、2,2,-雙(鄰氯苯基)_4,4,,5,5,_四苯基u,-聯 二咪唑、10-丁基_2_氣卩丫啶酮、2·乙基蒽醌 '苄、9,1〇_菲 醌、莰醌、苯基乙醛酸甲酯、茂鈦化合物等。 酸產生劑可舉例如·· 4_羥基苯基二平基鎏鹽對甲笨磺 酸鹽、4-羥基苯基二甲基鎏鹽六氟銻鹽、4_乙醯氧基苯基 二甲基鎏鹽對甲苯磺酸鹽、4-乙醯氧基苯基•甲基•苄基鎏 鹽六氟銻鹽、三苯基鎏鹽對甲苯磺酸鹽、三苯基鎏鹽六氟 銻鹽、二苯基碘鍚鹽對曱苯磺酸鹽、二苯基碘鍚鹽六氟銻 鹽等鐵鹽類、或硝基节甲苯磺醯鹽類、苯偶因曱苯磺醯鹽 類等。 狐 再者,活性自由基產生劑在上述化合物中,亦可為與 活性自由基同時產生酸的化合物,譬如三嗪系光聚合起始 劑亦可使用為酸產生劑。 聚合起始劑⑼含量係相對於黏結劑聚合物(B)與光聚 合性化合物(C)總計量100重量份,最好在〇」重量份以 上、20重量份以下,尤以i質量 里伤以上、1 5重量份以下為 佳。右光聚合起始劑含量在〇】t曰^ ▲ 在0.1重1份以上' 20重量份以 下的活’將有咼感度化且縮短蔽杏卩主p目 化短曝先時間而提昇生產性,此 卜亦不致因感度過tij而造成解德译丁技^ 佳狀況。 成解像度不佳的傾向,因而屬較 几徽性樹脂組成物中’亦可包含光 &起始助劑(G)。光聚合起始 起始劑⑼使用,乃為促進利用^人配先聚 来…“八一 合起始劑而開始聚合 先水合性化合物的聚合所採用之化合物。 315191 17 1326296 光聚合起始助劑(G)可舉例如:胺系化合物、烧氧基蒽 系化合物、噻噸酮系化合物等。 胺系化合物可舉例如:三乙醇胺、甲基二乙醇胺、三 異丙醇胺、4-二甲胺基苯曱酸曱酯、4_二曱胺苯曱酸乙醋、 4-二曱胺苯曱酸異戊酯、苯甲酸2_二甲胺乙酯、肛二甲胺 苯甲酸2-乙基己酯、N,N-二曱基對甲苯胺、4,41_雙(二曱胺 基) 一本曱_(俗稱「米希勒酮(Michler's ketone)」)、4 4,· 雙(二乙胺基)二笨甲酮、4,4’-雙(乙甲胺基)二苯曱酮等,其 中最好為4,4、雙(二乙胺基)二苯甲酮。 统氧基虚糸化合物可舉例如:9,10 -二曱氧基東、2乙 基-9,10-二甲氧基蒽、9,1〇_二乙氧基蒽、2_乙基_91〇_二乙 氧基蒽等。 ^ 噻噸酮系化合物可舉例如:2_異丙基噻噸鲷、仁異丙 基噻噸酮、2,4-二乙基噻噸酮、2,4_二氣噻噸酮、丨·氣_4丙 氧基噻噸酮等。 光聚合起始助劑(G)可單獨使用亦可組合2種以上使 用。此外,光聚合起始助劑(G)亦可使用市售者市隹的光 聚合起始助劑(G)可舉例如:商品名「EAB f f」(保土谷化 學工業(股)製)等。 二發明的著色光敏性樹脂組成物中’光聚合起始劑⑼ 與光聚合起始助劑(G)的組合,可舉例如下:二乙 — _,4,·雙(二乙胺基)二苯甲嗣、2_甲基|嗎琳代笨乙 基笨硫基)丙燒小嗣/4,4,_雙(二乙胺基)二笨甲剩,4'甲 2-曱基-1-苯基丙H,/4,4i_雙(二乙胺 尹工基' 本甲鲷、苄美 315191 18 一甲基縮_M,4,_雙(二乙胺基)二苯甲明' 2經基1甲基 苯甲酮、!-經基環己基苯酮/4,4、雙(二乙胺基)二笨;酮、 2-羥基曱基q-H-d•曱基乙 ^ /4 ^ _ π丞)本基]丙烷-1-酮的寡聚 ,[又(二乙胺基)二苯甲酮、2_节基_2二甲胺基 嗎琳代苯基)丁烧-1㈣,4、雙(二乙胺基)二苯甲酮等,最好 的組合為2-曱基-2-嗎啉代_1-(4 14甲基笨硫基)丙烷-1-酮 Μ,4·-雙(二乙胺基)二苯甲酮。 …當採用該等光聚合起始助劑⑹時,其使用量係對平均 每莫耳之光聚合起始劑(D),通常在10莫耳以下,最好為 0.01莫耳以上、5莫耳以下。 本發明所採用的溶劑⑻可舉例如:含丙二醇單甲喊錯 酸酷與4-經基-4-甲其〇 〇_、α θ 节基_2-戊酮的溶劑,在溶劑(E)中,亦可 3除上述2種以外的其他溶劑。其他溶劑可舉例如:除上 述以外的醚類、芳香族烴類、除上述以外㈣類、醇類、 酯類、醯胺類、N-甲基吡咯烷酮、二甲亞楓等。 鍵類可舉例如:四氫咲喃、四氫ϋ比喃、1,4-二錢、 乙二醇單甲驗、乙二醇單乙冑、乙二醇單丙喊、乙二醇單 丁醚、二乙二醇單甲w 喊、一乙二醇單乙喊、二乙二醇單丁 謎 '二乙二醇二甲_ '二乙二醇二乙醚、二乙二醇二丙越、 二乙二醇二丁越、而-fn。 丙一酵早乙醚醋酸酯、丙二醇單丙醚醋 酸醋、甲基溶纖劑醋酸酿、乙基溶纖劑醋酸醋、乙基卡必 醇醋酸酯、丁基卡必醇醋酸酯、6二醇甲醚醋酸酯、曱氧 基丁基醋酸醋、甲ϋ甘丄、β 氧基戊基醋酸酯、茴香喊、苯乙趟、甲 31519] 19 1326296 基茴香喊等。 芳香族烴類可舉例如:苯、甲苯、二甲笨、均三甲苯 等。 _ 一 酮類可舉例如:丙酮、2-丁酮、2-戊_、q山細 λ JX m ' 戊酮、4-甲基_2-戊酮、環戊酮、環己酮等。 醇類可舉例如:曱醇、乙醇、丙醇、丁醇、己醇、環 己醇、乙二醇'丙三醇等。 酯類可舉例如:醋酸乙酯、醋酸正丁酯、醋酸異丁酷、 蟻酸戊酯、醋酸異戊酯、醋酸異丁酯、丙酸丁略、丁酸異 丙酯、丁酸乙酯、丁酸丁酯、烷基酯類、乳酸曱醋、乳酸 乙酯、經基醋酸曱酯、經基醋酸乙酯、經基错酸丁醋、甲 氧基醋酸曱酯、曱氧基醋酸乙酯 '甲氧基醋酸丁酿、乙氧 基醋酸甲酯、乙氧基醋酸乙酯、3-羥基丙酸甲黯、3_經基 丙酸乙酯、3 -曱氧基丙酸曱酯、3 -甲氧基丙酸乙酿、3·乙 氧基丙酸曱酷、3 -乙氧基丙酸乙醋、2 -沒基丙酸甲g旨、2_ 經基丙酸乙醋、2 -經基丙酸丙S旨、2 -曱氧基丙酸甲醋、2-甲氧基丙酸乙酯、2-甲氧基丙酸丙酯、2-乙氧基丙酸曱酯、 2 -乙氧基丙酸乙酯、2 -經基-2-甲基丙酸甲酯、2 -經基-2-甲 基丙酸乙酯、2-甲氧基-2-甲基丙酸曱酯、2-乙氧基-2-曱基 丙酸乙酯、丙酸甲酯、丙_酸乙酯、丙酮酸丙酯、乙醯 醋酸甲酯、乙醯醋酸乙酯、2 - —氧丁酸曱酯、2 - —氧丁酸 乙酯、3-甲氧基丁基醋酸酯、3-甲基-3-甲氧基丁基醋酸酯、 γ - 丁内SI等。 醯胺類可舉例如:Ν,Ν-二曱基曱醯胺' Ν,Ν-二曱基乙 20 315191 醯胺等。 邊等之中,最好合併使用2_ μ 甘从 G虱基丙酸乙酯。 上述其他溶劑可單獨使用, 著色光敏性樹脂組成物(總量合使用2種以上。 為7〇質量%以上、95質量%以下的浴劑⑻含量,最好 90皙景〇/ w τ电从 尤以75質量〇/〇以上、 貝量/〇 U下為佳。若溶劑含 旦^ 3里在7〇質量%以上' 95質 里%的話,塗布時的平坦性將 貝 之ρ Α # 且在形成彩色濾光片 趨6 m二® 具有顯示特性趨於良好的 趨向,因而屬較佳狀況。 溶劑(Ε)中的4-羥基-4-甲美,上 田〇/ 〒基-2-戊_含量,最好為3質 ! “上,量%以下,尤以5質量%以上、%質量% 以下為佳,更以8質量%以上、2〇質量%以下為更佳。 溶劑(E)最好實質的由丙二醇單甲喊醋㈣與心經基_ 4_甲基-2-戊酮所構成。 本發明的著色光敏性樹脂組成㈣,亦可再含有界面 活性劑(F)。界面活性劑(F)可舉例如:由石夕酮系界面活性 劑、氟系界面活性劑、及含氣原子的石夕I系界面活性劑所 構成組群中,至少選擇其中1種。 矽酮系界面活性劑可舉例如··具矽氧烷鍵結的界面活 性劑等。具體而言,可舉例如:德雷矽酮(商品名,音 譯)DC3PA、同 SH7PA、同 DC11PA、同 SH21PA、同 SH28PA ' 同29SHPA、同SH30PA、聚醚改質矽油SH84〇〇(商品名: 德雷矽酮(股)製);KP32 卜 KP322、KP323、KP324、KP326、、 KP3 40、、KP3 4】(信越矽酮公司製);TSF400、TSF401、 21 315191 1326296 TSF410 、 TSF4300 、 TSF4440 、 TSF4445 、 TSF-4446 、 TSF445 2 ' TSF4460(GE 東芝矽酮(股)製)等。 氟系界面活性劑可舉例如:具氟碳鏈的界面活性劑 等。具體而言’可舉例如:福羅納德(註冊商標,音 譯)FC43〇、同FC431(住友3M(股)製);美佳發克(註冊商 標,音譯)F142D ' 同 F171、同 F172、同 F173、同 F177、 同F 183、同R30(大曰本油墨化學工業(股)製);艾福德布(註 冊商標’音譯)EF301、同EF303、同EF351、同EF352(新 秋田化成(股)製);桑福龍(註冊商標’音譯)S381、同s382、 同SC101、同SC105(旭玻璃(股)製);E5844[(股)大金精細 化學研究所製];BM-looo、BM_11〇〇(均為商品名:
Chemie公司製)等。 含氟原子的矽酮系界面活性劑可舉例如:具矽氧烷鍵 結與氟碳鏈的界面活性劑等。具體而言,可舉例如佳 發克(註冊商標,音譯)R08、同BL2〇、同F475 '同Η”、 同F443(大曰本油墨化學工業(股)製)等。 該等界面活性劑可單獨使用,亦可組合使用2種以 界面活性劑(F)含量’係相對於著色光敏性樹脂 [⑷至⑻總計量]i f量份’最好在q嶋$質量份 〇·"量份以下’尤以在0.001質量份以上、。5質量广以 圭。右界面活性劑(F)含量在〇 _5質量 I…下的"’其平坦性有變佳的傾向,因而屬較佳狀 315191 22 1326296 本發明的著色光敏性樹脂組成物,亦可 旁·填充劑、 除黏結劑聚合物以外的高分子化合物、密接促進劑 化劑、紫外線吸收劑、抗凝聚劑、有機酸、有機胺化合^氧 硬化劑等添加劑。 ° 、 填充劑可舉例如:玻璃、氧化鋁等微粒子。 ’可舉例如:聚 t氟院基丙稀酸 除黏結劑聚合物以外的高分子化合物 乙烯醇、聚丙烯酸、聚乙二醇單烷基醚、 酯等。 密接促進劑可舉例如:乙烯基三甲氧基矽烷、乙烯基 三乙氧基矽烷、乙烯基三(2_甲氧基乙氧基)矽烷、N(2胺 基乙基)-3-胺基丙基甲基二甲氧基石夕烧、Ν_(2·胺基乙基) 3-胺基丙基X甲氧基石夕⑦、3_胺基丙基三乙氧基石夕燒、 锿氧丙氧基丙基三甲氧基矽烷、3_環氧丙氧基甲基二甲氧 基矽烷' 2·(3,4-環氧基環己基)乙基三甲氧基矽烷、3氯丙 基甲基二甲氧基矽烷、3·氯丙基三甲氧基矽烷、3-甲基丙 烯氧基丙基二甲氧基矽烷、3_巯基丙基三甲氧基矽烷等。 抗氧化劑可舉例如·· 4,4,_硫代雙(6_第三丁基_3甲基苯 酚)、2,6-二第三丁基甲基苯酚等。 紫外線吸收劑可舉例如:2_(2·羥基_3第三丁基_5甲 基笨基)-5-氣苯并三唑等苯并三唑系; 2-羥基-4-辛氧基二苯甲酮等二笨甲酮系; 2,4-二第三丁基苯基-3,5_二第三丁基_4_羥基苯甲酸酯 等笨甲酸酯系; 二苯基-1,3,5-三嗪-2-基)-5-己氧基苯酚等三嗪 23 3)5191 1326296 系等。 抗凝聚劑可舉例如:聚丙歸酸納等。 有機酸可舉例如:甲酸' ^ ^醋酸、丙酸、丁酸、吉草酸、 一 、二乙基醋酸、庚酸'辛酸 羧酸類; 节k等脂肪族早 己二酸、庚二酸、 甲基丙二酸、乙基 四甲基琥珀酸、環 .酸、反丁烯二酸、 草酸、丙二酸、琥柏酸、戊二酸 辛二酸、壬二酸' 癸二酸、巴西二酸 丙二酸、二甲基丙二酸、甲基琥轴酸 an衣康酸、檸康酸、順丁烯 中康酸等脂肪族二羧酸類; 均丙三甲酸、良自吾缺 苯甲辦" 樟腦三酸等脂肪族三… -甲:甲本酸、括茗酸、2,3-二甲基笨基酸、35-一甲基苯甲酸等芳香族單缓酸類; , 酞酸、間苯二甲酴、科纪_ # 偏料 一曱®文專芳香族二羧酸類; 芳香族聚㈣類等。 h均本四甲酸| 有機胺化合物可舉例如:正丙 異丁胺、第二丁胺、第三丁胺、正戊胺二"丁胺、 正辛胺、正壬胺、正㈣、正十戍二正己胺、正庚胺、 烷胺類; 、 十烷胺、正十二烷胺等單 袁己胺、2 -甲基環己胺、3曱其 胺等軍環烧胺類; T…胺、”基環己 甲乙胺、二乙胺、甲基正丙胺、乙基正丙胺 '二 ' …胺、二正丁胺、二異丁胺 '二第二丁胺、二第三丁
3J519I 24 1326296 胺、二正戍胺、二正己胺等二烷胺類; 曱基環己胺'乙基環己胺等單烷基單環烷胺類; 一 %己胺荨一環院胺類; 二曱乙胺、甲基二乙胺、三乙胺、二曱基正丙胺、二 乙基正丙胺、曱基二正丙胺、乙基二正丙胺、三正丙胺、 三異丙胺、二正丁胺、三異丁胺、三第二丁胺、三第三丁 胺、三正戊胺、三正己胺等三烷胺類; 二甲基,己胺、二乙基環己胺等二烧基單環烧胺類; 甲基-環己胺、乙基一環己胺、三環己胺等單烧基二 環烷胺類; 2- 胺基乙醇' 3-胺基小丙醇、卜胺基_2丙醇、4_胺基 小丁醇、5_胺基小戊醇、6_胺基小己醇等單燒醇胺類; 4 -胺基-1 -環己醇等單環烧醇胺類; 乙醇胺一正丙醇胺、二異丙醇胺'二正丁醇胺、 '異丁醇胺、二正Λ酿脸、-T: j 於 叹畔胺—正己醇胺等二烷醇胺類; 二(4-環己醇)胺等二環烷醇胺類; -乙醇胺 '三正丙醇胺 '三異丙醇胺、三正丁醇胺、 三異:醇胺、三正戊醇胺、三正己醇胺等三烷醇胺類; 二(4-環己醇)胺等三環烷醇胺類; 3- 胺基-i,2-丙二醇、2_胺基],丙二醇' 4_胺基"_ 丁一醇、4-胺基-α 丁二醇、3·二甲胺基…丙二醇、^ 一乙胺基·12—丙二醇、2_二 胺基-1,3-丙一醇、2-二乙胺 土 ,_丙二醇等胺基鏈院二醇類; 4胺基-1,2-環己二醇、4_胺基],3環己二醇等胺基環 315191 25 1326296 烷二醇類; 1-胺基環戊酮甲醇、4 -胺基環戊酮甲醇等含胺基之環 烷酮曱醇類; 1-胺基$哀己嗣甲醇、4 -胺基環己鋼曱醇、4 -二甲基胺 基環戊烧曱醇、4 -二乙基胺基環戊燒甲醇、4 -二曱基胺基 環己烷曱醇、4-二乙基胺基環己烷曱醇等含胺基之環燒甲 醇類; /3 -丙胺酸、2-胺基丁酸、3-胺基丁酸、4-胺基丁酸、 2-胺基異丁酸、3-胺基異乙酸、2-胺基戊酸、5-胺基戊酸、 6-胺基己酸、1-胺基環丙羧酸、1-胺基環己羧酸' 4_胺基環 己羧酸等胺基羧酸類; 苯胺、鄰曱基苯胺、間甲基苯胺、對甲基苯胺、對乙 基苯胺、對正丙基苯胺、對異丙基苯胺、對正丁基苯胺、 對第三丁基苯胺、萘胺、2_萘胺、N,N_二曱基苯胺、N,N_ 二乙基苯胺、對曱基-N,N-二甲基笨胺等芳香族胺類; 鄰胺基卞醇、間胺基卞醇、對胺基节醇 '對二甲胺基 〒醇、對二乙胺基苄醇等胺基苄醇類; 鄰胺基笨酚 '間胺基苯酚、對胺基苯酚、對二甲胺基 苯酚、對二乙胺基苯酚等胺基苯酚類; 間胺基笨曱酸、對胺基笨曱酸、對二甲胺基笨甲酸、 對二乙胺基苯曱酸等胺基苯甲酸類等。 硬化劑可舉例如:經加熱而與黏結劑聚合物中的敌基 進行反應俾可交聯黏結劑聚合物的化合物,經單獨聚合而 可獲得使著色圖案硬化的化合物等。上述化合物可舉例 26 315191 1326296 如:環氧化合物、氧雜環丁炫化合物等,最好採用氧雜環 丁燒化合物。 紅在此,環氧化合物可舉例如:聯苯酚八系環氧樹脂、 ^匕聯苯酴A系環氧樹脂、聯苯# F系環氧樹脂、氯化聯 =酚F系環氧樹脂、酚醛清漆型環氧樹脂、其他芳香族系 環氧樹脂、脂環族系環氧樹脂、雜環環氧樹脂、縮水甘油 =系樹脂 '縮水甘油胺系樹脂、環氧化油等環氧樹脂或該 專%氧樹脂的漠化衍生物、環氧樹脂及其漠化衍生物之外 2脂肪族、脂環族或芳香族的環氧化合物、丁二烯的(共) 2物之裱乳化物、異戊二烯的(共)聚物之環氧化物、(甲 ^)。丙烯酸縮水甘油醋的(共)聚物、異氰酸三縮水甘油醋 〒上雜環丁院可舉例如:碳酸醋雙(氧雜環丁院)、苯二 土又(虱雜% 丁烷)、己二酸酯雙(氧 酸醋雙(氧雜環-)、環己二《雙(氧雜ST二 氧雜Γ二t著色光敏性樹脂組成物係含有環氧化合物、 之環氧基r氧二==劑時,亦可含有使環氧化合物 聚合而得之= 物之氧雜環丁院骨架進行開環 多元叛酸‘述化合物可舉例如:多元議、 二甲可舉例如m甲紐酸、間苯 類;,’4,4·二本甲_酸等芳香族多元叛酸 31519] 27 1326296 琥珀g义戍一自义、己二酸、丨2 3 , 义 ,2,3,4-丁四綾酸、順丁铋 二酸、反丁烯二酸'衣庫舻笙 、丁烯 a义4月日肪知多元羧酸類; 六氫鄰苯二甲酸、34_田且 ^ ,4_ 一甲基四氫鄰苯二曱酸、‘_ 間苯二曱酸、六氫對笨_ τ夂虱 本一甲酸、1,2,4-環戊三羧酸 環己三羧酸、環戊四羧酸 ,2,4_ 丨,乙4,5-%己四羧酸等 兀羧酸類等。 曰展私夕 多元羧酸酐類可舉你,丨士n •而+ μ —, 牛例如.酞酸酐、均笨四曱酸酐、偏 本二酸酐、3,3,,4,4,_二笨甲嗣 偏 酸酐類; ㈣-酐專方香私多元羧 衣康酸酐、琥珀酸酐、癉漆 仏工 棹康酸酐、十二碳烯琥珀酸酐、 均丙二曱酸酐、順丁烯二 久針1,2,3,4-丁四羧酸二酐箄 肪族多元羧酸酐類; 时寺月s 六氫酞酸酐、3,4--甲1 m ^ , 一甲基四虱舦酸酐、1,2,4-環戊烷= 羧酸酐、1,2,4-環己烷二羧 m ^ 竣酸針、環戊烷四羧酸二酐、 i,2,4,5-環己烷四羧酸二 « . 5_降冰片烯-2,3-二羧基酸酐、 甲基内亞甲基四氫苯野等脂環族多元_類; 乙SI雙(偏本二酸)、甘油三(偏苯三酸等 羧酸酐類等。 s i <_ 上述緩酸軒類亦可括 iS # 知用市售的環氧樹脂硬化劑。上述 衣氧祕脂硬化劑’可舉例. „nn j如.商叩名「雅德佳哈德納ΕΗ- 7〇〇 j (旭電化工業(股)製)、 立 )商叩名「理佳德HH」(商品名, 日#)(新曰本理化(股)製 ^ ;商。口名「MH-700」(新日本理 化(股)製)等。 上述硬化劑可單猸 使用’亦可組合使用2種或2種以 315191 28 丄326296 上。 調製本發明之著色光敏性樹脂組成物的方法,可舉例 如.在溶劑(E)中並存著顏料分散劑使顏料等著色劑(a)分 散’俾調製均句粒徑的著色劑(A)分散液’然後再於溶劑中 溶解黏結劑聚合物(B)、光聚合性化合物(c)、光聚合起始 劑(D)及配合需要而溶解其他添加劑等與上述著色劑(a) 分散液混合,配合需要再添加溶劑的方法等。 依此方式所獲得著色光敏性樹脂組成物係經流通、保 管之後,再提供給彩色遽光片之製造。在上述流 链 常保存於一定溫度中’此溫度通常為。: 製起,^ Μ °雖從著色光㈣成物之調 供給形色濾光片之製造(如23。〔:)為止,此期間 越短越好,但是最好著$ I " 少”固月期間,能維二=樹脂組成物從其調製起至 色遽光片的性能形成與剛調製當時相同品質之彩 呼估^者^著色絲性樹脂組成㈣發之際,於其先行 5子估令,若確認上述3個月〜 、兀仃 拉長。為此便m 疋性的話,開發期間將 二此更執…估長期安定性的溫度, 皿度,提昇至如4〇t至 甲 期間而進行評估的方法。卑加速時經變化’縮短保存 而上述長期安定性的評估 色光敏性樹脂組成物之 °牛例如.採用以著 變化率係可用下示式!求得。,·“示的方法專。黏度
3J5I9I 29 黏度變化率(%) = x 1 00 (式1 ) 77 1承在—定溫 h係開始保存前所測得黏度 度中保持一定期間後所測得黏度。) 為計异出上述黏度變化率 定 定 又化羊而測量黏度。黏度係在 及/皿(如23C)中,嬖如可垃田r ^ A ° #木用E型黏度計攪拌器,依 轉速(如50rpm)進行測量。 黏度變化率最好在3%以下。若在3%以下的話,便可 依同與著色光敏性樹脂組成物剛調製時的性能,形成平坦 性佳且無異物的彩色濾光片。 一。再者’本發明的著色光敏性樹脂組成物,豸常係封入 谷器中’再提供給流通、保管。 採用本發明的著色光敏性樹脂M成物形成彩色滤光片 之圖案的方法’可舉例士。:將本發明的著色光敏性樹脂袓 蝴如red)塗布於基板上,再去除溶劑等揮發成分而形成 著色層’ϋ隔著光罩對該著色層進行曝光並顯影的方法。 其中’基板可舉例如:玻璃基板、石夕基板、聚碳酸醋 基板聚gs基板、芳香族聚醯胺基板、聚醯胺醯亞胺基板、 聚醯亞胺基板、Al基板、GaAs基板等表面平坦的基板等。 該等基板亦可施行如矽烷偶合劑等藥物的藥物處理、 電漿處理、離子電鍍處理、濺鍍處理、氣相反應處理、真 空蒸鍍處理等前處理。 再者’在該等基板上,亦可形成其他著色圖案。 當基板採用矽基板等時,亦可在矽基板等表面上形成 315J9) 30 丄 電荷耦合元件(CCD)'薄膜電晶體(TFT)等。 、在2著色光敏性樹脂組成物塗布於上述基板(包括形 成-他著色圖案的基板)上,最好採用習知的旋塗機、省液 塗布機(其中’尤以無旋轉塗布機為佳)塗布於基板等之 ,接著再對'谷劑等揮發成分進行加熱使揮發。加熱乃通 常在40。(:至12(rc程度下施行i至5分鐘程度。 依此的話,便可在基板或已形成其他著色圖案的基板 上’形成平坦性佳之由著色光敏性樹脂組成㈣形份所構 成著色層。 對所形成的著色層隔著光罩進行曝光、顯影。 在+光方面,可採用!線(波長365nm)、h線、g線等, 但是最好採用1線(波長365nm)。在卜線(波長365細)的光 源方面,最好採用超高壓水銀燈(屋西歐電機(股)製;只8_ 75 105AA 0P1)等,照射光量通常為5〇至4〇〇mj/cm2程度。 顯影通常乃利用浸潰於顯影液中而實施。顯影液可舉 例如.氫氧化鈉 '氫氧化鉀、碳酸鈉、丁基萘磺酸鈉 '氫 氧四甲基敍(TMAH)等。尤其以㈣依質量分率計,氯氧化 鉀0.05%、丁基萘磺酸鈉〇 2%的顯影液為佳。 在顯影後,配合需要亦可利用純水進行洗淨,然後在 18〇°C至24(TC下施行10至6〇分鐘程度的加熱處理。 依此便形成著色圖案(1)(如red)。 然後,在著色圖案(1)上,採用著色光敏性樹脂組成物 (如Green),如同上述形成著色圖案(2)(如:Green)。更於 著色圖案(2)上,採用著色光敏性樹脂組成物(如⑴,如 315191 31 1326296 同上述形成著色圖案(3)(如:Biue) ^依此便可製造標的之 彩色濾光片》 在依上述所獲得彩色濾光片上,可將ITO、配向膜、 經塗佈步驟處理過的基板,與TFT基板隔著隔板而貼合, 並利用注入液晶便可製造液晶顯示裝置。 實施例 在上述中’雖針對本發明的實施形態進行說明,惟上 述所揭示的本發明實施形態,充其量僅止於例式而已,本 發明的範圍並非限定於該等實施形態。本發明的範圍乃依 申請專利範圍所示,甚至包含申請專利範圍中所記載的均 等涵義與範圍内之所有改變。以下,藉由實施例更加詳細 說明本發明,惟本發明並不僅限於該等實施例。 本只加例中所採用的成分乃如下示,以下有簡略表示 的情況。 (A-1)著色劑:C.I.顏料紅254 (B) 黏結劑聚合物:甲基丙烯酸與曱基丙烯酸苄酯之共 聚物[甲基丙烯酸單位與甲基丙烯酸苄酯單位之比,依物質 置比(莫耳比)計,為30 : 70,酸值i 13,聚苯乙烯換算重 量平均分子量為30,000] (C) 光聚合性化合物:二季戊四醇六丙稀酸酯 (D-1)光聚合起始劑:2-曱基·2-嗎啉代_ι_(4-甲基笨碎 基)丙烷-1-酮 (D-2)光聚合起始劑:2,4-雙(三氯甲基)_6_胡椒基_ 1,3,5-三嗪 315191 32 I326296 (G-υ光聚合起始助劑:2,4•二乙基嚷嘲調 (E-D溶劑:丙二醇單甲喊醋酸醋 (E-2)_ 基+甲基I戍酮
All 1 [著色光敏性樹脂組成物1之調製] (A-1) 7.98質量份 聚醋系顏料分散劑 2.3 9質量广 (B) 5.40質量份 (C) 3.60質量份 (D-1) 0.54質量份 (D-2) 0.54質量份 (G-1) 0.54質量份 (E-1) 76.54 質量份 (E-2) 2_37質量份 將上述成分予以混合而獲得著色光敏性樹脂組成物 [黏度變化率] 著色光敏性樹脂組成物 [乾燥異物] 之黏度變化率,如表1所示。 在30mL旋轉蓋開啟式褐色瓶中,封入著色光 敏性樹脂組成物1並密閉’經上下激烈振動之後,將上述 褐色瓶在23t:中保# i個月。在開啟上述褐色瓶之際並 未發現在t色光敏性樹脂組成⑱中有&燥異物沉殿現象, 且在瓶蓋口螺紋處並未發現到乾燥異物。 實施例2 315191 33 1326296 [著色光敏性樹脂組成物2之調製] (Α-1) 7·98質量份 聚醋系顏料分散劑 2 · 3 9質量份 (Β) 5.40質量份 (C) 3.60質量份 (D-1) 0.54質量份 (D-2) 0.54質量份 (G-1) 0.54質量份 (Ε-1) 71.01 質量份 (Ε-2) 7.90質量份 將上述成分予以混合而獲得著色光敏性樹脂組成物2。 [黏度變化率] 著色光敏性樹脂組成物2之斑痒嫩方 人切z之黏度變化率,如表〗所示。 [乾燥異物] 除以採用著色光敏性樹脂組成物2取代著色光敏性樹 脂組成物1之外,其餘均如同實施例i進行評彳卜在著色 光敏性樹脂組成物中並未發頰仏 ^ 不赞現乾燥異物沉澱現象,且在瓶 盍口螺紋處並未發現到乾燥異物。 實施例3 [著色光敏性樹脂組成物3之調製] (A-1) 7.98質量份 聚酯系顏料分散劑 2 · 3 9質量份 (B) 5.40質量份 (C) 3·60質量份 315191 34 1326296 (D_l) 0_54質量份 (D-2) 0.54質量份 (G-l) 0·54質量份 (E-l) 63.11 質量份 (Ε_2) 13.80 質量份 將上述成分予 [黏度變化率] 以混合而獲得著色光敏性樹 脂組成物3。 者色光敏性樹脂組成物 [乾燥異物] 之黏度變化率,如表1所示。 t除以採用著色光敏性樹脂組成物3取代著色光敏性樹 月曰組成物1之外,其餘均如同實施例1進行評估。在著色 光敏性樹脂組成物中並未發現乾燥異物沉澱現象,且在瓶 盍口螺紋處並未發現到乾燥異物。 實施例4 [著色光敏性樹脂組成物4之調製] (A-1) 7.98質量份 聚酯系顏料分散劑 2 · 3 9質量份 (B) 5.40質量份 (C) 3.60質量份 (D-1) 0_54質量份 (D-2) 〇·54質量份 (G-1) 0.54質量份 (E-1) 47.31 質量份 (E-2) 31.60 質量份 315191 35 將上述成分予以混合而獲得著声 又忖有巴尤敏性樹脂組成物4。
[黏度變化率J 著色光敏性樹脂組成物4之黏度變化率,如表”斤示。 [乾燥異物] 除以採用著色光敏性樹脂組成物4取代著色光敏性樹 腊組成物1之外,其餘均如同實施例丨進行評h在著色 光敏性樹脂組成物中並夫縣_ @ s。 一 X T 1禾發現乾燥異物沉澱現象,且在瓶 蓋口螺紋處並未發現到乾燥異物。 比較例1 [著色光敏性樹脂組成物5之調製] (Α-1) 7.98質量份 聚酯系顏料分散劑 2 · 3 9質量份 (Β) 5.40質量份 (C) 3.60質量份 (D-1) 〇,54質量份 〇)·2) 0.54質量份 (G-1) 0.54質量份 (E-Ι) 78.91 質量份 將上述成分予以混合而獲得著色光敏性樹脂組成物5。 [點度變化率] 著色光敏性樹脂組成物5之黏度變化率,如表1所示。 [乾燥異物] 除以採用著色光敏性樹脂組成物5取代著色光敏性樹 脂組成物1之外,其餘均如同實施例1進行評估。在著色 36 315191 1326296 燥異物沉殿現象 但在瓶 光敏性樹脂組成物中雖未發現乾 蓋口螺紋處卻發現到乾燥異物。 比較例2 [考色光敏性樹脂組成物6之調製] 除將4_經基·4_甲基_2•戊嗣改為丙二醇單甲喊之外, 其餘均如同實施例i,獲得著色光敏性樹脂组成物6。 [黏度變化率] 著色光敏性樹脂組成物6之黏度變化率,如表〗所示。 [乾燥異物] 除以採用著色光敏性樹脂組成物6取代著色光敏性樹 脂組成物丨之外,其餘均如同實施例丨進行評估。在著色 光敏性樹脂組成物中雖未發現乾燥異物沉澱現象,但在瓶 蓋口螺紋處卻發現到乾燥異物。 表1 黏度變化率(%) 乾燥異物 40°C X 1 週 2 3 °C X 1個月 實施例1 2.0 2.0 無 實施例2 2.8 2.5 無 實施例3 2.5 2.1 益 實施例4 2.9 Γ 2.5 無 比較例1 2.8 3.2 有 比較例2 10.4 6.2 有 依照本發明的話’可提供長期安定性優越的著色光敏性樹 脂組成物。本發明的著色光敏性樹脂組成物乃因為長期安 疋性優越’因此若使用於狹縫式塗佈機(slit coater)中的 話’便可獲得平坦性良好的塗膜。 37 315191
Claims (1)
1326296 公告本 §9年 第92130729號專利申請案 (99年2月5曰) 拾、申讀專魏範圆 1· 一種著色光敏性樹脂組成物,係含有著色劑(Α)、黏結 劑聚合物(Β)、光聚合性化合物(C)、光聚合起始劑(D)、 及含量為70質量%以上、8 5質量%以下之溶劑(ε);其 中,溶劑(Ε)係含有:丙二醇單曱醚醋酸酯與4_羥基_4· 甲基-2-戊酮。 2.如申請專利範圍第1項之組成物,其中,溶劑(Ε)係實 質的由丙二醇單曱醚醋酸酯與‘羥基_4_甲基_2•戊酮所 構成。 3.如申D青專利範圍第1或2項之組成物,其中,溶劑(ε ) 中之4-羥基-4-甲基_2_戊酮含量,係3質量%以上、4〇 質量%以下。 4. 一種圖案之形成方法,係將申請專利範圍第丨至3項中 任:項之組成物,塗布於基板上,經去除揮發成分而形 成者色I II·隔著光罩對該著色層進行曝 。 5· -種圖案.,係依申請專利範圍第4項之方法所::者 6. 一種彩色濾光片’係含有申請專利範圍第5項之圖案者。 7. -種液晶顯示裝置,係由具有申請專利範圍“項之彩 色濾光片所構成。 315191修正版 38
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