JPS59189340A - 高感度光重合開始剤組成物 - Google Patents

高感度光重合開始剤組成物

Info

Publication number: JPS59189340A
Authority: JP; Japan
Prior art keywords: org; peroxide; compounds; dye; initiator composition
Prior art date: 1983-04-13
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

Application number

JP6379683A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0365541B2 (fr

Inventor

Tsugio Yamaoka

亜夫山岡

Kenichi Koseki

小関　健一

Yoshitaka Goto

後藤　義隆

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

NOF Corp

Original Assignee

NOF Corp

Nippon Oil and Fats Co Ltd

Priority date (The priority date 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 date listed.)

1983-04-13

Filing date

1983-04-13

Publication date

1984-10-26

1983-04-13 Application filed by NOF Corp, Nippon Oil and Fats Co Ltd filed Critical NOF Corp

1983-04-13 Priority to JP6379683A priority Critical patent/JPS59189340A/ja

1984-10-26 Publication of JPS59189340A publication Critical patent/JPS59189340A/ja

1991-10-14 Publication of JPH0365541B2 publication Critical patent/JPH0365541B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 24
239000003999 initiator Substances 0.000 title claims abstract description 21
230000035945 sensitivity Effects 0.000 title description 11
150000001875 compounds Chemical class 0.000 claims abstract description 26
239000000975 dye Substances 0.000 claims abstract description 19
DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 claims abstract description 3
239000001017 thiazole dye Substances 0.000 claims abstract description 3
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims abstract 2
150000001451 organic peroxides Chemical class 0.000 claims description 7
LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical compound O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 claims 2
229940075420 xanthine Drugs 0.000 claims 1
-1 3,3,5-trimethylcyclohexanone peroxide Chemical class 0.000 abstract description 8
150000002978 peroxides Chemical class 0.000 abstract description 7
UICXTANXZJJIBC-UHFFFAOYSA-N 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(OO)CCCCC1 UICXTANXZJJIBC-UHFFFAOYSA-N 0.000 abstract description 2
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 abstract description 2
239000001018 xanthene dye Substances 0.000 abstract description 2
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 abstract 1
POSWICCRDBKBMH-UHFFFAOYSA-N dihydroisophorone Natural products CC1CC(=O)CC(C)(C)C1 POSWICCRDBKBMH-UHFFFAOYSA-N 0.000 abstract 1
230000000977 initiatory effect Effects 0.000 abstract 1
QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 abstract 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 9
239000000463 material Substances 0.000 description 8
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 3
ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical class C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 3
239000002904 solvent Substances 0.000 description 3
YKTNISGZEGZHIS-UHFFFAOYSA-N 2-$l^{1}-oxidanyloxy-2-methylpropane Chemical group CC(C)(C)O[O] YKTNISGZEGZHIS-UHFFFAOYSA-N 0.000 description 2
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-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
239000004342 Benzoyl peroxide Substances 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
206010034972 Photosensitivity reaction Diseases 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
150000008064 anhydrides 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
235000019400 benzoyl peroxide Nutrition 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
238000007865 diluting Methods 0.000 description 2
AUZONCFQVSMFAP-UHFFFAOYSA-N disulfiram Chemical compound CCN(CC)C(=S)SSC(=S)N(CC)CC AUZONCFQVSMFAP-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
229910052753 mercury Inorganic materials 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000000178 monomer Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
230000000649 photocoagulation Effects 0.000 description 2
229920002120 photoresistant polymer Polymers 0.000 description 2
230000036211 photosensitivity Effects 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 1
KDGNCLDCOVTOCS-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy propan-2-yl carbonate Chemical compound CC(C)OC(=O)OOC(C)(C)C KDGNCLDCOVTOCS-UHFFFAOYSA-N 0.000 description 1
ZORJPNCZZRLEDF-UHFFFAOYSA-N (3-methoxy-3-methylbutoxy)carbonyloxy (3-methoxy-3-methylbutyl) carbonate Chemical compound COC(C)(C)CCOC(=O)OOC(=O)OCCC(C)(C)OC ZORJPNCZZRLEDF-UHFFFAOYSA-N 0.000 description 1
RIPYNJLMMFGZSX-UHFFFAOYSA-N (5-benzoylperoxy-2,5-dimethylhexan-2-yl) benzenecarboperoxoate Chemical compound C=1C=CC=CC=1C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C1=CC=CC=C1 RIPYNJLMMFGZSX-UHFFFAOYSA-N 0.000 description 1
NALFRYPTRXKZPN-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane Chemical compound CC1CC(C)(C)CC(OOC(C)(C)C)(OOC(C)(C)C)C1 NALFRYPTRXKZPN-UHFFFAOYSA-N 0.000 description 1
BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
KABXCMUKNKDRHI-UHFFFAOYSA-N 1,2-dimethoxypropan-2-yl hydroxy carbonate Chemical compound COCC(C)(OC)OC(=O)OO KABXCMUKNKDRHI-UHFFFAOYSA-N 0.000 description 1
MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
HQOVXPHOJANJBR-UHFFFAOYSA-N 2,2-bis(tert-butylperoxy)butane Chemical compound CC(C)(C)OOC(C)(CC)OOC(C)(C)C HQOVXPHOJANJBR-UHFFFAOYSA-N 0.000 description 1
DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
VGZZAZYCLRYTNQ-UHFFFAOYSA-N 2-ethoxyethoxycarbonyloxy 2-ethoxyethyl carbonate Chemical compound CCOCCOC(=O)OOC(=O)OCCOCC VGZZAZYCLRYTNQ-UHFFFAOYSA-N 0.000 description 1
BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
RPBWMJBZQXCSFW-UHFFFAOYSA-N 2-methylpropanoyl 2-methylpropaneperoxoate Chemical compound CC(C)C(=O)OOC(=O)C(C)C RPBWMJBZQXCSFW-UHFFFAOYSA-N 0.000 description 1
KFGFVPMRLOQXNB-UHFFFAOYSA-N 3,5,5-trimethylhexanoyl 3,5,5-trimethylhexaneperoxoate Chemical compound CC(C)(C)CC(C)CC(=O)OOC(=O)CC(C)CC(C)(C)C KFGFVPMRLOQXNB-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
XYFRHHAYSXIKGH-UHFFFAOYSA-N 3-(5-methoxy-2-methoxycarbonyl-1h-indol-3-yl)prop-2-enoic acid Chemical compound C1=C(OC)C=C2C(C=CC(O)=O)=C(C(=O)OC)NC2=C1 XYFRHHAYSXIKGH-UHFFFAOYSA-N 0.000 description 1
VDQNOOZIDCTAPX-UHFFFAOYSA-N 3-butylperoxycarbonylbenzenecarboperoxoic acid Chemical group CCCCOOC(=O)C1=CC=CC(C(=O)OO)=C1 VDQNOOZIDCTAPX-UHFFFAOYSA-N 0.000 description 1
MKTOIPPVFPJEQO-UHFFFAOYSA-N 4-(3-carboxypropanoylperoxy)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OOC(=O)CCC(O)=O MKTOIPPVFPJEQO-UHFFFAOYSA-N 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
208000023514 Barrett esophagus Diseases 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
244000028419 Styrax benzoin Species 0.000 description 1
235000000126 Styrax benzoin Nutrition 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
235000008411 Sumatra benzointree Nutrition 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Natural products CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
LHMRXAIRPKSGDE-UHFFFAOYSA-N benzo[a]anthracene-7,12-dione Chemical compound C1=CC2=CC=CC=C2C2=C1C(=O)C1=CC=CC=C1C2=O LHMRXAIRPKSGDE-UHFFFAOYSA-N 0.000 description 1
229960002130 benzoin Drugs 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
BXIQXYOPGBXIEM-UHFFFAOYSA-N butyl 4,4-bis(tert-butylperoxy)pentanoate Chemical compound CCCCOC(=O)CCC(C)(OOC(C)(C)C)OOC(C)(C)C BXIQXYOPGBXIEM-UHFFFAOYSA-N 0.000 description 1
UPIWXMRIPODGLE-UHFFFAOYSA-N butyl benzenecarboperoxoate Chemical group CCCCOOC(=O)C1=CC=CC=C1 UPIWXMRIPODGLE-UHFFFAOYSA-N 0.000 description 1
JWKNCJFGBOQAQL-UHFFFAOYSA-N butyl dodecaneperoxoate Chemical group CCCCCCCCCCCC(=O)OOCCCC JWKNCJFGBOQAQL-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001728 carbonyl compounds Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
SPTHWAJJMLCAQF-UHFFFAOYSA-M ctk4f8481 Chemical compound [O-]O.CC(C)C1=CC=CC=C1C(C)C SPTHWAJJMLCAQF-UHFFFAOYSA-M 0.000 description 1
230000001186 cumulative effect Effects 0.000 description 1
XJOBOFWTZOKMOH-UHFFFAOYSA-N decanoyl decaneperoxoate Chemical compound CCCCCCCCCC(=O)OOC(=O)CCCCCCCCC XJOBOFWTZOKMOH-UHFFFAOYSA-N 0.000 description 1
LDCRTTXIJACKKU-ONEGZZNKSA-N dimethyl fumarate Chemical compound COC(=O)\C=C\C(=O)OC LDCRTTXIJACKKU-ONEGZZNKSA-N 0.000 description 1
229960004419 dimethyl fumarate Drugs 0.000 description 1
LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
235000019382 gum benzoic Nutrition 0.000 description 1
150000002366 halogen compounds Chemical class 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
238000001093 holography Methods 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000000976 ink Substances 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
229910001507 metal halide Inorganic materials 0.000 description 1
150000005309 metal halides Chemical class 0.000 description 1
238000000034 method Methods 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000003973 paint Substances 0.000 description 1
QUPCNWFFTANZPX-UHFFFAOYSA-M paramenthane hydroperoxide Chemical compound [O-]O.CC(C)C1CCC(C)CC1 QUPCNWFFTANZPX-UHFFFAOYSA-M 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
YPVDWEHVCUBACK-UHFFFAOYSA-N propoxycarbonyloxy propyl carbonate Chemical compound CCCOC(=O)OOC(=O)OCCC YPVDWEHVCUBACK-UHFFFAOYSA-N 0.000 description 1
229910052709 silver Inorganic materials 0.000 description 1
239000004332 silver Substances 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
150000003464 sulfur compounds Chemical class 0.000 description 1
PFBLRDXPNUJYJM-UHFFFAOYSA-N tert-butyl 2-methylpropaneperoxoate Chemical compound CC(C)C(=O)OOC(C)(C)C PFBLRDXPNUJYJM-UHFFFAOYSA-N 0.000 description 1
BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
229940035339 tri-chlor Drugs 0.000 description 1
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
229910052721 tungsten Inorganic materials 0.000 description 1
239000010937 tungsten Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
229910052724 xenon Inorganic materials 0.000 description 1
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene 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
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
- G03F7/031—Organic compounds not covered by group G03F7/029

Landscapes

Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
General Physics & Mathematics (AREA)
Polymerisation Methods In General (AREA)

JP6379683A 1983-04-13 1983-04-13 高感度光重合開始剤組成物 Granted JPS59189340A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP6379683A JPS59189340A (ja)	1983-04-13	1983-04-13	高感度光重合開始剤組成物

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP6379683A JPS59189340A (ja)	1983-04-13	1983-04-13	高感度光重合開始剤組成物

Publications (2)

Publication Number	Publication Date
JPS59189340A true JPS59189340A (ja)	1984-10-26
JPH0365541B2 JPH0365541B2 (fr)	1991-10-14

Family

ID=13239694

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP6379683A Granted JPS59189340A (ja)	1983-04-13	1983-04-13	高感度光重合開始剤組成物

Country Status (1)

Country	Link
JP (1)	JPS59189340A (fr)

Cited By (28)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61213838A (ja) *	1985-03-20	1986-09-22	Nippon Oil & Fats Co Ltd	感光性平版印刷版
JPS62263202A (ja) *	1986-05-08	1987-11-16	Unitika Ltd	光重合性組成物
JPS63132902A (ja) *	1986-11-22	1988-06-04	Nippon Oil & Fats Co Ltd	光重合開始剤組成物
JPS63144342A (ja) *	1986-12-09	1988-06-16	Nippon Oil & Fats Co Ltd	ドライフイルムフオトレジスト
US4766055A (en) *	1985-08-01	1988-08-23	Nippon Paint Co., Ltd.	Photopolymerizable composition containing a certain xanthene or thioxanthene dyestuff
JPS6488444A (en) *	1987-09-29	1989-04-03	Fuji Photo Film Co Ltd	Photopolymerizable composition
JPH0527422A (ja) *	1991-07-24	1993-02-05	Toyo Ink Mfg Co Ltd	可視光感光性樹脂組成物
JPH05107758A (ja) *	1991-10-14	1993-04-30	Fuji Photo Film Co Ltd	光重合性組成物
EP0695971A1 (fr)	1994-08-03	1996-02-07	Fuji Photo Film Co., Ltd.	Plaque d'impression photolithographique
EP0704764A1 (fr)	1994-09-05	1996-04-03	Mitsubishi Chemical Corporation	Composition photopolymerisable et plaque d'impression lithographique photosensible
EP0780731A2 (fr)	1995-12-22	1997-06-25	Mitsubishi Chemical Corporation	Composition photopolymérisable pour filtre couleur, filtre couleur et dispositif d'affichage à cristaux liquides
EP1626309A2 (fr)	2004-03-25	2006-02-15	Fuji Photo Film Co., Ltd.	Matériau pour l'enregistrement de hologrammes, méthode pour l'enregistrement de hologrammes et élément optique holographique
EP1635219A1 (fr)	2004-08-27	2006-03-15	Fuji Photo Film Co., Ltd.	Plaque d'impression lithographique photosensible
EP1757984A1 (fr)	2005-08-22	2007-02-28	Fuji Photo Film Co., Ltd.	Plaque d'impression lithographique photosensible
WO2008108406A1 (fr) *	2007-03-05	2008-09-12	Fujifilm Corporation	Composé pour résine photosensible, solution de résine photosensible, et procédé de gravure utilisant la solution de résine photosensible
EP2042532A2 (fr)	2007-09-28	2009-04-01	FUJIFILM Corporation	Composition polymérisable et précurseur de plaque d'impression planographique l'utilisant, résine polyréthane soluble dans l'alcali, procédé de production de ce composé
JP2009203349A (ja) *	2008-02-28	2009-09-10	Fujifilm Corp	フォトレジスト用化合物、フォトレジスト液、およびこれを用いるエッチング方法
WO2009119610A1 (fr)	2008-03-25	2009-10-01	富士フイルム株式会社	Procédé de production d’une plaque d'impression lithographique
EP2107089A1 (fr)	2005-06-13	2009-10-07	Toshiba TEC Kabushiki Kaisha	Encre à jet d'encre, procédé d'enregistrement à jet d'encre, procédé d'évaluation d'encre à jet d'encre, et procédé de fabrication d'encre à jet d'encre
EP2109000A1 (fr)	2004-09-10	2009-10-14	FUJIFILM Corporation	Polymère ayant un groupement polymérisable, composition polymérisable, précurseur de plaque d'impression planographique et méthode d'impression planographique
EP2128704A2 (fr)	2008-05-29	2009-12-02	Fujifilm Corporation	Liquide de traitement pour le développement de plaques d'impression lithographique et procédé de fabrication de plaques d'impression lithographique
EP2131239A1 (fr)	2008-05-29	2009-12-09	Fujifilm Corporation	Liquide de traitement pour le développement de plaques d'impression lithographique et procédé de fabrication de plaques d'impression lithographique
EP2157478A2 (fr)	2008-08-22	2010-02-24	Fujifilm Corporation	Procédé de fabrication d'une plaque d'impression lithographique
WO2010021364A1 (fr)	2008-08-22	2010-02-25	富士フイルム株式会社	Procédé de fabrication d'une plaque d'impression lithographique
EP2159640A1 (fr)	2008-08-29	2010-03-03	Fujifilm Corporation	Procédé de préparation de plaque d'impression lithographique
WO2013039235A1 (fr)	2011-09-15	2013-03-21	富士フイルム株式会社	Procédé de recyclage d'eaux usées produites par un procédé de fabrication de plaque
WO2013065853A1 (fr)	2011-11-04	2013-05-10	富士フイルム株式会社	Procédé de recyclage d'une solution résiduaire de traitement de fabrication de plaque
WO2023113043A1 (fr)	2021-12-17	2023-06-22	大日本印刷株式会社	Stratifié d'hologramme en volume, procédé de production de stratifié d'hologramme en volume, feuille de transfert d'hologramme en volume, étiquette d'hologramme en volume, feuille d'hologramme en volume pour incorporation, carte et produit de type autocollant d'hologramme

Citations (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS49115312A (fr) *	1973-02-20	1974-11-05
JPS5212825A (en) *	1975-07-21	1977-01-31	Toyobo Co Ltd	Visible light sensitive composition
JPS5289915A (en) *	1976-01-23	1977-07-28	Mitsubishi Paper Mills Ltd	Image forming method
JPS539519A (en) *	1976-07-14	1978-01-28	Ricoh Co Ltd	Photosensitive material for forming color image
JPS54151024A (en) *	1978-05-18	1979-11-27	Fuji Photo Film Co Ltd	Photopolymerizable composition
JPS5888739A (ja) *	1981-11-12	1983-05-26	ザ・ミ−ド・コ−ポレ−シヨン	転写画像形成系

1983
- 1983-04-13 JP JP6379683A patent/JPS59189340A/ja active Granted

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS49115312A (fr) *	1973-02-20	1974-11-05
JPS5212825A (en) *	1975-07-21	1977-01-31	Toyobo Co Ltd	Visible light sensitive composition
JPS5289915A (en) *	1976-01-23	1977-07-28	Mitsubishi Paper Mills Ltd	Image forming method
JPS539519A (en) *	1976-07-14	1978-01-28	Ricoh Co Ltd	Photosensitive material for forming color image
JPS54151024A (en) *	1978-05-18	1979-11-27	Fuji Photo Film Co Ltd	Photopolymerizable composition
JPS5888739A (ja) *	1981-11-12	1983-05-26	ザ・ミ−ド・コ−ポレ−シヨン	転写画像形成系

Cited By (29)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61213838A (ja) *	1985-03-20	1986-09-22	Nippon Oil & Fats Co Ltd	感光性平版印刷版
US4766055A (en) *	1985-08-01	1988-08-23	Nippon Paint Co., Ltd.	Photopolymerizable composition containing a certain xanthene or thioxanthene dyestuff
JPS62263202A (ja) *	1986-05-08	1987-11-16	Unitika Ltd	光重合性組成物
JPS63132902A (ja) *	1986-11-22	1988-06-04	Nippon Oil & Fats Co Ltd	光重合開始剤組成物
JPS63144342A (ja) *	1986-12-09	1988-06-16	Nippon Oil & Fats Co Ltd	ドライフイルムフオトレジスト
JPS6488444A (en) *	1987-09-29	1989-04-03	Fuji Photo Film Co Ltd	Photopolymerizable composition
JPH0527422A (ja) *	1991-07-24	1993-02-05	Toyo Ink Mfg Co Ltd	可視光感光性樹脂組成物
JPH05107758A (ja) *	1991-10-14	1993-04-30	Fuji Photo Film Co Ltd	光重合性組成物
EP0695971A1 (fr)	1994-08-03	1996-02-07	Fuji Photo Film Co., Ltd.	Plaque d'impression photolithographique
EP0704764A1 (fr)	1994-09-05	1996-04-03	Mitsubishi Chemical Corporation	Composition photopolymerisable et plaque d'impression lithographique photosensible
EP0780731A2 (fr)	1995-12-22	1997-06-25	Mitsubishi Chemical Corporation	Composition photopolymérisable pour filtre couleur, filtre couleur et dispositif d'affichage à cristaux liquides
EP1626309A2 (fr)	2004-03-25	2006-02-15	Fuji Photo Film Co., Ltd.	Matériau pour l'enregistrement de hologrammes, méthode pour l'enregistrement de hologrammes et élément optique holographique
EP1635219A1 (fr)	2004-08-27	2006-03-15	Fuji Photo Film Co., Ltd.	Plaque d'impression lithographique photosensible
EP3182204A1 (fr)	2004-09-10	2017-06-21	FUJIFILM Corporation	Polymère doté d'un groupe polymérisable, composition polymérisable, précurseur de plaque d'impression planographique et procédé d'impression planographique l'utilisant
EP2109000A1 (fr)	2004-09-10	2009-10-14	FUJIFILM Corporation	Polymère ayant un groupement polymérisable, composition polymérisable, précurseur de plaque d'impression planographique et méthode d'impression planographique
EP2107089A1 (fr)	2005-06-13	2009-10-07	Toshiba TEC Kabushiki Kaisha	Encre à jet d'encre, procédé d'enregistrement à jet d'encre, procédé d'évaluation d'encre à jet d'encre, et procédé de fabrication d'encre à jet d'encre
EP1757984A1 (fr)	2005-08-22	2007-02-28	Fuji Photo Film Co., Ltd.	Plaque d'impression lithographique photosensible
WO2008108406A1 (fr) *	2007-03-05	2008-09-12	Fujifilm Corporation	Composé pour résine photosensible, solution de résine photosensible, et procédé de gravure utilisant la solution de résine photosensible
EP2042532A2 (fr)	2007-09-28	2009-04-01	FUJIFILM Corporation	Composition polymérisable et précurseur de plaque d'impression planographique l'utilisant, résine polyréthane soluble dans l'alcali, procédé de production de ce composé
JP2009203349A (ja) *	2008-02-28	2009-09-10	Fujifilm Corp	フォトレジスト用化合物、フォトレジスト液、およびこれを用いるエッチング方法
WO2009119610A1 (fr)	2008-03-25	2009-10-01	富士フイルム株式会社	Procédé de production d’une plaque d'impression lithographique
EP2128704A2 (fr)	2008-05-29	2009-12-02	Fujifilm Corporation	Liquide de traitement pour le développement de plaques d'impression lithographique et procédé de fabrication de plaques d'impression lithographique
EP2131239A1 (fr)	2008-05-29	2009-12-09	Fujifilm Corporation	Liquide de traitement pour le développement de plaques d'impression lithographique et procédé de fabrication de plaques d'impression lithographique
EP2157478A2 (fr)	2008-08-22	2010-02-24	Fujifilm Corporation	Procédé de fabrication d'une plaque d'impression lithographique
WO2010021364A1 (fr)	2008-08-22	2010-02-25	富士フイルム株式会社	Procédé de fabrication d'une plaque d'impression lithographique
EP2159640A1 (fr)	2008-08-29	2010-03-03	Fujifilm Corporation	Procédé de préparation de plaque d'impression lithographique
WO2013039235A1 (fr)	2011-09-15	2013-03-21	富士フイルム株式会社	Procédé de recyclage d'eaux usées produites par un procédé de fabrication de plaque
WO2013065853A1 (fr)	2011-11-04	2013-05-10	富士フイルム株式会社	Procédé de recyclage d'une solution résiduaire de traitement de fabrication de plaque
WO2023113043A1 (fr)	2021-12-17	2023-06-22	大日本印刷株式会社	Stratifié d'hologramme en volume, procédé de production de stratifié d'hologramme en volume, feuille de transfert d'hologramme en volume, étiquette d'hologramme en volume, feuille d'hologramme en volume pour incorporation, carte et produit de type autocollant d'hologramme

Also Published As

Publication number	Publication date
JPH0365541B2 (fr)	1991-10-14

Publication	Publication Date	Title
JPS59189340A (ja)	1984-10-26	高感度光重合開始剤組成物
US4940648A (en)	1990-07-10	Increased sensitivity photoinitiation compositions
JP5617941B2 (ja)	2014-11-05	感光性樹脂組成物、感光性エレメント、レジストパターンの形成方法、及び、プリント配線板の製造方法
JP5051299B2 (ja)	2012-10-17	感光性樹脂組成物、感光性エレメント、レジストパターンの製造方法、及びプリント配線板の製造方法
JPS591504A (ja)	1984-01-06	光重合開始剤組成物
JPS621641B2 (fr)	1987-01-14
KR101514900B1 (ko)	2015-04-23	감광성 수지 조성물, 및 이를 이용한 감광성 엘리먼트, 레지스트 패턴의 형성 방법 및 프린트 배선판의 제조 방법
JP6022749B2 (ja)	2016-11-09	感光性樹脂組成物、感光性エレメント、レジストパターンの製造方法、リードフレームの製造方法及びプリント配線板の製造方法
JPS59140203A (ja)	1984-08-11	高感度光開始剤組成物
JP2018524285A (ja)	2018-08-30	ピラゾリン類増感剤及びその製造方法並びに使用
JPH0611765B2 (ja)	1994-02-16	光重合開始剤組成物
JPS6076503A (ja)	1985-05-01	高感度光開始剤組成物
JPS63168403A (ja)	1988-07-12	光重合性組成物
JPS627703A (ja)	1987-01-14	光重合開始剤組成物
JPH02279702A (ja)	1990-11-15	光重合開始剤組成物
JPS63132902A (ja)	1988-06-04	光重合開始剤組成物
JP7715912B1 (ja)	2025-07-30	感光性樹脂組成物及びレジストパターンの形成方法
JPS63278906A (ja)	1988-11-16	光重合開始剤組成物
JPS63278907A (ja)	1988-11-16	光重合開始剤組成物
JPH0463882B2 (fr)	1992-10-13
JPS63278905A (ja)	1988-11-16	光重合開始剤組成物
JPS63278908A (ja)	1988-11-16	光重合開始剤組成物
JPS6194040A (ja)	1986-05-12	非銀塩感光性フイルム
JPS63278904A (ja)	1988-11-16	光重合開始剤組成物
JPS63265901A (ja)	1988-11-02	光重合開始剤組成物