JPH0410482B2 - - Google Patents
Info
- Publication number
- JPH0410482B2 JPH0410482B2 JP58184924A JP18492483A JPH0410482B2 JP H0410482 B2 JPH0410482 B2 JP H0410482B2 JP 58184924 A JP58184924 A JP 58184924A JP 18492483 A JP18492483 A JP 18492483A JP H0410482 B2 JPH0410482 B2 JP H0410482B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- fluoroborate
- perchlorate
- bis
- carbon atoms
- 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.)
- Expired - Lifetime
Links
- -1 halofenyl group Chemical group 0.000 claims description 90
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 20
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 239000000975 dye Substances 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical group C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 7
- 125000003277 amino group Chemical group 0.000 claims description 4
- 125000000524 functional group Chemical group 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical group [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000005469 ethylenyl group Chemical group 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims description 2
- 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 description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000006501 nitrophenyl group Chemical group 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical class C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 claims description 2
- 229910052711 selenium Chemical group 0.000 claims description 2
- 239000011669 selenium Chemical group 0.000 claims description 2
- 125000005504 styryl group Chemical group 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- 239000001017 thiazole dye Substances 0.000 claims description 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims description 2
- 239000001018 xanthene dye Substances 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 14
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 14
- 230000035945 sensitivity Effects 0.000 description 12
- 125000003118 aryl group Chemical group 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 9
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 6
- 125000005843 halogen group Chemical group 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 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
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-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
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-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
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-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
- 229910052783 alkali metal Chemical group 0.000 description 3
- 150000001340 alkali metals Chemical group 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
- 239000012965 benzophenone Substances 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920002120 photoresistant polymer Polymers 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
- JCTIGQULNYPZDU-UHFFFAOYSA-M 2,4,6-triphenylselenopyran-1-ium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=[se+]C(C=2C=CC=CC=2)=C1 JCTIGQULNYPZDU-UHFFFAOYSA-M 0.000 description 2
- WPFBPHJBJLQPBB-UHFFFAOYSA-M 2,6-bis(4-ethylphenyl)-4-(4-pentoxyphenyl)pyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OCCCCC)=CC=C1C1=CC(C=2C=CC(CC)=CC=2)=[O+]C(C=2C=CC(CC)=CC=2)=C1 WPFBPHJBJLQPBB-UHFFFAOYSA-M 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
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- CLEKZIKTEHRDNU-UHFFFAOYSA-N 2-tert-butylperoxycarbonyl-4-(3-tert-butylperoxycarbonyl-4-carboxybenzoyl)benzoic acid Chemical compound C1=C(C(O)=O)C(C(=O)OOC(C)(C)C)=CC(C(=O)C=2C=C(C(C(O)=O)=CC=2)C(=O)OOC(C)(C)C)=C1 CLEKZIKTEHRDNU-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
- 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
- DPEQODCLVGYAFD-UHFFFAOYSA-M [O-]Cl(=O)(=O)=O.C1=CC(N(C)C)=CC=C1C=CC1=CC(C=2C=CC=CC=2)=CC(C=2C=CC=CC=2)=[S+]1 Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(N(C)C)=CC=C1C=CC1=CC(C=2C=CC=CC=2)=CC(C=2C=CC=CC=2)=[S+]1 DPEQODCLVGYAFD-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 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 2
- 239000004305 biphenyl Substances 0.000 description 2
- VRZQMDDQCTXMKG-UHFFFAOYSA-N bis(2-phenylpropan-2-yl) 4-[3,4-bis(2-phenylpropan-2-ylperoxycarbonyl)benzoyl]benzene-1,2-dicarboperoxoate Chemical compound C=1C=CC=CC=1C(C)(C)OOC(=O)C1=CC=C(C(=O)C=2C=C(C(C(=O)OOC(C)(C)C=3C=CC=CC=3)=CC=2)C(=O)OOC(C)(C)C=2C=CC=CC=2)C=C1C(=O)OOC(C)(C)C1=CC=CC=C1 VRZQMDDQCTXMKG-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
- KGGOIDKBHYYNIC-UHFFFAOYSA-N ditert-butyl 4-[3,4-bis(tert-butylperoxycarbonyl)benzoyl]benzene-1,2-dicarboperoxoate Chemical compound C1=C(C(=O)OOC(C)(C)C)C(C(=O)OOC(C)(C)C)=CC=C1C(=O)C1=CC=C(C(=O)OOC(C)(C)C)C(C(=O)OOC(C)(C)C)=C1 KGGOIDKBHYYNIC-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000003999 initiator Substances 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
- 238000000034 method Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 150000001451 organic peroxides Chemical class 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
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000000126 substance Substances 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
- 229910052724 xenon Inorganic materials 0.000 description 2
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
- 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
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- DVWQSKNALFXODO-UHFFFAOYSA-M 2,4,6-triphenylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=[O+]C(C=2C=CC=CC=2)=C1 DVWQSKNALFXODO-UHFFFAOYSA-M 0.000 description 1
- UAMORFUEIWNPCP-UHFFFAOYSA-M 2,4,6-triphenylthiopyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=[S+]C(C=2C=CC=CC=2)=C1 UAMORFUEIWNPCP-UHFFFAOYSA-M 0.000 description 1
- NILKBBWMPNIUNJ-UHFFFAOYSA-L 2,4,6-triphenylthiopyrylium;sulfate Chemical compound [O-]S([O-])(=O)=O.C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=[S+]C(C=2C=CC=CC=2)=C1.C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=[S+]C(C=2C=CC=CC=2)=C1 NILKBBWMPNIUNJ-UHFFFAOYSA-L 0.000 description 1
- KCUZJXQSQWBZJP-UHFFFAOYSA-M 2,4,6-tris(4-methoxyphenyl)pyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OC)=CC=C1C1=CC(C=2C=CC(OC)=CC=2)=[O+]C(C=2C=CC(OC)=CC=2)=C1 KCUZJXQSQWBZJP-UHFFFAOYSA-M 0.000 description 1
- ZPPDJOXVSLMNQK-UHFFFAOYSA-M 2,4-bis(4-butylphenyl)-6-(4-nitrophenyl)pyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(CCCC)=CC=C1C1=CC(C=2C=CC(CCCC)=CC=2)=[O+]C(C=2C=CC(=CC=2)[N+]([O-])=O)=C1 ZPPDJOXVSLMNQK-UHFFFAOYSA-M 0.000 description 1
- KWVPJUOCWQHWNW-UHFFFAOYSA-M 2,6-bis(4-ethylphenyl)-4-(4-methoxyphenyl)pyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(CC)=CC=C1C1=CC(C=2C=CC(OC)=CC=2)=CC(C=2C=CC(CC)=CC=2)=[O+]1 KWVPJUOCWQHWNW-UHFFFAOYSA-M 0.000 description 1
- SASYSCKFTPSEEG-UHFFFAOYSA-M 2,6-bis(4-ethylphenyl)-4-phenylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(CC)=CC=C1C1=CC(C=2C=CC=CC=2)=CC(C=2C=CC(CC)=CC=2)=[O+]1 SASYSCKFTPSEEG-UHFFFAOYSA-M 0.000 description 1
- ISQCVWDIPCTVMG-UHFFFAOYSA-M 2,6-bis(4-ethylphenyl)-4-phenylselenopyran-1-ium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(CC)=CC=C1C1=CC(C=2C=CC=CC=2)=CC(C=2C=CC(CC)=CC=2)=[se+]1 ISQCVWDIPCTVMG-UHFFFAOYSA-M 0.000 description 1
- PPDDORXLKBMVKB-UHFFFAOYSA-M 2,6-bis(4-methoxyphenyl)-4-(4-pentoxyphenyl)pyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OCCCCC)=CC=C1C1=CC(C=2C=CC(OC)=CC=2)=[O+]C(C=2C=CC(OC)=CC=2)=C1 PPDDORXLKBMVKB-UHFFFAOYSA-M 0.000 description 1
- KJPZZUGNDANJPH-UHFFFAOYSA-M 2,6-bis(4-methoxyphenyl)-4-methylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OC)=CC=C1C1=CC(C)=CC(C=2C=CC(OC)=CC=2)=[O+]1 KJPZZUGNDANJPH-UHFFFAOYSA-M 0.000 description 1
- BXUXWKVZQIPOBA-UHFFFAOYSA-M 2,6-bis(4-methoxyphenyl)-4-phenylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OC)=CC=C1C1=CC(C=2C=CC=CC=2)=CC(C=2C=CC(OC)=CC=2)=[O+]1 BXUXWKVZQIPOBA-UHFFFAOYSA-M 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
- GODBBAPLWRHHEO-UHFFFAOYSA-M 2-(3,4-dichlorophenyl)-4-(4-methoxyphenyl)-6-phenylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OC)=CC=C1C1=CC(C=2C=CC=CC=2)=[O+]C(C=2C=C(Cl)C(Cl)=CC=2)=C1 GODBBAPLWRHHEO-UHFFFAOYSA-M 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
- KSBYUGGJNCFDTQ-UHFFFAOYSA-M 2-(4-ethoxyphenyl)-4,6-diphenylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OCC)=CC=C1C1=CC(C=2C=CC=CC=2)=CC(C=2C=CC=CC=2)=[O+]1 KSBYUGGJNCFDTQ-UHFFFAOYSA-M 0.000 description 1
- FIGCIUZPWFBMSS-UHFFFAOYSA-M 2-(4-methoxyphenyl)-4,6-diphenylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OC)=CC=C1C1=CC(C=2C=CC=CC=2)=CC(C=2C=CC=CC=2)=[O+]1 FIGCIUZPWFBMSS-UHFFFAOYSA-M 0.000 description 1
- ZCAGMOQODTVCKE-UHFFFAOYSA-M 2-(4-methoxyphenyl)-4,6-diphenylselenopyran-1-ium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OC)=CC=C1C1=CC(C=2C=CC=CC=2)=CC(C=2C=CC=CC=2)=[se+]1 ZCAGMOQODTVCKE-UHFFFAOYSA-M 0.000 description 1
- XCJVVYBYCKCSRZ-UHFFFAOYSA-M 2-(4-pentoxyphenyl)-4,6-diphenylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC(OCCCCC)=CC=C1C1=CC(C=2C=CC=CC=2)=CC(C=2C=CC=CC=2)=[O+]1 XCJVVYBYCKCSRZ-UHFFFAOYSA-M 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZUVQWJLVHOMYQT-UHFFFAOYSA-M 2-[2-(3,4-diethoxyphenyl)ethenyl]-4,6-diphenylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=C(OCC)C(OCC)=CC=C1C=CC1=CC(C=2C=CC=CC=2)=CC(C=2C=CC=CC=2)=[O+]1 ZUVQWJLVHOMYQT-UHFFFAOYSA-M 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
- 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
- RFKUPJUWGRZWAV-UHFFFAOYSA-M 4-(2,4-dichlorophenyl)-2,6-diphenylpyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.ClC1=CC(Cl)=CC=C1C1=CC(C=2C=CC=CC=2)=[O+]C(C=2C=CC=CC=2)=C1 RFKUPJUWGRZWAV-UHFFFAOYSA-M 0.000 description 1
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- 150000005309 metal halides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 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
- 239000003973 paint Substances 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
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- NTQLADLBRQMNQJ-UHFFFAOYSA-M pyrylium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC=[O+]C=C1 NTQLADLBRQMNQJ-UHFFFAOYSA-M 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
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- RPMXRFYVVKQQJK-UHFFFAOYSA-N tris(2-methylbutan-2-yl) 5-[4-(2-methylbutan-2-ylperoxycarbonyl)benzoyl]cyclohexa-2,4-diene-1,1,2-tricarboperoxoate Chemical compound C1C(C(=O)OOC(C)(C)CC)(C(=O)OOC(C)(C)CC)C(C(=O)OOC(C)(C)CC)=CC=C1C(=O)C1=CC=C(C(=O)OOC(C)(C)CC)C=C1 RPMXRFYVVKQQJK-UHFFFAOYSA-N 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
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Polymerisation Methods In General (AREA)
- Paints Or Removers (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18492483A JPS6076503A (ja) | 1983-10-03 | 1983-10-03 | 高感度光開始剤組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18492483A JPS6076503A (ja) | 1983-10-03 | 1983-10-03 | 高感度光開始剤組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6076503A JPS6076503A (ja) | 1985-05-01 |
| JPH0410482B2 true JPH0410482B2 (ko) | 1992-02-25 |
Family
ID=16161711
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18492483A Granted JPS6076503A (ja) | 1983-10-03 | 1983-10-03 | 高感度光開始剤組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6076503A (ko) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6281403A (ja) * | 1985-10-04 | 1987-04-14 | Nippon Oil & Fats Co Ltd | 光重合開始剤組成物 |
| CA1284740C (en) * | 1985-11-20 | 1991-06-11 | Peter Gottschalk | Photosensitive materials containing ionic dye compounds as initiators |
| JPH0827539B2 (ja) * | 1987-09-28 | 1996-03-21 | 富士写真フイルム株式会社 | 光重合性組成物 |
| JP2704407B2 (ja) * | 1987-09-29 | 1998-01-26 | 富士写真フイルム株式会社 | 光重合性組成物 |
| JPH07103171B2 (ja) * | 1988-05-13 | 1995-11-08 | 日本ペイント株式会社 | 光重合性組成物 |
| US5773194A (en) | 1995-09-08 | 1998-06-30 | Konica Corporation | Light sensitive composition, presensitized lithographic printing plate and image forming method employing the printing plate |
| JP2005309359A (ja) | 2004-03-25 | 2005-11-04 | Fuji Photo Film Co Ltd | ホログラム記録材料、ホログラム記録方法、光記録媒体、３次元ディスプレイホログラムおよびホログラフィック光学素子。 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59197401A (ja) * | 1983-04-26 | 1984-11-09 | Nippon Oil & Fats Co Ltd | 光重合開始剤 |
-
1983
- 1983-10-03 JP JP18492483A patent/JPS6076503A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59197401A (ja) * | 1983-04-26 | 1984-11-09 | Nippon Oil & Fats Co Ltd | 光重合開始剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6076503A (ja) | 1985-05-01 |
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