JPS6076735A - 光硬化樹脂組成物 - Google Patents

光硬化樹脂組成物

Info

Publication number: JPS6076735A
Authority: JP; Japan
Prior art keywords: resin composition; merocyanine; initiator; represented; compound
Prior art date: 1983-10-04
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

JP18559783A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0336421B2 (fr

Inventor

Kunihiro Ichimura

市村　国宏

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.)

National Institute of Advanced Industrial Science and Technology AIST

Original Assignee

Agency of Industrial Science and Technology

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.)

1983-10-04

Filing date

1983-10-04

Publication date

1985-05-01

1983-10-04 Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology

1983-10-04 Priority to JP18559783A priority Critical patent/JPS6076735A/ja

1985-05-01 Publication of JPS6076735A publication Critical patent/JPS6076735A/ja

1991-05-31 Publication of JPH0336421B2 publication Critical patent/JPH0336421B2/ja

Status Granted legal-status Critical Current

Links

239000011342 resin composition Substances 0.000 title claims abstract description 11
239000003999 initiator Substances 0.000 claims abstract description 14
150000001875 compounds Chemical class 0.000 claims abstract description 9
125000005520 diaryliodonium group Chemical group 0.000 claims abstract description 8
125000000217 alkyl group Chemical group 0.000 claims abstract description 3
IRFSXVIRXMYULF-UHFFFAOYSA-N 1,2-dihydroquinoline Chemical group C1=CC=C2C=CCNC2=C1 IRFSXVIRXMYULF-UHFFFAOYSA-N 0.000 claims abstract 2
AEKNYBWUEYNWMJ-QWOOXDRHSA-N Pramiconazole Chemical class O=C1N(C(C)C)CCN1C1=CC=C(N2CCN(CC2)C=2C=CC(OC[C@@H]3O[C@](CN4N=CN=C4)(CO3)C=3C(=CC(F)=CC=3)F)=CC=2)C=C1 AEKNYBWUEYNWMJ-QWOOXDRHSA-N 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 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 abstract description 11
239000000203 mixture Substances 0.000 abstract description 10
239000000463 material Substances 0.000 abstract description 9
230000035945 sensitivity Effects 0.000 abstract description 8
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract description 6
MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical compound [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 abstract description 3
238000000034 method Methods 0.000 abstract description 3
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 abstract description 2
OZLBDYMWFAHSOQ-UHFFFAOYSA-N diphenyliodanium Chemical compound C=1C=CC=CC=1[I+]C1=CC=CC=C1 OZLBDYMWFAHSOQ-UHFFFAOYSA-N 0.000 abstract description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical group C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 abstract 1
230000015572 biosynthetic process Effects 0.000 abstract 1
238000002156 mixing Methods 0.000 abstract 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
229920005989 resin Polymers 0.000 description 6
239000011347 resin Substances 0.000 description 6
-1 hexafluorophosphate salt Chemical class 0.000 description 5
229920000642 polymer Polymers 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-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
229910052724 xenon Inorganic materials 0.000 description 3
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 3
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
IWTYTFSSTWXZFU-UHFFFAOYSA-N 3-chloroprop-1-enylbenzene Chemical compound ClCC=CC1=CC=CC=C1 IWTYTFSSTWXZFU-UHFFFAOYSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
230000000977 initiatory effect Effects 0.000 description 2
238000004519 manufacturing process Methods 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
239000000178 monomer Substances 0.000 description 2
238000006303 photolysis reaction Methods 0.000 description 2
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 2
VPQAFOWBKWKVQQ-UHFFFAOYSA-N (4-methoxyphenyl)methyl-phenyliodanium Chemical compound C1=CC(OC)=CC=C1C[I+]C1=CC=CC=C1 VPQAFOWBKWKVQQ-UHFFFAOYSA-N 0.000 description 1
QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-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
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
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
229930195725 Mannitol Natural products 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-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
206010034972 Photosensitivity reaction Diseases 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
MWPUSWNISCYUNR-UHFFFAOYSA-N bis(3-nitrophenyl)iodanium Chemical compound [O-][N+](=O)C1=CC=CC([I+]C=2C=C(C=CC=2)[N+]([O-])=O)=C1 MWPUSWNISCYUNR-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000000470 constituent Substances 0.000 description 1
FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
125000005044 dihydroquinolinyl group Chemical class N1(CC=CC2=CC=CC=C12)* 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical group I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000000976 ink Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
150000002605 large molecules Chemical class 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
239000000594 mannitol Substances 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 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
OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-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
108091008695 photoreceptors Proteins 0.000 description 1
229920002120 photoresistant polymer Polymers 0.000 description 1
230000036211 photosensitivity Effects 0.000 description 1
230000015843 photosynthesis, light reaction Effects 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
125000003367 polycyclic group Chemical group 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
LLLCSBYSPJHDJX-UHFFFAOYSA-M potassium;2-methylprop-2-enoate Chemical compound [K+].CC(=C)C([O-])=O LLLCSBYSPJHDJX-UHFFFAOYSA-M 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
QLCKHRQGBNMBPB-UHFFFAOYSA-M sodium;3,4-dihydro-2h-pyran-2-carboxylate Chemical compound [Na+].[O-]C(=O)C1CCC=CO1 QLCKHRQGBNMBPB-UHFFFAOYSA-M 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
238000012719 thermal polymerization Methods 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
125000004953 trihalomethyl group Chemical group 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000005406 washing Methods 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
- G03F7/029—Inorganic compounds; Onium compounds; Organic compounds having hetero atoms other than oxygen, nitrogen or sulfur

Landscapes

Physics & Mathematics (AREA)
Chemical & Material Sciences (AREA)
Inorganic Chemistry (AREA)
Spectroscopy & Molecular Physics (AREA)
General Physics & Mathematics (AREA)
Polymerisation Methods In General (AREA)

JP18559783A 1983-10-04 1983-10-04 光硬化樹脂組成物 Granted JPS6076735A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP18559783A JPS6076735A (ja)	1983-10-04	1983-10-04	光硬化樹脂組成物

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP18559783A JPS6076735A (ja)	1983-10-04	1983-10-04	光硬化樹脂組成物

Publications (2)

Publication Number	Publication Date
JPS6076735A true JPS6076735A (ja)	1985-05-01
JPH0336421B2 JPH0336421B2 (fr)	1991-05-31

Family

ID=16173581

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP18559783A Granted JPS6076735A (ja)	1983-10-04	1983-10-04	光硬化樹脂組成物

Country Status (1)

Country	Link
JP (1)	JPS6076735A (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS63261352A (ja) *	1987-04-20	1988-10-28	Fuji Photo Film Co Ltd	感光性組成物
JPH01287105A (ja) *	1988-05-13	1989-11-17	Nippon Paint Co Ltd	光重合性組成物
WO1992013008A1 (fr) *	1991-01-22	1992-08-06	Nippon Paint Co., Ltd.	Composition photopolymerisable
JPH05107758A (ja) *	1991-10-14	1993-04-30	Fuji Photo Film Co Ltd	光重合性組成物
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 (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS50122936A (fr) *	1974-03-01	1975-09-26
JPS51100716A (fr) *	1975-01-27	1976-09-06	Ici Ltd
JPS5322597A (en) *	1976-07-09	1978-03-02	Gen Electric	Hardenable composite
JPS54151024A (en) *	1978-05-18	1979-11-27	Fuji Photo Film Co Ltd	Photopolymerizable composition
JPS5784451A (en) *	1980-09-23	1982-05-26	Gen Electric	Dry film resist and use thereof

1983
- 1983-10-04 JP JP18559783A patent/JPS6076735A/ja active Granted

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS50122936A (fr) *	1974-03-01	1975-09-26
JPS51100716A (fr) *	1975-01-27	1976-09-06	Ici Ltd
JPS5322597A (en) *	1976-07-09	1978-03-02	Gen Electric	Hardenable composite
JPS54151024A (en) *	1978-05-18	1979-11-27	Fuji Photo Film Co Ltd	Photopolymerizable composition
JPS5784451A (en) *	1980-09-23	1982-05-26	Gen Electric	Dry film resist and use thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS63261352A (ja) *	1987-04-20	1988-10-28	Fuji Photo Film Co Ltd	感光性組成物
JPH01287105A (ja) *	1988-05-13	1989-11-17	Nippon Paint Co Ltd	光重合性組成物
WO1992013008A1 (fr) *	1991-01-22	1992-08-06	Nippon Paint Co., Ltd.	Composition photopolymerisable
US5368990A (en) *	1991-01-22	1994-11-29	Nippon Paint Co., Ltd.	Photopolymerizable composition
JPH05107758A (ja) *	1991-10-14	1993-04-30	Fuji Photo Film Co Ltd	光重合性組成物
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
JPH0336421B2 (fr)	1991-05-31

Publication	Publication Date	Title
US4416975A (en)	1983-11-22	Photopolymerization process employing compounds containing acryloyl groups and maleimide groups
US4269933A (en)	1981-05-26	Methods of developing photopolymerizable compositions containing an 0-nitroaromatic compound as photoinhibitor
US4696888A (en)	1987-09-29	Light-sensitive compounds possessing trichloromethyl groups, a process for their production and light-sensitive mixtures containing these compounds
US4413052A (en)	1983-11-01	Photopolymerization process employing compounds containing acryloyl group and anthryl group
US3885964A (en)	1975-05-27	Photoimaging process using nitroso dimer
JPS63178105A (ja)	1988-07-22	光重合性組成物
JPH0273813A (ja)	1990-03-13	光重合可能な混合物および光重合可能な記録材料
JPS6088005A (ja)	1985-05-17	光硬化樹脂組成物
KR102061130B1 (ko)	2020-02-20	피라졸린계 증감제 및 그 제조방법과 응용
US4198242A (en)	1980-04-15	Photopolymerizable composition containing an o-nitroaromatic compound as photoinhibitor
US3901705A (en)	1975-08-26	Method of using variable depth photopolymerization imaging systems
US4029505A (en)	1977-06-14	Method of producing positive polymer images
JPS6076735A (ja)	1985-05-01	光硬化樹脂組成物
CA1103084A (fr)	1981-06-16	Traduction non-disponible
JPS60247639A (ja)	1985-12-07	光不溶性感光材料
JPS6076740A (ja)	1985-05-01	可視光感光性樹脂組成物
JPH02292278A (ja)	1990-12-03	感光性ビス‐トリクロロメチル‐ｓ‐トリアジン類、それらの製造方法およびそれらの化合物を含有する感光性組成物
JPS60257444A (ja)	1985-12-19	光架橋性感光材料
JPH0362163B2 (fr)	1991-09-25
JPS6078442A (ja)	1985-05-04	光硬化性樹脂組成物
JPS60258204A (ja)	1985-12-20	光硬化樹脂組成物
JPH02157760A (ja)	1990-06-18	光重合性組成物
JPS6096604A (ja)	1985-05-30	光不溶性樹脂組成物
JPS60112802A (ja)	1985-06-19	光増感高分子とその製法
JPS6032176B2 (ja)	1985-07-26	光重合性組成物