JPS6088005A - 光硬化樹脂組成物 - Google Patents

光硬化樹脂組成物

Info

Publication number: JPS6088005A
Authority: JP; Japan
Prior art keywords: resin composition; photopolymerization initiator; photocurable resin; formula; photosensitive
Prior art date: 1983-10-21
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

JP19808583A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0362162B2 (fr

Inventor

Kunihiro Ichimura

市村　国宏

Keiichi Fujii

圭一藤井

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.)

1983-10-21

Filing date

1983-10-21

Publication date

1985-05-17

1983-10-21 Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology

1983-10-21 Priority to JP19808583A priority Critical patent/JPS6088005A/ja

1985-05-17 Publication of JPS6088005A publication Critical patent/JPS6088005A/ja

1991-09-25 Publication of JPH0362162B2 publication Critical patent/JPH0362162B2/ja

Status Granted legal-status Critical Current

Links

239000011342 resin composition Substances 0.000 title claims description 15
150000001875 compounds Chemical class 0.000 claims abstract description 12
239000003999 initiator Substances 0.000 claims abstract description 12
CDSULTPOCMWJCM-UHFFFAOYSA-N 4h-chromene-2,3-dione Chemical class C1=CC=C2OC(=O)C(=O)CC2=C1 CDSULTPOCMWJCM-UHFFFAOYSA-N 0.000 claims abstract description 8
125000005520 diaryliodonium group Chemical group 0.000 claims description 5
238000006116 polymerization reaction Methods 0.000 claims description 2
239000000203 mixture Substances 0.000 abstract description 5
125000000217 alkyl group Chemical group 0.000 abstract description 4
125000003545 alkoxy group Chemical group 0.000 abstract description 3
150000003839 salts Chemical class 0.000 abstract description 3
125000003118 aryl group Chemical group 0.000 abstract description 2
125000004663 dialkyl amino group Chemical group 0.000 abstract description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 2
229910017048 AsF6 Inorganic materials 0.000 abstract 1
239000000463 material Substances 0.000 description 10
230000035945 sensitivity Effects 0.000 description 10
-1 coumarin compound Chemical class 0.000 description 8
229920000642 polymer Polymers 0.000 description 5
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
229920005989 resin Polymers 0.000 description 4
239000011347 resin Substances 0.000 description 4
IWTYTFSSTWXZFU-UHFFFAOYSA-N 3-chloroprop-1-enylbenzene Chemical compound ClCC=CC1=CC=CC=C1 IWTYTFSSTWXZFU-UHFFFAOYSA-N 0.000 description 3
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
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 3
235000001671 coumarin Nutrition 0.000 description 3
229960000956 coumarin Drugs 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
OZLBDYMWFAHSOQ-UHFFFAOYSA-N diphenyliodanium Chemical compound C=1C=CC=CC=1[I+]C1=CC=CC=C1 OZLBDYMWFAHSOQ-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
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-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
238000000354 decomposition reaction Methods 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002366 halogen compounds Chemical class 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
230000000977 initiatory effect Effects 0.000 description 2
MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical compound [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 description 2
150000002576 ketones Chemical class 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
229920002554 vinyl polymer Polymers 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
WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-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
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
VAPQAGMSICPBKJ-UHFFFAOYSA-N 2-nitroacridine Chemical compound C1=CC=CC2=CC3=CC([N+](=O)[O-])=CC=C3N=C21 VAPQAGMSICPBKJ-UHFFFAOYSA-N 0.000 description 1
JQYDECSZBZCKFQ-UHFFFAOYSA-N 3-acetyl-7-(diethylamino)chromen-2-one Chemical compound C1=C(C(C)=O)C(=O)OC2=CC(N(CC)CC)=CC=C21 JQYDECSZBZCKFQ-UHFFFAOYSA-N 0.000 description 1
CPVJWBWVJUAOMV-UHFFFAOYSA-N 3-benzoyl-7-(diethylamino)chromen-2-one Chemical compound O=C1OC2=CC(N(CC)CC)=CC=C2C=C1C(=O)C1=CC=CC=C1 CPVJWBWVJUAOMV-UHFFFAOYSA-N 0.000 description 1
SANIRTQDABNCHF-UHFFFAOYSA-N 7-(diethylamino)-3-[7-(diethylamino)-2-oxochromene-3-carbonyl]chromen-2-one Chemical compound C1=C(N(CC)CC)C=C2OC(=O)C(C(=O)C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=CC2=C1 SANIRTQDABNCHF-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
WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 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
CVMOPKROILOZFI-UHFFFAOYSA-N O=S(=O)=Cl Chemical group O=S(=O)=Cl CVMOPKROILOZFI-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
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 1
239000002253 acid Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001555 benzenes Chemical class 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
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
150000001649 bromium compounds Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
229930016911 cinnamic acid Natural products 0.000 description 1
235000013985 cinnamic acid Nutrition 0.000 description 1
239000003086 colorant Substances 0.000 description 1
150000004775 coumarins Chemical group 0.000 description 1
125000000332 coumarinyl group Chemical group O1C(=O)C(=CC2=CC=CC=C12)* 0.000 description 1
125000006371 dihalo methyl group Chemical group 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
239000011521 glass Substances 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 class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000000976 ink Substances 0.000 description 1
230000001678 irradiating effect Effects 0.000 description 1
150000002605 large molecules Chemical class 0.000 description 1
229920002521 macromolecule Polymers 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
238000000034 method Methods 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-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
125000006372 monohalo methyl group Chemical group 0.000 description 1
239000000178 monomer Substances 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
YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-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
238000006303 photolysis reaction Methods 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
230000000704 physical effect Effects 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 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
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000003756 stirring Methods 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
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
239000002966 varnish Substances 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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

Landscapes

Polymerisation Methods In General (AREA)

JP19808583A 1983-10-21 1983-10-21 光硬化樹脂組成物 Granted JPS6088005A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP19808583A JPS6088005A (ja)	1983-10-21	1983-10-21	光硬化樹脂組成物

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP19808583A JPS6088005A (ja)	1983-10-21	1983-10-21	光硬化樹脂組成物

Publications (2)

Publication Number	Publication Date
JPS6088005A true JPS6088005A (ja)	1985-05-17
JPH0362162B2 JPH0362162B2 (fr)	1991-09-25

Family

ID=16385254

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP19808583A Granted JPS6088005A (ja)	1983-10-21	1983-10-21	光硬化樹脂組成物

Country Status (1)

Country	Link
JP (1)	JPS6088005A (fr)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS63180946A (ja) *	1987-01-22	1988-07-26	Nippon Paint Co Ltd	高感度光重合性組成物
JPH02144539A (ja) *	1988-11-28	1990-06-04	Sumitomo Bakelite Co Ltd	感光性樹脂組成物
JPH02238002A (ja) *	1989-03-10	1990-09-20	Nippon Paint Co Ltd	感光性組成物
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
US6171759B1 (en)	1992-05-14	2001-01-09	Brother Kogyo Kabushiki Kaisha	Photocurable composition
WO2007123183A1 (fr)	2006-04-19	2007-11-01	Mitsubishi Chemical Corporation	Dispositif d'affichage d'images couleur
EP2078978A2 (fr)	2004-04-26	2009-07-15	Mitsubishi Chemical Corporation	LCD rétroéclairage comprenant un LED avec émission de lumière adaptée et des filtres de couleur convenables
WO2009099211A1 (fr)	2008-02-07	2009-08-13	Mitsubishi Chemical Corporation	Dispositif émettant de la lumière à semi-conducteur, dispositif de rétroéclairage, dispositif d'affichage d'image en couleur et luminophore utilisé pour ces dispositifs
US7727679B2 (en)	2005-01-07	2010-06-01	Nitto Denko Corporation	Optical refractive index-modifying polymer composition, hologram recording material and method of controlling refractive index
WO2013016973A1 (fr) *	2011-07-29	2013-02-07	华中科技大学	Système photoamorceur sensible au visible pour la préparation d'un matériau polymère optique holographique à haute efficacité de diffraction
EP3147335A1 (fr)	2015-09-23	2017-03-29	BYK-Chemie GmbH	Compositions colorantes contenant des agents mouillants et/ou dispersants à faible indice d'amine
KR101869388B1 (ko)	2017-05-15	2018-06-21	한국화학연구원	광이성화 디페닐아세틸렌-아조벤젠 중합성 메조겐 화합물 및 이를 포함하는 고분자
KR20180117828A (ko)	2017-04-20	2018-10-30	한국화학연구원	아조벤젠 화합물 및 이를 포함하는 홀로그램 기록용 조성물
WO2019096891A1 (fr)	2017-11-15	2019-05-23	Byk-Chemie Gmbh	Copolymère bloc
WO2019096893A1 (fr)	2017-11-15	2019-05-23	Byk-Chemie Gmbh	Copolymère séquencé

Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS52112681A (en) *	1976-02-02	1977-09-21	Eastman Kodak Co	Sensitive composition
JPS5815503A (ja) *	1981-07-20	1983-01-28	Fuji Photo Film Co Ltd	光重合性組成物

1983
- 1983-10-21 JP JP19808583A patent/JPS6088005A/ja active Granted

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS52112681A (en) *	1976-02-02	1977-09-21	Eastman Kodak Co	Sensitive composition
JPS5815503A (ja) *	1981-07-20	1983-01-28	Fuji Photo Film Co Ltd	光重合性組成物

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS63180946A (ja) *	1987-01-22	1988-07-26	Nippon Paint Co Ltd	高感度光重合性組成物
JPH02144539A (ja) *	1988-11-28	1990-06-04	Sumitomo Bakelite Co Ltd	感光性樹脂組成物
JPH02238002A (ja) *	1989-03-10	1990-09-20	Nippon Paint Co Ltd	感光性組成物
US6171759B1 (en)	1992-05-14	2001-01-09	Brother Kogyo Kabushiki Kaisha	Photocurable composition
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
EP2078978A2 (fr)	2004-04-26	2009-07-15	Mitsubishi Chemical Corporation	LCD rétroéclairage comprenant un LED avec émission de lumière adaptée et des filtres de couleur convenables
US7727679B2 (en)	2005-01-07	2010-06-01	Nitto Denko Corporation	Optical refractive index-modifying polymer composition, hologram recording material and method of controlling refractive index
WO2007123183A1 (fr)	2006-04-19	2007-11-01	Mitsubishi Chemical Corporation	Dispositif d'affichage d'images couleur
WO2009099211A1 (fr)	2008-02-07	2009-08-13	Mitsubishi Chemical Corporation	Dispositif émettant de la lumière à semi-conducteur, dispositif de rétroéclairage, dispositif d'affichage d'image en couleur et luminophore utilisé pour ces dispositifs
EP3045965A1 (fr)	2008-02-07	2016-07-20	Mitsubishi Chemical Corporation	Luminophore au fluorure émettant du rouge et active par mn4+
WO2013016973A1 (fr) *	2011-07-29	2013-02-07	华中科技大学	Système photoamorceur sensible au visible pour la préparation d'un matériau polymère optique holographique à haute efficacité de diffraction
US9753431B2 (en)	2011-07-29	2017-09-05	Huazhong University Of Science And Technology	Visible light photoinitiating system for preparing high diffraction efficiency hologram optical polymer material
EP3147335A1 (fr)	2015-09-23	2017-03-29	BYK-Chemie GmbH	Compositions colorantes contenant des agents mouillants et/ou dispersants à faible indice d'amine
KR20180117828A (ko)	2017-04-20	2018-10-30	한국화학연구원	아조벤젠 화합물 및 이를 포함하는 홀로그램 기록용 조성물
KR101869388B1 (ko)	2017-05-15	2018-06-21	한국화학연구원	광이성화 디페닐아세틸렌-아조벤젠 중합성 메조겐 화합물 및 이를 포함하는 고분자
WO2019096891A1 (fr)	2017-11-15	2019-05-23	Byk-Chemie Gmbh	Copolymère bloc
WO2019096893A1 (fr)	2017-11-15	2019-05-23	Byk-Chemie Gmbh	Copolymère séquencé

Also Published As

Publication number	Publication date
JPH0362162B2 (fr)	1991-09-25

Publication	Publication Date	Title
US4416975A (en)	1983-11-22	Photopolymerization process employing compounds containing acryloyl groups and maleimide groups
US4413052A (en)	1983-11-01	Photopolymerization process employing compounds containing acryloyl group and anthryl group
US4269933A (en)	1981-05-26	Methods of developing photopolymerizable compositions containing an 0-nitroaromatic compound as photoinhibitor
US3885964A (en)	1975-05-27	Photoimaging process using nitroso dimer
JPS6088005A (ja)	1985-05-17	光硬化樹脂組成物
HK78590A (en)	1990-10-05	Light-sensitive compounds containing trichloromethyl groups, process for their preparation and light-sensitive mixture containing these compounds
CN105182688B (zh)	2019-11-12	感光性树脂组合物、感光性元件、抗蚀剂图形的制造方法以及印刷电路板的制造方法
JPH01152109A (ja)	1989-06-14	光重合性組成物
JP5344034B2 (ja)	2013-11-20	感光性樹脂組成物、並びにこれを用いた感光性エレメント、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
JP2839974B2 (ja)	1998-12-24	厚膜感光性印刷版用光重合性組成物及びそれを用いた厚膜感光性印刷版の製造方法
US4978604A (en)	1990-12-18	Process for forming images
JP2024051000A (ja)	2024-04-10	感光性樹脂積層体およびその製造方法
US4198242A (en)	1980-04-15	Photopolymerizable composition containing an o-nitroaromatic compound as photoinhibitor
JPH05255420A (ja)	1993-10-05	光重合性組成物の改良された増感
CA1103084A (fr)	1981-06-16	Traduction non-disponible
JPH0336421B2 (fr)	1991-05-31
JP2003262956A (ja)	2003-09-19	感光性樹脂組成物、これを用いた感光性エレメント、レジストパターンの製造法及びプリント配線板の製造法
JPS60257444A (ja)	1985-12-19	光架橋性感光材料
JPS6092302A (ja)	1985-05-23	光不溶性樹脂組成物
JP3111708B2 (ja)	2000-11-27	光重合性組成物及び光重合性エレメント
JP2001174992A (ja)	2001-06-29	感光性樹脂組成物、これを用いた感光性エレメント、レジストパターンの製造法及びプリント配線板の製造法
WO2022186389A1 (fr)	2022-09-09	Corps multicouche de résine photosensible et son procédé de production
JPH0362164B2 (fr)	1991-09-25
JP4201555B2 (ja)	2008-12-24	感光性樹脂組成物
JPH0344287B2 (fr)	1991-07-05