KR19990072925A - 착색된광경화성조성물 - Google Patents

착색된광경화성조성물 Download PDF

Info

Publication number: KR19990072925A
Authority: KR; South Korea
Prior art keywords: alkyl; compound; phenyl; formula; alkoxy
Prior art date: 1998-02-27

Application number

KR1019990006255A

Other languages

English (en)

Korean (ko)

Inventor

쾰러만프레드

콘티히파트릭

레파르트다비드게오르게

Original Assignee

에프. 아. 프라저, 에른스트 알테르 (에. 알테르), 한스 페터 비틀린 (하. 페. 비틀린), 피. 랍 보프, 브이. 스펜글러, 페. 아에글러

시바 스페셜티 케미칼스 홀딩 인크.

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.)

1998-02-27

Filing date

1999-02-25

Publication date

1999-09-27

1999-02-25 Application filed by 에프. 아. 프라저, 에른스트 알테르 (에. 알테르), 한스 페터 비틀린 (하. 페. 비틀린), 피. 랍 보프, 브이. 스펜글러, 페. 아에글러, 시바 스페셜티 케미칼스 홀딩 인크. filed Critical 에프. 아. 프라저, 에른스트 알테르 (에. 알테르), 한스 페터 비틀린 (하. 페. 비틀린), 피. 랍 보프, 브이. 스펜글러, 페. 아에글러

1999-09-27 Publication of KR19990072925A publication Critical patent/KR19990072925A/ko

Links

239000000203 mixture Substances 0.000 title claims abstract description 126
-1 benzoin derivative compounds Chemical class 0.000 claims abstract description 83
150000001875 compounds Chemical class 0.000 claims abstract description 73
239000000049 pigment Substances 0.000 claims abstract description 19
238000000576 coating method Methods 0.000 claims description 50
125000000217 alkyl group Chemical group 0.000 claims description 44
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 36
239000011248 coating agent Substances 0.000 claims description 28
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 24
125000003545 alkoxy group Chemical group 0.000 claims description 20
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 20
238000000034 method Methods 0.000 claims description 18
239000000758 substrate Substances 0.000 claims description 18
239000001257 hydrogen Substances 0.000 claims description 17
229910052739 hydrogen Inorganic materials 0.000 claims description 17
229920000642 polymer Polymers 0.000 claims description 16
125000004414 alkyl thio group Chemical group 0.000 claims description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
229910052736 halogen Inorganic materials 0.000 claims description 11
150000002367 halogens Chemical class 0.000 claims description 11
150000002431 hydrogen Chemical class 0.000 claims description 11
235000010290 biphenyl Nutrition 0.000 claims description 10
239000004305 biphenyl Substances 0.000 claims description 10
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 10
125000001624 naphthyl group Chemical group 0.000 claims description 10
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 10
238000007650 screen-printing Methods 0.000 claims description 9
125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 8
GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 claims description 8
239000004408 titanium dioxide Substances 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
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125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
125000000753 cycloalkyl group Chemical group 0.000 claims description 6
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CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 claims description 4
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125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 3
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230000001678 irradiating effect Effects 0.000 claims description 3
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235000021286 stilbenes Nutrition 0.000 claims description 3
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 2
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150000001721 carbon Chemical group 0.000 claims description 2
235000001671 coumarin Nutrition 0.000 claims description 2
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239000012463 white pigment Substances 0.000 claims description 2
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ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 1
229960000956 coumarin Drugs 0.000 claims 1
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
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QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 7
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QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 6
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical group CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
230000000996 additive effect Effects 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 6
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125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000007645 offset printing Methods 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000013307 optical fiber Substances 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
SOWBFZRMHSNYGE-UHFFFAOYSA-N oxamic acid Chemical compound NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 description 1
150000002916 oxazoles Chemical class 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
239000003973 paint Substances 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
FZUGPQWGEGAKET-UHFFFAOYSA-N parbenate Chemical compound CCOC(=O)C1=CC=C(N(C)C)C=C1 FZUGPQWGEGAKET-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
150000004978 peroxycarbonates Chemical class 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229960000969 phenyl salicylate Drugs 0.000 description 1
150000003003 phosphines Chemical class 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
238000000016 photochemical curing Methods 0.000 description 1
230000036211 photosensitivity Effects 0.000 description 1
239000006223 plastic coating Substances 0.000 description 1
239000011120 plywood Substances 0.000 description 1
229920001603 poly (alkyl acrylates) Polymers 0.000 description 1
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001228 polyisocyanate Polymers 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920000909 polytetrahydrofuran Polymers 0.000 description 1
229920000166 polytrimethylene carbonate Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920001289 polyvinyl ether Polymers 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
150000004032 porphyrins Chemical class 0.000 description 1
238000004382 potting Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000013772 propylene glycol Nutrition 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
INCIMLINXXICKS-UHFFFAOYSA-M pyronin Y Chemical compound [Cl-].C1=CC(=[N+](C)C)C=C2OC3=CC(N(C)C)=CC=C3C=C21 INCIMLINXXICKS-UHFFFAOYSA-M 0.000 description 1
FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
238000003847 radiation curing Methods 0.000 description 1
230000002285 radioactive effect Effects 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000007763 reverse roll coating Methods 0.000 description 1
PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
238000006798 ring closing metathesis reaction Methods 0.000 description 1
239000005060 rubber Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000003678 scratch resistant effect Effects 0.000 description 1
DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
238000004904 shortening Methods 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
238000004528 spin coating Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000002344 surface layer Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000010345 tape casting Methods 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
150000003577 thiophenes Chemical class 0.000 description 1
YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical class C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
AYNNSCRYTDRFCP-UHFFFAOYSA-N triazene Chemical compound NN=N AYNNSCRYTDRFCP-UHFFFAOYSA-N 0.000 description 1
KKFOMYPMTJLQGA-UHFFFAOYSA-N tribenzyl phosphite Chemical compound C=1C=CC=CC=1COP(OCC=1C=CC=CC=1)OCC1=CC=CC=C1 KKFOMYPMTJLQGA-UHFFFAOYSA-N 0.000 description 1
TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
125000004953 trihalomethyl group Chemical group 0.000 description 1
CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
239000011345 viscous material Substances 0.000 description 1
238000004804 winding Methods 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1
238000004383 yellowing Methods 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
239000011787 zinc oxide 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
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
- G03F7/105—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having substances, e.g. indicators, for forming visible images
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
- 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

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Physics & Mathematics (AREA)
Life Sciences & Earth Sciences (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
General Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Inorganic Chemistry (AREA)
Architecture (AREA)
Structural Engineering (AREA)
Paints Or Removers (AREA)
Polymerisation Methods In General (AREA)
Medicinal Preparation (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Macromonomer-Based Addition Polymer (AREA)

KR1019990006255A 1998-02-27 1999-02-25 착색된광경화성조성물 KR19990072925A (ko)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH19980483/98		1998-02-27
CH48398		1998-02-27

Publications (1)

Publication Number	Publication Date
KR19990072925A true KR19990072925A (ko)	1999-09-27

Family

ID=4188042

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
KR1019990006255A KR19990072925A (ko)	1998-02-27	1999-02-25	착색된광경화성조성물

Country Status (5)

Country	Link
JP (1)	JPH11292910A (it)
KR (1)	KR19990072925A (it)
DE (1)	DE19907957A1 (it)
ES (1)	ES2153315B1 (it)
IT (1)	IT1309578B1 (it)

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KR100778199B1 (ko) *	2000-07-07	2007-11-27	린텍 가부시키가이샤	자외선-경화형 점착제 조성물 및 자외선-경화성 점착시트

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WO2001018130A1 (en) *	1999-09-02	2001-03-15	Gmbh Clariant	Method for brightening workpieces by powder coating
ATE253082T1 (de)	1999-12-08	2003-11-15	Ciba Sc Holding Ag	Neues photoinitiatorsystem aus phosphinoxidverbindungen und wenig gefärbte härtbare zusammensetzungen
GB2365430B (en)	2000-06-08	2002-08-28	Ciba Sc Holding Ag	Acylphosphine photoinitiators and intermediates
JP4993053B2 (ja) *	2001-02-27	2012-08-08	株式会社トクヤマ	歯科用硬化性組成物
ATE409708T1 (de)	2000-12-13	2008-10-15	Ciba Holding Inc	Oberflächenaktive photoinitiatoren
JP4812963B2 (ja) *	2001-05-18	2011-11-09	リンテック株式会社	半導体ウエハ加工用粘着シートおよび半導体ウエハの加工方法
DE10154420A1 (de) *	2001-11-06	2003-05-28	Carl V Ossietzky Uni Oldenburg	Lichthärtendes Kunststoffmaterial mit Indikator zur Anzeige des Aushärtungsgrades
CN1310707C (zh)	2002-01-29	2007-04-18	西巴特殊化学品控股有限公司	制备强附着涂层的方法
EP1349006B1 (en) *	2002-03-28	2013-09-25	Agfa Graphics N.V.	Photopolymerizable composition sensitized for the wavelength range from 300 to 450 nm.
JP2003313208A (ja) *	2002-04-19	2003-11-06	Meiko:Kk	光硬化性樹脂組成物
DE10307451A1 (de) *	2003-02-21	2004-09-16	Kodak Polychrome Graphics Gmbh	Strahlungsempfindliche Zusammensetzungen und darauf basierende bebilderbare Elemente
US7527916B2 (en) *	2003-09-22	2009-05-05	Agfa Graphics, N.V.	Photopolymerizable composition
JP4813900B2 (ja) *	2005-03-31	2011-11-09	株式会社イーテック	紫外線硬化型の紫外線遮蔽性を有する粘着剤・接着剤組成物
JP5255369B2 (ja) *	2007-09-25	2013-08-07	富士フイルム株式会社	光硬化性コーティング組成物、オーバープリント及びその製造方法
RU2528264C2 (ru) *	2009-02-09	2014-09-10	Хантсман Эдванст Матириалз (Свитзеленд) Гмбх	Порошковая покрывающая композиция
DE102012212429A1 (de)	2012-07-16	2014-01-16	Voco Gmbh	Dentalhandgerät, Verfahren und Verwendung desselben zum Aushärten lichthärtbaren Materials
WO2015104972A1 (ja) *	2014-01-08	2015-07-16	Dic株式会社	床材用活性エネルギー線硬化性組成物
CN107709371A (zh) *	2015-12-28	2018-02-16	积水化学工业株式会社	光固化性组合物以及电子部件的制造方法
JP6950257B2 (ja) *	2017-04-18	2021-10-13	コニカミノルタ株式会社	活性光線硬化型インクジェットインク
EP3681434A4 (en) *	2017-09-11	2021-04-07	3M Innovative Properties Company	RADIATION CURABLE COMPOSITIONS AND COMPOSITE ARTICLES MADE BY AN ADDITIVE MANUFACTURING PROCESS
CN107987209B (zh) *	2018-01-08	2023-05-02	无锡佶达德光电子技术有限公司	一种香豆素类聚合物半导体激光材料及其应用
ES2913237T3 (es) *	2018-12-21	2022-06-01	Ivoclar Vivadent Ag	Composiciones para la fabricación de piezas de trabajo dentales resistentes a la fractura mediante estereolitografía
EP3669856A1 (de)	2018-12-21	2020-06-24	Ivoclar Vivadent AG	Zusammensetzungen für die herstellung von transparenten dentalwerkstücken mittels stereolithographie
CN110105166A (zh) *	2019-04-30	2019-08-09	同济大学	含有二苯乙烯的α-羟基酮类化合物及其制备方法和应用
EP4085893A1 (de) *	2021-05-07	2022-11-09	Ivoclar Vivadent AG	Transparente, bruchzähe polymerisationsharze zur herstellung dentaler formkörper

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US5660968A (en) *	1995-05-05	1997-08-26	Bayer Corporation	Negative working, peel developeable, single sheet color proofing system with improved background color
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GB9605712D0 (en) *	1996-03-19	1996-05-22	Minnesota Mining & Mfg	Novel uv-curable compositions

1999
- 1999-02-24 DE DE19907957A patent/DE19907957A1/de not_active Withdrawn
- 1999-02-24 IT IT1999MI000376A patent/IT1309578B1/it active
- 1999-02-25 ES ES009900386A patent/ES2153315B1/es not_active Expired - Lifetime
- 1999-02-25 KR KR1019990006255A patent/KR19990072925A/ko not_active Application Discontinuation
- 1999-03-01 JP JP11052133A patent/JPH11292910A/ja active Pending

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR100778199B1 (ko) *	2000-07-07	2007-11-27	린텍 가부시키가이샤	자외선-경화형 점착제 조성물 및 자외선-경화성 점착시트

Also Published As

Publication number	Publication date
ES2153315B1 (es)	2001-09-01
ITMI990376A1 (it)	2000-08-24
IT1309578B1 (it)	2002-01-24
JPH11292910A (ja)	1999-10-26
ES2153315A1 (es)	2001-02-16
DE19907957A1 (de)	1999-09-02

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Date	Code	Title	Description
2004-02-26	WITN	Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid

Publication	Publication Date	Title
KR19990072925A (ko)	1999-09-27	착색된광경화성조성물
KR100548976B1 (ko)	2006-02-03	비휘발성 페닐글리옥살산 에스테르
JP4869463B2 (ja)	2012-02-08	光開始剤の組み合わせ
NL1005424C2 (nl)	1999-03-22	Alkylfenylbisacylfosfineoxiden en fotoinitiatormengsels.
KR100363978B1 (ko)	2003-02-17	알콕시페닐-치환비스아실포스핀옥시드
KR100903939B1 (ko)	2009-06-25	광개시제로서의 장파장 모노- 및 비스-아실포스핀 옥사이드 및 설파이드
US5942290A (en)	1999-08-24	Molecular complex compounds of acylphosphine oxide and α-hydroxy ketones as photoinitiators
US6057380A (en)	2000-05-02	Photogeneration of amines from α-aminoacetophenones
KR100829076B1 (ko)	2008-05-14	유기 금속성 모노아실알킬포스핀
KR100722179B1 (ko)	2007-05-29	광개시제 조성물
US20060160915A1 (en)	2006-07-20	Photocurable compositions
KR100358815B1 (ko)	2003-01-24	이합체성비스아실포스핀,옥사이드및술파이드화합물및이들화합물을포함하는조성물
KR20010062219A (ko)	2001-07-07	신규한 포스핀 옥사이드 광개시제 시스템 및 색상이 낮은경화성 조성물
US20020042022A1 (en)	2002-04-11	Alkylphenylbisacylphosphine oxides and photoinitiator mixtures
JP2000510884A (ja)	2000-08-22	重合性組成物
US5721292A (en)	1998-02-24	Acylphosphine oxides
KR20050044549A (ko)	2005-05-12	아실포스핀 및 이의 유도체의 멀티머 형태
KR100685153B1 (ko)	2007-02-22	광개시제 혼합물, 이를 포함하는 광중합성 조성물 및 이의 용도
MXPA97006542A (en)	1998-11-09	Compounds of molecular complex as photoinicided

KR19990072925A - 착색된광경화성조성물 - Google Patents

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