TW460450B - Specific non-volatile dimeric phenylglyoxalic ester compounds and photopolymerizable compositions comprising said compounds - Google Patents
Specific non-volatile dimeric phenylglyoxalic ester compounds and photopolymerizable compositions comprising said compounds Download PDFInfo
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- TW460450B TW460450B TW087100902A TW87100902A TW460450B TW 460450 B TW460450 B TW 460450B TW 087100902 A TW087100902 A TW 087100902A TW 87100902 A TW87100902 A TW 87100902A TW 460450 B TW460450 B TW 460450B
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- 239000000203 mixture Substances 0.000 title claims abstract description 104
- 150000001875 compounds Chemical class 0.000 title claims abstract description 90
- -1 ester compounds Chemical class 0.000 title claims description 121
- 239000001257 hydrogen Substances 0.000 claims abstract description 30
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 30
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 69
- 238000000576 coating method Methods 0.000 claims description 58
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 49
- 239000011248 coating agent Substances 0.000 claims description 38
- 125000003545 alkoxy group Chemical group 0.000 claims description 31
- 238000011049 filling Methods 0.000 claims description 30
- 230000002079 cooperative effect Effects 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 24
- 125000002947 alkylene group Chemical group 0.000 claims description 23
- 238000004519 manufacturing process Methods 0.000 claims description 22
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- 239000003999 initiator Substances 0.000 claims description 19
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- 239000000843 powder Substances 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
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- 150000002431 hydrogen Chemical class 0.000 claims description 13
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- 238000012360 testing method Methods 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
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- YLHXLHGIAMFFBU-UHFFFAOYSA-N methyl phenylglyoxalate Chemical compound COC(=O)C(=O)C1=CC=CC=C1 YLHXLHGIAMFFBU-UHFFFAOYSA-N 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
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- HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 claims 1
- 241000276498 Pollachius virens Species 0.000 claims 1
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 claims 1
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 23
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
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- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 6
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- FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical class OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 description 6
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- 239000002356 single layer Substances 0.000 description 1
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- 238000004528 spin coating Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010025 steaming Methods 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
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- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
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- 239000003826 tablet Substances 0.000 description 1
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- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
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- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical group Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-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
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
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- 235000021419 vinegar Nutrition 0.000 description 1
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- 238000004383 yellowing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- AKJVMGQSGCSQBU-UHFFFAOYSA-N zinc azanidylidenezinc Chemical compound [Zn++].[N-]=[Zn].[N-]=[Zn] AKJVMGQSGCSQBU-UHFFFAOYSA-N 0.000 description 1
- DTOSIQBPPRVQHS-UHFFFAOYSA-N α-Linolenic acid Chemical compound CCC=CCC=CCC=CCCCCCCCC(O)=O DTOSIQBPPRVQHS-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/738—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerisation Methods In General (AREA)
- Paints Or Removers (AREA)
- Holo Graphy (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Cosmetics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH19597 | 1997-01-30 |
Publications (1)
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|---|---|
| TW460450B true TW460450B (en) | 2001-10-21 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW087100902A TW460450B (en) | 1997-01-30 | 1998-01-23 | Specific non-volatile dimeric phenylglyoxalic ester compounds and photopolymerizable compositions comprising said compounds |
Country Status (14)
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|---|---|
| US (1) | US6048660A (enExample) |
| EP (1) | EP0956280B1 (enExample) |
| JP (1) | JP4171073B2 (enExample) |
| KR (1) | KR100548976B1 (enExample) |
| CN (1) | CN1157359C (enExample) |
| AU (1) | AU718619B2 (enExample) |
| BR (1) | BR9806940B1 (enExample) |
| CA (1) | CA2275667A1 (enExample) |
| DE (1) | DE69809029T2 (enExample) |
| DK (1) | DK0956280T3 (enExample) |
| ES (1) | ES2184233T3 (enExample) |
| TW (1) | TW460450B (enExample) |
| WO (1) | WO1998033761A1 (enExample) |
| ZA (1) | ZA98724B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI618721B (zh) * | 2012-10-19 | 2018-03-21 | 巴地斯顏料化工廠 | 混合光起始劑 |
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| US3532737A (en) * | 1967-02-02 | 1970-10-06 | Sterling Drug Inc | Esters of arylglyoxylic acids |
| US3754006A (en) * | 1967-02-02 | 1973-08-21 | Sterling Drug Inc | Esters and amides of substituted glyoxylic acids |
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| US3657325A (en) * | 1969-12-03 | 1972-04-18 | Sterling Drug Inc | Esters of substituted glyoxylic acids |
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| US4038164A (en) * | 1975-09-18 | 1977-07-26 | Stauffer Chemical Company | Photopolymerizable aryl and heterocyclic glyoxylate compositions and process |
| US3991416A (en) * | 1975-09-18 | 1976-11-09 | Hughes Aircraft Company | AC biased and resonated liquid crystal display |
| DE2825955A1 (de) * | 1978-06-14 | 1980-01-03 | Bayer Ag | Arylglyoxyloyloxyalkylacrylate und ihre verwendung in photopolymerisierbaren bindemitteln |
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| AU569084B2 (en) * | 1983-06-27 | 1988-01-21 | Stauffer Chemical Company | Photopolymerizable composition |
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| US5795581A (en) * | 1995-03-31 | 1998-08-18 | Sandia Corporation | Controlled release of molecular components of dendrimer/bioactive complexes |
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1998
- 1998-01-23 BR BRPI9806940-3A patent/BR9806940B1/pt not_active IP Right Cessation
- 1998-01-23 AU AU60963/98A patent/AU718619B2/en not_active Ceased
- 1998-01-23 TW TW087100902A patent/TW460450B/zh active
- 1998-01-23 JP JP53250998A patent/JP4171073B2/ja not_active Expired - Lifetime
- 1998-01-23 EP EP98905335A patent/EP0956280B1/en not_active Expired - Lifetime
- 1998-01-23 ES ES98905335T patent/ES2184233T3/es not_active Expired - Lifetime
- 1998-01-23 DK DK98905335T patent/DK0956280T3/da active
- 1998-01-23 CN CNB98801985XA patent/CN1157359C/zh not_active Expired - Lifetime
- 1998-01-23 WO PCT/EP1998/000351 patent/WO1998033761A1/en not_active Ceased
- 1998-01-23 KR KR1019997006856A patent/KR100548976B1/ko not_active Expired - Fee Related
- 1998-01-23 CA CA002275667A patent/CA2275667A1/en not_active Abandoned
- 1998-01-23 DE DE69809029T patent/DE69809029T2/de not_active Expired - Lifetime
- 1998-01-28 US US09/014,555 patent/US6048660A/en not_active Expired - Lifetime
- 1998-01-29 ZA ZA98724A patent/ZA98724B/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI618721B (zh) * | 2012-10-19 | 2018-03-21 | 巴地斯顏料化工廠 | 混合光起始劑 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2001511137A (ja) | 2001-08-07 |
| KR100548976B1 (ko) | 2006-02-03 |
| CN1157359C (zh) | 2004-07-14 |
| US6048660A (en) | 2000-04-11 |
| CN1244190A (zh) | 2000-02-09 |
| AU6096398A (en) | 1998-08-25 |
| ZA98724B (en) | 1998-07-30 |
| DK0956280T3 (da) | 2003-02-24 |
| ES2184233T3 (es) | 2003-04-01 |
| CA2275667A1 (en) | 1998-08-06 |
| WO1998033761A1 (en) | 1998-08-06 |
| BR9806940B1 (pt) | 2010-12-14 |
| BR9806940A (pt) | 2000-03-28 |
| DE69809029D1 (de) | 2002-12-05 |
| DE69809029T2 (de) | 2003-06-05 |
| JP4171073B2 (ja) | 2008-10-22 |
| EP0956280A1 (en) | 1999-11-17 |
| AU718619B2 (en) | 2000-04-20 |
| EP0956280B1 (en) | 2002-10-30 |
| KR20000070608A (ko) | 2000-11-25 |
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