JP2005523923A5 - - Google Patents
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- Publication number
- JP2005523923A5 JP2005523923A5 JP2003587844A JP2003587844A JP2005523923A5 JP 2005523923 A5 JP2005523923 A5 JP 2005523923A5 JP 2003587844 A JP2003587844 A JP 2003587844A JP 2003587844 A JP2003587844 A JP 2003587844A JP 2005523923 A5 JP2005523923 A5 JP 2005523923A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- formula
- alkoxy
- hydrogen
- independently
- 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.)
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- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 10
- 150000002431 hydrogen Chemical class 0.000 claims 8
- 239000000203 mixture Substances 0.000 claims 8
- 125000003545 alkoxy group Chemical group 0.000 claims 7
- 125000002947 alkylene group Chemical group 0.000 claims 7
- 150000001875 compounds Chemical class 0.000 claims 7
- 239000000463 material Substances 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- -1 phenylene, methyl-phenylene, cyclohexanediyl Chemical group 0.000 claims 7
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 6
- 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 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 239000000976 ink Substances 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 3
- 239000004305 biphenyl Substances 0.000 claims 3
- 235000010290 biphenyl Nutrition 0.000 claims 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 3
- 125000000466 oxiranyl group Chemical group 0.000 claims 3
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 3
- 238000002360 preparation method Methods 0.000 claims 3
- 238000007639 printing Methods 0.000 claims 3
- 125000005569 butenylene group Chemical group 0.000 claims 2
- 125000005622 butynylene group Chemical group 0.000 claims 2
- 238000000576 coating method Methods 0.000 claims 2
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims 2
- 125000004956 cyclohexylene group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 230000003287 optical effect Effects 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 229920000642 polymer Polymers 0.000 claims 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims 2
- 238000007650 screen-printing Methods 0.000 claims 2
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 claims 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 claims 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims 1
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 claims 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 claims 1
- HDYRYUINDGQKMC-UHFFFAOYSA-M acetyloxyaluminum;dihydrate Chemical compound O.O.CC(=O)O[Al] HDYRYUINDGQKMC-UHFFFAOYSA-M 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000008065 acid anhydrides Chemical class 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 claims 1
- 229940009827 aluminum acetate Drugs 0.000 claims 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- ITHZDDVSAWDQPZ-UHFFFAOYSA-L barium acetate Chemical compound [Ba+2].CC([O-])=O.CC([O-])=O ITHZDDVSAWDQPZ-UHFFFAOYSA-L 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- LHQLJMJLROMYRN-UHFFFAOYSA-L cadmium acetate Chemical compound [Cd+2].CC([O-])=O.CC([O-])=O LHQLJMJLROMYRN-UHFFFAOYSA-L 0.000 claims 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims 1
- 239000000292 calcium oxide Substances 0.000 claims 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 claims 1
- 239000008199 coating composition Substances 0.000 claims 1
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 claims 1
- 239000002131 composite material Substances 0.000 claims 1
- 238000002845 discoloration Methods 0.000 claims 1
- 238000005538 encapsulation Methods 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 239000003365 glass fiber Substances 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- NONOKGVFTBWRLD-UHFFFAOYSA-N isocyanatosulfanylimino(oxo)methane Chemical compound O=C=NSN=C=O NONOKGVFTBWRLD-UHFFFAOYSA-N 0.000 claims 1
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 claims 1
- JILPJDVXYVTZDQ-UHFFFAOYSA-N lithium methoxide Chemical compound [Li+].[O-]C JILPJDVXYVTZDQ-UHFFFAOYSA-N 0.000 claims 1
- LZWQNOHZMQIFBX-UHFFFAOYSA-N lithium;2-methylpropan-2-olate Chemical compound [Li+].CC(C)(C)[O-] LZWQNOHZMQIFBX-UHFFFAOYSA-N 0.000 claims 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 claims 1
- 239000011654 magnesium acetate Substances 0.000 claims 1
- 229940069446 magnesium acetate Drugs 0.000 claims 1
- 235000011285 magnesium acetate Nutrition 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 1
- 239000003094 microcapsule Substances 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- 125000001064 morpholinomethyl group Chemical group [H]C([H])(*)N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 claims 1
- 125000004957 naphthylene group Chemical group 0.000 claims 1
- 238000007645 offset printing Methods 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical compound OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 claims 1
- 235000011056 potassium acetate Nutrition 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 125000001422 pyrrolinyl group Chemical group 0.000 claims 1
- 230000033458 reproduction Effects 0.000 claims 1
- 239000001632 sodium acetate Substances 0.000 claims 1
- 235000017281 sodium acetate Nutrition 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 229920001187 thermosetting polymer Polymers 0.000 claims 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 claims 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 239000004246 zinc acetate Substances 0.000 claims 1
- YXWWEYJLDGSORF-UHFFFAOYSA-N [O-][NH+](c1ccccc1)[NH+]([O-])OCCO[NH+]([NH+](c1ccccc1)[O-])[O-] Chemical compound [O-][NH+](c1ccccc1)[NH+]([O-])OCCO[NH+]([NH+](c1ccccc1)[O-])[O-] YXWWEYJLDGSORF-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH7172002 | 2002-04-26 | ||
| PCT/EP2003/004035 WO2003091287A1 (en) | 2002-04-26 | 2003-04-17 | Incorporable photoinitiator |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005523923A JP2005523923A (ja) | 2005-08-11 |
| JP2005523923A5 true JP2005523923A5 (https=) | 2006-06-01 |
| JP4451137B2 JP4451137B2 (ja) | 2010-04-14 |
Family
ID=29256413
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003587844A Expired - Lifetime JP4451137B2 (ja) | 2002-04-26 | 2003-04-17 | 配合可能な光開始剤 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7588880B2 (https=) |
| EP (1) | EP1499645B1 (https=) |
| JP (1) | JP4451137B2 (https=) |
| KR (1) | KR100979660B1 (https=) |
| CN (1) | CN1307207C (https=) |
| AT (1) | ATE320452T1 (https=) |
| AU (1) | AU2003233984A1 (https=) |
| BR (1) | BR0309779B1 (https=) |
| CA (1) | CA2483004A1 (https=) |
| DE (1) | DE60304035T2 (https=) |
| DK (1) | DK1499645T3 (https=) |
| ES (1) | ES2259413T3 (https=) |
| MX (1) | MXPA04010254A (https=) |
| PL (1) | PL207511B1 (https=) |
| RU (1) | RU2320641C2 (https=) |
| TW (1) | TW200305582A (https=) |
| WO (1) | WO2003091287A1 (https=) |
| ZA (1) | ZA200407897B (https=) |
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|---|---|---|---|---|
| US7642296B2 (en) | 2004-04-19 | 2010-01-05 | Ciba Specialty Chemicals Corporation | Photoinitiators |
| FR2871898B1 (fr) * | 2004-06-18 | 2006-09-08 | Alcatel Sa | Composant a fibre optique et fibre optique associee |
| US8414982B2 (en) * | 2004-12-22 | 2013-04-09 | Basf Se | Process for the production of strongly adherent coatings |
| US20070012208A1 (en) * | 2005-07-13 | 2007-01-18 | Byungwoo Cho | Offset printing system |
| US20100022676A1 (en) * | 2006-10-03 | 2010-01-28 | Jonathan Rogers | Photocurable compositions comprising a photoinitiator of the phenylglyoxylate type |
| EP2157614B1 (en) * | 2007-05-30 | 2017-03-01 | Nissan Chemical Industries, Ltd. | Gate insulating film forming agent for thin-film transistor |
| ITVA20070073A1 (it) * | 2007-09-17 | 2009-03-18 | Lamberti Spa | Fotoiniziatori per reticolazione indotta dalla luce |
| CN101583908B (zh) * | 2007-11-20 | 2012-12-26 | 日立化成工业株式会社 | 感光性树脂组合物、感光性树脂固化物、感光性树脂膜、感光性树脂膜固化物和使用它们得到的光波导 |
| JP5192277B2 (ja) * | 2008-04-14 | 2013-05-08 | シャープ株式会社 | 固体撮像装置の製造方法 |
| US7970247B2 (en) * | 2008-09-12 | 2011-06-28 | Draka Comteq B.V. | Buffer tubes for mid-span storage |
| US8401353B2 (en) * | 2008-09-12 | 2013-03-19 | Draka Comteq B.V. | Optical fiber cable assembly |
| RU2465888C1 (ru) * | 2008-11-11 | 2012-11-10 | Колгейт-Палмолив Компани | Композиция с красящим веществом для указания степени покрытия |
| WO2010077132A1 (en) | 2008-12-31 | 2010-07-08 | Draka Comteq B.V. | Uvled apparatus for curing glass-fiber coatings |
| DE102009001966A1 (de) | 2009-03-30 | 2010-10-07 | Evonik Röhm Gmbh | Beschichtungszusammensetzung,(Meth)acryl-Polymer und Monomermischung zur Herstellung des(Meth)acryl-Polymers |
| US20100276059A1 (en) * | 2009-04-30 | 2010-11-04 | Dong Tian | UVV curable coating compositions and method for coating flooring and other substrates with same |
| US8625945B1 (en) | 2009-05-13 | 2014-01-07 | Draka Comteq, B.V. | Low-shrink reduced-diameter dry buffer tubes |
| US8625944B1 (en) | 2009-05-13 | 2014-01-07 | Draka Comteq, B.V. | Low-shrink reduced-diameter buffer tubes |
| CN101811968B (zh) * | 2010-02-09 | 2014-07-30 | 深圳市有为化学技术有限公司 | 多官能团化苯甲酰甲酸羟基酮酯类化合物及含有该类化合物的光引发剂 |
| EP2388239B1 (en) | 2010-05-20 | 2017-02-15 | Draka Comteq B.V. | Curing apparatus employing angled UV-LEDs |
| US8871311B2 (en) | 2010-06-03 | 2014-10-28 | Draka Comteq, B.V. | Curing method employing UV sources that emit differing ranges of UV radiation |
| EP2418183B1 (en) | 2010-08-10 | 2018-07-25 | Draka Comteq B.V. | Method for curing coated glass fibres providing increased UVLED intensitiy |
| SG190259A1 (en) * | 2010-11-12 | 2013-06-28 | Coloplast As | Novel polymeric photoinitiators |
| MX352264B (es) * | 2011-10-06 | 2017-11-16 | Firmenich & Cie | Latex fotolabil para la liberacion de perfumes. |
| JP6139551B2 (ja) * | 2011-12-01 | 2017-05-31 | スリーエム イノベイティブ プロパティズ カンパニー | 一成分自己接着性歯科用組成物、その製造方法、及び使用 |
| BR112015022854A2 (pt) | 2013-03-14 | 2017-07-18 | Alkermes Pharma Ireland Ltd | pró-farmacos de fumaratos e uso do mesmo no tratamento de várias doenças |
| US8669281B1 (en) | 2013-03-14 | 2014-03-11 | Alkermes Pharma Ireland Limited | Prodrugs of fumarates and their use in treating various diseases |
| WO2015067478A1 (de) * | 2013-11-05 | 2015-05-14 | Construction Research & Technology Gmbh | Neue bindemittelsysteme |
| CN103709036B (zh) * | 2013-12-03 | 2015-07-29 | 天津久日化学股份有限公司 | 双官能团苯甲酰基甲酸羟基酮酯类化合物及含该类化合物的光引发剂 |
| JP6337135B2 (ja) | 2014-02-24 | 2018-06-06 | アルカーメス ファーマ アイルランド リミテッド | フマル酸エステルのスルホンアミドプロドラッグ及びスルフィンアミドプロドラッグ並びに種々の疾患の治療におけるその使用 |
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| JP6659048B2 (ja) * | 2014-08-17 | 2020-03-04 | ディーエスエム アイピー アセッツ ビー．ブイ．Ｄｓｍ Ｉｐ Ａｓｓｅｔｓ Ｂ．Ｖ． | 光ファイバー用の単色化学線硬化性被覆 |
| JP7118580B2 (ja) * | 2014-08-26 | 2022-08-16 | キヤノン株式会社 | 光硬化性組成物、これを用いた硬化物パターンの製造方法、光学部品の製造方法、回路基板の製造方法、およびインプリント用モールドの製造方法 |
| CN104387576B (zh) * | 2014-11-19 | 2016-06-29 | 浙江皇马科技股份有限公司 | 一种缩水甘油醚基封端烯丙醇无规聚醚的制备方法 |
| KR101685520B1 (ko) | 2014-12-10 | 2016-12-12 | 고오 가가쿠고교 가부시키가이샤 | 액상 솔더 레지스트 조성물 및 피복 프린트 배선판 |
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| CN106905147A (zh) * | 2017-02-21 | 2017-06-30 | 怀化金鑫新材料有限公司 | 光引发剂苯甲酰甲酸二甘醇酯的合成新工艺 |
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| CN116425634A (zh) * | 2023-04-18 | 2023-07-14 | 浙江东海新材料科技股份有限公司 | 一种混合酯类光引发剂的合成方法及产品 |
| CN118027806B (zh) * | 2024-02-01 | 2024-08-09 | 江苏大自然智能家居有限公司 | 一种木地板用水性uv光固化涂料及其制备方法 |
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| TW328535B (en) * | 1993-07-02 | 1998-03-21 | Novartis Ag | Functional photoinitiators and their manufacture |
| TW460509B (en) * | 1996-07-12 | 2001-10-21 | Ciba Sc Holding Ag | Curing process for cationically photocurable formulations |
| EP0849300A1 (de) * | 1996-12-19 | 1998-06-24 | Basf Aktiengesellschaft | Polyurethane mit kovalent gebundenen Photoinitiatoreinheiten |
| EP0956280B1 (en) * | 1997-01-30 | 2002-10-30 | Ciba SC Holding AG | Non-volatile phenylglyoxalic esters |
| DE19913353A1 (de) | 1999-03-24 | 2000-09-28 | Basf Ag | Verwendung von Phenylglyoxalsäureestern als Photoinitiatoren |
| DE10002089A1 (de) * | 2000-01-19 | 2001-07-26 | Basf Ag | Witterungsstabile, strahlungshärtbare Polyurethane |
| CN1250513C (zh) * | 2000-06-23 | 2006-04-12 | 西巴特殊化学品控股有限公司 | 羟苯基羧酸酯的制备方法 |
| TW557298B (en) * | 2000-08-14 | 2003-10-11 | Ciba Sc Holding Ag | A compound, a photopolymerizible composition, a process for producing coatings and a method for causing a photoinitiator to accumulate at the surface of coatings |
| TWI244495B (en) * | 2000-08-14 | 2005-12-01 | Ciba Sc Holding Ag | Process for producing coatings siloxane photoinitiators |
| US8003169B2 (en) * | 2002-04-19 | 2011-08-23 | Basf Se | Curing of coating induced by plasma |
| DE10223614A1 (de) * | 2002-05-27 | 2003-12-11 | Basf Ag | Strahlungshärtbare wässrige Dispersionen |
-
2003
- 2003-04-17 CN CNB038093413A patent/CN1307207C/zh not_active Expired - Lifetime
- 2003-04-17 DE DE60304035T patent/DE60304035T2/de not_active Expired - Lifetime
- 2003-04-17 AU AU2003233984A patent/AU2003233984A1/en not_active Abandoned
- 2003-04-17 AT AT03727317T patent/ATE320452T1/de not_active IP Right Cessation
- 2003-04-17 RU RU2004134570/04A patent/RU2320641C2/ru not_active IP Right Cessation
- 2003-04-17 ES ES03727317T patent/ES2259413T3/es not_active Expired - Lifetime
- 2003-04-17 DK DK03727317T patent/DK1499645T3/da active
- 2003-04-17 PL PL371516A patent/PL207511B1/pl unknown
- 2003-04-17 MX MXPA04010254A patent/MXPA04010254A/es active IP Right Grant
- 2003-04-17 KR KR1020047017189A patent/KR100979660B1/ko not_active Expired - Fee Related
- 2003-04-17 US US10/512,300 patent/US7588880B2/en not_active Expired - Lifetime
- 2003-04-17 BR BRPI0309779-0B1A patent/BR0309779B1/pt not_active IP Right Cessation
- 2003-04-17 JP JP2003587844A patent/JP4451137B2/ja not_active Expired - Lifetime
- 2003-04-17 CA CA002483004A patent/CA2483004A1/en not_active Abandoned
- 2003-04-17 EP EP03727317A patent/EP1499645B1/en not_active Expired - Lifetime
- 2003-04-17 WO PCT/EP2003/004035 patent/WO2003091287A1/en not_active Ceased
- 2003-04-25 TW TW092109781A patent/TW200305582A/zh unknown
-
2004
- 2004-09-30 ZA ZA200407897A patent/ZA200407897B/xx unknown
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