JP2005509685A5 - - Google Patents
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- Publication number
- JP2005509685A5 JP2005509685A5 JP2003545667A JP2003545667A JP2005509685A5 JP 2005509685 A5 JP2005509685 A5 JP 2005509685A5 JP 2003545667 A JP2003545667 A JP 2003545667A JP 2003545667 A JP2003545667 A JP 2003545667A JP 2005509685 A5 JP2005509685 A5 JP 2005509685A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- unsubstituted
- substituted
- phenyl
- hydrogen
- 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.)
- Pending
Links
- 125000000217 alkyl group Chemical group 0.000 claims 56
- 229910052739 hydrogen Inorganic materials 0.000 claims 31
- 239000001257 hydrogen Substances 0.000 claims 30
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 30
- 150000002431 hydrogen Chemical class 0.000 claims 28
- 229910052717 sulfur Inorganic materials 0.000 claims 25
- 229910052760 oxygen Inorganic materials 0.000 claims 23
- -1 biphenylyl Chemical group 0.000 claims 19
- 229910052736 halogen Inorganic materials 0.000 claims 18
- 150000002367 halogens Chemical class 0.000 claims 18
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims 15
- 150000001875 compounds Chemical group 0.000 claims 14
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 9
- 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 9
- 239000000463 material Substances 0.000 claims 8
- 125000003545 alkoxy group Chemical group 0.000 claims 7
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 7
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 6
- 125000001624 naphthyl group Chemical group 0.000 claims 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims 6
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 5
- 238000000576 coating method Methods 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- 125000000623 heterocyclic group Chemical group 0.000 claims 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 4
- 125000002947 alkylene group Chemical group 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 239000011248 coating agent Substances 0.000 claims 4
- 125000005647 linker group Chemical group 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- 235000010290 biphenyl Nutrition 0.000 claims 3
- 239000004305 biphenyl Substances 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 3
- 229920000642 polymer Polymers 0.000 claims 3
- 238000007639 printing Methods 0.000 claims 3
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 2
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims 2
- PCPQWYHRMVULIX-UHFFFAOYSA-P [1-[2,3-dihydroxy-4-[4-(oxoazaniumylmethylidene)pyridin-1-yl]butyl]pyridin-4-ylidene]methyl-oxoazanium;dinitrate Chemical compound [O-][N+]([O-])=O.[O-][N+]([O-])=O.C1=CC(=C[NH+]=O)C=CN1CC(O)C(O)CN1C=CC(=C[NH+]=O)C=C1 PCPQWYHRMVULIX-UHFFFAOYSA-P 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 239000000178 monomer Substances 0.000 claims 2
- 230000003287 optical effect Effects 0.000 claims 2
- 125000001422 pyrrolinyl group Chemical group 0.000 claims 2
- 238000007650 screen-printing Methods 0.000 claims 2
- 125000006656 (C2-C4) alkenyl group Chemical group 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
- 241000257303 Hymenoptera Species 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000004450 alkenylene group Chemical group 0.000 claims 1
- 125000004419 alkynylene group Chemical group 0.000 claims 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims 1
- 125000004350 aryl cycloalkyl group Chemical group 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
- 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- 238000004061 bleaching Methods 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000002131 composite material Substances 0.000 claims 1
- 125000004956 cyclohexylene group Chemical group 0.000 claims 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims 1
- 239000005548 dental material Substances 0.000 claims 1
- 238000005538 encapsulation Methods 0.000 claims 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims 1
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 1
- 239000011152 fibreglass Substances 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
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 230000001678 irradiating effect Effects 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
- 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
- 238000007645 offset printing Methods 0.000 claims 1
- 239000013307 optical fiber Substances 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 239000000758 substrate Substances 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
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01811113 | 2001-11-20 | ||
| PCT/EP2002/012680 WO2003044030A1 (en) | 2001-11-20 | 2002-11-13 | Multimer forms of acylphosphines and their derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005509685A JP2005509685A (ja) | 2005-04-14 |
| JP2005509685A5 true JP2005509685A5 (enExample) | 2005-12-22 |
Family
ID=8184252
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003545667A Pending JP2005509685A (ja) | 2001-11-20 | 2002-11-13 | アシルホスフィン及びその誘導体のマルチマー形態 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7109250B2 (enExample) |
| EP (1) | EP1446410A1 (enExample) |
| JP (1) | JP2005509685A (enExample) |
| KR (1) | KR20050044549A (enExample) |
| CN (1) | CN1589276A (enExample) |
| AU (1) | AU2002366198A1 (enExample) |
| BR (1) | BR0214324A (enExample) |
| CA (1) | CA2467576A1 (enExample) |
| MX (1) | MXPA04004729A (enExample) |
| WO (1) | WO2003044030A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7196228B2 (en) * | 2002-06-11 | 2007-03-27 | Ciba Specialty Chemicals Corporation | Multimer forms of mono-and bis-acylphosphine oxides |
| EP1658245B1 (en) * | 2003-08-29 | 2017-11-29 | IGM Malta Limited | Optical fiber coatings |
| DE602005026156D1 (de) * | 2004-11-23 | 2011-03-10 | Basf Se | Bisacylphosphane und ihre verwendung als photoinitiatoren, verfahren zur herstellung von acylphosphanen |
| US7547735B1 (en) | 2006-12-04 | 2009-06-16 | Henkel Corporation | UV curable compositions |
| KR102135300B1 (ko) * | 2012-10-01 | 2020-08-27 | 에테하 취리히 | 아실포스판의 제조 방법 |
| JP6599446B2 (ja) * | 2014-05-30 | 2019-10-30 | アイジーエム レシンス イタリア ソチエタ レスポンサビリタ リミタータ | 多官能性アシルホスフィンオキシド光重合開始剤 |
| JP7036506B2 (ja) * | 2015-12-08 | 2022-03-15 | スリーエム イノベイティブ プロパティズ カンパニー | 二成分自己接着性歯科用組成物、保存安定性開始剤系、及びそれらの使用 |
| CN105334697B (zh) * | 2015-12-08 | 2019-10-11 | 深圳市华星光电技术有限公司 | 光刻胶组合物及彩色滤光片的制作方法 |
| EP3409680B1 (en) * | 2017-05-30 | 2021-01-06 | IGM Group B.V. | Synthesis of bis(acyl)phosphines by activation of unreactive metal phosphides |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4265723A (en) * | 1979-07-06 | 1981-05-05 | Basf Aktiengesellschaft | Photocurable molding, impregnating and coating compositions |
| DE3034697A1 (de) * | 1980-09-15 | 1982-05-06 | Basf Ag, 6700 Ludwigshafen | Acylphosphinsulfidverbindungen, ihre herstellung und verwendung |
| EP0736540A3 (de) * | 1989-08-04 | 1997-06-18 | Ciba Geigy | Mono- und Diacylphosphinoxide |
| US5218009A (en) | 1989-08-04 | 1993-06-08 | Ciba-Geigy Corporation | Mono- and di-acylphosphine oxides |
| TW303379B (enExample) | 1994-03-02 | 1997-04-21 | Ciba Sc Holding Ag | |
| DE19618720A1 (de) * | 1995-05-12 | 1996-11-14 | Ciba Geigy Ag | Bisacyl-bisphosphine, -oxide und -sulfide |
| US6075065A (en) * | 1996-12-20 | 2000-06-13 | Takeda Chemical Industries, Ltd. | Photocurable resin composition and a method for producing the same |
| AU7084798A (en) * | 1997-04-22 | 1998-11-13 | Dsm N.V. | Liquid curable resin composition |
| JP2001200007A (ja) * | 2000-01-19 | 2001-07-24 | Shin Etsu Chem Co Ltd | 光硬化性樹脂組成物及び光ファイバー用被覆材 |
| GB2360283B (en) * | 2000-02-08 | 2002-08-21 | Ciba Sc Holding Ag | Monoacylarylphosphines and acylphosphine oxides and sulphides |
| GB2365430B (en) | 2000-06-08 | 2002-08-28 | Ciba Sc Holding Ag | Acylphosphine photoinitiators and intermediates |
| EP1578987A2 (en) * | 2001-08-03 | 2005-09-28 | Diversa Corporation | Epoxide hydrolases, nucleic acids encoding them and methods for making and using them |
-
2002
- 2002-11-13 EP EP02790367A patent/EP1446410A1/en not_active Withdrawn
- 2002-11-13 CN CNA028229142A patent/CN1589276A/zh active Pending
- 2002-11-13 KR KR1020047007699A patent/KR20050044549A/ko not_active Withdrawn
- 2002-11-13 MX MXPA04004729A patent/MXPA04004729A/es unknown
- 2002-11-13 US US10/495,958 patent/US7109250B2/en not_active Expired - Fee Related
- 2002-11-13 AU AU2002366198A patent/AU2002366198A1/en not_active Abandoned
- 2002-11-13 WO PCT/EP2002/012680 patent/WO2003044030A1/en not_active Ceased
- 2002-11-13 JP JP2003545667A patent/JP2005509685A/ja active Pending
- 2002-11-13 CA CA002467576A patent/CA2467576A1/en not_active Abandoned
- 2002-11-13 BR BR0214324-0A patent/BR0214324A/pt not_active Application Discontinuation
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