JP2003522227A5 - - Google Patents
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- Publication number
- JP2003522227A5 JP2003522227A5 JP2001557879A JP2001557879A JP2003522227A5 JP 2003522227 A5 JP2003522227 A5 JP 2003522227A5 JP 2001557879 A JP2001557879 A JP 2001557879A JP 2001557879 A JP2001557879 A JP 2001557879A JP 2003522227 A5 JP2003522227 A5 JP 2003522227A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- groups
- aryl
- alkyl
- isocyanate
- 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
- -1 cycloalkynyl Chemical group 0.000 description 19
- 125000003118 aryl group Chemical group 0.000 description 15
- 238000000034 method Methods 0.000 description 14
- 125000000217 alkyl group Chemical group 0.000 description 11
- 229910052739 hydrogen Inorganic materials 0.000 description 11
- 239000001257 hydrogen Substances 0.000 description 11
- 125000003342 alkenyl group Chemical group 0.000 description 10
- 125000000304 alkynyl group Chemical group 0.000 description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
- 125000000392 cycloalkenyl group Chemical group 0.000 description 8
- 125000000753 cycloalkyl group Chemical group 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 125000002877 alkyl aryl group Chemical group 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 125000003710 aryl alkyl group Chemical group 0.000 description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 6
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 4
- 125000005041 acyloxyalkyl group Chemical group 0.000 description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 4
- 125000004171 alkoxy aryl group Chemical group 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 125000005083 alkoxyalkoxy group Chemical group 0.000 description 4
- 125000006575 electron-withdrawing group Chemical group 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 125000005113 hydroxyalkoxy group Chemical group 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 150000004714 phosphonium salts Chemical class 0.000 description 4
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 description 4
- 125000001174 sulfone group Chemical group 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 4
- 125000004423 acyloxy group Chemical group 0.000 description 3
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 125000000547 substituted alkyl group Chemical group 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 125000004945 acylaminoalkyl group Chemical group 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003302 alkenyloxy group Chemical group 0.000 description 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 description 2
- 125000005133 alkynyloxy group Chemical group 0.000 description 2
- HXBPYFMVGFDZFT-UHFFFAOYSA-N allyl isocyanate Chemical compound C=CCN=C=O HXBPYFMVGFDZFT-UHFFFAOYSA-N 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 125000005128 aryl amino alkyl group Chemical group 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 125000004465 cycloalkenyloxy group Chemical group 0.000 description 2
- 125000000000 cycloalkoxy group Chemical group 0.000 description 2
- 125000004984 dialkylaminoalkoxy group Chemical group 0.000 description 2
- 125000005020 hydroxyalkenyl group Chemical group 0.000 description 2
- 125000005016 hydroxyalkynyl group Chemical group 0.000 description 2
- 125000005027 hydroxyaryl group Chemical group 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002560 nitrile group Chemical group 0.000 description 2
- 150000001282 organosilanes Chemical class 0.000 description 2
- 125000005375 organosiloxane group Chemical group 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical class C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 125000003106 haloaryl group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen(.) Chemical compound [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003512 tertiary amines Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00300942 | 2000-02-07 | ||
| EP00300942.0 | 2000-02-07 | ||
| PCT/GB2001/000519 WO2001057048A1 (en) | 2000-02-07 | 2001-02-07 | Silicon containing compounds from michael - type addition reactions useful as monomers and macromers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003522227A JP2003522227A (ja) | 2003-07-22 |
| JP2003522227A5 true JP2003522227A5 (enExample) | 2012-06-28 |
Family
ID=8172685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001557879A Pending JP2003522227A (ja) | 2000-02-07 | 2001-02-07 | シリコン含有化合物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7064174B2 (enExample) |
| EP (1) | EP1255761B1 (enExample) |
| JP (1) | JP2003522227A (enExample) |
| AT (1) | ATE303391T1 (enExample) |
| AU (1) | AU3383901A (enExample) |
| DE (1) | DE60113066T2 (enExample) |
| WO (1) | WO2001057048A1 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60010644T2 (de) * | 2000-02-07 | 2005-05-19 | Biocompatibles Uk Ltd., Farnham | Silizium enthaltende Verbindungen hergestellt durch Michael Addition als Monomere und Macromere |
| JP4245336B2 (ja) * | 2002-11-25 | 2009-03-25 | 株式会社資生堂 | ホスホリルコリン基を有するポリシロキサン及びその製造方法 |
| CN100549018C (zh) * | 2003-12-02 | 2009-10-14 | 株式会社资生堂 | 含有磷酸胆碱基的化合物及包含该化合物的表面改性剂 |
| US8231218B2 (en) | 2006-06-15 | 2012-07-31 | Coopervision International Holding Company, Lp | Wettable silicone hydrogel contact lenses and related compositions and methods |
| US7540609B2 (en) | 2006-06-15 | 2009-06-02 | Coopervision International Holding Company, Lp | Wettable silicone hydrogel contact lenses and related compositions and methods |
| US7572841B2 (en) | 2006-06-15 | 2009-08-11 | Coopervision International Holding Company, Lp | Wettable silicone hydrogel contact lenses and related compositions and methods |
| US20080004413A1 (en) * | 2006-06-30 | 2008-01-03 | Derek Schorzman | Carboxylic M2Dx-like siloxanyl monomers |
| US8168738B2 (en) * | 2006-09-21 | 2012-05-01 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| US8349066B2 (en) * | 2006-09-21 | 2013-01-08 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| US20090111912A1 (en) * | 2006-09-21 | 2009-04-30 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| US7868120B2 (en) * | 2006-09-21 | 2011-01-11 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| US20090078156A1 (en) * | 2006-09-21 | 2009-03-26 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| US20080075871A1 (en) * | 2006-09-21 | 2008-03-27 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| SG11201400281PA (en) | 2011-09-01 | 2014-08-28 | Vertellus Specialties Inc | Biocompatible material |
| EP2751153A1 (en) * | 2011-09-01 | 2014-07-09 | Vertellus Specialties Inc. | Methods for producing biocompatible materials |
| GB201119363D0 (en) * | 2011-11-10 | 2011-12-21 | Vertellus Specialities Inc | Polymerisable material |
| US9200119B2 (en) * | 2012-11-09 | 2015-12-01 | Momentive Performance Materials Inc. | Silicon-containing zwitterionic linear copolymer composition |
| WO2019107322A1 (ja) * | 2017-11-28 | 2019-06-06 | 三井化学株式会社 | （メタ）アクリレート、モノマー組成物、該組成物から得られた歯科材料およびその製造方法 |
| EP3648227B1 (en) * | 2017-12-01 | 2022-08-10 | LG Energy Solution, Ltd. | Gel polymer electrolyte composition and lithium secondary battery including the same |
| US11342585B2 (en) * | 2017-12-01 | 2022-05-24 | Lg Energy Solution, Ltd. | Gel polymer electrolyte composition and lithium secondary battery including the same |
| US11316194B2 (en) * | 2018-01-03 | 2022-04-26 | Lg Energy Solution, Ltd. | Gel polymer electrolyte composition, gel polymer electrolyte prepared thereby, and lithium secondary battery including the gel polymer electrolyte |
| JP7591863B2 (ja) * | 2019-03-19 | 2024-11-29 | 信越化学工業株式会社 | オルガノポリシロキサン、紫外線硬化性シリコーン組成物及び硬化物 |
| KR20240051184A (ko) * | 2021-08-31 | 2024-04-19 | 니치유 가부시키가이샤 | 포스포릴콜린기와 수산기를 갖는 폴리디메틸실록산 함유 모노머 |
| JPWO2023033013A1 (enExample) * | 2021-08-31 | 2023-03-09 |
Family Cites Families (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2924588A (en) | 1957-04-22 | 1960-02-09 | Dow Corning | Organosiloxane alcohols |
| US3146250A (en) | 1961-10-11 | 1964-08-25 | Dow Corning | Nitrogen-containing cyclic silanes, their preparation and hydrolysis |
| EP0032622B1 (en) | 1979-12-20 | 1985-08-14 | Dennis Chapman | Polymerisable phospholipids and polymers thereof, methods for their preparation, methods for their use in coating substrates and forming liposomes and the resulting coated substrates and liposome compositions |
| US4486577A (en) | 1982-10-12 | 1984-12-04 | Ciba-Geigy Corporation | Strong, silicone containing polymers with high oxygen permeability |
| US4507466A (en) | 1983-01-07 | 1985-03-26 | The Dow Chemical Corporation | Dense star polymers having core, core branches, terminal groups |
| US5380904A (en) | 1984-01-20 | 1995-01-10 | Biocompatibles Ltd. | Process for rendering a surface biocompatible, and articles containing the same |
| JPH0627196B2 (ja) | 1984-03-12 | 1994-04-13 | 大日本印刷株式会社 | 放射線硬化性有機珪素化合物の製造法 |
| DE3417912C1 (de) | 1984-05-15 | 1985-07-25 | Goldschmidt Ag Th | Betaingruppen enthaltende Siloxane,deren Herstellung und Verwendung in kosmetischen Zubereitungen |
| CA1257727A (en) | 1984-12-18 | 1989-07-18 | Chi-Long Lee | Hydrophilic silicone-organic copolymer elastomers |
| US4606933A (en) * | 1985-09-25 | 1986-08-19 | Sws Silicones Corporation | Acrylate-functional organopolysiloxanes |
| US4697026A (en) | 1986-01-06 | 1987-09-29 | Dow Corning Corporation | Acryl functional silicone compounds |
| US4734475A (en) | 1986-12-15 | 1988-03-29 | Ciba-Geigy Corporation | Wettable surface modified contact lens fabricated from an oxirane containing hydrophobic polymer |
| JPH0618866B2 (ja) * | 1986-12-22 | 1994-03-16 | 鐘淵化学工業株式会社 | 常温硬化性樹脂の製造法 |
| US5712327A (en) | 1987-01-07 | 1998-01-27 | Chang; Sing-Hsiung | Soft gas permeable contact lens having improved clinical performance |
| US4918210A (en) | 1987-01-20 | 1990-04-17 | Fenton William N | Zwitterionic polysiloxane compositions |
| US4780515A (en) | 1987-02-05 | 1988-10-25 | Bausch & Lomb Incorporated | Continuous-wear lenses having improved physical properties |
| US5070169A (en) | 1988-02-26 | 1991-12-03 | Ciba-Geigy Corporation | Wettable, flexible, oxygen permeable contact lens containing block copolymer polysiloxane-polyoxyalkylene backbone units and use thereof |
| US4912240A (en) | 1988-08-01 | 1990-03-27 | Dow Corning Corporation | Organofunctional betaine modified siloxanes |
| US4962178A (en) | 1988-11-03 | 1990-10-09 | Ciba-Geigy Corporation | Novel polysiloxane-polyurethanes and contact lens thereof |
| CA2015903A1 (en) | 1989-05-12 | 1990-11-12 | Andrew B. Auerbach | Grafting of amine functional polymers onto functionalized oxymethylene polymers and the resulting graft polymers thereof |
| US5010141A (en) | 1989-10-25 | 1991-04-23 | Ciba-Geigy Corporation | Reactive silicone and/or fluorine containing hydrophilic prepolymers and polymers thereof |
| DE69101464T2 (de) * | 1990-04-26 | 1994-07-14 | Ciba Geigy | Ungesättigte Harnstoff-Polysiloxane. |
| GB9023498D0 (en) | 1990-10-29 | 1990-12-12 | Biocompatibles Ltd | Soft contact lens material |
| ATE190988T1 (de) | 1991-07-05 | 2000-04-15 | Biocompatibles Ltd | Polymere oberflächenbeschichtungszusammensetzungen |
| DK0818479T3 (da) * | 1991-08-08 | 2001-01-15 | Biocompatibles Ltd | Polymere overfladecoatinger |
| GB9118597D0 (en) | 1991-08-30 | 1991-10-16 | Biocompatibles Ltd | Polymer treatments |
| EP0603268B1 (en) | 1991-09-12 | 1996-12-18 | BAUSCH & LOMB INCORPORATED | Wettable silicone hydrogel compositions and methods |
| US5352714A (en) | 1991-11-05 | 1994-10-04 | Bausch & Lomb Incorporated | Wettable silicone hydrogel compositions and methods for their manufacture |
| EP0611379B1 (en) | 1991-11-05 | 1996-05-29 | BAUSCH & LOMB INCORPORATED | Wettable silicone hydrogel compositions and methods for their manufacture |
| US5296144A (en) | 1992-01-02 | 1994-03-22 | World Trade Corporation | Composite membrane of a hydrophilic asymmetric membrane coated with an organosiloxane block copolymer |
| US5194251A (en) | 1992-02-10 | 1993-03-16 | Dow Corning Corporation | Hair treatment with zwitterionomeric siloxanes |
| DE69324249D1 (de) | 1992-04-24 | 1999-05-06 | Biocompatibles Ltd | Metall beschichtungen |
| GB9301701D0 (en) | 1993-01-28 | 1993-03-17 | Biocompatibles Ltd | New zwitterionic materials |
| GB9301702D0 (en) | 1993-01-28 | 1993-03-17 | Biocompatibles Ltd | New materials |
| US5321108A (en) | 1993-02-12 | 1994-06-14 | Bausch & Lomb Incorporated | Fluorosilicone hydrogels |
| US5550219A (en) | 1993-10-20 | 1996-08-27 | Siltech Inc. | Silicone polymers |
| US5405983A (en) | 1993-12-28 | 1995-04-11 | Mona Industries, Inc. | Silicone modified phospholipid compositions |
| US5792827A (en) | 1994-01-13 | 1998-08-11 | Basf Lacke + Farben, Ag | Addition products, radiation-curable surface coating compositions based on the addition products and their use for woodcoating and papercoating |
| US5760100B1 (en) | 1994-09-06 | 2000-11-14 | Ciba Vision Corp | Extended wear ophthalmic lens |
| US6194539B1 (en) | 1994-11-22 | 2001-02-27 | Daicel Chemical Industries, Inc. | Polylactone having amino groups, a process for the preparation thereof, a compound having amino group, a composition for coatings, a composition for printing inks |
| US5786086A (en) | 1996-01-02 | 1998-07-28 | Union Camp Corporation | Conductive wire coating |
| US5602224A (en) | 1996-03-19 | 1997-02-11 | Siltech Inc. | Silicone alkyl quats |
| JPH09291135A (ja) | 1996-04-26 | 1997-11-11 | Toyo Ink Mfg Co Ltd | 硬化剤及びそれを含む硬化性樹脂組成物 |
| US5739192A (en) * | 1996-11-20 | 1998-04-14 | Dow Corning Corporation | Polysiloxane copolymers from Michael Adduct reactions |
| US6136943A (en) | 1997-09-01 | 2000-10-24 | Toyo Ink Mfg. Co., Ltd. | Multi-branched compounds and curable composition |
| DE19803468A1 (de) * | 1998-01-29 | 1999-08-05 | Wacker Chemie Gmbh | Durch Michael-Addition-ähnliche Reaktionen vernetzte Aminosiliconölemulsionen |
-
2001
- 2001-02-07 EP EP01905867A patent/EP1255761B1/en not_active Expired - Lifetime
- 2001-02-07 AU AU33839/01A patent/AU3383901A/en not_active Abandoned
- 2001-02-07 DE DE60113066T patent/DE60113066T2/de not_active Expired - Lifetime
- 2001-02-07 JP JP2001557879A patent/JP2003522227A/ja active Pending
- 2001-02-07 US US10/203,203 patent/US7064174B2/en not_active Expired - Lifetime
- 2001-02-07 AT AT01905867T patent/ATE303391T1/de not_active IP Right Cessation
- 2001-02-07 WO PCT/GB2001/000519 patent/WO2001057048A1/en not_active Ceased
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