JP2002506070A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2002506070A5 JP2002506070A5 JP2000535640A JP2000535640A JP2002506070A5 JP 2002506070 A5 JP2002506070 A5 JP 2002506070A5 JP 2000535640 A JP2000535640 A JP 2000535640A JP 2000535640 A JP2000535640 A JP 2000535640A JP 2002506070 A5 JP2002506070 A5 JP 2002506070A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- group
- substituted
- formula
- 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.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 description 12
- -1 amino, hydroxy Chemical group 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229910004013 NO 2 Inorganic materials 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 125000000304 alkynyl group Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 125000003884 phenylalkyl group Chemical group 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 101100516563 Caenorhabditis elegans nhr-6 gene Proteins 0.000 description 1
- SYNHCENRCUAUNM-UHFFFAOYSA-N Nitrogen mustard N-oxide hydrochloride Chemical group Cl.ClCC[N+]([O-])(C)CCCl SYNHCENRCUAUNM-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98810194.5 | 1998-03-09 | ||
| EP98810194 | 1998-03-09 | ||
| PCT/EP1999/001233 WO1999046261A1 (en) | 1998-03-09 | 1999-02-26 | Nitroxyl derivatives with glycidyl or alkylcarbonyl groups as initiators for radical polymerisation |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002506070A JP2002506070A (ja) | 2002-02-26 |
| JP2002506070A5 true JP2002506070A5 (enExample) | 2006-04-13 |
| JP4584448B2 JP4584448B2 (ja) | 2010-11-24 |
Family
ID=8235977
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000535640A Expired - Fee Related JP4584448B2 (ja) | 1998-03-09 | 1999-02-26 | ラジカル重合開始剤としてのグリシジル又はアルキルカルボニル基を有するニトロキシル誘導体 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6566468B1 (enExample) |
| EP (1) | EP1071681B1 (enExample) |
| JP (1) | JP4584448B2 (enExample) |
| AU (1) | AU2929699A (enExample) |
| CA (1) | CA2321792C (enExample) |
| DE (1) | DE69933020T2 (enExample) |
| TW (1) | TW495515B (enExample) |
| WO (1) | WO1999046261A1 (enExample) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG82601A1 (en) | 1998-03-09 | 2001-08-21 | Ciba Sc Holding Ag | 1-alkoxy-polyalkyl-piperidine derivatives and their use as polymerization regulators |
| TWI225483B (en) * | 1998-10-16 | 2004-12-21 | Ciba Sc Holding Ag | Heterocyclic alkoxyamines as regulators in controlled radical polymerization process |
| US6472486B2 (en) | 1999-03-09 | 2002-10-29 | Symyx Technologies, Inc. | Controlled stable free radical emulsion polymerization processes |
| EP1165625A1 (en) | 1999-03-09 | 2002-01-02 | Symyx Technologies, Inc. | Controlled free radical emulsion and water-based polymerizations and seeded methodologies |
| CA2375806A1 (en) * | 1999-07-02 | 2001-01-11 | Ciba Specialty Chemicals Holding Inc. | Mono and multifunctional alkoxyamines for the preparation of functionalized macromers |
| US6716948B1 (en) | 1999-07-31 | 2004-04-06 | Symyx Technologies, Inc. | Controlled-architecture polymers and use thereof as separation media |
| EP1203054B1 (en) * | 1999-08-12 | 2004-11-03 | Ciba SC Holding AG | Polymer blends with improved impact resistance |
| TW546311B (en) * | 1999-11-25 | 2003-08-11 | Ciba Sc Holding Ag | Composition and method for color improvement of nitroxyl containing polymers |
| JP2001253916A (ja) * | 2000-03-10 | 2001-09-18 | Nippon Chem Ind Co Ltd | フルオロアルキル基含有ホスホン酸オリゴマー類およびその製造方法、並びにその用途 |
| TW572896B (en) * | 2000-05-26 | 2004-01-21 | Ciba Sc Holding Ag | Process for the synthesis of amine ethers from secondary amino oxides |
| US20030031675A1 (en) | 2000-06-06 | 2003-02-13 | Mikesell Glen E. | B7-related nucleic acids and polypeptides useful for immunomodulation |
| TWI274053B (en) * | 2000-12-14 | 2007-02-21 | Ciba Sc Holding Ag | N-alkoxy-4,4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization |
| US6544304B2 (en) | 2001-04-02 | 2003-04-08 | Ciba Specialty Chemicals Corporation | Candle wax stabilized with morpholinones |
| US7868171B2 (en) * | 2001-11-12 | 2011-01-11 | Ciba Specialty Chemicals Corp. | N-alkoxy-4, 4-dioxy-polyalkyl-piperidines as radical polymerization initiators |
| WO2003075091A1 (en) * | 2002-03-05 | 2003-09-12 | Ciba Specialty Chemicals Holding Inc. | Colour photographic recording material |
| WO2004022617A1 (en) * | 2002-09-04 | 2004-03-18 | Ciba Specialty Chemicals Holding Inc. | Method of producing comb or star copolymers using epoxy-functionalized nitroxylethers |
| EP1543077A1 (en) * | 2002-09-26 | 2005-06-22 | Ciba SC Holding AG | Thermoplastic compositions with enhanced melt flow and compatibility |
| WO2004069887A2 (en) * | 2003-02-10 | 2004-08-19 | Ciba Specialty Chemicals Holding Inc. | Comb copolymers with defined side chains and process for their manufacture |
| US6967228B2 (en) | 2003-05-01 | 2005-11-22 | Firestone Polymers, Llc | Stable free radical polymers |
| US20060079624A1 (en) * | 2004-10-08 | 2006-04-13 | Hildeberto Nava | Crosslinkable polymer systems |
| US20060173142A1 (en) * | 2005-02-01 | 2006-08-03 | Hildeberto Nava | Functionalized thermosetting resin systems |
| ATE482985T1 (de) * | 2005-04-04 | 2010-10-15 | Basf Se | Verfahren zur herstellung von stern- und blockcopolymeren über epoxidfunktionelle alkoxyamine |
| US7279527B2 (en) | 2005-04-22 | 2007-10-09 | Bridgestone Corporation | Method of converting anionic living end to protected free radical living end and applications thereof |
| US8357759B2 (en) * | 2005-08-26 | 2013-01-22 | CID Centro de Investigación y Desarrollo Tecnológico S.A. de C.V. | Reactive block copolymers |
| US20100311920A1 (en) * | 2005-08-26 | 2010-12-09 | Cid Centro De Investigacion Y Desarrollo Tecnologico Sa De Cv | Using Reactive Block Copolymers as Chain Extenders and Surface Modifiers |
| WO2008003619A2 (en) | 2006-07-06 | 2008-01-10 | Ciba Holding Inc. | Encapsulated dispersions comprising electrophoretically mobile organic colorants |
| US20100311849A1 (en) * | 2006-08-23 | 2010-12-09 | Cid Centro De Investigacion Y Desarrollo Tecnologico Sa De Cv | Using Reactive Block Copolymers as Chain Extenders and Surface Modifiers |
| US7985826B2 (en) | 2006-12-22 | 2011-07-26 | Reichhold, Inc. | Molding resins using renewable resource component |
| US7396887B1 (en) | 2006-12-29 | 2008-07-08 | Bridgestone Corporation | Insitu removal of chelator from anionic polymerization reactions |
| US7737218B2 (en) | 2006-12-29 | 2010-06-15 | Bridgestone Corporation | Method for generating free radical capable polymers using tin or silicon halide compounds |
| US8030410B2 (en) | 2006-12-29 | 2011-10-04 | Bridgestone Corporation | Method for generating free radical capable polymers using carbonyl-containing compounds |
| US7560509B2 (en) | 2006-12-29 | 2009-07-14 | Bridgestone Corporation | Method of directing grafting by controlling the location of high vinyl segments in a polymer |
| CA2698832A1 (en) | 2007-09-07 | 2009-03-12 | Basf Se | Encapsulated dispersions comprising electrophoretically mobile organic colorants |
| CN106699639A (zh) * | 2016-12-22 | 2017-05-24 | 甘肃省化工研究院 | 一种光稳定剂hs‑112的合成方法 |
| WO2020094539A1 (de) * | 2018-11-05 | 2020-05-14 | Merck Patent Gmbh | In einer organischen elektronischen vorrichtung einsetzbare verbindungen |
| FR3152278A1 (fr) | 2023-08-24 | 2025-02-28 | Snf Sa | polymère hydrosoluble ramifié comme liant pour batterie |
| FR3152279A1 (fr) | 2023-08-24 | 2025-02-28 | Snf Sa | Polymere hydrosoluble comme liant pour batterie |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU571240B2 (en) | 1983-07-11 | 1988-04-14 | Commonwealth Scientific And Industrial Research Organisation | Alkoxy-amines, useful as initiators |
| JPS6089452A (ja) * | 1983-07-11 | 1985-05-20 | コモンウエルス サイエンテイフイツク アンド インダストリアル リサ−チ オ−ガニゼ−シヨン | 遊離基重合開始用化合物 |
| EP0155912A3 (de) * | 1984-03-20 | 1986-06-04 | Ciba-Geigy Ag | Strahlenstabilisierte polymere Zusammensetzungen |
| TW270131B (enExample) | 1993-07-13 | 1996-02-11 | Ciba Geigy | |
| WO1997036944A1 (en) | 1996-03-29 | 1997-10-09 | The Dow Chemical Company | In situ block copolymer formation during polymerization of a vinyl aromatic monomer |
| ATE210156T1 (de) | 1996-09-25 | 2001-12-15 | Akzo Nobel Nv | Nitroso verbindungen zur pseudo-lebenden radikalpolymerisation |
| TWI225483B (en) * | 1998-10-16 | 2004-12-21 | Ciba Sc Holding Ag | Heterocyclic alkoxyamines as regulators in controlled radical polymerization process |
-
1999
- 1999-01-18 TW TW088100735A patent/TW495515B/zh not_active IP Right Cessation
- 1999-02-26 DE DE69933020T patent/DE69933020T2/de not_active Expired - Lifetime
- 1999-02-26 WO PCT/EP1999/001233 patent/WO1999046261A1/en not_active Ceased
- 1999-02-26 EP EP99910286A patent/EP1071681B1/en not_active Expired - Lifetime
- 1999-02-26 AU AU29296/99A patent/AU2929699A/en not_active Abandoned
- 1999-02-26 CA CA002321792A patent/CA2321792C/en not_active Expired - Fee Related
- 1999-02-26 US US09/623,547 patent/US6566468B1/en not_active Expired - Fee Related
- 1999-02-26 JP JP2000535640A patent/JP4584448B2/ja not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2002506070A5 (enExample) | ||
| AU692979B2 (en) | Polymers based on block copolymers | |
| US6777513B1 (en) | Synthesis method for polymers by controlled radical polymerisation using halogenated xanthates | |
| US6878789B2 (en) | Preparation process of acrylic acid ester polymer | |
| JP2001316365A5 (enExample) | ||
| IE781059L (en) | Polysiloxane polymer, contact lens | |
| JPH09323993A5 (enExample) | ||
| CA2175655A1 (en) | Allylic chain transfer agents | |
| JP5647176B2 (ja) | 低い重合応力を有するラジカル重合性マクロ環状樹脂組成物 | |
| JP2001233915A5 (enExample) | ||
| ATE356835T1 (de) | Verfahren zur herstellung von homo- und copolymeren von ethylen | |
| AU2669401A (en) | Method for producing a composition that contains polymer ester compounds with long-chain alkyl groups, and use of such a composition | |
| ATE336520T1 (de) | Verfahren zur herstellung von homo- und copolymeren von ethylen | |
| WO2002030992A3 (en) | Multi-functional initiators for atom transfer radical (co)polymerization | |
| DE60238606D1 (de) | 4-imin-n-alkoxy- oder oxy-polyalkyl-piperidin-verboren | |
| JP2002535423A5 (enExample) | ||
| JPS591509A (ja) | 重合性高分子の製造方法 | |
| ITMI20021495A1 (it) | Procedimento per la preparazione di copolimeri a blocchi. | |
| DE60213992D1 (de) | Katalysator für die polymerisation und copolymerisation von ethylen | |
| JP2002533482A5 (enExample) | ||
| FR2879205B1 (fr) | Procede de preparation de plaques renforcees a l'impact par polymerisation radiculaire controlee | |
| GB1569027A (en) | Polymers comprising phospholene substituents | |
| FR2762604A1 (fr) | Procede et systeme d'amorcage pour la (co)polymerisation anionique de monomeres (meth)acryliques, vinylaromatiques et/ou dieniques | |
| ID20067A (id) | Proses pembuatan polimer anhidrida | |
| EP0818440A3 (en) | Azoamide compounds and their use as initiators for producing block copolymers |