JP2002525398A5 - - Google Patents
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- JP2002525398A5 JP2002525398A5 JP2000572265A JP2000572265A JP2002525398A5 JP 2002525398 A5 JP2002525398 A5 JP 2002525398A5 JP 2000572265 A JP2000572265 A JP 2000572265A JP 2000572265 A JP2000572265 A JP 2000572265A JP 2002525398 A5 JP2002525398 A5 JP 2002525398A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- aliphatic
- aromatic
- polymer
- 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
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- 229920000642 polymer Polymers 0.000 description 13
- 125000001931 aliphatic group Chemical group 0.000 description 12
- 239000000178 monomer Substances 0.000 description 12
- -1 amidino, 2-imidazolyl Chemical group 0.000 description 10
- 239000012634 fragment Substances 0.000 description 9
- 125000003118 aryl group Chemical group 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 239000003505 polymerization initiator Substances 0.000 description 6
- 125000002723 alicyclic group Chemical group 0.000 description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 5
- 239000003999 initiator Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 4
- 238000010560 atom transfer radical polymerization reaction Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- 230000000977 initiatory effect Effects 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
- 125000001589 carboacyl group Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- 125000006839 xylylene group Chemical group 0.000 description 2
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000002993 cycloalkylene group Chemical group 0.000 description 1
- 125000003073 divalent carboacyl group Chemical group 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Chemical group 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98810979.9 | 1998-09-29 | ||
| EP98810979 | 1998-09-29 | ||
| PCT/EP1999/006924 WO2000018807A1 (en) | 1998-09-29 | 1999-09-18 | Process for the preparation of polymers containing n→o terminal groups |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002525398A JP2002525398A (ja) | 2002-08-13 |
| JP2002525398A5 true JP2002525398A5 (enExample) | 2006-11-02 |
| JP4593786B2 JP4593786B2 (ja) | 2010-12-08 |
Family
ID=8236358
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000572265A Expired - Lifetime JP4593786B2 (ja) | 1998-09-29 | 1999-09-18 | Ｎ→ｏ末端基を含むポリマーの製造方法 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6433100B1 (enExample) |
| EP (1) | EP1153043B1 (enExample) |
| JP (1) | JP4593786B2 (enExample) |
| KR (1) | KR100559974B1 (enExample) |
| AT (1) | ATE279447T1 (enExample) |
| AU (1) | AU752451B2 (enExample) |
| BR (1) | BR9914104A (enExample) |
| CA (1) | CA2341384A1 (enExample) |
| DE (1) | DE69921194T2 (enExample) |
| WO (1) | WO2000018807A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1254185A1 (en) | 2000-01-11 | 2002-11-06 | Ciba SC Holding AG | Comb polymers from atrp macromonomers |
| FR2807439B1 (fr) * | 2000-04-07 | 2003-06-13 | Atofina | Polymeres multimodaux par polymerisation radicalaire controlee en presence d'alcoxyamines |
| US6740712B2 (en) * | 2001-01-29 | 2004-05-25 | Boehringer Ingelheim Pharma Kg | Polymers based on N-carbamyl-N'-dimethylsilyl methyl-piperazine traceless linkers for the solid phase synthesis of phenyl based libraries |
| US6849679B2 (en) | 2001-05-21 | 2005-02-01 | Ciba Specialty Chemicals Corporation | Pigment compositions with modified block copolymer dispersants |
| US6689844B2 (en) * | 2001-05-29 | 2004-02-10 | Rohmax Additives Gmbh | Process for synthesis of polymer compositions with reduced halogen content, polymer composition with reduced halogen content as well as use of this composition |
| US6787279B2 (en) | 2001-06-20 | 2004-09-07 | Lexmark International, Inc. | Random copolymers used as compatibilizers in toner compositions |
| DE60223689T2 (de) | 2001-07-05 | 2008-10-30 | Ciba Holding Inc. | Multifunktionale alkoxyamine auf grundlage von polyalkylpiperidinen, polyalkylpiperazinonen und polyalkylmorpholinonen, und deren verwendung als polymerisationsregulatoren/-initiatoren |
| WO2003095512A1 (en) * | 2002-05-08 | 2003-11-20 | Ciba Specialty Chemicals Holding Inc. | Polymers produced by atom transfer radical polymerisation technique with structurally modified terminal groups |
| CN100516155C (zh) * | 2003-12-10 | 2009-07-22 | 西巴特殊化学品控股有限公司 | 包含由硝酰基介导的聚合制备的流平剂的涂料组合物 |
| US20050184304A1 (en) * | 2004-02-25 | 2005-08-25 | Gupta Pavan O. | Large cavity wafer-level package for MEMS |
| JP5211439B2 (ja) * | 2005-06-21 | 2013-06-12 | 三菱化学株式会社 | ビニル系モノマーの重合方法及び重合体の製造方法 |
| US7517928B2 (en) * | 2005-11-07 | 2009-04-14 | Xerox Corporation | Siloxane-acrylate interpenetrating networks and methods for producing the same |
| EP2118150B1 (en) | 2007-02-14 | 2015-09-23 | Biocompatibles UK Limited | Derivatisation of biological molecules |
| WO2009077396A1 (en) * | 2007-12-18 | 2009-06-25 | Basf Se | Biodiesel cold flow improver |
| EP2260873B1 (en) | 2009-06-08 | 2019-07-24 | Biocompatibles UK Limited | Pcylation of proteins |
| CN102010490B (zh) * | 2010-10-12 | 2014-04-16 | 浙江大学 | 一种可降解多嵌段聚合物的制备方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| AU571240B2 (en) * | 1983-07-11 | 1988-04-14 | Commonwealth Scientific And Industrial Research Organisation | Alkoxy-amines, useful as initiators |
| US5322912A (en) * | 1992-11-16 | 1994-06-21 | Xerox Corporation | Polymerization processes and toner compositions therefrom |
| US5910549A (en) | 1996-08-22 | 1999-06-08 | Carnegie-Mellon University | Method for preparation of alkoxyamines from nitroxyl radicals |
| AU4773997A (en) | 1996-09-25 | 1998-04-17 | Akzo Nobel N.V. | No-compounds for pseudo-living radical polymerization |
| JPH10130314A (ja) * | 1996-10-25 | 1998-05-19 | Asahi Glass Co Ltd | ポリフルオロアルキル基含有ポリマーの製造法 |
| JPH10130347A (ja) * | 1996-10-25 | 1998-05-19 | Asahi Glass Co Ltd | ポリマーの製造法 |
| DE69710163T2 (de) * | 1996-12-02 | 2002-10-02 | Ondeo Nalco Energy Services, L.P. | Hemmung der Polymerisation von vinylaromatischen Monomeren |
| US6271340B1 (en) * | 1997-01-10 | 2001-08-07 | E. I. Du Pont De Nemours And Company | Method of controlling polymer molecular weight and structure |
| US6274683B1 (en) * | 1999-06-30 | 2001-08-14 | Uniroyal Chemical Company, Inc. | Test method for evaluating soluble polymer growth when recycling inhibitor streams |
-
1999
- 1999-09-18 AU AU59794/99A patent/AU752451B2/en not_active Ceased
- 1999-09-18 CA CA002341384A patent/CA2341384A1/en not_active Abandoned
- 1999-09-18 KR KR1020017003845A patent/KR100559974B1/ko not_active Expired - Fee Related
- 1999-09-18 BR BR9914104-3A patent/BR9914104A/pt not_active Application Discontinuation
- 1999-09-18 AT AT99969724T patent/ATE279447T1/de not_active IP Right Cessation
- 1999-09-18 US US09/763,432 patent/US6433100B1/en not_active Expired - Lifetime
- 1999-09-18 DE DE69921194T patent/DE69921194T2/de not_active Expired - Lifetime
- 1999-09-18 JP JP2000572265A patent/JP4593786B2/ja not_active Expired - Lifetime
- 1999-09-18 EP EP99969724A patent/EP1153043B1/en not_active Expired - Lifetime
- 1999-09-18 WO PCT/EP1999/006924 patent/WO2000018807A1/en not_active Ceased
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