JP2009508976A5 - - Google Patents
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- Publication number
- JP2009508976A5 JP2009508976A5 JP2008528465A JP2008528465A JP2009508976A5 JP 2009508976 A5 JP2009508976 A5 JP 2009508976A5 JP 2008528465 A JP2008528465 A JP 2008528465A JP 2008528465 A JP2008528465 A JP 2008528465A JP 2009508976 A5 JP2009508976 A5 JP 2009508976A5
- Authority
- JP
- Japan
- Prior art keywords
- acrylate
- alkyl
- meth
- polymer
- formula
- 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
- 229920000642 polymer Polymers 0.000 claims 13
- 125000000217 alkyl group Chemical group 0.000 claims 12
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 11
- -1 hydroxyalkyl ester Chemical class 0.000 claims 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 6
- 125000005907 alkyl ester group Chemical group 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 239000000178 monomer Substances 0.000 claims 4
- 150000003254 radicals Chemical class 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims 3
- 150000002431 hydrogen Chemical group 0.000 claims 3
- 239000003999 initiator Substances 0.000 claims 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- YLFIGGHWWPSIEG-UHFFFAOYSA-N aminoxyl Chemical group [O]N YLFIGGHWWPSIEG-UHFFFAOYSA-N 0.000 claims 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims 2
- 229920001577 copolymer Polymers 0.000 claims 2
- 239000012634 fragment Substances 0.000 claims 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 230000000379 polymerizing effect Effects 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 239000007858 starting material Substances 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 claims 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims 1
- MJPPGVVIDGQOQT-UHFFFAOYSA-N 2-bromo-5-(2-bromo-2-nitroethenyl)furan Chemical compound [O-][N+](=O)C(Br)=CC1=CC=C(Br)O1 MJPPGVVIDGQOQT-UHFFFAOYSA-N 0.000 claims 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 claims 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 claims 1
- FLCAEMBIQVZWIF-UHFFFAOYSA-N 6-(dimethylamino)-2-methylhex-2-enamide Chemical compound CN(C)CCCC=C(C)C(N)=O FLCAEMBIQVZWIF-UHFFFAOYSA-N 0.000 claims 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- 229920000028 Gradient copolymer Polymers 0.000 claims 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 1
- 150000001345 alkine derivatives Chemical class 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005262 alkoxyamine group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- LCIYFINKFGDAHD-UHFFFAOYSA-N azepane;3-nitrobenzoic acid Chemical compound C1CCCNCC1.OC(=O)C1=CC=CC([N+]([O-])=O)=C1 LCIYFINKFGDAHD-UHFFFAOYSA-N 0.000 claims 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 claims 1
- 125000004663 dialkyl amino group Chemical group 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 238000003379 elimination reaction Methods 0.000 claims 1
- 150000002191 fatty alcohols Chemical class 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 229920001519 homopolymer Polymers 0.000 claims 1
- 238000006459 hydrosilylation reaction Methods 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 229920006030 multiblock copolymer Polymers 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 claims 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- WPBNLDNIZUGLJL-UHFFFAOYSA-N prop-2-ynyl prop-2-enoate Chemical group C=CC(=O)OCC#C WPBNLDNIZUGLJL-UHFFFAOYSA-N 0.000 claims 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 claims 1
- 238000010526 radical polymerization reaction Methods 0.000 claims 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 claims 1
- 150000003440 styrenes Chemical class 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 claims 1
- 150000003672 ureas Chemical group 0.000 claims 1
- 238000009736 wetting Methods 0.000 claims 1
- 239000000080 wetting agent Substances 0.000 claims 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05107914 | 2005-08-30 | ||
| EP05107914.3 | 2005-08-30 | ||
| PCT/EP2006/065480 WO2007025885A1 (en) | 2005-08-30 | 2006-08-21 | Polymers obtained via nitroxyl radical polymerization |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009508976A JP2009508976A (ja) | 2009-03-05 |
| JP2009508976A5 true JP2009508976A5 (enExample) | 2009-10-08 |
| JP5399071B2 JP5399071B2 (ja) | 2014-01-29 |
Family
ID=35124618
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008528465A Expired - Fee Related JP5399071B2 (ja) | 2005-08-30 | 2006-08-21 | ニトロキシルラジカル重合により得られるポリマー |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7858694B2 (enExample) |
| EP (1) | EP1919962B1 (enExample) |
| JP (1) | JP5399071B2 (enExample) |
| KR (1) | KR101365953B1 (enExample) |
| CN (1) | CN100549034C (enExample) |
| AT (1) | ATE465183T1 (enExample) |
| BR (1) | BRPI0615603A2 (enExample) |
| DE (1) | DE602006013841D1 (enExample) |
| RU (1) | RU2425057C2 (enExample) |
| WO (1) | WO2007025885A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5539647B2 (ja) | 2005-05-26 | 2014-07-02 | チバ ホールディング インコーポレーテッド | スリップ及びレベリング剤 |
| ATE461230T1 (de) | 2006-05-18 | 2010-04-15 | Basf Se | Slip- und verlaufmittel |
| WO2009085754A1 (en) * | 2007-12-27 | 2009-07-09 | Bausch & Lomb Incorporated | Segmented interactive block copolymers |
| WO2009085759A1 (en) * | 2007-12-27 | 2009-07-09 | Bausch & Lomb Incorporated | Segmented reactive block copolymers |
| WO2009149001A1 (en) * | 2008-06-06 | 2009-12-10 | Union Carbide Chemicals & Plastics Technology Llc | Method for inhibiting scorch in crosslinkable compositions |
| DE102011005493A1 (de) * | 2011-03-14 | 2012-09-20 | Evonik Rohmax Additives Gmbh | Estergruppen-umfassende Copolymere und deren Verwendung in Schmiermitteln |
| FR3030525B1 (fr) * | 2014-12-18 | 2018-05-11 | Arkema France | Polymerisation radicalaire d'alcoxyamines a basse temperature |
| RU2642780C1 (ru) * | 2017-03-06 | 2018-01-26 | Федеральное государственное автономное образовательное учреждение высшего образования "Национальный исследовательский Нижегородский государственный университет им. Н.И. Лобачевского" | Способ получения линейных блок-сополимеров (мет)акриловых мономеров |
| WO2021209349A1 (en) * | 2020-04-14 | 2021-10-21 | Basf Se | An amine-modified polymer, a controlled free radical polymerization for preparing the same and implementations thereof |
| CN117062872A (zh) * | 2021-03-26 | 2023-11-14 | 巴斯夫欧洲公司 | 作为分散剂的包含聚丙烯酸系嵌段共聚物和芳族基聚氧化烯的聚合物组合物 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3486145T2 (de) * | 1983-07-11 | 1993-09-23 | Commw Scient Ind Res Org | Verfahren zur polymerisation und nach diesem verfahren hergestellte polymere. |
| RU2171262C2 (ru) * | 1995-11-04 | 2001-07-27 | Акцо Нобель Н.В. | Способ радикальной (со)полимеризации |
| US5844025A (en) * | 1996-12-02 | 1998-12-01 | Ciba Specialty Chemicals Corporation | 1,2-Bis-adducts of stable nitroxides with substituted ethylenes and stabilized compositions |
| US6281311B1 (en) * | 1997-03-31 | 2001-08-28 | Pmd Holdings Corp. | Controlled free radical polymerization process |
| FR2764892B1 (fr) * | 1997-06-23 | 2000-03-03 | Rhodia Chimie Sa | Procede de synthese de polymeres a blocs |
| CH693416A5 (de) * | 1998-03-09 | 2003-07-31 | Ciba Sc Holding Ag | 1-Alkoxypolyalkylpiperidinderivate und ihre Verwendung als Polymerisationsregler. |
| JP2001026610A (ja) | 1999-05-11 | 2001-01-30 | Sankyo Co Ltd | ポリマー製造方法及び重合メディエイター |
| TWI236482B (en) * | 2000-11-13 | 2005-07-21 | Ciba Sc Holding Ag | Process for the (co)polymerization of vinyl chloride in the presence of a stable free nitroxyl radical |
| ITMI20021495A1 (it) * | 2002-07-09 | 2002-10-08 | Polimeri Europa Spa | Procedimento per la preparazione di copolimeri a blocchi. |
| DE10236133A1 (de) * | 2002-08-07 | 2004-02-26 | Byk-Chemie Gmbh | Verwendung von Gradientencopolymeren als Dispergiermittel zur Behandlung von Pigmenten und Feststoffen |
| KR101123607B1 (ko) * | 2003-12-10 | 2012-03-21 | 시바 홀딩 인크 | 니트록실 매개되는 중합반응에 의해 제조된 균전제를함유하는 피복 조성물 |
-
2006
- 2006-08-21 AT AT06792913T patent/ATE465183T1/de not_active IP Right Cessation
- 2006-08-21 EP EP06792913A patent/EP1919962B1/en not_active Expired - Lifetime
- 2006-08-21 KR KR1020087007652A patent/KR101365953B1/ko not_active Expired - Fee Related
- 2006-08-21 DE DE602006013841T patent/DE602006013841D1/de not_active Expired - Lifetime
- 2006-08-21 WO PCT/EP2006/065480 patent/WO2007025885A1/en not_active Ceased
- 2006-08-21 US US11/991,113 patent/US7858694B2/en active Active
- 2006-08-21 BR BRPI0615603-7A patent/BRPI0615603A2/pt not_active IP Right Cessation
- 2006-08-21 RU RU2008111984/04A patent/RU2425057C2/ru not_active IP Right Cessation
- 2006-08-21 CN CNB2006800313917A patent/CN100549034C/zh not_active Expired - Fee Related
- 2006-08-21 JP JP2008528465A patent/JP5399071B2/ja not_active Expired - Fee Related
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