JP2005524743A5 - - Google Patents
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- Publication number
- JP2005524743A5 JP2005524743A5 JP2004503522A JP2004503522A JP2005524743A5 JP 2005524743 A5 JP2005524743 A5 JP 2005524743A5 JP 2004503522 A JP2004503522 A JP 2004503522A JP 2004503522 A JP2004503522 A JP 2004503522A JP 2005524743 A5 JP2005524743 A5 JP 2005524743A5
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- alkyl
- acrylic acid
- group
- ester
- 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
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 30
- 125000004432 carbon atom Chemical group C* 0.000 claims 24
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 22
- -1 alkyl acrylic acid Chemical compound 0.000 claims 14
- 229910052799 carbon Inorganic materials 0.000 claims 14
- 229920000642 polymer Polymers 0.000 claims 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 9
- 125000005250 alkyl acrylate group Chemical group 0.000 claims 6
- 125000005907 alkyl ester group Chemical group 0.000 claims 5
- 239000000178 monomer Substances 0.000 claims 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 229920001400 block copolymer Polymers 0.000 claims 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 3
- 239000000654 additive Substances 0.000 claims 3
- 230000000996 additive effect Effects 0.000 claims 3
- 239000003963 antioxidant agent Substances 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 238000010560 atom transfer radical polymerization reaction Methods 0.000 claims 3
- 150000001721 carbon Chemical group 0.000 claims 3
- 239000000314 lubricant Substances 0.000 claims 3
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 claims 2
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims 2
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 claims 2
- BEWCNXNIQCLWHP-UHFFFAOYSA-N 2-(tert-butylamino)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCNC(C)(C)C BEWCNXNIQCLWHP-UHFFFAOYSA-N 0.000 claims 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 2
- 239000005069 Extreme pressure additive Substances 0.000 claims 2
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 claims 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 239000007866 anti-wear additive Substances 0.000 claims 2
- 230000007797 corrosion Effects 0.000 claims 2
- 238000005260 corrosion Methods 0.000 claims 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
- 125000004185 ester group Chemical group 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 239000012634 fragment Substances 0.000 claims 2
- 239000001530 fumaric acid Substances 0.000 claims 2
- 239000003112 inhibitor Substances 0.000 claims 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 2
- 239000011976 maleic acid Substances 0.000 claims 2
- 239000006078 metal deactivator Substances 0.000 claims 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims 2
- 239000003505 polymerization initiator Substances 0.000 claims 2
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims 2
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims 1
- QLMGIWHWWWXXME-UHFFFAOYSA-N 2-(3,5-ditert-butyl-4-hydroxyphenyl)acetic acid Chemical compound CC(C)(C)C1=CC(CC(O)=O)=CC(C(C)(C)C)=C1O QLMGIWHWWWXXME-UHFFFAOYSA-N 0.000 claims 1
- QHVBLSNVXDSMEB-UHFFFAOYSA-N 2-(diethylamino)ethyl prop-2-enoate Chemical compound CCN(CC)CCOC(=O)C=C QHVBLSNVXDSMEB-UHFFFAOYSA-N 0.000 claims 1
- KDAKDBASXBEFFK-UHFFFAOYSA-N 2-(tert-butylamino)ethyl prop-2-enoate Chemical compound CC(C)(C)NCCOC(=O)C=C KDAKDBASXBEFFK-UHFFFAOYSA-N 0.000 claims 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims 1
- DBHUTHZPCWZNRW-UHFFFAOYSA-N 3-(3,5-dicyclohexyl-4-hydroxyphenyl)propanoic acid Chemical compound OC=1C(C2CCCCC2)=CC(CCC(=O)O)=CC=1C1CCCCC1 DBHUTHZPCWZNRW-UHFFFAOYSA-N 0.000 claims 1
- FLZYQMOKBVFXJS-UHFFFAOYSA-N 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoic acid Chemical compound CC1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O FLZYQMOKBVFXJS-UHFFFAOYSA-N 0.000 claims 1
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical class C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 claims 1
- LBSXSAXOLABXMF-UHFFFAOYSA-N 4-Vinylaniline Chemical compound NC1=CC=C(C=C)C=C1 LBSXSAXOLABXMF-UHFFFAOYSA-N 0.000 claims 1
- GQWAOUOHRMHSHL-UHFFFAOYSA-N 4-ethenyl-n,n-dimethylaniline Chemical compound CN(C)C1=CC=C(C=C)C=C1 GQWAOUOHRMHSHL-UHFFFAOYSA-N 0.000 claims 1
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- 229930185605 Bisphenol Natural products 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 230000003213 activating effect Effects 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 150000001350 alkyl halides Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000004103 aminoalkyl group Chemical group 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- 230000015556 catabolic process Effects 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 239000003610 charcoal Substances 0.000 claims 1
- 238000004132 cross linking Methods 0.000 claims 1
- 238000006731 degradation reaction Methods 0.000 claims 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 1
- 125000003827 glycol group Chemical group 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 230000000977 initiatory effect Effects 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 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
- 235000019260 propionic acid Nutrition 0.000 claims 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims 1
- 238000010526 radical polymerization reaction Methods 0.000 claims 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims 1
- 125000005353 silylalkyl group Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02405377 | 2002-05-08 | ||
| PCT/EP2003/004449 WO2003095512A1 (en) | 2002-05-08 | 2003-04-29 | Polymers produced by atom transfer radical polymerisation technique with structurally modified terminal groups |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005524743A JP2005524743A (ja) | 2005-08-18 |
| JP2005524743A5 true JP2005524743A5 (https=) | 2006-06-22 |
| JP4490260B2 JP4490260B2 (ja) | 2010-06-23 |
Family
ID=29414850
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004503522A Expired - Fee Related JP4490260B2 (ja) | 2002-05-08 | 2003-04-29 | 構造的に変性された末端基を使用した、原子移動ラジカル重合技術により製造されたポリマー |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7615522B2 (https=) |
| EP (1) | EP1501881B1 (https=) |
| JP (1) | JP4490260B2 (https=) |
| KR (1) | KR100956565B1 (https=) |
| CN (1) | CN1294172C (https=) |
| AT (1) | ATE462740T1 (https=) |
| AU (1) | AU2003229749B2 (https=) |
| BR (1) | BR0309831B1 (https=) |
| CA (1) | CA2483030C (https=) |
| DE (1) | DE60331906D1 (https=) |
| ES (1) | ES2342374T3 (https=) |
| TW (1) | TWI338696B (https=) |
| WO (1) | WO2003095512A1 (https=) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5078087B2 (ja) * | 2004-10-25 | 2012-11-21 | ザ ルブリゾル コーポレイション | 星形重合体およびそれらの組成物 |
| DE102005041528A1 (de) * | 2005-08-31 | 2007-03-01 | Rohmax Additives Gmbh | Öllösliche Polymere |
| WO2007127661A1 (en) * | 2006-04-24 | 2007-11-08 | The Lubrizol Corporation | Star polymer lubricating composition |
| ES2589952T3 (es) * | 2006-04-24 | 2016-11-17 | The Lubrizol Corporation | Composición lubricante de polímero de estrella |
| DE102008043674A1 (de) * | 2008-11-12 | 2010-05-20 | Evonik Röhm Gmbh | Verfahren zur Herstellung von Telechelen mit einer bimodalen Molekulkargewichtsverteilung |
| US8802606B2 (en) | 2010-08-06 | 2014-08-12 | Basf Se | Lubricant composition having improved antiwear properties |
| RU2545078C2 (ru) | 2009-08-07 | 2015-03-27 | Басф Се | Смазочная композиция, включающая алкилэфиркарбоновую кислоту |
| CN101845129B (zh) * | 2010-05-21 | 2012-07-04 | 中科院广州化学有限公司 | 有机硅(甲基)丙烯酸酯aba型嵌段共聚物及其制备方法和应用 |
| US8796189B2 (en) | 2011-10-14 | 2014-08-05 | Chevron U.S.A. Inc. | Gear lubricant |
| JP5822706B2 (ja) * | 2011-12-13 | 2015-11-24 | 株式会社Adeka | 潤滑油用摩擦摩耗低減剤及びそれを含有する潤滑油組成物 |
| US8802235B2 (en) | 2012-01-18 | 2014-08-12 | University Of Kansas | Drug and imaging agent delivery compositions and methods |
| CN103492441B (zh) * | 2012-02-03 | 2016-06-29 | 西奥公司 | 接枝到pvdf上的丙烯腈 |
| CN102861558B (zh) * | 2012-09-24 | 2014-06-04 | 浙江工商大学 | 聚丙烯腈螯合树脂金属吸附材料的制备方法 |
| CN103709335B (zh) * | 2013-12-27 | 2016-03-16 | 齐鲁工业大学 | pH响应接枝共聚物及其制备方法和用途 |
| CN103880996B (zh) * | 2014-01-13 | 2016-08-17 | 盐城工学院 | 聚4-乙烯基吡啶以及基于反相细乳液aget atrp体系合成聚4-乙烯基吡啶的方法 |
| CN109642179B (zh) * | 2016-08-15 | 2021-10-08 | 赢创运营有限公司 | 具有增强的破乳性能的官能聚(甲基)丙烯酸烷基酯 |
| CN106263924A (zh) * | 2016-08-25 | 2017-01-04 | 费孝锋 | 一种改良结构的桌布 |
| CN106213925A (zh) * | 2016-08-25 | 2016-12-14 | 费孝锋 | 一种改进后的餐桌布 |
| CN109134788B (zh) * | 2017-06-28 | 2022-03-11 | 中国石油化工股份有限公司 | 一种端羧基sbs、制备及其在沥青改性中的应用 |
| CN107880229B (zh) * | 2017-12-08 | 2020-12-15 | 万华化学集团股份有限公司 | 一种端基改性的聚丙烯酸酯嵌段共聚物的制备方法及其制得的聚丙烯酸酯嵌段共聚物 |
| CN108755141B (zh) * | 2018-06-29 | 2021-03-12 | 乌鲁木齐市华泰隆化学助剂有限公司 | 一种粘胶纤维纺丝油剂及其制备方法 |
| CN113121778B (zh) * | 2021-05-06 | 2022-08-05 | 福建师范大学泉港石化研究院 | 一种含有改性石墨烯的聚氨酯阻燃发泡材料及其制备方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0420793B1 (de) * | 1989-08-30 | 1993-11-10 | Ciba-Geigy Ag | Phenolische Verbindungen als Kettenabbrecher für die anionische Lösungspolymerisation von Dienen |
| CN1137938C (zh) * | 1997-07-28 | 2004-02-11 | 钟渊化学工业株式会社 | 可固化的粘合剂组合物 |
| WO1999007803A1 (fr) * | 1997-08-06 | 1999-02-18 | Kaneka Corporation | Composition auto-adhesive |
| CA2268950A1 (en) * | 1997-08-19 | 1999-02-25 | Infineum Holdings Bv | Functionalized polymers |
| ATE279447T1 (de) * | 1998-09-29 | 2004-10-15 | Ciba Sc Holding Ag | Verfahren zur herstellung von polymeren enthaltend endständige n-0 gruppen |
| US6403746B1 (en) * | 1999-11-30 | 2002-06-11 | Rohmax Additives Gmbh | Method for preparation of a composition that contains polymer ester compounds with long-chain alkyl residues and use of this composition |
| DE10052646A1 (de) * | 2000-10-24 | 2002-05-16 | Boettcher Henrik | Verfahren zur Herstellung von Funktionspolymeren sowie Schichten aus Funktionspolymeren auf Festkörperoberflächen über "lebende"/kontrollierte radikalische Polymerisation |
| US6576722B2 (en) * | 2000-12-13 | 2003-06-10 | Ppg Industries Ohio, Inc. | Acrylic-halogenated polyolefin copolymer adhesion promoters |
-
2003
- 2003-04-29 EP EP03722569A patent/EP1501881B1/en not_active Expired - Lifetime
- 2003-04-29 DE DE60331906T patent/DE60331906D1/de not_active Expired - Lifetime
- 2003-04-29 BR BRPI0309831-1B1A patent/BR0309831B1/pt not_active IP Right Cessation
- 2003-04-29 US US10/513,837 patent/US7615522B2/en not_active Expired - Fee Related
- 2003-04-29 CN CNB038103397A patent/CN1294172C/zh not_active Expired - Fee Related
- 2003-04-29 KR KR1020047017758A patent/KR100956565B1/ko not_active Expired - Fee Related
- 2003-04-29 ES ES03722569T patent/ES2342374T3/es not_active Expired - Lifetime
- 2003-04-29 AT AT03722569T patent/ATE462740T1/de not_active IP Right Cessation
- 2003-04-29 CA CA2483030A patent/CA2483030C/en not_active Expired - Fee Related
- 2003-04-29 JP JP2004503522A patent/JP4490260B2/ja not_active Expired - Fee Related
- 2003-04-29 AU AU2003229749A patent/AU2003229749B2/en not_active Ceased
- 2003-04-29 WO PCT/EP2003/004449 patent/WO2003095512A1/en not_active Ceased
- 2003-05-06 TW TW092112307A patent/TWI338696B/zh not_active IP Right Cessation
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