JP2007224303A5 - - Google Patents

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Publication number
JP2007224303A5
JP2007224303A5 JP2007041079A JP2007041079A JP2007224303A5 JP 2007224303 A5 JP2007224303 A5 JP 2007224303A5 JP 2007041079 A JP2007041079 A JP 2007041079A JP 2007041079 A JP2007041079 A JP 2007041079A JP 2007224303 A5 JP2007224303 A5 JP 2007224303A5
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Japan
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nitrile rubber
alkyl
aryl
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JP2007041079A
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Japanese (ja)
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JP5618455B2 (ja
JP2007224303A (ja
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Priority claimed from DE102006008521A external-priority patent/DE102006008521A1/de
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JP2007041079A 2006-02-22 2007-02-21 ニトリルゴムのメタセシスのための増大された活性を有する触媒の使用 Active JP5618455B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102006008521A DE102006008521A1 (de) 2006-02-22 2006-02-22 Verwendung von Katalysatoren mit erhöhter Aktivität für die NBR-Metathese
DE102006008521.3 2006-02-22

Publications (3)

Publication Number Publication Date
JP2007224303A JP2007224303A (ja) 2007-09-06
JP2007224303A5 true JP2007224303A5 (enExample) 2010-02-18
JP5618455B2 JP5618455B2 (ja) 2014-11-05

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ID=38068324

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JP2007041079A Active JP5618455B2 (ja) 2006-02-22 2007-02-21 ニトリルゴムのメタセシスのための増大された活性を有する触媒の使用

Country Status (11)

Country Link
US (4) US8609782B2 (enExample)
EP (1) EP1826220B1 (enExample)
JP (1) JP5618455B2 (enExample)
KR (1) KR101367536B1 (enExample)
CN (2) CN102199311A (enExample)
AT (1) ATE492567T1 (enExample)
BR (1) BRPI0700452A (enExample)
DE (2) DE102006008521A1 (enExample)
MX (1) MX2007002174A (enExample)
PL (1) PL1826220T3 (enExample)
TW (1) TWI402275B (enExample)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102006008520A1 (de) * 2006-02-22 2007-08-23 Lanxess Deutschland Gmbh Neue Katalysator-Systeme und deren Verwendung für Metathese-Reaktionen
DE102006008521A1 (de) * 2006-02-22 2007-08-23 Lanxess Deutschland Gmbh Verwendung von Katalysatoren mit erhöhter Aktivität für die NBR-Metathese
DE102006040569A1 (de) * 2006-08-30 2008-03-06 Lanxess Deutschland Gmbh Verfahren zum Metathese-Abbau von Nitrilkautschuken
DE102007039525A1 (de) * 2007-08-21 2009-02-26 Lanxess Deutschland Gmbh Verfahren zum Metathese-Abbau von Nitrilkautschuk
EP2143489A1 (de) * 2008-07-08 2010-01-13 Lanxess Deutschland GmbH Katalysator-Systeme und deren Verwendung für Metathese-Reaktionen
EP2289623A1 (en) * 2009-08-31 2011-03-02 LANXESS Deutschland GmbH Metathesis of nitrile rubbers in the presence of transition metal catalysts
WO2011023771A1 (en) * 2009-08-31 2011-03-03 Lanxess Deutschland Gmbh Vulcanizable polymer composition comprising a low molecular weight optionally hydrogenated nitrile rubber
EP2289621A1 (en) * 2009-08-31 2011-03-02 LANXESS Deutschland GmbH Process for the preparation of low molecular weight hydrogenated nitrile rubber
EP2289622A1 (en) * 2009-08-31 2011-03-02 LANXESS Deutschland GmbH Ruthenium based catalysts for the metathesis of nitrile rubbers
IN2012DN02284A (enExample) 2009-09-17 2015-08-21 Lanxess Deutschland Gmbh
EP2385074A1 (de) * 2010-05-07 2011-11-09 LANXESS Deutschland GmbH Nitrilkautschuke und deren Herstellung in organischen Lösungsmitteln
EP2298824A1 (de) * 2009-09-17 2011-03-23 LANXESS Deutschland GmbH Nitrilkautschuke und deren Herstellung in organischen Lösungsmitteln
WO2011079439A1 (en) * 2009-12-30 2011-07-07 Zannan Scitech Co., Ltd. Highly active metathesis catalysts selective for romp and rcm reactions
KR101589353B1 (ko) * 2010-07-28 2016-01-27 란세스 도이치란트 게엠베하 디엔-기재 중합체의 수소화
EP2418225A1 (de) 2010-08-09 2012-02-15 LANXESS Deutschland GmbH Teilhydrierte Nitrilkautschuke
EP2484700B1 (de) 2011-02-04 2013-10-09 LANXESS Deutschland GmbH Funktionalisierte Nitrilkautschuke und ihre Herstellung
WO2013056400A1 (en) * 2011-10-21 2013-04-25 Lanxess Deutschland Gmbh Catalyst compositions and their use for hydrogenation of nitrile rubber
CN104023845B (zh) * 2011-10-21 2016-10-05 朗盛德国有限责任公司 包括格鲁布斯-荷维达型络合物和末端烯烃的催化剂组合物及其用于氢化丁腈橡胶的用途
EP2676969B1 (en) * 2012-06-22 2016-06-01 University Of Waterloo Tandem metathesis and hydrogenation of diene-based polymers in latex
EP2725030A1 (en) 2012-10-29 2014-04-30 Umicore AG & Co. KG Ruthenium-based metathesis catalysts, precursors for their preparation and their use
TWI566835B (zh) 2014-12-25 2017-01-21 財團法人工業技術研究院 烯烴複分解觸媒及低分子量丁腈橡膠之製備方法
JP7248677B2 (ja) * 2017-12-08 2023-03-29 アランセオ・ドイチュランド・ゲーエムベーハー ルテニウム錯体触媒を使用してニトリルゴムを製造するためのプロセス
CN112088044B (zh) 2018-04-27 2023-10-24 阿朗新科德国有限责任公司 钌和锇催化剂用于丁腈橡胶复分解的用途
WO2020020629A1 (en) 2018-07-23 2020-01-30 Arlanxeo Deutschland Gmbh Use of catalysts for the metathesis of nitrile rubber
CN113164941B (zh) * 2018-12-12 2023-12-12 阿朗新科德国有限责任公司 含复分解催化剂和至少一种酚类化合物的催化剂体系及使用催化剂体系进行丁腈橡胶(nbr)的复分解的方法
US11827726B2 (en) 2018-12-17 2023-11-28 Arlanxeo Deutschland Gmbh Process for producing PEG acrylate-HNBR copolymer

Family Cites Families (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3700637A (en) * 1970-05-08 1972-10-24 Shell Oil Co Diene-nitrile rubbers
DE2539132C2 (de) 1975-09-03 1987-04-09 Bayer Ag, 5090 Leverkusen Verwendung hydrierter Dien-Copolymere als temperaturbeständige Materialien auf dem Dichtungssektor
CA1220300A (en) * 1982-12-08 1987-04-07 Polysar Limited Polymer hydrogenation process
CA1203047A (en) * 1982-12-08 1986-04-08 Hormoz Azizian Polymer hydrogenation process
DE3329974A1 (de) * 1983-08-19 1985-02-28 Bayer Ag, 5090 Leverkusen Herstellung von hydrierten nitrilkautschuken
DE3433392A1 (de) * 1984-09-12 1986-03-20 Bayer Ag, 5090 Leverkusen Hydrierung nitrilgruppenhaltiger ungesaettigter polymerer
DE3529252A1 (de) * 1985-08-16 1987-02-19 Bayer Ag Verfahren zur selektiven hydrierung ungesaettigter verbindungen
DE3540918A1 (de) * 1985-11-19 1987-05-21 Bayer Ag Verfahren zur selektiven hydrierung ungesaettigter verbindungen
DE3541689A1 (de) * 1985-11-26 1987-05-27 Bayer Ag Verfahren zur selektiven hydrierung nitrilgruppenhaltiger ungesaettigter polymerer
US4816525A (en) 1987-07-06 1989-03-28 University Of Waterloo Polymer hydrogenation process
DE3932019C1 (enExample) 1989-09-26 1991-05-08 Bayer Ag, 5090 Leverkusen, De
DE4025781A1 (de) 1990-08-15 1992-02-20 Bayer Ag Hydrierte butadien/isopren/(meth-)acrylnitril- copolymerisate
DE4032597A1 (de) * 1990-10-13 1992-04-16 Bayer Ag Rueckgewinnung von hydrierkatalysatoren aus loesungen von hydriertem nitrilkautschuk
CA2196061C (en) 1992-04-03 2000-06-13 Robert H. Grubbs High activity ruthenium or osmium metal carbene complexes for olefin metathesis reactions and synthesis thereof
US5831108A (en) 1995-08-03 1998-11-03 California Institute Of Technology High metathesis activity ruthenium and osmium metal carbene complexes
US6403802B1 (en) * 1998-09-10 2002-06-11 University Of New Orleans Research & Technology Foundation Use of catalyst system comprising nickel, palladium, or platinum and imidazoline-2-ylidene or imidazolidine-2-ylidene in amination reactions
JP4410422B2 (ja) 1999-05-24 2010-02-03 カリフォルニア インスティチュート オブ テクノロジー イミダゾリジンに基づく金属カルベンメタセシス触媒
WO2002000590A1 (en) * 2000-06-23 2002-01-03 California Institute Of Technology Synthesis of functionalized and unfunctionalized olefins via cross and ring-closing metathesis
CA2419485C (en) * 2000-08-10 2007-10-30 The Trustees Of Boston College Recyclable metathesis catalysts
CA2329844A1 (en) * 2000-12-28 2002-06-28 Bayer Inc. Esbo enhanced hydrogenation
US6838489B2 (en) * 2001-03-23 2005-01-04 Cymetech, Llc High activity metal carbene metathesis catalysts generated using a thermally activated N-heterocyclic carbene precursor
TW593386B (en) 2001-06-12 2004-06-21 Bayer Inc Process for the preparation of low molecular weight hydrogenated nitrile rubber
CA2350280A1 (en) 2001-06-12 2002-12-12 Bayer Inc. Low molecular weight hydrogenated nitrile rubber
US6841623B2 (en) 2001-06-29 2005-01-11 Bayer Inc. Low molecular weight nitrile rubber
EP1455937B1 (en) * 2001-11-15 2018-04-11 Materia, Inc. Chelating carbene ligand precursors and their use in the synthesis of metathesis catalysts
PL199412B1 (pl) * 2002-10-15 2008-09-30 Boehringer Ingelheim Int Nowe kompleksy rutenu jako (pre)katalizatory reakcji metatezy, pochodne 2-alkoksy-5-nitrostyrenu jako związki pośrednie i sposób ich wytwarzania
CA2409434A1 (en) * 2002-10-17 2004-04-17 Bayer Inc. Polymer blends comprising low molecular weight nitrile rubber
CA2413607A1 (en) * 2002-12-05 2004-06-05 Bayer Inc. Process for the preparation of low molecular weight hydrogenated nitrile rubber
CA2462005A1 (en) * 2004-02-23 2005-08-23 Bayer Inc. Process for the preparation of low molecular weight hydrogenated nitrile rubber
CA2462011A1 (en) * 2004-02-23 2005-08-23 Bayer Inc. Process for the preparation of low molecular weight nitrile rubber
KR101269568B1 (ko) * 2005-07-04 2013-06-04 자난 사이텍 컴퍼니 리미티드 루테늄 착물 리간드, 루테늄 착물, 고정 루테늄 착물 촉매및 그의 제조방법과 용도
EP1757623A1 (en) * 2005-07-14 2007-02-28 Lanxess Inc. Process for the preparation of low mooney nitrile terpolymers
ATE538139T1 (de) * 2005-08-30 2012-01-15 Lanxess Deutschland Gmbh Verwendung von katalysatoren für den metatheseabbau von nitrilkautschuk
DE102006008521A1 (de) * 2006-02-22 2007-08-23 Lanxess Deutschland Gmbh Verwendung von Katalysatoren mit erhöhter Aktivität für die NBR-Metathese

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