JP2005508883A - 六配位ルテニウム又はオスミウム金属カルベンメタセシス触媒 - Google Patents

六配位ルテニウム又はオスミウム金属カルベンメタセシス触媒 Download PDF

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Publication number
JP2005508883A
JP2005508883A JP2003516680A JP2003516680A JP2005508883A JP 2005508883 A JP2005508883 A JP 2005508883A JP 2003516680 A JP2003516680 A JP 2003516680A JP 2003516680 A JP2003516680 A JP 2003516680A JP 2005508883 A JP2005508883 A JP 2005508883A
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group
substituted
alkyl
independently
unsubstituted
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Japanese (ja)
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JP2005508883A5 (enExample
Inventor
グルブス，ロバート，エイチ．
サンフォード，メラニー，エス．
ムーア，ジェイソン，エル．
ラブ，ジェニファー，エー．
トゥーンカ，ティナ，エム．
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California Institute of Technology
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California Institute of Technology
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Priority claimed from US09/948,115 external-priority patent/US6610626B2/en
Priority claimed from US10/017,489 external-priority patent/US6759537B2/en
Priority claimed from US10/107,531 external-priority patent/US6838489B2/en
Priority claimed from US10/138,188 external-priority patent/US20030083445A1/en
Application filed by California Institute of Technology filed Critical California Institute of Technology
Publication of JP2005508883A publication Critical patent/JP2005508883A/ja
Publication of JP2005508883A5 publication Critical patent/JP2005508883A5/ja
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02—Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04—Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1815—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1825—Ligands comprising condensed ring systems, e.g. acridine, carbazole
    • B01J31/183—Ligands comprising condensed ring systems, e.g. acridine, carbazole with more than one complexing nitrogen atom, e.g. phenanthroline
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2265—Carbenes or carbynes, i.e.(image)
    • B01J31/2269—Heterocyclic carbenes
    • B01J31/2273—Heterocyclic carbenes with only nitrogen as heteroatomic ring members, e.g. 1,3-diarylimidazoline-2-ylidenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02—Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04—Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • C07C6/06—Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond at a cyclic carbon-to-carbon double bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
    • C07F15/002—Osmium compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
    • C07F15/0046—Ruthenium compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
    • C08G61/04—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms
    • C08G61/06—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/54—Metathesis reactions, e.g. olefin metathesis
    • B01J2231/543—Metathesis reactions, e.g. olefin metathesis alkene metathesis
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/46—Ruthenium, rhodium, osmium or iridium
    • B01J23/462—Ruthenium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/46—Ruthenium, rhodium, osmium or iridium
    • B01J23/466—Osmium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/821—Ruthenium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/825—Osmium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B01J31/28—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of the platinum group metals, iron group metals or copper
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/22—Organic complexes

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
JP2003516680A 2001-08-01 2002-06-14 六配位ルテニウム又はオスミウム金属カルベンメタセシス触媒 Withdrawn JP2005508883A (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US30980601P 2001-08-01 2001-08-01
US31497801P 2001-08-24 2001-08-24
US09/948,115 US6610626B2 (en) 2000-09-05 2001-09-05 Highly active metathesis catalysts generated in situ from inexpensive and air stable precursors
US10/017,489 US6759537B2 (en) 2001-03-23 2001-12-14 Hexacoordinated ruthenium or osmium metal carbene metathesis catalysts
US10/107,531 US6838489B2 (en) 2001-03-23 2002-03-25 High activity metal carbene metathesis catalysts generated using a thermally activated N-heterocyclic carbene precursor
US10/138,188 US20030083445A1 (en) 2001-03-23 2002-05-03 High activity metal carbene metathesis catalysts generated using a thermally activated N-heterocyclic carbene precursor
PCT/US2002/019167 WO2003011455A1 (en) 2001-08-01 2002-06-14 Hexacoordinated ruthenium or osmium metal carbene metathesis catalysts

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2009235547A Division JP5577069B2 (ja) 2001-08-01 2009-10-09 六配位ルテニウム又はオスミウム金属カルベンメタセシス触媒

Publications (2)

Publication Number Publication Date
JP2005508883A true JP2005508883A (ja) 2005-04-07
JP2005508883A5 JP2005508883A5 (enExample) 2006-01-05

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JP2003516680A Withdrawn JP2005508883A (ja) 2001-08-01 2002-06-14 六配位ルテニウム又はオスミウム金属カルベンメタセシス触媒

Country Status (6)

Country Link
EP (1) EP1423195B1 (enExample)
JP (1) JP2005508883A (enExample)
CN (1) CN1265882C (enExample)
CA (1) CA2455893C (enExample)
MX (1) MXPA04001004A (enExample)
WO (1) WO2003011455A1 (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008285546A (ja) * 2007-05-16 2008-11-27 Okayama Univ 開環メタセシス重合触媒および開環メタセシス重合体の製造方法
JP2011523625A (ja) * 2008-04-09 2011-08-18 マテリア， インコーポレイテッド 置換された骨格を有するｎ−ヘテロ環状カルベンリガンドを有するルテニウムオレフィン複分解触媒

Families Citing this family (69)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7598330B2 (en) 2002-04-05 2009-10-06 California Institute Of Technology Cross-metathesis of olefins directly substituted with an electron-withdrawing group using transition metal carbene catalysts
RU2326733C1 (ru) * 2007-03-29 2008-06-20 ООО "Объединенный центр исследований и разработок" Каталитическая композиция для получения эфиров акриловой кислоты по реакции метатезиса диалкилмалеатов с этиленом
DE102007039526A1 (de) 2007-08-21 2009-02-26 Lanxess Deutschland Gmbh Katalysator-Systeme und deren Verwendung für Metathese-Reaktionen
DE102007039695A1 (de) 2007-08-22 2009-02-26 Lanxess Deutschland Gmbh Katalysatoren für Metathese-Reaktionen
EP2027920B1 (de) 2007-08-21 2014-10-08 LANXESS Deutschland GmbH Katalysatoren für Metathese-Reaktionen
ATE467644T1 (de) 2007-08-21 2010-05-15 Lanxess Deutschland Gmbh Metathese eines nitrilkautschuks in gegenwart von übergangsmetallkomplexkatalysatoren
DE102007039525A1 (de) 2007-08-21 2009-02-26 Lanxess Deutschland Gmbh Verfahren zum Metathese-Abbau von Nitrilkautschuk
DE102007039527A1 (de) 2007-08-21 2009-02-26 Lanxess Deutschland Gmbh Katalysatoren für Metathese-Reaktionen
EP2147721A1 (de) 2008-07-08 2010-01-27 Lanxess Deutschland GmbH Katalysator-Systeme und deren Verwendung für Metathese-Reaktionen
CN101665567B (zh) * 2008-09-01 2011-11-23 南京工业大学 卡宾衍生物催化的环状化合物可调控开环聚合方法
CN104211735B (zh) * 2008-09-27 2018-01-30 赞南科技(上海)有限公司 一种金属络合物配体、金属络合物及其制备方法和应用、高分子聚合物及其制备方法和应用
EP2379616A1 (en) 2009-01-21 2011-10-26 Henkel AG & Co. KGaA Olefin metathesis polymerisation
EP2280017B1 (en) * 2009-07-21 2013-01-02 Rimtec Corporation Catalytic complex for olefin metathesis reactions, process for the preparation thereof and use thereof
EP2289620A1 (en) 2009-08-31 2011-03-02 LANXESS Deutschland GmbH Process for the preparation of hydrogenated nitrile rubber
KR101405744B1 (ko) 2009-08-31 2014-06-10 란세스 도이치란트 게엠베하 저분자량의 임의로 수소화된 니트릴 고무를 포함하는 가황성 중합체 조성물
EP2289623A1 (en) 2009-08-31 2011-03-02 LANXESS Deutschland GmbH Metathesis of nitrile rubbers in the presence of transition metal catalysts
PL2506972T3 (pl) 2009-12-03 2019-09-30 Umicore Ag & Co. Kg Nośnikowe katalizatory metatezy olefin
WO2011139704A2 (en) * 2010-04-27 2011-11-10 The Regents Of The University Of California Crystalline 1h-1,2,3-triazol-5-ylidenes
EP2395034A1 (de) 2010-06-14 2011-12-14 LANXESS Deutschland GmbH Blends aus teilhydriertem Nitrilkautschuk und Silikonkautschuk, darauf basierende vulkanisierbaren Mischungen und Vulkanisate
EP2418225A1 (de) 2010-08-09 2012-02-15 LANXESS Deutschland GmbH Teilhydrierte Nitrilkautschuke
BR112013004244A2 (pt) 2010-08-23 2016-07-26 Materia Inc modificações de fluxo vartim sistemas de resina de baixa viscosidade
US8455412B2 (en) 2010-08-31 2013-06-04 Biosynthetic Technologies, Llc Acetic acid-capped estolide base oils and methods of making the same
EP2484700B1 (de) 2011-02-04 2013-10-09 LANXESS Deutschland GmbH Funktionalisierte Nitrilkautschuke und ihre Herstellung
US10457597B2 (en) 2011-06-17 2019-10-29 Materia, Inc. Adhesion promoters and gel-modifiers for olefin metathesis compositions
AU2012271204B2 (en) 2011-06-17 2016-12-22 Biosynthetic Technologies, Llc Grease compositions comprising estolide base oils
JP5976807B2 (ja) 2011-08-15 2016-08-24 ザ・ガヴァニング・カウンシル・オヴ・ユニヴァーシティー・オヴ・トロント ルテニウム系錯体触媒
WO2013056459A1 (en) 2011-10-21 2013-04-25 Lanxess Deutschland Gmbh Catalyst compositions and their use for hydrogenation of nitrile rubber
WO2013056400A1 (en) 2011-10-21 2013-04-25 Lanxess Deutschland Gmbh Catalyst compositions and their use for hydrogenation of nitrile rubber
WO2013056461A1 (en) 2011-10-21 2013-04-25 Lanxess Deutschland Gmbh Catalyst compositions and their use for hydrogenation of nitrile rubber
SG10201600292YA (en) 2011-12-19 2016-02-26 Biosynthetic Technologies Llc Processes For Preparing Estolide Base Oils And Oligomeric Compounds That Include Cross Metathesis
WO2013098056A1 (en) 2011-12-28 2013-07-04 Lanxess Deutschland Gmbh Purification of optionally hydrogenated nitrile rubber
WO2013098052A2 (en) 2011-12-28 2013-07-04 Lanxess Deutschland Gmbh Metathesis of nitrile rubbers in the presence of transition metal complex catalysts
EP2614887A1 (en) 2012-01-12 2013-07-17 Lanxess Deutschland GmbH Ruthenium-based complex catalysts
EP2641909A1 (en) 2012-03-19 2013-09-25 LANXESS Deutschland GmbH Transition metal P-N complexes as polymerization catalysts
WO2013159365A1 (en) 2012-04-28 2013-10-31 Lanxess Deutschland Gmbh Hydrogenation of nitrile rubber
US20150152283A1 (en) 2012-06-12 2015-06-04 Materia, Inc. Method and composition for improving adhesion of metathesis compositions to substrates
SG11201602875QA (en) 2012-06-18 2016-05-30 Biosynthetic Technologies Llc Processes of preparing estolide compounds that include removing sulfonate residues
EP2676971B1 (en) 2012-06-22 2015-04-08 University Of Waterloo Hydrogenation of a diene-based polymer latex
EP2676969B1 (en) 2012-06-22 2016-06-01 University Of Waterloo Tandem metathesis and hydrogenation of diene-based polymers in latex
US9234985B2 (en) 2012-08-01 2016-01-12 California Institute Of Technology Birefringent polymer brush structures formed by surface initiated ring-opening metathesis polymerization
WO2014022482A1 (en) 2012-08-01 2014-02-06 California Institute Of Technology Solvent-free enyne metathesis polymerization
US9527982B2 (en) 2012-12-19 2016-12-27 Materia, Inc. Storage stable adhesion promoter compositions for cyclic olefin resin compositions
CN103936793B (zh) 2013-01-10 2017-02-08 光明创新（武汉）有限公司 含卡宾配体的催化剂及其制备方法与其在复分解反应中的应用
WO2014134333A1 (en) 2013-02-27 2014-09-04 Materia, Inc. Metal carbene olefin metathesis two catalyst composition
US9598531B2 (en) 2013-02-27 2017-03-21 Materia, Inc. Olefin metathesis catalyst compositions comprising at least two metal carbene olefin metathesis catalysts
MX2015011454A (es) 2013-03-15 2016-05-31 Materia Inc Revestimiento en molde de polimeros romp.
EP2984055B1 (en) 2013-04-09 2018-10-17 Materia, Inc. Preparation of surfactants via cross-metathesis
US9758445B2 (en) 2013-04-09 2017-09-12 Materia, Inc. Preparation of surfactants via cross-metathesis
BR112015025850B1 (pt) 2013-04-09 2021-11-03 Materia, Inc Método para produzir pelo menos um produto de metátese cruzada
WO2014186631A1 (en) * 2013-05-15 2014-11-20 California Institute Of Technology Highly z-selective and enantioselective ring opening/cross metathesis
US20160244632A1 (en) 2013-06-24 2016-08-25 Materia, Inc. Thermal insulation
ES2992740T3 (en) 2013-07-03 2024-12-17 Materia Inc Liquid molding compositions
EP3041812B1 (en) 2013-09-04 2022-08-10 California Institute of Technology Functionalized linear and cyclic polyolefins
EP3052666B1 (en) 2013-09-30 2021-01-06 The Research Foundation for the State University of New York System and method for removing transition metals from solution
EP3092204A4 (en) 2014-01-10 2017-12-20 Materia, Inc. Method and composition for improving adhesion of metathesis compositions to substrates
WO2015130802A1 (en) 2014-02-27 2015-09-03 Materia, Inc. Adhesion promoter compositions for cyclic olefin resin compositions
CN103980317B (zh) * 2014-05-28 2017-01-25 南开大学 联吡啶四齿配体钌络合物及其制备方法和应用
EP3164409B1 (en) 2014-07-03 2021-09-01 Guang Ming Innovation Company (Wuhan) Group 8 transition metal catalysts and method for making same and process for use of same in metathesis reaction
EP3034486A1 (de) 2014-12-16 2016-06-22 LANXESS Deutschland GmbH 1,3-Butadien-Synthese
EP3256505B1 (en) 2015-02-12 2023-11-29 Materia, Inc. Cyclic olefin resin compositions comprising functional elastomers
CA2975259C (en) 2015-02-14 2023-03-14 Materia, Inc. Romp polymers having improved resistance to hydrocarbon fluids
US10774035B2 (en) 2016-09-23 2020-09-15 Umicore Ag & Co. Kg Preparation of amino acids and amino acid derivatives
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
EP3781309A1 (en) 2018-04-20 2021-02-24 ARLANXEO Deutschland GmbH Hydrogenation catalyst compositions and their use for hydrogenation of nitrile rubber
CN110694692B (zh) * 2018-07-09 2021-08-06 沈阳中化农药化工研发有限公司 一种空气稳定型催化剂及其制备和催化生成n1-取代吡唑类衍生物的应用
JP7434277B2 (ja) 2018-07-23 2024-02-20 アランセオ・ドイチュランド・ゲーエムベーハー ニトリルゴムの水素化
WO2020120207A2 (en) 2018-12-12 2020-06-18 Arlanxeo Deutschland Gmbh Catalyst system containing a metathesis catalyst and at least one phenolic compound and a process for metathesis of nitrile-butadiene rubber (nbr) using the catalyst system
CA3122882A1 (en) 2018-12-17 2020-06-25 Arlanxeo Deutschland Gmbh Process for preparing hnbr solutions with alternative solvents
TWI723817B (zh) * 2020-03-20 2021-04-01 國家中山科學研究院 開環移位聚合反應之新型釕金屬錯合物

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998039346A1 (en) * 1997-03-06 1998-09-11 Ciba Specialty Chemicals Holding Inc. New catalysts
US6107420A (en) * 1998-07-31 2000-08-22 California Institute Of Technology Thermally initiated polymerization of olefins using Ruthenium or osmium vinylidene complexes

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5312940A (en) 1992-04-03 1994-05-17 California Institute Of Technology Ruthenium and osmium metal carbene complexes for olefin metathesis polymerization
US5710298A (en) 1992-04-03 1998-01-20 California Institute Of Technology Method of preparing ruthenium and osmium carbene complexes
EP0773948A4 (en) 1992-04-03 1998-09-02 California Inst Of Techn HIGHLY ACTIVE RUTHENIUM OR OSMIUM METAL CARBEN COMPLEXES FOR OLEFIN METHETHESE REACTIONS AND THEIR SYNTHESIS
US5831108A (en) 1995-08-03 1998-11-03 California Institute Of Technology High metathesis activity ruthenium and osmium metal carbene complexes
US5939504A (en) 1995-12-07 1999-08-17 Advanced Polymer Technologies Method for extending the pot life of an olefin metathesis polymerization reaction
US6020443A (en) 1996-02-08 2000-02-01 Advanced Polymer Technologies, Inc. Polymerization of low grade DCPD monomers using an olefin metathesis catalyst
US6310121B1 (en) * 1996-12-02 2001-10-30 Cymetech, Llc Polymeric composites including dicyclopentadiene and related monomers
EP1036081B1 (en) * 1997-12-04 2002-07-17 Ciba SC Holding AG Heterocyclyl ligand containing ruthenium and osmium catalysts
DE19815275B4 (de) 1998-04-06 2009-06-25 Evonik Degussa Gmbh Alkylidenkomplexe des Rutheniums mit N-heterozyklischen Carbenliganden und deren Verwendung als hochaktive, selektive Katalysatoren für die Olefin-Metathese
WO2000043343A2 (en) 1999-01-26 2000-07-27 California Institute Of Technology Novel methods for cross-metathesis of terminal olefins
DE60039166D1 (de) 1999-03-31 2008-07-24 California Inst Of Techn Mit triazolydin-liganden koordinierte rutheniummetall-alkyliden-komplexe die hohe olefin-metathese-aktivität aufweisen
US7329758B1 (en) 1999-05-24 2008-02-12 California Institute Of Technology Imidazolidine-based metal carbene metathesis catalysts
IL153578A0 (en) 2000-06-23 2003-07-06 California Inst Of Techn Synthesis of functionalized and unfunctionalized olefins via cross and ring-closing metathesis
WO2002020535A1 (en) 2000-09-05 2002-03-14 California Institute Of Technology Highly active metathesis catalysts generated in situ from inexpensive and air stable precursors
US20030083445A1 (en) 2001-03-23 2003-05-01 Grubbs Robert H. High activity metal carbene metathesis catalysts generated using a thermally activated N-heterocyclic carbene precursor
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
CA2973417C (en) 2015-01-16 2023-09-12 Beaulieu International Group Nv Covering panel and process of producing covering panels

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998039346A1 (en) * 1997-03-06 1998-09-11 Ciba Specialty Chemicals Holding Inc. New catalysts
US6107420A (en) * 1998-07-31 2000-08-22 California Institute Of Technology Thermally initiated polymerization of olefins using Ruthenium or osmium vinylidene complexes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008285546A (ja) * 2007-05-16 2008-11-27 Okayama Univ 開環メタセシス重合触媒および開環メタセシス重合体の製造方法
JP2011523625A (ja) * 2008-04-09 2011-08-18 マテリア， インコーポレイテッド 置換された骨格を有するｎ−ヘテロ環状カルベンリガンドを有するルテニウムオレフィン複分解触媒

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