ATE219091T1 - Hochwirksame kationische ruthenium und osmiumkomplexe für die metathesereaktionen - Google Patents

Hochwirksame kationische ruthenium und osmiumkomplexe für die metathesereaktionen

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Publication number
ATE219091T1
ATE219091T1 AT98965675T AT98965675T ATE219091T1 AT E219091 T1 ATE219091 T1 AT E219091T1 AT 98965675 T AT98965675 T AT 98965675T AT 98965675 T AT98965675 T AT 98965675T AT E219091 T1 ATE219091 T1 AT E219091T1
Authority
AT
Austria
Prior art keywords
metathesis
reactions
catalysts
types
olefins
Prior art date
Application number
AT98965675T
Other languages
English (en)
Inventor
Alois Fuerstner
Kohlenforschung
Pierre Dixneuf
Christian Bruneau
Michel Picquet
Rainer Kunz
Original Assignee
Studiengesellschaft Kohle Mbh
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Studiengesellschaft Kohle Mbh filed Critical Studiengesellschaft Kohle Mbh
Application granted granted Critical
Publication of ATE219091T1 publication Critical patent/ATE219091T1/de

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2265Carbenes or carbynes, i.e.(image)
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2282Unsaturated compounds used as ligands
    • B01J31/2295Cyclic compounds, e.g. cyclopentadienyls
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/0006Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
    • C07F15/002Osmium compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/0006Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
    • C07F15/0046Ruthenium compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/10Polymerisation reactions involving at least dual use catalysts, e.g. for both oligomerisation and polymerisation
    • B01J2231/14Other (co) polymerisation, e.g. of lactides or epoxides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/50Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/54Metathesis reactions, e.g. olefin metathesis
    • B01J2231/543Metathesis reactions, e.g. olefin metathesis alkene metathesis
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/825Osmium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/22Organic complexes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/24Phosphines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
AT98965675T 1997-12-03 1998-11-17 Hochwirksame kationische ruthenium und osmiumkomplexe für die metathesereaktionen ATE219091T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP97121228A EP0921129A1 (de) 1997-12-03 1997-12-03 Hochwirksame kationische Ruthenium- und Osmiumkomplexe für die Olefinmetathese-Reaktionen
PCT/EP1998/007364 WO1999028330A1 (en) 1997-12-03 1998-11-17 Highly active cationic ruthenium and osmium complexes for olefin metathesis reactions

Publications (1)

Publication Number Publication Date
ATE219091T1 true ATE219091T1 (de) 2002-06-15

Family

ID=8227727

Family Applications (1)

Application Number Title Priority Date Filing Date
AT98965675T ATE219091T1 (de) 1997-12-03 1998-11-17 Hochwirksame kationische ruthenium und osmiumkomplexe für die metathesereaktionen

Country Status (7)

Country Link
US (1) US6590048B1 (de)
EP (2) EP0921129A1 (de)
JP (1) JP2001525330A (de)
AT (1) ATE219091T1 (de)
CA (1) CA2312755A1 (de)
DE (1) DE69806053T2 (de)
WO (1) WO1999028330A1 (de)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7507854B2 (en) 1998-09-01 2009-03-24 Materia, Inc. Impurity reduction in Olefin metathesis reactions
US6696597B2 (en) 1998-09-01 2004-02-24 Tilliechem, Inc. Metathesis syntheses of pheromones or their components
US6900347B2 (en) 1998-09-01 2005-05-31 Tilliechem, Inc. Impurity inhibition in olefin metathesis reactions
ATE438462T1 (de) 1998-09-10 2009-08-15 Univ New Orleans Foundation Katalysatorkomplex mit phenylindenyliden-ligand
WO2001046096A1 (en) * 1999-12-21 2001-06-28 Sasol Technology (Pty) Ltd Metathesis process for converting short chain olefins to longer chain olefins
US6610626B2 (en) * 2000-09-05 2003-08-26 Cymetech, Llp Highly active metathesis catalysts generated in situ from inexpensive and air stable precursors
DE10113963A1 (de) * 2001-03-22 2002-09-26 Haarmann & Reimer Gmbh Verfahren zur Herstellung von 15-Pentadecanolid
BE1014952A3 (nl) * 2001-10-03 2004-07-06 Ineos Nv Katalysator op basis van schiffse base ruthenium of osmium complexen, de vervaardiging en het gebruik daarvan in olefine metathese, atrp en kharasch reacties.
AU2003213017A1 (en) * 2002-02-11 2003-09-04 The Trustees Of Dartmouth College Systems and methods for modifying an ice-to-object interface
US7348290B2 (en) * 2002-03-11 2008-03-25 Japan Science And Technology Agency Arene-ruthenium complexes immobilized on polymers, catalysts consisting of the complexes, and processes for organic syntheses with the same
US6939982B2 (en) * 2002-05-15 2005-09-06 The Trustees Of Boston College Recyclable chiral metathesis catalysts
US7094898B2 (en) * 2003-05-29 2006-08-22 University Of Ottawa Ruthenium compounds, their production and use
DE10344690A1 (de) * 2003-09-25 2005-04-14 Basf Ag Verfahren zur Herstellung von 1,7-Octadien und dessen Verwendung
EP1765839B1 (de) * 2004-06-09 2017-01-25 UTI Limited Partnership Einen kationischen substituenten enthaltende übergangsmetallcarbenkomplexe als katalysatoren von olefin-metathesereaktionen
US8241575B2 (en) 2008-01-28 2012-08-14 The Johns Hopkins University Molecularly imprinted polymer sensor device
EP2276725B1 (de) * 2008-04-11 2012-07-04 F. Hoffmann-La Roche AG Neue ruthen-komplexe als katalysatoren für metathesereaktionen
FR2939331B1 (fr) 2008-12-10 2012-08-10 Inst Francais Du Petrole Composition catalytique et procede de metathese de corps gras insature
JP5454764B2 (ja) * 2009-03-09 2014-03-26 国立大学法人 千葉大学 ビアリール化合物を製造する方法
US8863345B2 (en) * 2009-12-18 2014-10-21 Colgate-Palmolive Company Oral care implement having a closed-loop arrangement of cleaning elements
US8656638B2 (en) * 2010-03-25 2014-02-25 Cheryl D. Stevenson Compounds and processes that generate cyclopropenes and substituted cyclopropenes on demand
CN103974772B (zh) * 2011-10-21 2017-03-29 阿朗新科德国有限责任公司 包括钌或锇卡宾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
WO2013056461A1 (en) * 2011-10-21 2013-04-25 Lanxess Deutschland Gmbh Catalyst compositions and their use for hydrogenation of nitrile rubber
US8604148B2 (en) 2011-11-29 2013-12-10 Exxonmobil Chemical Patents Inc. Functionalization of vinyl terminated polymers by ring opening cross metathesis
EP2785763A4 (de) * 2011-11-29 2015-06-03 Exxonmobil Chem Patents Inc Funktionalisierung von vinylterminierten polymeren durch ringöffnungs-kreuzmetathese
EP2778154A1 (de) 2013-03-13 2014-09-17 Evonik Industries AG In situ Generierung von Ruthenium-Katalysatoren zur Olefin-Metathese
EP2933274A1 (de) 2014-04-16 2015-10-21 Evonik Degussa GmbH Verfahren zur Herstellung von Polymeren mittels ringöffnender Polymerisation
KR102702569B1 (ko) 2017-12-08 2024-09-06 아란세오 도이치란드 게엠베하 루테늄 착물 촉매를 사용하여 니트릴 고무를 생성하기 위한 방법

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3067031B2 (ja) * 1992-04-03 2000-07-17 カリフォルニア インスティチュート オブ テクノロジー オレフィンメタセシス重合方法
US5312940A (en) * 1992-04-03 1994-05-17 California Institute Of Technology Ruthenium and osmium metal carbene complexes for olefin metathesis polymerization
DE4447066A1 (de) * 1994-12-29 1996-07-04 Hoechst Ag Heterocyclische Carbene enthaltende Metallkomplexverbindungen
US5831108A (en) * 1995-08-03 1998-11-03 California Institute Of Technology High metathesis activity ruthenium and osmium metal carbene complexes
US5936100A (en) * 1996-12-16 1999-08-10 Studiengesellschaft Kohle Mbh Synthesis of functionalized macrocycles by ring closing metathesis

Also Published As

Publication number Publication date
CA2312755A1 (en) 1999-06-10
EP1037897B1 (de) 2002-06-12
WO1999028330A1 (en) 1999-06-10
EP1037897A1 (de) 2000-09-27
DE69806053T2 (de) 2003-01-23
US6590048B1 (en) 2003-07-08
JP2001525330A (ja) 2001-12-11
EP0921129A1 (de) 1999-06-09
DE69806053D1 (de) 2002-07-18

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