DE60323373D1 - Phosphor enthaltende ligande für metathese katalysatoren - Google Patents

Phosphor enthaltende ligande für metathese katalysatoren

Info

Publication number
DE60323373D1
DE60323373D1 DE60323373T DE60323373T DE60323373D1 DE 60323373 D1 DE60323373 D1 DE 60323373D1 DE 60323373 T DE60323373 T DE 60323373T DE 60323373 T DE60323373 T DE 60323373T DE 60323373 D1 DE60323373 D1 DE 60323373D1
Authority
DE
Germany
Prior art keywords
phosphorus
containing ligands
metathesis catalysts
metathesis
catalyst
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.)
Expired - Fee Related
Application number
DE60323373T
Other languages
English (en)
Inventor
Catherine Lynn Dwyer
Ann Elizabeth Cather Mcconnell
Grant Stephen Forman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sasol Technology (UK) Ltd
Original Assignee
Sasol Technology (UK) Ltd
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 Sasol Technology (UK) Ltd filed Critical Sasol Technology (UK) Ltd
Application granted granted Critical
Publication of DE60323373D1 publication Critical patent/DE60323373D1/de
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • 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
    • B01J31/2419Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising P as ring member
    • 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
    • B01J31/24Phosphines, 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
    • B01J31/2442Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/2461Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as ring members in the condensed ring system or in a further ring
    • B01J31/248Bridged ring systems, e.g. 9-phosphabicyclononane
    • 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
    • C07F15/0046Ruthenium compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/02Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
    • C08G61/04Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms
    • C08G61/06Macromolecular 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
    • C08G61/08Macromolecular 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 of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
    • 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, 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
    • 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
    • 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)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
DE60323373T 2002-07-05 2003-07-04 Phosphor enthaltende ligande für metathese katalysatoren Expired - Fee Related DE60323373D1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ZA200205387 2002-07-05
PCT/ZA2003/000087 WO2004005223A1 (en) 2002-07-05 2003-07-04 Phosphorus containing ligands for metathesis catalysts

Publications (1)

Publication Number Publication Date
DE60323373D1 true DE60323373D1 (de) 2008-10-16

Family

ID=30116347

Family Applications (1)

Application Number Title Priority Date Filing Date
DE60323373T Expired - Fee Related DE60323373D1 (de) 2002-07-05 2003-07-04 Phosphor enthaltende ligande für metathese katalysatoren

Country Status (8)

Country Link
US (1) US7276616B2 (de)
EP (1) EP1519904B1 (de)
AT (1) ATE407106T1 (de)
AU (1) AU2003249331B2 (de)
CA (1) CA2490144A1 (de)
DE (1) DE60323373D1 (de)
MY (1) MY130628A (de)
WO (1) WO2004005223A1 (de)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0514612D0 (en) * 2005-07-15 2005-08-24 Sasol Technology Uk Ltd The use of a phosphorus containing ligand and a cyclic organic ligand in a metathesis catalyst
MX2011005524A (es) 2008-11-26 2011-06-06 Elevance Renewable Sciences Metodos para producir turbosina a partir de cargas de alimentacion de aceite natural a traves de reacciones de metatesis.
MX2011005525A (es) 2008-11-26 2011-06-06 Elevance Renewable Sciences Metodos para producir turbosina a partir de cargas de alimentacion de aceite natural a traves de reacciones de division por oxigeno.
US9365487B2 (en) 2009-10-12 2016-06-14 Elevance Renewable Sciences, Inc. Methods of refining and producing dibasic esters and acids from natural oil feedstocks
US9000246B2 (en) 2009-10-12 2015-04-07 Elevance Renewable Sciences, Inc. Methods of refining and producing dibasic esters and acids from natural oil feedstocks
US9382502B2 (en) 2009-10-12 2016-07-05 Elevance Renewable Sciences, Inc. Methods of refining and producing isomerized fatty acid esters and fatty acids from natural oil feedstocks
JP6224896B2 (ja) 2009-10-12 2017-11-01 エレバンス・リニューアブル・サイエンシズ,インコーポレーテッド 天然油供給原料から燃料を精製および製造する方法
US9051519B2 (en) 2009-10-12 2015-06-09 Elevance Renewable Sciences, Inc. Diene-selective hydrogenation of metathesis derived olefins and unsaturated esters
US9222056B2 (en) 2009-10-12 2015-12-29 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US9169447B2 (en) 2009-10-12 2015-10-27 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US9175231B2 (en) 2009-10-12 2015-11-03 Elevance Renewable Sciences, Inc. Methods of refining natural oils and methods of producing fuel compositions
US8735640B2 (en) 2009-10-12 2014-05-27 Elevance Renewable Sciences, Inc. Methods of refining and producing fuel and specialty chemicals from natural oil feedstocks
US9169174B2 (en) 2011-12-22 2015-10-27 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9139493B2 (en) 2011-12-22 2015-09-22 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9133416B2 (en) 2011-12-22 2015-09-15 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9388098B2 (en) 2012-10-09 2016-07-12 Elevance Renewable Sciences, Inc. Methods of making high-weight esters, acids, and derivatives thereof
WO2017129440A1 (en) * 2016-01-27 2017-08-03 Basf Se Process for the generation of thin inorganic films

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3420898A (en) 1965-03-29 1969-01-07 Shell Oil Co Single stage hydroformylation of olefins to alcohols
WO2000058322A1 (en) * 1999-03-31 2000-10-05 California Institute Of Technology Novel ruthenium metal alkylidene complexes coordinated with triazolylidene ligands that exhibit high olefin metathesis activity
WO2002014248A2 (en) 2000-08-14 2002-02-21 Sasol Technology (Proprietary) Limited Bicyclic phosphin comprising hydroformylation catalyst and use thereof in production of oxygenated products

Also Published As

Publication number Publication date
US20050283026A1 (en) 2005-12-22
US7276616B2 (en) 2007-10-02
AU2003249331A1 (en) 2004-01-23
ATE407106T1 (de) 2008-09-15
EP1519904B1 (de) 2008-09-03
CA2490144A1 (en) 2004-01-15
AU2003249331B2 (en) 2009-03-05
WO2004005223A1 (en) 2004-01-15
MY130628A (en) 2007-07-31
EP1519904A1 (de) 2005-04-06

Similar Documents

Publication Publication Date Title
DE60323373D1 (de) Phosphor enthaltende ligande für metathese katalysatoren
Rodriguez-Ruiz et al. Recent developments in alkene hydro-functionalisation promoted by homogeneous catalysts based on earth abundant elements: formation of C–N, C–O and C–P bond
WO2007010453A3 (en) Transition metal compounds having a cyclic phosphorus-containing ligand and a cyclic organic ligand for use in metathesis reactions
ATE512945T1 (de) Metallkomplexe und deren verwendung in der olefinmetathese und atom- oder gruppenübertragungsreaktionen
Gomez-Suarez et al. Influence of a very bulky N-heterocyclic carbene in gold-mediated catalysis
Zhang et al. Reductive C–C coupling by desulfurizing gold-catalyzed photoreactions
Burks et al. Catalytic enantioselective diboration, disilation and silaboration: new opportunities for asymmetric synthesis
Intrieri et al. Highly diastereoselective cyclopropanation of α-methylstyrene catalysed by a C 2-symmetrical chiral iron porphyrin complex
WO2002083742A3 (en) Group 8 transition metal carbene complexes as enantioselective olefin metathesis catalysts
MX2010008110A (es) Catalizadores para reacciones de metatesis incluyendo metatesis de olefina enantioselectiva, y metodos relacionados.
WO2004101581A3 (en) Nitrogen-containing monodentate phosphines and their use in catalysis
ATE222918T1 (de) Liganden und komplexe zur enantioselektiven hydrierung
SG169326A1 (en) Organometallic ruthenium complexes and related methods for the preparation of tetra-substituted and other hindered olefins
WO2008010961A3 (en) Synthesis of terminal alkenes from internal alkenes and ethylene via olefin metathesis
MXPA04001348A (es) NUEVOS COMPUESTOS DE FOSFITOS Y SUS COMPLEJOS METaLICOS.
DE502004011288D1 (de) Auf basis von phosphoramiditliganden
DE59912097D1 (de) Alkylidenkomplexe des rutheniums mit n-heterozyklischen carbenliganden; verwendung als katalysatoren für die olefin-metathese
CA2502342A1 (en) Ruthenium complexes as (pre)catalysts for metathesis reactions
NZ704603A (en) Phosphine ligands for catalytic reactions
Matsuda et al. Rhodium-catalysed intramolecular trans-bis-silylation of alkynes to synthesise 3-silyl-1-benzosiloles
WO2004076464A3 (en) Optically active phosphites and phosphoramidites and their use in asymmetric reactions
AR036636A1 (es) Fosfonita i, su uso como ligando en complejos de metal de transicion, dichos complejos, procedimiento para la obtencion de estos ultimos, uso de complejos de metal transitorio como catalizador y procedimientos para la adicion de acido cianhidrico a un doble enlace olefinico y para la isomerizacion d
Demir et al. Synthesis of rhodium complexes derived from benzimidazolin-2-ylidene ligands and first used for the addition of arylboron to benzonitriles
DK1047669T3 (da) Perfluor-N-alkylsulfonsyrederivater
ATE356662T1 (de) Neue nickel-, palladium- und platin- carbenkomplexe, ihre herstellung und verwendung in katalytischen reaktionen

Legal Events

Date Code Title Description
8364 No opposition during term of opposition
8339 Ceased/non-payment of the annual fee