AU2002210819A1 - Imidazolium salts and their use of these ionic liquids as a solvent - Google Patents

Imidazolium salts and their use of these ionic liquids as a solvent

Info

Publication number
AU2002210819A1
AU2002210819A1 AU2002210819A AU1081902A AU2002210819A1 AU 2002210819 A1 AU2002210819 A1 AU 2002210819A1 AU 2002210819 A AU2002210819 A AU 2002210819A AU 1081902 A AU1081902 A AU 1081902A AU 2002210819 A1 AU2002210819 A1 AU 2002210819A1
Authority
AU
Australia
Prior art keywords
olefins
hydrogenation
reaction
solvent
reactions
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.)
Abandoned
Application number
AU2002210819A
Inventor
Jean-Marie Basset
Yves Chauvin
Lionel Magna
Gerald Peter Niccolai
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.)
Centre National de la Recherche Scientifique CNRS
Original Assignee
Centre National de la Recherche Scientifique CNRS
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 Centre National de la Recherche Scientifique CNRS filed Critical Centre National de la Recherche Scientifique CNRS
Publication of AU2002210819A1 publication Critical patent/AU2002210819A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/10Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
    • 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
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235Nitrogen containing compounds
    • B01J31/0239Quaternary ammonium 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
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235Nitrogen containing compounds
    • B01J31/0244Nitrogen containing compounds with nitrogen contained as ring member in aromatic compounds or moieties, e.g. pyridine
    • 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
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0278Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre
    • B01J31/0281Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member
    • B01J31/0284Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member of an aromatic ring, e.g. pyridinium
    • 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
    • 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
    • B01J31/40Regeneration or reactivation
    • B01J31/4015Regeneration or reactivation of catalysts containing metals
    • B01J31/4023Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper
    • B01J31/4038Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper containing noble metals
    • 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
    • B01J31/40Regeneration or reactivation
    • B01J31/4015Regeneration or reactivation of catalysts containing metals
    • B01J31/4053Regeneration or reactivation of catalysts containing metals with recovery of phosphorous catalyst system constituents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/48Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
    • C07F5/022Boron compounds without C-boron linkages
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0803Compounds with Si-C or Si-Si linkages
    • C07F7/081Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • C07F7/0814Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
    • 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
    • B01J2231/20Olefin oligomerisation or telomerisation
    • 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
    • B01J2531/824Palladium
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/54Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Gas Separation By Absorption (AREA)

Abstract

New 1,2,3- or 1,2,3,4- or 1,2,3,4,5- substituted imidazolium salts and their uses as solvent in catalyzed organic reactions, as well as compositions containing them and a transition metal compound. They can be used in the following reactions : the telomerisation of conjugated dienes, the dimerisation of olefins, the oligomerisation of olefins, the polymerization of olefins, the alkylation of olefins, the hydrogenation of olefins, the olefin metathesis, the hydroformylation of olefins, the ring-closing metathesis of olefins, the ring-opening metathesis polymerisation of olefins, the symetric or asymetric epoxidation of olefins (including heteroatom substituted olefins) and the cyclopropanation of olefins, the condensation reaction, the hydrogenation reaction, the isomerization reaction, the Suzuki cross-coupling reactions, the amination reaction, the partial oxidation of alkancs, the kinetic resolution of racemic mixtures, the hydrogenation of imines, the hydrogenation of ketones, the transfer hydrogenation and the hydroxylation of aromatic organic compounds.
AU2002210819A 2000-10-27 2001-10-25 Imidazolium salts and their use of these ionic liquids as a solvent Abandoned AU2002210819A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP20000403008 EP1201657B1 (en) 2000-10-27 2000-10-27 Imidazolium salts and the use of these ionic liquids as a solvent and as a catalyst
EP00403008 2000-10-27
PCT/IB2001/002003 WO2002034722A1 (en) 2000-10-27 2001-10-25 Imidazolium salts and their use of these ionic liquids as a solvent

Publications (1)

Publication Number Publication Date
AU2002210819A1 true AU2002210819A1 (en) 2002-05-06

Family

ID=8173924

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2002210819A Abandoned AU2002210819A1 (en) 2000-10-27 2001-10-25 Imidazolium salts and their use of these ionic liquids as a solvent

Country Status (8)

Country Link
US (1) US7915426B2 (en)
EP (2) EP1201657B1 (en)
JP (2) JP2004512325A (en)
AT (1) ATE266008T1 (en)
AU (1) AU2002210819A1 (en)
CA (1) CA2427048C (en)
DE (1) DE60010472T2 (en)
WO (1) WO2002034722A1 (en)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4214997B2 (en) * 2002-07-26 2009-01-28 和光純薬工業株式会社 Ionic liquid osmium oxide
DE10240098B4 (en) * 2002-08-30 2006-04-06 Roche Diagnostics Gmbh Process for the synthesis and selective biocatalytic modification of peptides, peptide mimetics and proteins
DE10241555A1 (en) * 2002-09-07 2004-03-18 Basf Ag Process for carrying out chemical reactions in the liquid phase in the presence of a catalyst and a 1,3-substituted imidazolium salt
WO2004078811A1 (en) * 2003-02-25 2004-09-16 Nisshinbo Industries,Inc. Solvent for polymerization reaction and process for producing polymer
DE10333239A1 (en) 2003-07-21 2005-03-10 Basf Ag Process for the preparation of purified 1,3-substituted imidazolium salts
EP1658262B1 (en) * 2003-08-27 2013-02-20 proionic Production of Ionic Substances GmbH & Co KG Method for producing ionic liquids, ionic solids or mixtures thereof
TW200526587A (en) * 2003-09-05 2005-08-16 Univ Alabama Ionic liquids containing secondary hydroxyl-groups and a method for their preparation
FR2866345B1 (en) * 2004-02-13 2006-04-14 Inst Francais Du Petrole PROCESS FOR TREATING NATURAL GAS WITH EXTRACTION OF THE SOLVENT CONTAINED IN PURIFIED NATURAL GAS
WO2005105756A1 (en) * 2004-04-28 2005-11-10 Kaneka Corporation Ionic liquid and process for producing the same
KR100739452B1 (en) 2004-04-29 2007-07-18 인하대학교 산학협력단 A Process for Preparing ?-Alkylpyrrole Compounds
DE102004043632A1 (en) * 2004-09-07 2006-03-09 Basf Ag Process for the preparation of heterocyclic quaternary ammonium and / or guanidinium compounds
GB0422447D0 (en) * 2004-10-08 2004-11-10 Univ Cambridge Tech Use of ionic liquids
US7737102B2 (en) 2004-11-01 2010-06-15 The Procter & Gamble Company Ionic liquids derived from functionalized anionic surfactants
US7776810B2 (en) 2004-11-01 2010-08-17 The Procter & Gamble Company Compositions containing ionic liquid actives
US20060090777A1 (en) 2004-11-01 2006-05-04 Hecht Stacie E Multiphase cleaning compositions having ionic liquid phase
US7939485B2 (en) 2004-11-01 2011-05-10 The Procter & Gamble Company Benefit agent delivery system comprising ionic liquid
JP4706267B2 (en) * 2005-01-25 2011-06-22 トヨタ自動車株式会社 Multi-substituted imidazolium molten salt and its use
US7786065B2 (en) 2005-02-18 2010-08-31 The Procter & Gamble Company Ionic liquids derived from peracid anions
GB2427192A (en) * 2005-06-17 2006-12-20 Johnson Matthey Plc A process for the oxidation of an alkyl-group containing substrate in the presence of an ionic liquid
DE102005032838A1 (en) * 2005-07-14 2007-02-08 Merck Patent Gmbh Mixture of onium alkyl sulfonates and onium alkyl sulfites
DE102005032837A1 (en) * 2005-07-14 2007-02-08 Merck Patent Gmbh Process for the preparation of onium alkyl sulfites
DE102005032836A1 (en) 2005-07-14 2007-01-18 Merck Patent Gmbh Process for the preparation of onium alkyl sulfonates
US7528287B2 (en) * 2005-09-22 2009-05-05 E.I. Du Pont De Nemours And Company Preparation of poly(tetramethylene) glycol
US7544813B2 (en) * 2005-09-22 2009-06-09 E.I. Du Pont De Nemours And Company Ionic liquids
WO2007038360A2 (en) * 2005-09-22 2007-04-05 E. I. Du Pont De Nemours And Company Preparation of polytrimethylene ether glycol and copolymers thereof
US8232265B2 (en) * 2005-10-07 2012-07-31 Board Of Trustees Of The University Of Alabama Multi-functional ionic liquid compositions for overcoming polymorphism and imparting improved properties for active pharmaceutical, biological, nutritional, and energetic ingredients
JP4753796B2 (en) * 2006-05-26 2011-08-24 日本合成化学工業株式会社 Urethane (meth) acrylate compound, active energy ray-curable resin composition and coating agent using the same
JP2008133248A (en) * 2006-10-24 2008-06-12 Sanyo Chem Ind Ltd Method for producing imidazolium salt
CN101215262B (en) * 2007-01-05 2010-06-23 中国纺织科学研究院 Ionic liquid and its preparing process and use
JP4815604B2 (en) * 2007-01-30 2011-11-16 国立大学法人 新潟大学 Method for producing biaryl compound
DE102007040333A1 (en) * 2007-08-24 2009-02-26 Rheinisch-Westfälische Technische Hochschule Aachen Catalyst composition for enantioselective hydrogenation of unsaturated compounds, e.g. olefins, comprises a transition metal component, a tropoisomeric or racemic chiral ligand and a chiral ionic liquid
KR100963402B1 (en) 2007-12-04 2010-06-14 성균관대학교산학협력단 Process for the hydrogenation of aromatic compounds
US9260397B2 (en) * 2008-01-30 2016-02-16 Technische Universitaet Dresden Salts comprising aryl-alkyl-substituted imidazolium and triazolium cations and the use thereof
US9592268B2 (en) 2011-05-23 2017-03-14 Cornell University Endothelium protective materials and methods of use
US20130099156A1 (en) * 2011-10-25 2013-04-25 Christoph Stock Use of liquid compositions comprising imidazolium salts as operating materials
WO2013098052A2 (en) 2011-12-28 2013-07-04 Lanxess Deutschland Gmbh Metathesis of nitrile rubbers in the presence of transition metal complex catalysts
WO2014009350A1 (en) * 2012-07-11 2014-01-16 Basf Se Performing a hydrocarbon conversion or processing a hydrocarbon conversion in devices having a surface made of nonmetallic materials
CN102786474A (en) * 2012-08-22 2012-11-21 林州市科能材料科技有限公司 Synthetic method of thiocyanate ionic liquid
US20150094486A1 (en) * 2013-09-27 2015-04-02 Uop Llc Active ionic liquid mixtures for oxidizing alkylaromatic compounds
US10208391B2 (en) 2014-10-17 2019-02-19 Ut-Battelle, Llc Aluminum trihalide-neutral ligand ionic liquids and their use in aluminum deposition
CN104496928A (en) * 2014-11-21 2015-04-08 绍兴佳华高分子材料股份有限公司 Method for preparing quaternary ammonium salt ionic liquid without halogen ions and sodium ions
WO2018090199A1 (en) * 2016-11-15 2018-05-24 广东莱佛士制药技术有限公司 Method for preparing isophorone
CN111836849B (en) * 2018-03-09 2023-04-07 巴斯夫欧洲公司 Process for producing fibers, films and moldings of polybenzazole polymer (P)
CN114478216A (en) * 2020-11-13 2022-05-13 辽宁众辉生物科技有限公司 Novel synthesis method of 1-acetyl-1-chlorocyclopropane

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2508420A1 (en) * 1975-02-27 1976-09-09 Goldschmidt Ag Th QUATERNAERE IMIDAZOLIUM JOINTS
DE2510525C3 (en) * 1975-03-11 1978-03-30 Th. Goldschmidt Ag, 4300 Essen 2-alkyl imidazolium quaternary salts
DE2706839A1 (en) * 1977-02-17 1978-08-24 Bayer Ag AGENTS FOR REGULATING PLANT GROWTH
DE2829137C2 (en) * 1978-07-03 1982-09-16 Th. Goldschmidt Ag, 4300 Essen Use of 1,3-di-n-decyl-2-methyl-imidazolium chloride or bromide as microbicides
DE3442172A1 (en) * 1983-11-30 1985-06-05 Allied Corp., Morristown, N.J. MELTED, NON-AQUEOUS ELECTROLYTE COMPOSITION
JPH01135662A (en) * 1987-11-24 1989-05-29 Seiko Epson Corp Thermal printer
JPH02305988A (en) * 1989-05-18 1990-12-19 Mitsubishi Petrochem Co Ltd Composition having low melting point and aluminum electroplating method with bath of this composition
US5041194A (en) 1989-05-18 1991-08-20 Mitsubishi Petrochemical Co., Ltd. Aluminum electroplating method
JPH08509242A (en) * 1994-02-10 1996-10-01 ビーピー ケミカルズ リミテッド Ionic liquid
EP0718288B8 (en) * 1994-12-21 2005-10-26 Hydro Quebec Liquid hydrophobic salts, their preparation and their use in electrochemistry
US5827602A (en) * 1995-06-30 1998-10-27 Covalent Associates Incorporated Hydrophobic ionic liquids
JPH1135662A (en) * 1997-07-14 1999-02-09 Mitsui Chem Inc Lactic acid and lactic acid oligomer and production of polylactic acid using the same
JP3817045B2 (en) * 1997-09-12 2006-08-30 四国化成工業株式会社 Molten salt type polymer electrolyte
DE69934170T2 (en) * 1998-02-03 2007-09-27 Acep Inc., Montreal NEW MATERIALS SUITABLE AS ELECTROLYTIC SOLUBILISTS

Also Published As

Publication number Publication date
WO2002034722A1 (en) 2002-05-02
CA2427048C (en) 2011-07-05
CA2427048A1 (en) 2002-05-02
DE60010472D1 (en) 2004-06-09
EP1328518A1 (en) 2003-07-23
DE60010472T2 (en) 2005-05-19
JP5642995B2 (en) 2014-12-17
EP1201657B1 (en) 2004-05-06
JP2010215638A (en) 2010-09-30
US7915426B2 (en) 2011-03-29
JP2004512325A (en) 2004-04-22
ATE266008T1 (en) 2004-05-15
US20040026666A1 (en) 2004-02-12
EP1201657A1 (en) 2002-05-02

Similar Documents

Publication Publication Date Title
AU2002210819A1 (en) Imidazolium salts and their use of these ionic liquids as a solvent
Bertozzi et al. Highly enantioselective regiodivergent and catalytic parallel kinetic resolution
Prakash et al. Gallium (III) triflate: An efficient and a sustainable Lewis acid catalyst for organic synthetic transformations
Grotjahn et al. Extensive isomerization of alkenes using a bifunctional catalyst: an alkene zipper
Walker et al. Palladium‐Catalyzed Direct C H Functionalization of Benzoquinone
BR0005637A (en) Process for hydroformylation of olefins
WO2000050470A3 (en) Catalysts containing n-pyrrolyl substituted nitrogen donors
WO2001083571A3 (en) Catalysts containing n-pyrrolyl substituted nitrogen donors
BR9915991A (en) Heterogeneous olefin polymerization catalyst and processes for the preparation of a heterogeneous olefin polymerization catalyst, for the homo or copolymerization of an olefin and for the production of an olefin polymer, and, use of a catalyst
BR9506039A (en) Components and catalysts for olefin polymerization
EP2943499B1 (en) Catalyst complexes with carbene ligand and method for making same and use in metathesis reaction
WO1993020111A3 (en) Ruthenium and osmium metal carbene complexes for olefin metathesis polymerization
WO2003042135A3 (en) P-chiral phospholanes and phosphocyclic compounds and their use in asymmetric catalytic reactions
BR0010376A (en) Multi-stage process for the (co) polymerization of olefins, catalytic components and polymeric composition
Castarlenas et al. Allenylidene–ruthenium complexes as versatile precatalysts for alkene metathesis reactions
Albright et al. Superelectrophilic Fe (III)–ion pairs as stronger Lewis acid catalysts for (E)-selective intermolecular carbonyl–olefin metathesis
Wei et al. Hexafluoroisopropanol-promoted disulfidation and diselenation of alkyne, alkene, and allene
Dinh et al. Alkyl–aryl coupling catalyzed by tandem systems of pincer-ligated iridium complexes and zeolites
Pai et al. Friedel-Crafts Benzylation of Arenes Using FeCl3 Impregnated Montmorillonite K10.
Dardir et al. Synthesis of triarylmethanes via palladium-catalyzed Suzuki–Miyaura reactions of diarylmethyl esters
ITMI931466A1 (en) CATALYSTS FOR THE (CO) POLYMERIZATION OF ETHYLENE
BR0016134B1 (en) compounds, catalyst for the olefin polymerization and processes for the preparation of compounds and a catalyst and for the polymerization of olefins.
Alizadeh et al. Green and fast synthesis of 2-arylidene-indan-1, 3-diones using a task-specific ionic liquid
Kikuchi et al. Cycloaddition of cyclopropenes with alkynes via carbon–carbon double bond cleavage enabled by a ruthenium catalyst: Synthesis of cyclopentadienes and cycloheptatrienes
Song et al. Stereoselective Synthesis of trans-Stilbenes through Silver-Catalyzed Self-Coupling of N-Triftosylhydrazones: An Experimental and Theoretical Study