ATE349407T1 - Zusammensetzungen, die ionische flüssigkeiten enthalten, und deren vewendungen, insbesondere in der organischen synthese - Google Patents

Zusammensetzungen, die ionische flüssigkeiten enthalten, und deren vewendungen, insbesondere in der organischen synthese

Info

Publication number
ATE349407T1
ATE349407T1 AT03798215T AT03798215T ATE349407T1 AT E349407 T1 ATE349407 T1 AT E349407T1 AT 03798215 T AT03798215 T AT 03798215T AT 03798215 T AT03798215 T AT 03798215T AT E349407 T1 ATE349407 T1 AT E349407T1
Authority
AT
Austria
Prior art keywords
functional
organic synthesis
compositions containing
ionic liquids
containing ionic
Prior art date
Application number
AT03798215T
Other languages
English (en)
Inventor
Michel Vaultier
Said Gmouh
Original Assignee
Centre Nat Rech Scient
Univ Rennes
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 Nat Rech Scient, Univ Rennes filed Critical Centre Nat Rech Scient
Application granted granted Critical
Publication of ATE349407T1 publication Critical patent/ATE349407T1/de

Links

Classifications

    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277—Catalysts 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
    • B01J31/0278—Catalysts 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
    • B01J31/0281—Catalysts 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
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235—Nitrogen containing compounds
    • B01J31/0239—Quaternary ammonium 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
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277—Catalysts 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
    • B01J31/0287—Catalysts 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 atoms other than nitrogen as cationic centre
    • B01J31/0288—Phosphorus
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
    • 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
    • B01J31/30—Halides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B37/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving either the formation of a carbon-to-carbon bond between two carbon atoms not directly linked already or the disconnection of two directly linked carbon atoms
    • C07B37/02—Addition
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B37/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving either the formation of a carbon-to-carbon bond between two carbon atoms not directly linked already or the disconnection of two directly linked carbon atoms
    • C07B37/04—Substitution
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B37/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving either the formation of a carbon-to-carbon bond between two carbon atoms not directly linked already or the disconnection of two directly linked carbon atoms
    • C07B37/10—Cyclisation
    • C07B37/12—Diels-Alder reactions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/03—Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C67/347—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
    • 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
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32—Addition reactions to C=C or C-C triple bonds
    • B01J2231/324—Cyclisations via conversion of C-C multiple to single or less multiple bonds, e.g. cycloadditions
    • B01J2231/326—Diels-Alder or other [4+2] cycloadditions, e.g. hetero-analogues
    • 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
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/34—Other additions, e.g. Monsanto-type carbonylations, addition to 1,2-C=X or 1,2-C-X triplebonds, additions to 1,4-C=C-C=X or 1,4-C=-C-X triple bonds with X, e.g. O, S, NH/N
    • B01J2231/341—1,2-additions, e.g. aldol or Knoevenagel condensations
    • 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
    • B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/42—Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
    • B01J2231/4205—C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type
    • B01J2231/4211—Suzuki-type, i.e. RY + R'B(OR)2, in which R, R' are optionally substituted alkyl, alkenyl, aryl, acyl and Y is the leaving group
    • 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
    • B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/42—Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
    • B01J2231/4205—C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type
    • B01J2231/4261—Heck-type, i.e. RY + C=C, in which R is aryl
    • 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
    • B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/42—Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
    • B01J2231/4205—C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type
    • B01J2231/4266—Sonogashira-type, i.e. RY + HC-CR' triple bonds, in which R=aryl, alkenyl, alkyl and R'=H, alkyl or aryl
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0215—Sulfur-containing compounds
    • B01J31/0222—Sulfur-containing compounds comprising sulfonyl groups
    • B01J31/0224—Sulfur-containing compounds comprising sulfonyl groups being perfluorinated, i.e. comprising at least one perfluorinated moiety as substructure in case of polyfunctional compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00—Systems containing two condensed rings
    • C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
    • C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Lubricants (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)
AT03798215T 2002-09-26 2003-09-23 Zusammensetzungen, die ionische flüssigkeiten enthalten, und deren vewendungen, insbesondere in der organischen synthese ATE349407T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0211910A FR2845084B1 (fr) 2002-09-26 2002-09-26 Compositions contenant des liquides ioniques et leurs utilisations, notamment en synthese organique

Publications (1)

Publication Number Publication Date
ATE349407T1 true ATE349407T1 (de) 2007-01-15

Family

ID=31985248

Family Applications (1)

Application Number Title Priority Date Filing Date
AT03798215T ATE349407T1 (de) 2002-09-26 2003-09-23 Zusammensetzungen, die ionische flüssigkeiten enthalten, und deren vewendungen, insbesondere in der organischen synthese

Country Status (9)

Country Link
US (2) US20060128996A1 (de)
EP (1) EP1542942B1 (de)
JP (1) JP2006500418A (de)
AT (1) ATE349407T1 (de)
AU (1) AU2003276363A1 (de)
CA (1) CA2500206C (de)
DE (1) DE60310737T2 (de)
FR (1) FR2845084B1 (de)
WO (1) WO2004029004A1 (de)

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7888412B2 (en) * 2004-03-26 2011-02-15 Board Of Trustees Of The University Of Alabama Polymer dissolution and blend formation in ionic liquids
FR2872715B1 (fr) * 2004-07-08 2006-11-17 Commissariat Energie Atomique Microreacteur goutte
GB0500028D0 (en) * 2005-01-04 2005-02-09 Univ Belfast Base stable ionic liquids
GB0500029D0 (en) 2005-01-04 2005-02-09 Univ Belfast Basic ionic liquids
FR2882057B1 (fr) * 2005-02-16 2012-11-23 Aventis Pharma Sa Synthese peptidique sur supports solubles de types sels d'onium
WO2006096963A1 (en) * 2005-03-15 2006-09-21 Mcgill University Ionic liquid supported synthesis
AU2006246838B2 (en) * 2005-05-20 2010-12-02 Wacker Chemie Ag A process for continuous carbonylation by supported ionic Liquid-Phase catalysis
CA2614117A1 (en) * 2005-06-29 2007-01-11 The University Of Alabama Ionic liquid reconstituted cellulose composites as solid support matrices
US8883193B2 (en) 2005-06-29 2014-11-11 The University Of Alabama Cellulosic biocomposites as molecular scaffolds for nano-architectures
KR100843594B1 (ko) * 2005-09-07 2008-07-03 주식회사 엘지화학 액상 산화 반응을 이용한 알데히드 화합물로부터의유기산의 제조 방법
US7737106B2 (en) * 2005-11-29 2010-06-15 The Procter & Gamble Company Process for making an ionic liquid comprising ion actives
JP5142178B2 (ja) 2006-03-10 2013-02-13 独立行政法人科学技術振興機構 イオン性液体で被覆された固定化ルイス酸触媒、及びその使用
EP1911829A1 (de) * 2006-10-10 2008-04-16 The Queen's University of Belfast Entsäuerungsverfahren für Rohöl
WO2007138307A2 (en) * 2006-05-25 2007-12-06 The Queen's University Of Belfast Process for removing sulfur-containing acids from crude oil
GB0612305D0 (en) * 2006-06-21 2006-08-02 Leuven K U Res & Dev Novel ionic liquids
WO2008003836A1 (fr) * 2006-07-05 2008-01-10 Centre National De La Recherche Scientifique Utilisation de sels d'onium fonctionnalisés pour la synthèse de peptides
WO2008012758A2 (en) * 2006-07-24 2008-01-31 The Procter & Gamble Company Process for epimerising cyclohexenyl ketones and its application in aldol condensation process
EP2254871B1 (de) * 2008-01-30 2016-11-09 Technische Universität Dresden Salze mit aryl-alkyl-substituierten imidazolium-und triazoliumkationen als ionische flüssigkeiten
WO2009105236A1 (en) 2008-02-19 2009-08-27 The Board Of Trustees Of The University Of Alabama Ionic liquid systems for the processing of biomass, their components and/or derivatives, and mixtures thereof
FR2930247B1 (fr) * 2008-04-21 2012-12-07 Commissariat Energie Atomique Sels d'onium et leur utilisation pour la detection et le dosage des metaux.
WO2010017564A1 (en) * 2008-08-08 2010-02-11 University Of Toledo Boron selective ionic liquids and polymeric ionic liquids, methods of making and methods of use thereof
US7700529B1 (en) * 2008-10-14 2010-04-20 International Flavors & Fragrances Inc. Isomers of bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester and their use in perfume compositions
US8114823B2 (en) 2008-10-14 2012-02-14 International Flavors & Fragrances Inc. Isomers of bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester and their use in perfume compositions
WO2010078300A1 (en) 2008-12-29 2010-07-08 The Board Of Trustees Of The University Of Alabama Dual functioning ionic liquids and salts thereof
US9096743B2 (en) 2009-06-01 2015-08-04 The Board Of Trustees Of The University Of Alabama Process for forming films, fibers, and beads from chitinous biomass
US8784691B2 (en) 2009-07-24 2014-07-22 Board Of Trustees Of The University Of Alabama Conductive composites prepared using ionic liquids
US9394375B2 (en) 2011-03-25 2016-07-19 Board Of Trustees Of The University Of Alabama Compositions containing recyclable ionic liquids for use in biomass processing
DE102011080230A1 (de) * 2011-08-01 2013-02-07 Helmholtz-Zentrum Dresden - Rossendorf E.V. Extraktion von Edelmetall(ionen) mittels ionischer Flüssigkeiten
CN102731370B (zh) * 2012-07-13 2013-10-16 黑龙江大学 离子液体的制备方法及应用离子液体钯碳催化合成联苯类化合物的方法
BR112016009482B8 (pt) * 2013-11-05 2022-12-06 Construction Research & Technology Gmbh Composição de revestimento, uso de uma composição de revestimento, processo para preparação de uma composição de revestimento e método para cura de uma composição de revestimento
JP6489910B2 (ja) * 2014-05-15 2019-03-27 キヤノン株式会社 ヒドロキシ化合物、イオン導電剤、および導電性樹脂組成物
JP6478775B2 (ja) 2014-05-15 2019-03-06 キヤノン株式会社 アミン化合物及びイオン導電剤、導電性樹脂組成物
US10100131B2 (en) 2014-08-27 2018-10-16 The Board Of Trustees Of The University Of Alabama Chemical pulping of chitinous biomass for chitin
US10011931B2 (en) 2014-10-06 2018-07-03 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing dyed and welded substrates
US10982381B2 (en) 2014-10-06 2021-04-20 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing welded substrates
GB2538758A (en) 2015-05-27 2016-11-30 Green Lizard Tech Ltd Process for removing chloropropanols and/or glycidol
EP3098292A1 (de) 2015-05-27 2016-11-30 Evonik Degussa GmbH Verfahren zum raffinieren von glyceridöl mit einer behandlung mit basischem quaternärem ammoniumsalz
EP3098293A1 (de) 2015-05-27 2016-11-30 Evonik Degussa GmbH Verfahren zur entfernung von metall aus einem metallhaltigen glyceridöl mit einer behandlung aus basischem quaternärem ammoniumsalz
DE102015212749A1 (de) 2015-07-08 2017-01-12 Evonik Degussa Gmbh Verfahren zur Entfeuchtung von feuchten Gasgemischen
US11766835B2 (en) 2016-03-25 2023-09-26 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing welded substrates
CN113930874B (zh) 2016-05-03 2022-11-01 天然纤维焊接股份有限公司 用于生产染色的焊接基质的方法、工艺和设备
EP3257568B1 (de) 2016-06-14 2019-09-18 Evonik Degussa GmbH Verfahren zur entfeuchtung von feuchten gasgemischen mit ionischen flüssigkeiten
DE102016210478A1 (de) 2016-06-14 2017-12-14 Evonik Degussa Gmbh Verfahren zur Entfeuchtung von feuchten Gasgemischen
DE102016210484A1 (de) 2016-06-14 2017-12-14 Evonik Degussa Gmbh Verfahren zur Entfeuchtung von feuchten Gasgemischen
US10927191B2 (en) 2017-01-06 2021-02-23 The Board Of Trustees Of The University Of Alabama Coagulation of chitin from ionic liquid solutions using kosmotropic salts
WO2018236445A2 (en) 2017-03-24 2018-12-27 The Board Of Trustees Of The University Of Alabama Metal particle-chitin composite materials and methods of making thereof
EP3483237A1 (de) 2017-11-10 2019-05-15 Evonik Degussa GmbH Verfahren zur extraktion von fettsäuren aus triglyceridölen
TWI829660B (zh) 2017-11-11 2024-01-21 美商天然纖維焊接股份有限公司 紗與熔接紗
CN113385225B (zh) * 2021-06-18 2022-11-18 抚顺东科新能源科技有限公司 一种超分子离子液体催化剂及其制备方法与应用
CN115433126B (zh) * 2022-08-12 2023-10-20 浙江工业大学 一种功能化喹啉类比色离子探针及其合成方法与应用
CN116393167B (zh) * 2023-03-09 2024-08-16 新疆至臻化工工程研究中心有限公司 一种用于草酸二甲酯与乙醇酯交换反应的离子液体催化剂

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4463071A (en) * 1983-11-30 1984-07-31 Allied Corporation Secondary batteries using room-temperature molten non-aqueous electrolytes containing 1,2,3-trialkylimidazolium halides or 1,3-dialkylimidazolium halide
US6030917A (en) * 1996-07-23 2000-02-29 Symyx Technologies, Inc. Combinatorial synthesis and analysis of organometallic compounds and catalysts
US20020010291A1 (en) * 1998-12-04 2002-01-24 Vince Murphy Ionic liquids and processes for production of high molecular weight polyisoolefins
JP2001247542A (ja) * 2000-03-06 2001-09-11 Central Glass Co Ltd ヘテロ環化合物の製造方法
JP4011830B2 (ja) * 2000-06-20 2007-11-21 独立行政法人科学技術振興機構 Ｎ−アルコキシアルキルイミダゾリウム塩、該イミダゾリウム塩からなるイオン液体ならびにイオン性ゲル
JP3541223B2 (ja) * 2001-03-08 2004-07-07 東北大学長 イオン性液体中でのＰｄ／Ｃ触媒を用いたＨｅｃｋ反応

Also Published As

Publication number Publication date
FR2845084B1 (fr) 2009-07-17
EP1542942B1 (de) 2006-12-27
JP2006500418A (ja) 2006-01-05
DE60310737T2 (de) 2008-03-20
DE60310737D1 (de) 2007-02-08
CA2500206C (fr) 2013-06-11
AU2003276363A1 (en) 2004-04-19
US20090326228A1 (en) 2009-12-31
AU2003276363A8 (en) 2004-04-19
WO2004029004A1 (fr) 2004-04-08
US9452425B2 (en) 2016-09-27
CA2500206A1 (fr) 2004-04-08
EP1542942A1 (de) 2005-06-22
FR2845084A1 (fr) 2004-04-02
US20060128996A1 (en) 2006-06-15

Similar Documents

Publication Publication Date Title
ATE349407T1 (de) Zusammensetzungen, die ionische flüssigkeiten enthalten, und deren vewendungen, insbesondere in der organischen synthese
BRPI0706947B8 (pt) método de preparação de uma composição de micropartícula
BR0213877A (pt) Compostos orgânicos
Ghovanloo et al. The Effects of Amiodarone and N-Desethylamiodarone on Cardiac Voltage-Gated Sodium Channels
BRPI0414858A (pt) métodos para preparação de corpos de óleo compreendendo ingredientes ativos
BRPI0606302A2 (pt) Uso de um líquido iônico, e, líquido iônico básico
BRPI0613429A2 (pt) inibidores de histona desacetilase
WO2005065398A3 (en) Synthesis of ionic liquids
MX2007013065A (es) Derivados de dihidrobenzofurano y usos de los mismos.
BRPI0601896A (pt) composições que contêm microgéis e agentes espessantes
BR112014000688B8 (pt) Composições pesticidas, e processo para controle de pestes
ATE337305T1 (de) Halogenfreie ionische flüssigkeiten
BRPI0507947A (pt) processo para preparação de borracha nitrìlica de baixo peso molecular
BR0308191A (pt) Fluidos de hidrocarbonetos aperfeiçoados
ES2335410T8 (es) Derivados de aminopropanol.
ZA202204076B (en) Compositions having pesticidal utility and processes related thereto
DE60141351D1 (de) Derivate von 4-hydroxybutansäure und deren höheren homologen als liganden von g-hydroxybutyrat- (gbh-)rezeptoren, pharmazeutische zusammensetzungen, die diese enthalten, und pharmazeutische anwendungen
ATE394358T1 (de) Verwendung funktionalisierter oniumsalze als lösliche träger für die organische synthese
WO2006114186A3 (de) Wasser-in-öl suspoemulsionen
GT200000003A (es) Heterociclos arilimino 2 - substituidos y composiciones que los contienen, para usar como agentes de unionde receptores de progesterona.
Chaudhari et al. Preparative-scale synthesis of amino coumarins through new sequential nitration and reduction protocol
ES2187184T3 (es) Fosfoepoxidos, procedimiento de fabricacion y aplicaciones.
BR0111669A (pt) Novos compostos
DK1960077T3 (da) Kationudvekslings-forskydningskromatografifremgangsmåde og kationiske, organiske forbindelser til anvendelse som forskydningsforbindelser i kationudvekslings-forskydningskromatografifremgangsmåde
Cichewicz et al. A revised amino group pKa for prymnesins does not provide decisive evidence for a pH-dependent mechanism of Prymnesium parvum’s toxicity

Legal Events

Date Code Title Description
RER Ceased as to paragraph 5 lit. 3 law introducing patent treaties