ES2044587T3 - Procedimiento de sintesis de sulfonilimiduros. - Google Patents
Procedimiento de sintesis de sulfonilimiduros.Info
- Publication number
- ES2044587T3 ES2044587T3 ES90907110T ES90907110T ES2044587T3 ES 2044587 T3 ES2044587 T3 ES 2044587T3 ES 90907110 T ES90907110 T ES 90907110T ES 90907110 T ES90907110 T ES 90907110T ES 2044587 T3 ES2044587 T3 ES 2044587T3
- Authority
- ES
- Spain
- Prior art keywords
- atoms
- carbon
- sulfonylimidide
- radicals
- formula
- 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 - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/38—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reaction of ammonia or amines with sulfonic acids, or with esters, anhydrides, or halides thereof
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/16—Cells with non-aqueous electrolyte with organic electrolyte
- H01M6/162—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte
- H01M6/166—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte by the solute
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/18—Cells with non-aqueous electrolyte with solid electrolyte
- H01M6/181—Cells with non-aqueous electrolyte with solid electrolyte with polymeric electrolytes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Electrochemistry (AREA)
- Engineering & Computer Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Secondary Cells (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
EL INVENTO TIENE POR OBJETO UN PROCESO DE SINTESIS DE SULFONILIMIDURAS. EL PROCESO DE SINTESIS DE SULFONILIMIDURAS DE FORMULA GENERAL M [CRSO2)2N]Y EN LA CUAL M REPRESENTA UN METAL ESCOGIDO ENTRE LOS METALES ALCALINOS, METALES ALCALINO-TERREOS, TIERRAS VARAS, AL, SC, Y Y TH, R REPRESENTA UN RADICAL MONOVALENTE ESCOGIDO ENTRE LOS RADICALES ALIFATICOS, TENIENDO DE 1 A 8 ATOMOS DE CARBONO, LINEALES O RAMIFICADOS, LOS RADICALES ALICICLICOS TIENEN DE 3 A 8 ATOMOS DE CARBONO, LOS RADICALES ARILICOS TIENEN DE 3 A 8 ATOMOS DE CARBONO E "Y" ES UN NUMERO IGUAL A LA VALENCIA DE M, ESTA CARACTERIZADO EN QUE SE HACE REACCIONAR UN NITRURO IONICO DE FORMULA M3NY EN LA CUAL M E "Y" TIENEN LA SIGNIFICACION DADA MAS ARRIBA, CON UN HALOGENURO DE SULFONILO RESPONDIENDO A LA FORMULA RSO2X EN LA CUAL R TIENE LA SIGNIFICACION DADA MAS ARRIBA Y X ESTA ESCOGIDO ENTRE F O CL, EN UN DISOLVENTE APROTICO POLAR.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8904504A FR2645533B1 (fr) | 1989-04-06 | 1989-04-06 | Procede de synthese de sulfonylimidures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2044587T3 true ES2044587T3 (es) | 1994-01-01 |
Family
ID=9380429
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES90907110T Expired - Lifetime ES2044587T3 (es) | 1989-04-06 | 1990-04-05 | Procedimiento de sintesis de sulfonilimiduros. |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5072040A (es) |
| EP (1) | EP0419647B1 (es) |
| JP (1) | JPH04501118A (es) |
| CA (1) | CA2030809A1 (es) |
| DE (1) | DE69003063T2 (es) |
| ES (1) | ES2044587T3 (es) |
| FR (1) | FR2645533B1 (es) |
| WO (1) | WO1990011999A1 (es) |
Families Citing this family (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2683524A1 (fr) * | 1991-11-08 | 1993-05-14 | Centre Nat Rech Scient | Derives des bis(perfluorosulfonyl)methanes, leur procede de preparation, et leurs utilisations . |
| US5883220A (en) * | 1992-01-12 | 1999-03-16 | Centre National De La Recherche Scientifique | Redox copolymers and their use in preparing mixed conduction materials |
| FR2687671B1 (fr) * | 1992-02-21 | 1994-05-20 | Centre Nal Recherc Scientifique | Monomeres derives de sultones perhalogenees et polymeres obtenus a partir de ces monomeres. |
| US5627292A (en) * | 1992-02-21 | 1997-05-06 | Centre National De La Recherche Scientifique | Monomers derived from perhalogenated sultones and polymers obtained from these monomers |
| FR2693731B1 (fr) * | 1992-07-15 | 1994-10-21 | Centre Nat Rech Scient | Copolymères d'oxirane et de dioxolane, leur procédé de préparation et matériaux à conduction ionique les contenant. |
| US5508130A (en) * | 1992-07-22 | 1996-04-16 | Golovin; Milton N. | Solid electrolytes containing LiN(SO2 CF3)2 and a triglyme-carbonate solvent, and electrochemical cells produced therefrom |
| FR2694758B1 (fr) * | 1992-08-14 | 1994-10-21 | Centre Nat Rech Scient | Copolymères réticulablres obtenus par polycondensation et matériau à conduction ionique les contenant. |
| US5403957A (en) * | 1992-10-20 | 1995-04-04 | Wagner; William J. | Method for preparing N-fluorosulfonimides |
| DE4313664C2 (de) * | 1993-04-20 | 1996-12-05 | Schering Ag | N-Fluormethansulfonimid, Verfahren zu seiner Herstellung sowie dessen Verwendung |
| FR2713646B1 (fr) * | 1993-12-09 | 1996-02-23 | Centre Nat Rech Scient | Procédé de préparation d'un terpolymère du type poly(oxyalkylène) par hydrogénation. |
| DE69413020T2 (de) * | 1994-07-12 | 1999-02-18 | Imation Corp., Oakdale, Minn. | Antistatischer Röntgenstrahlenverstärkungsschirm mit Sulfonylmethid- und Sulfonylimidlithiumsalzen |
| FR2723098B1 (fr) * | 1994-07-28 | 1996-10-04 | Centre Nat Rech Scient | Materiau macromoleculaire comportant des substituants ioniques et son utilisation dans les systemes electrochimiques |
| US5514493A (en) * | 1995-03-06 | 1996-05-07 | Minnesota Mining And Manufacturing Company | Perfluoroalkylsulfonates, sulfonimides, and sulfonyl methides, and electrolytes containing them |
| US5874616A (en) * | 1995-03-06 | 1999-02-23 | Minnesota Mining And Manufacturing Company | Preparation of bis (fluoroalkylenesulfonyl) imides and (fluoroalkysulfony) (fluorosulfonyl) imides |
| US5691081A (en) * | 1995-09-21 | 1997-11-25 | Minnesota Mining And Manufacturing Company | Battery containing bis(perfluoroalkylsulfonyl)imide and cyclic perfluoroalkylene disulfonylimide salts |
| US5652072A (en) * | 1995-09-21 | 1997-07-29 | Minnesota Mining And Manufacturing Company | Battery containing bis(perfluoroalkylsulfonyl)imide and cyclic perfluoroalkylene disulfonylimide salts |
| JP3750179B2 (ja) * | 1996-03-22 | 2006-03-01 | 三菱化学株式会社 | 有機酸リチウム塩の精製方法 |
| US5962546A (en) * | 1996-03-26 | 1999-10-05 | 3M Innovative Properties Company | Cationically polymerizable compositions capable of being coated by electrostatic assistance |
| DE69618019T2 (de) * | 1996-03-26 | 2002-08-01 | Minnesota Mining And Mfg. Co., Saint Paul | Kationisch polymerisierbare zusmmensetzungen, die zur beschichtung in einem elektrostatischen verfahren verwendet werden können |
| JP4124487B2 (ja) | 1996-12-30 | 2008-07-23 | イドロ―ケベック | 五員環アニオン塩又はテトラアザペンタレン誘導体と、イオン伝導性物質としてのそれらの使用 |
| US5723630A (en) * | 1997-02-18 | 1998-03-03 | Minnesota Mining And Manufacturing Company | Process for preparing fluorinated beta-sultones |
| RU2114824C1 (ru) * | 1997-04-17 | 1998-07-10 | Ангарский электролизный химический комбинат | Способ получения бис(трифторметансульфонил)имида |
| FR2763331B1 (fr) | 1997-05-16 | 1999-06-25 | Rhodia Chimie Sa | Procede de synthese de sulfonimides et de leurs sels |
| DE19733948A1 (de) * | 1997-08-06 | 1999-02-11 | Merck Patent Gmbh | Verfahren zur Herstellung von Perfluoralkan-1-sulfonyl(perfluoralkylsulfonyl) imid-N-sulfonyl enthaltende Methanide, Imide und Sulfonate, und Perfluoralkan-1-N-(sulfonylbis(perfluoralkylsulfonyl)methaniden) |
| JP4859264B2 (ja) | 1997-12-01 | 2012-01-25 | アセップ・インク | 過弗素化されたスルホン塩類、およびイオン性伝導材料としてのそれらの使用 |
| KR100559110B1 (ko) | 1997-12-10 | 2006-03-13 | 미네소타 마이닝 앤드 매뉴팩춰링 캄파니 | 전기화학 시스템에서의 비스(퍼플루오로알킬설포닐)이미드 계면활성제 염 |
| US6063522A (en) * | 1998-03-24 | 2000-05-16 | 3M Innovative Properties Company | Electrolytes containing mixed fluorochemical/hydrocarbon imide and methide salts |
| AU3115500A (en) | 1998-12-09 | 2000-06-26 | B.F. Goodrich Company, The | In mold addition polymerization of norbornene-type monomers using group 10 metal complexes |
| US6252111B1 (en) * | 1999-02-16 | 2001-06-26 | Central Glass Company, Limited | Method for producing sulfonimide or its salt |
| US6355735B1 (en) | 1999-08-17 | 2002-03-12 | 3M Innovative Properties Company | Semi-interpenetrating polymer network from epoxy monomer and olefin |
| US6372829B1 (en) | 1999-10-06 | 2002-04-16 | 3M Innovative Properties Company | Antistatic composition |
| US6587628B1 (en) | 1999-11-22 | 2003-07-01 | 3M Innovative Properties Company | Optical fiber with improved strength in high humidity/high temperature environments |
| CN1402705A (zh) * | 1999-12-02 | 2003-03-12 | 纳幕尔杜邦公司 | 由磺酰氟制备二酰亚胺的方法 |
| US6592988B1 (en) | 1999-12-29 | 2003-07-15 | 3M Innovative Properties Company | Water-and oil-repellent, antistatic composition |
| US6518347B1 (en) | 2000-12-27 | 2003-02-11 | 3M Innovative Properties Company | Flame retardant carbonate polymers and use thereof |
| US6545109B2 (en) | 2001-06-29 | 2003-04-08 | 3M Innovative Properties Company | Imide salts as emulsifiers for the polymerization of fluoroolefins |
| US6895156B2 (en) | 2001-10-09 | 2005-05-17 | 3M Innovative Properties Company | Small diameter, high strength optical fiber |
| US6727386B2 (en) | 2001-10-25 | 2004-04-27 | 3M Innovative Properties Company | Aromatic imide and aromatic methylidynetrissulfonyl compounds and method of making |
| US6863838B2 (en) * | 2001-10-25 | 2005-03-08 | 3M Innovative Properties Company | Zwitterionic imides |
| US20030162099A1 (en) | 2002-02-28 | 2003-08-28 | Bowden William L. | Non-aqueous electrochemical cell |
| US20040137324A1 (en) * | 2002-12-27 | 2004-07-15 | Masaharu Itaya | Electrolyte for nanaqueous battery, method for producing the same, and electrolytic solution for nonaqueous battery |
| US20040265733A1 (en) * | 2003-06-30 | 2004-12-30 | Houlihan Francis M. | Photoacid generators |
| US20050287441A1 (en) * | 2004-06-23 | 2005-12-29 | Stefano Passerini | Lithium polymer electrolyte batteries and methods of making |
| US7285356B2 (en) | 2004-07-23 | 2007-10-23 | The Gillette Company | Non-aqueous electrochemical cells |
| US7598002B2 (en) * | 2005-01-11 | 2009-10-06 | Material Methods Llc | Enhanced electrochemical cells with solid-electrolyte interphase promoters |
| US7479348B2 (en) | 2005-04-08 | 2009-01-20 | The Gillette Company | Non-aqueous electrochemical cells |
| US20110300367A1 (en) | 2010-06-07 | 2011-12-08 | Ching-Kee Chien | Optical Fiber With Photoacid Coating |
| WO2012128964A1 (en) | 2011-03-08 | 2012-09-27 | Trinapco, Inc. | Method of making fluorosulfonylamine |
| EP2864128A1 (en) | 2012-06-21 | 2015-04-29 | 3M Innovative Properties Company | A static dissipating laser engravable film |
| KR102115384B1 (ko) | 2012-11-16 | 2020-05-26 | 트리나프코 인크. | 테트라부틸암모늄 비스(플루오로술포닐)이미드 및 관련 염의 합성 |
| US9322986B2 (en) | 2013-06-24 | 2016-04-26 | Corning Incorporated | Optical fiber coating for short data network |
| CN105947998B (zh) * | 2016-04-29 | 2018-05-15 | 金国范 | 一种利用氮化锂制备双氟磺酰亚胺锂盐的方法 |
| CN120413753A (zh) | 2018-05-04 | 2025-08-01 | 尤米科尔公司 | 包含氟化电解质的Ni基锂离子二次蓄电池 |
| PL3788667T3 (pl) | 2018-05-04 | 2025-04-22 | Umicore | Wtórna bateria na bazie litu i tlenku kobaltu zawierająca fluorowany elektrolit i materiał elektrody dodatniej do zastosowań wysokonapięciowych |
| EP3788671A1 (en) | 2018-05-04 | 2021-03-10 | Solvay Sa | Non-aqueous liquid electrolyte composition |
| CN109369474B (zh) * | 2018-12-29 | 2021-02-05 | 江苏华盛锂电材料股份有限公司 | 一种二(三氟甲基磺酰)亚胺锂盐的制备方法 |
| CN109776362B (zh) | 2019-03-08 | 2022-02-15 | 如鲲(山东)新材料科技有限公司 | 一种双三氟磺酰亚胺盐的新工艺 |
| FR3095204A1 (fr) | 2019-04-16 | 2020-10-23 | Sce France | Solvants carbonates pour électrolytes non aqueux, électrolytes non aqueux et dispositifs électrochimiques, et leurs procédés de fabrication |
| WO2021031430A1 (en) * | 2019-08-22 | 2021-02-25 | Fujian Yongjing Technology Co., Ltd | New process for the synthesis of fluorinated conductive salts for lithium ion batteries |
| CN113135555B (zh) * | 2021-04-28 | 2022-12-02 | 多氟多新材料股份有限公司 | 一种双氟磺酰亚胺锂的制备方法 |
| CN116969867A (zh) * | 2023-06-16 | 2023-10-31 | 中船(邯郸)派瑞特种气体股份有限公司 | 一种双三氟甲磺酰亚胺的制备方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1249259B (de) * | 1966-04-14 | 1967-09-07 | Farbenfabriken Bayer Aktiengesellschaft, Leverkusen | Verfahren zur Herstellung von N'-substituierten N-(Amidosulfonyl)-sulfonsäureamiden |
| DE1265157B (de) * | 1966-11-30 | 1968-04-04 | Henkel & Cie Gmbh | Verfahren zur Herstellung aliphatischer und aliphatisch-aromatischer Disulfimide |
| DE2239817A1 (de) * | 1972-08-12 | 1974-02-21 | Bayer Ag | Bis-perfluoralkansulfonsaeureimide sowie verfahren zu ihrer herstellung |
| DE2639473C2 (de) * | 1976-09-02 | 1986-03-27 | Bayer Ag, 5090 Leverkusen | Alkoxylierte Perfluoralkansulfonamide und deren Quaternierungsprodukte, Verfahren zu deren Herstellung und deren Verwendung |
| FR2527602A1 (fr) * | 1982-06-01 | 1983-12-02 | Anvar | Bis perhalogenoacyl- ou sulfonyl- imidures de metaux alcalins, leurs solutions solides avec des matieres plastiques et leur application a la constitution d'elements conducteurs pour des generateurs electrochimiques |
| US4697011A (en) * | 1985-07-24 | 1987-09-29 | Research Corporation | N-fluoro-N-perfluoromethyl sulfonamides |
-
1989
- 1989-04-06 FR FR8904504A patent/FR2645533B1/fr not_active Expired - Lifetime
-
1990
- 1990-04-05 JP JP2506618A patent/JPH04501118A/ja active Pending
- 1990-04-05 EP EP90907110A patent/EP0419647B1/fr not_active Expired - Lifetime
- 1990-04-05 DE DE90907110T patent/DE69003063T2/de not_active Expired - Fee Related
- 1990-04-05 CA CA002030809A patent/CA2030809A1/fr not_active Abandoned
- 1990-04-05 ES ES90907110T patent/ES2044587T3/es not_active Expired - Lifetime
- 1990-04-05 WO PCT/FR1990/000240 patent/WO1990011999A1/fr not_active Ceased
- 1990-04-05 US US07/613,642 patent/US5072040A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US5072040A (en) | 1991-12-10 |
| EP0419647A1 (fr) | 1991-04-03 |
| WO1990011999A1 (fr) | 1990-10-18 |
| FR2645533A1 (fr) | 1990-10-12 |
| DE69003063T2 (de) | 1994-03-17 |
| JPH04501118A (ja) | 1992-02-27 |
| DE69003063D1 (de) | 1993-10-07 |
| FR2645533B1 (fr) | 1991-07-12 |
| CA2030809A1 (fr) | 1990-10-07 |
| EP0419647B1 (fr) | 1993-09-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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