TW449942B - Cyano-substituted methide and amide salts - Google Patents
Cyano-substituted methide and amide salts Download PDFInfo
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- TW449942B TW449942B TW088114037A TW88114037A TW449942B TW 449942 B TW449942 B TW 449942B TW 088114037 A TW088114037 A TW 088114037A TW 88114037 A TW88114037 A TW 88114037A TW 449942 B TW449942 B TW 449942B
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- -1 amide salts Chemical class 0.000 title claims abstract description 89
- 125000005525 methide group Chemical class 0.000 title abstract 3
- 239000003792 electrolyte Substances 0.000 claims abstract description 100
- 150000003839 salts Chemical class 0.000 claims abstract description 98
- 150000001875 compounds Chemical class 0.000 claims description 53
- 125000004432 carbon atom Chemical group C* 0.000 claims description 47
- 150000001768 cations Chemical class 0.000 claims description 44
- 125000001931 aliphatic group Chemical group 0.000 claims description 41
- 239000011159 matrix material Substances 0.000 claims description 26
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 22
- 125000003118 aryl group Chemical group 0.000 claims description 22
- 230000002079 cooperative effect Effects 0.000 claims description 22
- 229920000642 polymer Polymers 0.000 claims description 22
- 229910052799 carbon Inorganic materials 0.000 claims description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 229910052731 fluorine Inorganic materials 0.000 claims description 16
- 125000001183 hydrocarbyl group Chemical class 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 15
- 125000001153 fluoro group Chemical group F* 0.000 claims description 14
- 125000005842 heteroatom Chemical group 0.000 claims description 14
- 125000005647 linker group Chemical group 0.000 claims description 14
- 125000004122 cyclic group Chemical group 0.000 claims description 11
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 7
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
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- PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 claims 2
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- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 1
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- 238000006471 dimerization reaction Methods 0.000 description 1
- YOTZYFSGUCFUKA-UHFFFAOYSA-N dimethylphosphine Chemical compound CPC YOTZYFSGUCFUKA-UHFFFAOYSA-N 0.000 description 1
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- 150000002170 ethers Chemical class 0.000 description 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
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- 229910052740 iodine Inorganic materials 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910001540 lithium hexafluoroarsenate(V) Inorganic materials 0.000 description 1
- IIPYXGDZVMZOAP-UHFFFAOYSA-N lithium nitrate Inorganic materials [Li+].[O-][N+]([O-])=O IIPYXGDZVMZOAP-UHFFFAOYSA-N 0.000 description 1
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- LPNBBFKOUUSUDB-UHFFFAOYSA-M p-toluate Chemical compound CC1=CC=C(C([O-])=O)C=C1 LPNBBFKOUUSUDB-UHFFFAOYSA-M 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
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- 229910052702 rhenium Inorganic materials 0.000 description 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
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- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical class O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
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- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
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- SLVAEVYIJHDKRO-UHFFFAOYSA-N trifluoromethanesulfonyl fluoride Chemical compound FC(F)(F)S(F)(=O)=O SLVAEVYIJHDKRO-UHFFFAOYSA-N 0.000 description 1
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- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides 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
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides 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
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/09—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton the carbon skeleton being further substituted by at least two halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0565—Polymeric materials, e.g. gel-type or solid-type
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
- H01M10/0568—Liquid materials characterised by the solutes
-
- 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
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Inorganic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Secondary Cells (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
- Conductive Materials (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/139,315 US6294289B1 (en) | 1998-08-25 | 1998-08-25 | Cyano-substituted methide and amide salts |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW449942B true TW449942B (en) | 2001-08-11 |
Family
ID=22486067
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW088114037A TW449942B (en) | 1998-08-25 | 1999-08-17 | Cyano-substituted methide and amide salts |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6294289B1 (enExample) |
| EP (1) | EP1108270B1 (enExample) |
| JP (1) | JP2002523879A (enExample) |
| KR (1) | KR20010072928A (enExample) |
| AU (1) | AU5334699A (enExample) |
| CA (1) | CA2340379A1 (enExample) |
| DE (1) | DE69937455T2 (enExample) |
| TW (1) | TW449942B (enExample) |
| WO (1) | WO2000011742A1 (enExample) |
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| 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 |
| 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 |
| SE518564C2 (sv) * | 1999-12-20 | 2002-10-22 | Ericsson Telefon Ab L M | Polymer elektrolyt, battericell innefattande elektrolyten, förfarande för framställning av elektrolyten samt användning av elektrolyten och battericellen |
| AU2000253140A1 (en) * | 2000-01-11 | 2001-07-24 | 3M Innovative Properties Company | Perfluoroalkanesulfonate salts in electrochemical systems |
| US6699623B1 (en) | 2000-04-26 | 2004-03-02 | E. I. Du Pont De Nemours And Company | High performance lithium or lithium ion cell |
| CA2419226A1 (en) * | 2000-08-18 | 2002-03-21 | University Of North Carolina At Chapel Hill | Compositions of nucleic acids that form molten phases and methods of use thereof |
| KR20040005831A (ko) * | 2000-10-06 | 2004-01-16 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 고성능 리튬 또는 리튬 이온 전지 |
| US6518347B1 (en) | 2000-12-27 | 2003-02-11 | 3M Innovative Properties Company | Flame retardant carbonate polymers and use thereof |
| US20030054172A1 (en) * | 2001-05-10 | 2003-03-20 | 3M Innovative Properties Company | Polyoxyalkylene ammonium salts and their use as antistatic agents |
| JP2003203674A (ja) * | 2001-10-29 | 2003-07-18 | Sanyo Electric Co Ltd | 非水電解質二次電池 |
| US6740413B2 (en) | 2001-11-05 | 2004-05-25 | 3M Innovative Properties Company | Antistatic compositions |
| US6924329B2 (en) * | 2001-11-05 | 2005-08-02 | 3M Innovative Properties Company | Water- and oil-repellent, antistatic compositions |
| CN1449069A (zh) * | 2002-04-02 | 2003-10-15 | 株式会社日本触媒 | 电解质溶液用材料及其用途 |
| AU2003280692A1 (en) * | 2002-10-31 | 2004-05-25 | Mitsubishi Chemical Corporation | Electrolyte for electrolytic capacitor, electrolytic capacitor and process for producing tetrafluoroaluminate salt of organic onium |
| US8124869B2 (en) * | 2003-01-15 | 2012-02-28 | Nippon Shokubai Co., Ltd. | Dye-sensitized type solar cell |
| KR20070013326A (ko) * | 2004-05-10 | 2007-01-30 | 가부시키가이샤 닛폰 쇼쿠바이 | 전해액용 재료, 이온 재료 함유 조성물 및 그 사용 |
| KR100746479B1 (ko) * | 2005-09-15 | 2007-08-03 | 주식회사 엘지화학 | 비수전해액 첨가제 및 이를 이용한 전기 화학 소자 |
| US7541492B2 (en) * | 2005-10-26 | 2009-06-02 | Toyota Jidosha Kabushiki Kaisha | Perfluoroalkanesulfonamide compounds |
| US7718319B2 (en) | 2006-09-25 | 2010-05-18 | Board Of Regents, The University Of Texas System | Cation-substituted spinel oxide and oxyfluoride cathodes for lithium ion batteries |
| US8415070B2 (en) * | 2006-12-21 | 2013-04-09 | E I Du Pont De Nemours And Company | Partially fluorinated cyclic ionic polymers and membranes |
| US7456314B2 (en) * | 2006-12-21 | 2008-11-25 | E.I. Du Pont De Nemours And Company | Partially fluorinated ionic compounds |
| TW200909549A (en) * | 2007-04-13 | 2009-03-01 | 3M Innovative Properties Co | Antistatic optically clear pressure sensitive adhesive |
| KR20110008028A (ko) * | 2008-03-07 | 2011-01-25 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 대전 방지 블록 코폴리머 감압성 접착제 및 물품 |
| US9350017B2 (en) | 2010-11-12 | 2016-05-24 | A123 Systems Llc | High performance lithium or lithium ion cell |
| US9263731B2 (en) | 2010-11-12 | 2016-02-16 | A123 Systems Llc | High performance lithium or lithium ion cell |
| CN105580184B (zh) * | 2013-09-25 | 2019-03-12 | 国立大学法人东京大学 | 非水电解质二次电池 |
| WO2015045387A1 (ja) * | 2013-09-25 | 2015-04-02 | 国立大学法人東京大学 | 非水電解質二次電池 |
| WO2015045386A1 (ja) * | 2013-09-25 | 2015-04-02 | 国立大学法人東京大学 | 非水系二次電池 |
| CN104953177A (zh) * | 2014-03-26 | 2015-09-30 | 中国科学院福建物质结构研究所 | 一种高温型锂电池电解液 |
| JP6067631B2 (ja) * | 2014-08-06 | 2017-01-25 | トヨタ自動車株式会社 | フッ化物イオン電池用電解液およびフッ化物イオン電池 |
| KR102586005B1 (ko) * | 2022-09-13 | 2023-10-06 | 제이엘켐 주식회사 | 리튬 이차 전지용 술포닐계 첨가제, 이를 포함하는 리튬 이차 전지용 전해액 및 이를 포함하는 리튬 이차 전지 |
| CN119798123A (zh) * | 2023-01-05 | 2025-04-11 | 清华大学 | 内盐型有机锂盐及其制备方法、锂电池电解液和锂电池 |
| CN116621743B (zh) * | 2023-04-24 | 2025-09-02 | 清华大学 | 含氰基锂盐及其制备方法和锂电池电解液、锂电池 |
| FR3161982A1 (fr) * | 2024-05-06 | 2025-11-07 | Commissariat à l'énergie atomique et aux énergies alternatives | Nouveau sel organique de métal alcalin et son utilisation dans des électrolytes pour batteries |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE118433C (de) | 1899-07-16 | 1901-03-05 | Ernst Leitz | Sphärisch chromatisch und astigmatisch korrigirtes Objektiv |
| US5232940A (en) | 1985-12-20 | 1993-08-03 | Hatton Leslie R | Derivatives of N-phenylpyrazoles |
| DE3545594A1 (de) | 1985-12-21 | 1987-06-25 | Roehm Gmbh | Natriummethacryloylcyanamid und seine verwendung als polymerisierbares monomeres |
| US5273840A (en) | 1990-08-01 | 1993-12-28 | Covalent Associates Incorporated | Methide salts, formulations, electrolytes and batteries formed therefrom |
| FR2683524A1 (fr) | 1991-11-08 | 1993-05-14 | Centre Nat Rech Scient | Derives des bis(perfluorosulfonyl)methanes, leur procede de preparation, et leurs utilisations . |
| 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 |
-
1998
- 1998-08-25 US US09/139,315 patent/US6294289B1/en not_active Expired - Lifetime
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1999
- 1999-08-04 KR KR1020017002354A patent/KR20010072928A/ko not_active Ceased
- 1999-08-04 EP EP99938974A patent/EP1108270B1/en not_active Expired - Lifetime
- 1999-08-04 WO PCT/US1999/017616 patent/WO2000011742A1/en not_active Ceased
- 1999-08-04 DE DE69937455T patent/DE69937455T2/de not_active Expired - Lifetime
- 1999-08-04 CA CA002340379A patent/CA2340379A1/en not_active Abandoned
- 1999-08-04 AU AU53346/99A patent/AU5334699A/en not_active Abandoned
- 1999-08-04 JP JP2000566911A patent/JP2002523879A/ja not_active Withdrawn
- 1999-08-17 TW TW088114037A patent/TW449942B/zh not_active IP Right Cessation
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|---|---|
| WO2000011742A1 (en) | 2000-03-02 |
| US6294289B1 (en) | 2001-09-25 |
| DE69937455D1 (de) | 2007-12-13 |
| DE69937455T2 (de) | 2008-08-21 |
| AU5334699A (en) | 2000-03-14 |
| CA2340379A1 (en) | 2000-03-02 |
| JP2002523879A (ja) | 2002-07-30 |
| KR20010072928A (ko) | 2001-07-31 |
| EP1108270A1 (en) | 2001-06-20 |
| EP1108270B1 (en) | 2007-10-31 |
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