CA2340379A1 - Cyano-substituted methide and amide salts - Google Patents
Cyano-substituted methide and amide salts Download PDFInfo
- Publication number
- CA2340379A1 CA2340379A1 CA002340379A CA2340379A CA2340379A1 CA 2340379 A1 CA2340379 A1 CA 2340379A1 CA 002340379 A CA002340379 A CA 002340379A CA 2340379 A CA2340379 A CA 2340379A CA 2340379 A1 CA2340379 A1 CA 2340379A1
- Authority
- CA
- Canada
- Prior art keywords
- group
- compound
- carbon atoms
- electrolyte
- perfluorinated
- 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
Links
- -1 amide salts Chemical class 0.000 title claims abstract description 103
- 125000005525 methide group Chemical class 0.000 title abstract description 9
- 239000003792 electrolyte Substances 0.000 claims abstract description 93
- 150000003839 salts Chemical class 0.000 claims abstract description 84
- 125000004432 carbon atom Chemical group C* 0.000 claims description 44
- 150000001768 cations Chemical class 0.000 claims description 34
- LGRLWUINFJPLSH-UHFFFAOYSA-N methanide Chemical compound [CH3-] LGRLWUINFJPLSH-UHFFFAOYSA-N 0.000 claims description 31
- 150000001875 compounds Chemical class 0.000 claims description 28
- 125000001931 aliphatic group Chemical group 0.000 claims description 27
- 239000011159 matrix material Substances 0.000 claims description 25
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 21
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- 150000002430 hydrocarbons Chemical class 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 229910052757 nitrogen Inorganic materials 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- 125000001153 fluoro group Chemical group F* 0.000 claims description 11
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 125000005647 linker group Chemical group 0.000 claims description 11
- 239000004215 Carbon black (E152) Substances 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 125000005842 heteroatom Chemical group 0.000 claims description 9
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 125000005003 perfluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 claims description 3
- 125000001183 hydrocarbyl group Chemical class 0.000 claims 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 150000001408 amides Chemical class 0.000 abstract description 18
- 125000004093 cyano group Chemical group *C#N 0.000 abstract description 7
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- 238000010494 dissociation reaction Methods 0.000 abstract description 2
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- 229910052782 aluminium Inorganic materials 0.000 description 19
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- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 18
- 239000007787 solid Substances 0.000 description 17
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- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 7
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- 229920001577 copolymer Polymers 0.000 description 5
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 5
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- 229940021013 electrolyte solution Drugs 0.000 description 5
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- 238000005481 NMR spectroscopy Methods 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
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- 229910052739 hydrogen Inorganic materials 0.000 description 4
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- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- BOXSCYUXSBYGRD-UHFFFAOYSA-N cyclopenta-1,3-diene;iron(3+) Chemical compound [Fe+3].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 BOXSCYUXSBYGRD-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 210000001787 dendrite Anatomy 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
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- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical group FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 239000004811 fluoropolymer Substances 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052808 lithium carbonate 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
- UGEOMRBXRFUYJH-UHFFFAOYSA-N lithium;1,1,1-trifluoro-n-(trifluoromethylsulfonyl)methanesulfonamide Chemical compound [Li].FC(F)(F)S(=O)(=O)NS(=O)(=O)C(F)(F)F UGEOMRBXRFUYJH-UHFFFAOYSA-N 0.000 description 1
- ACFSQHQYDZIPRL-UHFFFAOYSA-N lithium;bis(1,1,2,2,2-pentafluoroethylsulfonyl)azanide Chemical compound [Li+].FC(F)(F)C(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)C(F)(F)F ACFSQHQYDZIPRL-UHFFFAOYSA-N 0.000 description 1
- QSZMZKBZAYQGRS-UHFFFAOYSA-N lithium;bis(trifluoromethylsulfonyl)azanide Chemical compound [Li+].FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F QSZMZKBZAYQGRS-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
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- 239000012528 membrane Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical compound C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 229960001027 opium Drugs 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 150000002924 oxiranes Chemical group 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
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- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002627 poly(phosphazenes) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
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- 238000007790 scraping Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
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- 150000003457 sulfones Chemical class 0.000 description 1
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- 229920001897 terpolymer Polymers 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 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
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229910000314 transition metal oxide Inorganic materials 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
- 238000005829 trimerization reaction Methods 0.000 description 1
- DSROZUMNVRXZNO-UHFFFAOYSA-K tris[(1-naphthalen-1-yl-3-phenylnaphthalen-2-yl)oxy]alumane Chemical compound C=1C=CC=CC=1C=1C=C2C=CC=CC2=C(C=2C3=CC=CC=C3C=CC=2)C=1O[Al](OC=1C(=C2C=CC=CC2=CC=1C=1C=CC=CC=1)C=1C2=CC=CC=C2C=CC=1)OC(C(=C1C=CC=CC1=C1)C=2C3=CC=CC=C3C=CC=2)=C1C1=CC=CC=C1 DSROZUMNVRXZNO-UHFFFAOYSA-K 0.000 description 1
- 238000004832 voltammetry Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/139,315 | 1998-08-25 | ||
| US09/139,315 US6294289B1 (en) | 1998-08-25 | 1998-08-25 | Cyano-substituted methide and amide salts |
| PCT/US1999/017616 WO2000011742A1 (en) | 1998-08-25 | 1999-08-04 | Cyano-substituted methide and amide salts |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2340379A1 true CA2340379A1 (en) | 2000-03-02 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002340379A Abandoned CA2340379A1 (en) | 1998-08-25 | 1999-08-04 | 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 |
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|---|---|---|---|---|
| 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
-
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
Also Published As
| Publication number | Publication date |
|---|---|
| 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 |
| JP2002523879A (ja) | 2002-07-30 |
| KR20010072928A (ko) | 2001-07-31 |
| EP1108270A1 (en) | 2001-06-20 |
| TW449942B (en) | 2001-08-11 |
| EP1108270B1 (en) | 2007-10-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued | ||
| FZDE | Discontinued |
Effective date: 20090804 |