KR960034167A - 퍼플루오로알킬술포네이트, 술폰이미드 및 술포닐 메티드, 및 이들을 함유하는 전해질 - Google Patents
퍼플루오로알킬술포네이트, 술폰이미드 및 술포닐 메티드, 및 이들을 함유하는 전해질 Download PDFInfo
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- KR960034167A KR960034167A KR1019960005285A KR19960005285A KR960034167A KR 960034167 A KR960034167 A KR 960034167A KR 1019960005285 A KR1019960005285 A KR 1019960005285A KR 19960005285 A KR19960005285 A KR 19960005285A KR 960034167 A KR960034167 A KR 960034167A
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- 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
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- 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
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- 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
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- 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
- H01M6/04—Cells with aqueous electrolyte
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- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
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Abstract
본 발명은 하기 식(1) 및 (2)의 화합물, 매체중에 이들 화합물로 이루어진 군중에서 선택됨 염을 포함하는 전해질 조성물 및 이 전해질 조성물을 포함하는 배터리에 관한 것이다;
상기 식에서, -X-는 -O-, -N-SO2Rf 3또는 (Rf 5SO2)(SO2Rf 4)이고; Z는 -CF2-, -O-,NRf 8- 또는 -SF4, -이며; Rf 1및 Rf 2는 독립적으로 -CF3, 또는 -CmF2m +1, -(CF2)q-SO2-X-M+이고; Rf 3, Rf 4및 Rf 5는 독립적으로 -CF3, -CmF2m +1, -(CF2)4-SO2-X-M+,또는이며; Rf 8은 -CF3, -CmF2m +1, 또는 -(CF2)4-SO2-X-M+이고; Rf 6및 Rf 7은 독립적으로 식 CrF2r을 가진 퍼플루오로알킬렌 부위이며; n은 1~4이고; r은 1~4이며; m은 1~12이고; q는 1~4이며; 및 M+은 반대이온이다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (7)
- 매체중에 하기 식(1) 및 (2)의 화합물로 이루어진 군중에서 선택됨 염을 포함하는 전해질 조성물;상기 식에서, -X-는 -O-, -N-SO2Rf 3또는 (Rf 5SO2)(SO2Rf 4)이고; Z는 -CF2-, -O-,NRf 8- 또는 -SF4, -이며; Rf 1및 Rf 2는 독립적으로 -CF3, -CmF2m +1, 또는 -(CF2)q-SO2-X-M+이고; Rf 3, Rf 4및 Rf 5는 독립적으로 -CF3, -CmF2m +1, -(CF2)4-SO2-X-M+,또는이며; Rf 8은 -CF3, -CmF2m +1, 또는 -(CF2)4-SO2-X-M+이고; Rf 6및 Rf 7은 독립적으로 식 CrF2r을 가진 퍼플루오로알킬렌 부위이며; n은 1~4이고; r은 1~4이며; m은 1~12이고; q는 1~4이며; 및 M+은 반대이온이다.
- 제1항에 있어서, 상기M+가 알카리 금속, 알칼리 토금속, 전이 금속, 회유토, NH(4-j)Rj +, RjC(NH(2-j)Rj)2및 C(NH(2-j)Rj)3 +(식중, j는 0~2이고, Rj는 -H, 알킬기, 옥스알킬기 또는 아릴기임)로 이루어진 군중에서 선택된 것인 전해질 조성물.
- 제1항에 있어서, 상기 염이 하기 식 (3) 내지 (10)의 화합물로 이루어진 군중에서 선택된 것인 전해질 조성물;
- 제1항에 있어서, M+FB4 -; M+SbF6 -; M+AsF6 -; M+C1O4 -; M+C-(SO2CF3)3; M+PE6 -; CF3SO3 -M+; (CF3SO2)2N-M+(식중, M+는 반대이온임); 및 이들의 배합물로 이루어진 군중에서 선택됨을 염의 추가로 포함하는 전해질 조성물.
- 하나 이상의 양의 전극; 하나 이상의 음의 전극; 및 매체중에 하기 식(1) 및 (2)로 이루어진 군중에서 선택된 염을 포함하는 전해질을 포함한 배터리;상기 식에서, -X-는 -O-, -N-SO2Rf 3또는 (Rf 5SO2)(SO2Rf 4)이고; Z는 -CF2-, -O-,NRf 8- 또는 -SF4, -이며; Rf 1및 Rf 2는 독립적으로 -CF3, -CmF2m +1, 또는 -(CF2)q-SO2-X-M+이고; Rf 3, Rf 4및 Rf 5는 독립적으로 -CF3, -CmF2m +1, -(CF2)4-SO2-X-M+,또는이며; Rf 8은 -CF3, -CmF2m +1, 또는 -(CF2)4-SO2-X-M+이고; Rf 6및 Rf 7은 독립적으로 식 -CrF2r을 가진 퍼플루오로알킬렌 부위이며; n은 1~4이고; r은 1~4이며; m은 1~12이고; q는 1~4이며; 및 M+은 반대이온이다.
- 하기 식 (1) 및 (2)의 화합물로 이루어진 군중에서 선택된 염;상기 식에서, -X-는 -O-, -N-SO2Rf 3또는 (Rf 5SO2)(SO2Rf 4)이고; Z는 -CF2-, -O-,NRf 8- 또는 -SF4, -이며; Rf 1및 Rf 2는 독립적으로 -CF3, -CmF2m +1, 또는 -(CF2)q-SO2-X-M+이고; Rf 3, Rf 4및 Rf 5는 독립적으로 -CF3, -CmF2m +1, -(CF2)4-SO2-X-M+,또는이며; Rf 8은 -CF3, -CmF2m +1, 또는 -(CF2)4-SO2-X-M+이고; Q는 -O-, -N-SO2Rf 3또는 (Rf 5SO2)(SO2Rf 4)이며; Rf 6및 Rf 7은 독립적으로 식 CrF2r을 가진 퍼플루오로알킬렌 부위이며; n은 1~4이고; r은 1~4이며; m은 1~12이고; q는 1~4이며; 및 M+은 반대이온이다.
- 제6항에 있어서, 하기 식(5), (6), (7), (8) 및 (9)의 화합물로 군중에서 선택된 염;※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/398,859 | 1995-03-06 | ||
US08/398,859 US5514493A (en) | 1995-03-06 | 1995-03-06 | Perfluoroalkylsulfonates, sulfonimides, and sulfonyl methides, and electrolytes containing them |
Publications (1)
Publication Number | Publication Date |
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KR960034167A true KR960034167A (ko) | 1996-10-22 |
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KR1019960005285A KR960034167A (ko) | 1995-03-06 | 1996-02-29 | 퍼플루오로알킬술포네이트, 술폰이미드 및 술포닐 메티드, 및 이들을 함유하는 전해질 |
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Country | Link |
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US (1) | US5514493A (ko) |
EP (1) | EP0731518B1 (ko) |
JP (1) | JP3926864B2 (ko) |
KR (1) | KR960034167A (ko) |
CA (1) | CA2169034A1 (ko) |
DE (1) | DE69609542T2 (ko) |
ES (1) | ES2149393T3 (ko) |
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JPS63126212A (ja) * | 1986-11-14 | 1988-05-30 | 松下電器産業株式会社 | 固体電解コンデンサ |
US5256821A (en) * | 1988-10-05 | 1993-10-26 | Societe Nationale Elf Aquitaine | Method of synthesis of sulphonylimides |
FR2645533B1 (fr) * | 1989-04-06 | 1991-07-12 | Centre Nat Rech Scient | Procede de synthese de sulfonylimidures |
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 . |
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. |
DE4217366A1 (de) * | 1992-05-26 | 1993-12-02 | Bayer Ag | Imide und deren Salze sowie deren Verwendung |
US5506073A (en) * | 1992-06-22 | 1996-04-09 | Arizona State University (Arizona Board Of Regents, A Body Corporate Acting On Behalf Of Arizona State University) | Lithium ion conducting electrolytes |
US5352547A (en) * | 1992-08-27 | 1994-10-04 | Hitachi Maxell, Ltd. | Organic electrolytic solution and organic electrolytic solution cell |
-
1995
- 1995-03-06 US US08/398,859 patent/US5514493A/en not_active Expired - Lifetime
-
1996
- 1996-02-07 CA CA002169034A patent/CA2169034A1/en not_active Abandoned
- 1996-02-29 JP JP04341096A patent/JP3926864B2/ja not_active Expired - Lifetime
- 1996-02-29 KR KR1019960005285A patent/KR960034167A/ko not_active Application Discontinuation
- 1996-03-05 ES ES96103424T patent/ES2149393T3/es not_active Expired - Lifetime
- 1996-03-05 EP EP96103424A patent/EP0731518B1/en not_active Expired - Lifetime
- 1996-03-05 DE DE69609542T patent/DE69609542T2/de not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP3926864B2 (ja) | 2007-06-06 |
DE69609542T2 (de) | 2001-04-05 |
ES2149393T3 (es) | 2000-11-01 |
JPH08268998A (ja) | 1996-10-15 |
EP0731518B1 (en) | 2000-08-02 |
CA2169034A1 (en) | 1996-09-07 |
DE69609542D1 (de) | 2000-09-07 |
EP0731518A1 (en) | 1996-09-11 |
US5514493A (en) | 1996-05-07 |
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