JP6498668B2 - 二重結合含有基を含むフッ化カーボネート、その製造方法、及びその使用 - Google Patents
二重結合含有基を含むフッ化カーボネート、その製造方法、及びその使用 Download PDFInfo
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- JP6498668B2 JP6498668B2 JP2016524814A JP2016524814A JP6498668B2 JP 6498668 B2 JP6498668 B2 JP 6498668B2 JP 2016524814 A JP2016524814 A JP 2016524814A JP 2016524814 A JP2016524814 A JP 2016524814A JP 6498668 B2 JP6498668 B2 JP 6498668B2
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- Prior art keywords
- alkylene
- carbonate
- compound
- compound according
- general formula
- Prior art date
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- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 52
- 239000003792 electrolyte Substances 0.000 claims description 47
- 239000000203 mixture Substances 0.000 claims description 45
- 239000002904 solvent Substances 0.000 claims description 35
- 229910001416 lithium ion Inorganic materials 0.000 claims description 23
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 claims description 21
- 239000000654 additive Substances 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 15
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 14
- 125000005275 alkylenearyl group Chemical group 0.000 claims description 13
- 230000000996 additive effect Effects 0.000 claims description 12
- 125000005218 alkyleneheteroaryl group Chemical group 0.000 claims description 12
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 11
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 10
- JDZCKJOXGCMJGS-UHFFFAOYSA-N [Li].[S] Chemical compound [Li].[S] JDZCKJOXGCMJGS-UHFFFAOYSA-N 0.000 claims description 10
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- 229910052744 lithium Inorganic materials 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 claims description 6
- HCUYBXPSSCRKRF-UHFFFAOYSA-N diphosgene Chemical compound ClC(=O)OC(Cl)(Cl)Cl HCUYBXPSSCRKRF-UHFFFAOYSA-N 0.000 claims description 6
- UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 claims description 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 4
- XKAFKUGMXFMRCC-UHFFFAOYSA-N 1,1-diphenylurea Chemical compound C=1C=CC=CC=1N(C(=O)N)C1=CC=CC=C1 XKAFKUGMXFMRCC-UHFFFAOYSA-N 0.000 claims description 3
- GWEHVDNNLFDJLR-UHFFFAOYSA-N Carbanilide Natural products C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 claims description 3
- IYRWEQXVUNLMAY-UHFFFAOYSA-N carbonyl fluoride Chemical compound FC(F)=O IYRWEQXVUNLMAY-UHFFFAOYSA-N 0.000 claims description 3
- BPQPBEVHMFRECG-UHFFFAOYSA-N fluoro formate Chemical compound FOC=O BPQPBEVHMFRECG-UHFFFAOYSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000004776 1-fluoroethyl group Chemical group [H]C([H])([H])C([H])(F)* 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- JKJWYKGYGWOAHT-UHFFFAOYSA-N bis(prop-2-enyl) carbonate Chemical compound C=CCOC(=O)OCC=C JKJWYKGYGWOAHT-UHFFFAOYSA-N 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- -1 copper anions Chemical class 0.000 description 20
- 238000000034 method Methods 0.000 description 11
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 125000003118 aryl group Chemical group 0.000 description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- YZMJSEAMPXECSW-UHFFFAOYSA-N 1-fluoroethyl phenyl carbonate Chemical compound CC(F)OC(=O)Oc1ccccc1 YZMJSEAMPXECSW-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 229910013870 LiPF 6 Inorganic materials 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 229910012258 LiPO Inorganic materials 0.000 description 5
- 239000003990 capacitor Substances 0.000 description 5
- 125000001072 heteroaryl group Chemical group 0.000 description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 4
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 3
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 description 2
- NAKBHPIDKQIZDG-UHFFFAOYSA-N 1-fluoroethyl carbonofluoridate Chemical compound CC(F)OC(F)=O NAKBHPIDKQIZDG-UHFFFAOYSA-N 0.000 description 2
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000006245 Carbon black Super-P Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- 229910012851 LiCoO 2 Inorganic materials 0.000 description 2
- 239000004813 Perfluoroalkoxy alkane Substances 0.000 description 2
- 229920006373 Solef Polymers 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 2
- PIQRQRGUYXRTJJ-UHFFFAOYSA-N fluoromethyl methyl carbonate Chemical compound COC(=O)OCF PIQRQRGUYXRTJJ-UHFFFAOYSA-N 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 235000015110 jellies Nutrition 0.000 description 2
- 239000008274 jelly Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920011301 perfluoro alkoxyl alkane Polymers 0.000 description 2
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 1
- 125000006636 (C3-C8) cycloalkylcarbonyl group Chemical group 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
- NRKYWOKHZRQRJR-UHFFFAOYSA-N 2,2,2-trifluoroacetamide Chemical compound NC(=O)C(F)(F)F NRKYWOKHZRQRJR-UHFFFAOYSA-N 0.000 description 1
- LRTRRTZWJXMMGS-UHFFFAOYSA-N 2,2-difluoroethyl ethenyl carbonate Chemical compound FC(F)COC(=O)OC=C LRTRRTZWJXMMGS-UHFFFAOYSA-N 0.000 description 1
- WXVCMUWGHFXASO-UHFFFAOYSA-N 2,2-difluoroethyl ethyl carbonate Chemical compound CCOC(=O)OCC(F)F WXVCMUWGHFXASO-UHFFFAOYSA-N 0.000 description 1
- VGKKQOMMALQKIC-UHFFFAOYSA-N 2,2-difluoroethyl fluoromethyl carbonate Chemical compound FCOC(=O)OCC(F)F VGKKQOMMALQKIC-UHFFFAOYSA-N 0.000 description 1
- 125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 description 1
- QOARFWDBTJVWJG-UHFFFAOYSA-N 2,2-difluoroethyl methyl carbonate Chemical compound COC(=O)OCC(F)F QOARFWDBTJVWJG-UHFFFAOYSA-N 0.000 description 1
- ZJVUKUFQQGRGIJ-UHFFFAOYSA-N 2,2-difluoroethyl phenyl carbonate Chemical compound FC(F)COC(=O)OC1=CC=CC=C1 ZJVUKUFQQGRGIJ-UHFFFAOYSA-N 0.000 description 1
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 description 1
- XVUMEEAIPCCPHI-UHFFFAOYSA-N 2-fluoroethyl fluoromethyl carbonate Chemical compound FCCOC(=O)OCF XVUMEEAIPCCPHI-UHFFFAOYSA-N 0.000 description 1
- NOLGJZJMWUDWQW-UHFFFAOYSA-N 2-fluoroethyl methyl carbonate Chemical compound COC(=O)OCCF NOLGJZJMWUDWQW-UHFFFAOYSA-N 0.000 description 1
- UKJOHKQKTGJHRX-UHFFFAOYSA-N 2-fluoroethyl phenyl carbonate Chemical compound FCCOC(=O)OC1=CC=CC=C1 UKJOHKQKTGJHRX-UHFFFAOYSA-N 0.000 description 1
- SBLRHMKNNHXPHG-UHFFFAOYSA-N 4-fluoro-1,3-dioxolan-2-one Chemical compound FC1COC(=O)O1 SBLRHMKNNHXPHG-UHFFFAOYSA-N 0.000 description 1
- BUPLCMMXKFWTTA-UHFFFAOYSA-N 4-methylidene-1,3-dioxetan-2-one Chemical compound C=C1OC(=O)O1 BUPLCMMXKFWTTA-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229910017008 AsF 6 Inorganic materials 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 229910020366 ClO 4 Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 229910015015 LiAsF 6 Inorganic materials 0.000 description 1
- 229910013063 LiBF 4 Inorganic materials 0.000 description 1
- 229910013684 LiClO 4 Inorganic materials 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 125000005910 alkyl carbonate group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910021383 artificial graphite Inorganic materials 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- WLLOZRDOFANZMZ-UHFFFAOYSA-N bis(2,2,2-trifluoroethyl) carbonate Chemical compound FC(F)(F)COC(=O)OCC(F)(F)F WLLOZRDOFANZMZ-UHFFFAOYSA-N 0.000 description 1
- UYFISINJOLGYBJ-UHFFFAOYSA-N bis(2,2-difluoroethyl) carbonate Chemical compound FC(F)COC(=O)OCC(F)F UYFISINJOLGYBJ-UHFFFAOYSA-N 0.000 description 1
- YZWIIIGEQKTIMS-UHFFFAOYSA-N bis(2-fluoroethyl) carbonate Chemical compound FCCOC(=O)OCCF YZWIIIGEQKTIMS-UHFFFAOYSA-N 0.000 description 1
- IUXMJLLWUTWQFX-UHFFFAOYSA-N bis(methylsulfanyl)methanone Chemical compound CSC(=O)SC IUXMJLLWUTWQFX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000011889 copper foil Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 description 1
- 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
- 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
- 238000006731 degradation reaction Methods 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- VWCDXEKXDIWXKI-UHFFFAOYSA-N difluoromethyl ethyl carbonate Chemical compound CCOC(=O)OC(F)F VWCDXEKXDIWXKI-UHFFFAOYSA-N 0.000 description 1
- VDGKFLGYHYBDQC-UHFFFAOYSA-N difluoromethyl methyl carbonate Chemical compound COC(=O)OC(F)F VDGKFLGYHYBDQC-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000012983 electrochemical energy storage Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- DPGXGQNEWAAUKM-UHFFFAOYSA-N ethenyl 2,2,2-trifluoroethyl carbonate Chemical compound FC(F)(F)COC(=O)OC=C DPGXGQNEWAAUKM-UHFFFAOYSA-N 0.000 description 1
- JCBADTLNWNTCNV-UHFFFAOYSA-N ethenyl 2-fluoroethyl carbonate Chemical compound FCCOC(=O)OC=C JCBADTLNWNTCNV-UHFFFAOYSA-N 0.000 description 1
- BDNXATXQVYVLCI-UHFFFAOYSA-N ethenyl fluoromethyl carbonate Chemical compound FCOC(=O)OC=C BDNXATXQVYVLCI-UHFFFAOYSA-N 0.000 description 1
- XLHKMGHXUXYDQJ-UHFFFAOYSA-N ethyl 2-fluoroethyl carbonate Chemical compound CCOC(=O)OCCF XLHKMGHXUXYDQJ-UHFFFAOYSA-N 0.000 description 1
- UHHPUKUEMKPCII-UHFFFAOYSA-N ethyl fluoromethyl carbonate Chemical compound CCOC(=O)OCF UHHPUKUEMKPCII-UHFFFAOYSA-N 0.000 description 1
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 description 1
- ZPBVUMUIOIGYRV-UHFFFAOYSA-N ethyl trifluoromethyl carbonate Chemical compound CCOC(=O)OC(F)(F)F ZPBVUMUIOIGYRV-UHFFFAOYSA-N 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- KUPHFFIERSZZDV-UHFFFAOYSA-N fluoromethyl phenyl carbonate Chemical compound FCOC(=O)OC1=CC=CC=C1 KUPHFFIERSZZDV-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 239000002608 ionic liquid Substances 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 238000004502 linear sweep voltammetry Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910021450 lithium metal oxide Inorganic materials 0.000 description 1
- GBPVMEKUJUKTBA-UHFFFAOYSA-N methyl 2,2,2-trifluoroethyl carbonate Chemical compound COC(=O)OCC(F)(F)F GBPVMEKUJUKTBA-UHFFFAOYSA-N 0.000 description 1
- CXHHBNMLPJOKQD-UHFFFAOYSA-M methyl carbonate Chemical compound COC([O-])=O CXHHBNMLPJOKQD-UHFFFAOYSA-M 0.000 description 1
- YSYBYIDPNZPQLJ-UHFFFAOYSA-N methyl trifluoromethyl carbonate Chemical compound COC(=O)OC(F)(F)F YSYBYIDPNZPQLJ-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- AJFDBNQQDYLMJN-UHFFFAOYSA-N n,n-diethylacetamide Chemical compound CCN(CC)C(C)=O AJFDBNQQDYLMJN-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000004971 nitroalkyl group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 150000005677 organic carbonates Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000003880 polar aprotic solvent Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- JJKUOVDAMCXQFK-UHFFFAOYSA-H ruthenium(3+);tricarbonate Chemical compound [Ru+3].[Ru+3].[O-]C([O-])=O.[O-]C([O-])=O.[O-]C([O-])=O JJKUOVDAMCXQFK-UHFFFAOYSA-H 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000001075 voltammogram Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Images
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/96—Esters of carbonic or haloformic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/02—Preparation of esters of carbonic or haloformic acids from phosgene or haloformates
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- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
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- H01—ELECTRIC ELEMENTS
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Description
R1R2CF−O−C(O)−O−R3
(式中、
R1及びR2は、独立して、H、F、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、及び
R3は二重結合含有基である)
の化合物に関する。
R1R2CF−O−C(O)F
のフルオロホルメートを一般式
R3−OH
のアルコールと反応させる工程を含む一般式
R1R2CF−O−C(O)−O−R3
の化合物の製造方法であって、
式中、
R1はH、F、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、
R2はHであり、及び
R3は二重結合含有基である、製造方法に関する。
R1R2CF−OH
の化合物と反応させて、一般式
R1R2CF−O−C(O)X
の中間体を形成する第1の工程と、一般式
R1R2CF−O−C(O)X
の中間体を一般式
R3−OH
の化合物と反応させる第2の工程とを含む一般式
R1R2CF−O−C(O)−O−R3
の化合物の製造方法であって、
式中、
R1及びR2は、独立して、H、F、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、
R3は二重結合含有基であり、及び
X−は脱離基であり、好ましくは、X−は塩化物又はフッ化物である、製造方法に関する。
R3−OH
の化合物と反応させて、一般式
R3−O−C(O)X
の中間体を形成する第1の工程と、一般式
R3−O−C(O)X
の中間体を一般式
R1R2CF−OH
の化合物と反応させる第2の工程とを含む一般式
R1R2CF−O−C(O)−O−R3
の化合物の製造方法であって、
式中、
R1及びR2は、独立して、H、F、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、
R3は二重結合含有基であり、及び
X−は脱離基であり、好ましくは、X−は塩化物又はフッ化物である、製造方法に関する。
R1R2CF−O−C(O)−O−R3
(式中、
R1及びR2は、独立して、H、F、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、及び
R3は二重結合含有基である)
の化合物の使用である。
加熱したダブルマントル、還流コンデンサー、及びメカニカルスターラーを備えた2.5lのパーフルオロアルコキシアルカンの反応器に、1023gの1−フルオロエチルフルオロホルメートを入れた(国際公開第2011/006822号に記載の通り調製)。3℃まで材料を冷却した後、231gのピリジンと517gのアリルアルコールとの混合物を2時間かけてゆっくり添加した。反応温度は60℃未満に維持した。室温に冷却した後、混合物をクエン酸溶液で2回洗浄した(30%の脱イオン水)。生成物を無色液体として得た(収率:91%、GC純度>95%)。生成物は、任意選択的には蒸留によって更に精製されて、GC純度>99.9%で生成物を得ることができる。
加熱したダブルマントル、還流コンデンサー、及びメカニカルスターラーを備えた2.5lのパーフルオロアルコキシアルカンの反応器に、1007gの1−フルオロエチルフルオロホルメートを入れた(国際公開第2011/006822号に記載の通り調製)。3℃まで材料を冷却した後、238gのピリジンと819gのフェノールとの混合物を2時間かけてゆっくり添加した。反応温度は45℃未満に維持した。室温に冷却した後、混合物をクエン酸溶液で3回洗浄した(30%の脱イオン水)。生成物を無色液体として得た(収率:81%、GC純度>94%)。生成物は、任意選択的には蒸留及び/又は結晶化によって精製されて、GC純度>99.9%で生成物を得ることができる。
試験システム:正極として[LiCoO2:Super−P(登録商標)(MMM Carbon、Belgiumから入手可能な導電性カーボンブラック):PVdF(Solvay Specialty PolymersのSolef(登録商標)5130)バインダー=92:4:4(重量%)]及び負極として[SCMG−AR(登録商標)(昭和電工株式会社から入手可能な人工グラファイト):Super−P(登録商標)(MMM Carbon、Belgiumから入手可能な導電性カーボンブラック):PVdF(Solvay Specialty PolymersのSolef(登録商標)5130)バインダー=90:4:6(重量%)]からなるパウチフルセル。ポリエチレンをセパレーターとして使用した。標準電解質組成物[(1.0MのLiPF6/エチレンカーボネート+ジメチルカーボネート(1:2(v/v)]をこれに使用し、本発明によるフッ化添加剤を乾燥した室内雰囲気下にて加えた。
以下のように3つの電極を含むビーカー型セルにおいて試験を実施した。
a)参照電極としてLi金属
b)作用電極としてLiCoO2
c)対極としてLi金属
曲線(1):標準電解質
曲線(2):1重量%の1−フルオロエチルフェニルカーボネートを有する標準電解質
曲線(3):1重量%のアリル 1−フルオロエチルカーボネートを有する標準電解質
Claims (13)
- 一般式(I)
R1R2CF−O−C(O)−O−R3
(式中、
R1は、H、F、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、
R2は、H、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、及び
R3はアルケニルである)
の化合物。 - R3はアリルである、請求項1に記載の化合物。
- R2はHである、請求項1又は2に記載の化合物。
- R1は、H又はアルキル基である、請求項1〜3のいずれか一項に記載の化合物。
- R1はメチルであり、R2はHであり、R3はアリルであり、及び前記化合物は(1−フルオロエチル)アリルカーボネートである、請求項1〜4のいずれか一項に記載の化合物。
- 一般式(II)
R1R2CF−O−C(O)F
のフルオロホルマートを一般式(III)
R3−OH
のアルコールと反応させる工程を含む、請求項1〜5のいずれか一項に記載の化合物の製造方法であって、
式中、
R1はH、F、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、
R2はHであり、及び
R3はアルケニルである、製造方法。 - ホスゲン又はホスゲン類似体を一般式(IV)
R1R2CF−OH
の化合物と反応させて、一般式(V)
R1R2CF−O−C(O)X
の中間体を形成する第1の工程と、前記一般式(V)の前記中間体を一般式(VI)
R3−OH
の化合物と反応させる第2の工程とを含む、請求項1〜5のいずれか一項に記載の化合物の製造方法であって、
式中、
R1は、H、F、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、
R2は、H、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、
R3はアルケニルであり、
X−は脱離基であり、ホスゲン類似体が、ジフルオロホスゲン(FC(O)F)、トリクロロメチルクロロホルメート(「ジホスゲン」)、ビス(トリクロロメチル)カーボネート(「トリホスゲン」)、S,S−ジメチルジチオカーボネート(DMDTC)、カルボニルジイミダゾール(CDI)、N,N−ジフェニル尿素及びそれらの組合せからなる群から選択される、製造方法。 - ホスゲン又はホスゲン類似体を一般式(VI)
R3−OH
の化合物と反応させて、一般式(VII)
R3−O−C(O)X
の中間体を形成する第1の工程と、前記一般式(VII)の前記中間体を一般式(VIII))
R1R2CF−OH
の化合物と反応させる第2の工程とを含む、請求項1〜5のいずれか一項に記載の化合物の製造方法であって、
式中、
R1は、H、F、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、
R2は、H、アルキル、シクロアルキル、アルキレン−アリール、又はアルキレン−ヘテロアリールであり、
R3はアルケニルであり、
X−は脱離基であり、ホスゲン類似体が、ジフルオロホスゲン(FC(O)F)、トリクロロメチルクロロホルメート(「ジホスゲン」)、ビス(トリクロロメチル)カーボネート(「トリホスゲン」)、S,S−ジメチルジチオカーボネート(DMDTC)、カルボニルジイミダゾール(CDI)、N,N−ジフェニル尿素及びそれらの組合せからなる群から選択される、製造方法。 - リチウムイオン電池、リチウム空気電池、リチウム硫黄電池、スーパーキャパシタ、又はハイブリッドスーパーキャパシタ用の溶媒添加物又は溶媒としての請求項1〜5のいずれか一項に記載の化合物の使用。
- リチウムイオン電池に有用な少なくとも1種の溶媒を含有し、請求項1〜5のいずれか1項に記載の少なくとも1種の化合物を更に含有する、リチウムイオン電池用、リチウム空気電池用、リチウム硫黄電池用、スーパーキャパシタ用、又はハイブリッドスーパーキャパシタ用の溶媒組成物。
- 請求項1〜5のいずれか1項に記載の少なくとも1種の化合物と、リチウムイオン電池又はスーパーキャパシタに有用な少なくとも1種の溶媒と、少なくとも1種の電解質塩とを含有する、リチウムイオン電池用、リチウム空気電池用、リチウム硫黄電池用、スーパーキャパシタ用、又はハイブリッドスーパーキャパシタ用の電解質組成物。
- 請求項1〜5のいずれか1項に記載の少なくとも1種の化合物を含むリチウムイオン電池、リチウム空気電池、リチウム硫黄電池、スーパーキャパシタ、又はハイブリッドスーパーキャパシタ。
- Liイオン電池、Li空気電池、又はLi硫黄電池用の電解質組成物における、電解質組成物中の成分としての、請求項1〜5のいずれか一項に記載の化合物の使用であって、請求項1〜5のいずれか一項に記載の化合物の濃度は、前記電解質組成物の総重量に対して、1〜15重量%である、使用。
Applications Claiming Priority (3)
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EP13175668.6A EP2824096A1 (en) | 2013-07-09 | 2013-07-09 | Fluorinated carbonates comprising double bond-containing groups, methods for their manufacture and uses thereof |
EP13175668.6 | 2013-07-09 | ||
PCT/EP2014/064734 WO2015004195A1 (en) | 2013-07-09 | 2014-07-09 | Fluorinated carbonates comprising double bond-containing groups, methods for their manufacture and uses thereof |
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JP2016531093A JP2016531093A (ja) | 2016-10-06 |
JP6498668B2 true JP6498668B2 (ja) | 2019-04-10 |
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US (2) | US20160145190A1 (ja) |
EP (2) | EP2824096A1 (ja) |
JP (1) | JP6498668B2 (ja) |
KR (1) | KR20160029065A (ja) |
CN (1) | CN105377807A (ja) |
CA (1) | CA2916831A1 (ja) |
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WO (1) | WO2015004195A1 (ja) |
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KR20170095324A (ko) * | 2014-12-18 | 2017-08-22 | 솔베이(소시에떼아노님) | 플루오르화 카보네이트를 포함하는 전해질 조성물 및 이를 포함하는 배터리 |
US10105609B2 (en) | 2015-03-31 | 2018-10-23 | Universal City Studios Llc | System and method for positioning vehicles of an amusement park attraction |
US10707531B1 (en) | 2016-09-27 | 2020-07-07 | New Dominion Enterprises Inc. | All-inorganic solvents for electrolytes |
EP3309143A1 (en) * | 2016-10-17 | 2018-04-18 | Solvay SA | Method for producing fluoroformate compounds |
KR102239499B1 (ko) * | 2019-06-24 | 2021-04-13 | 삼화페인트공업주식회사 | 플루오로설포닐기를 함유하는 카보네이트 화합물, 이의 제조방법 및 용도 |
CN114597489A (zh) * | 2022-03-22 | 2022-06-07 | 香河昆仑新能源材料股份有限公司 | 一种含氟代苯碳酸酯的电解液及由该电解液组成的电池 |
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US3702870A (en) * | 1969-05-21 | 1972-11-14 | Us Agriculture | Fluorinated alcoholates |
US4022609A (en) * | 1972-10-24 | 1977-05-10 | Ppg Industries, Inc. | Herbicidal fluorinated carbonates |
JPS6023664B2 (ja) * | 1979-06-25 | 1985-06-08 | 株式会社トクヤマ | 有機カ−ボネ−トの分離方法 |
FR2600058B1 (fr) * | 1986-06-13 | 1988-08-19 | Poudres & Explosifs Ste Nale | Procede de preparation d'esters organiques alpha-halogenes de l'acide carbonique |
DE19858924A1 (de) | 1998-12-19 | 2000-06-21 | Aventis Res & Tech Gmbh & Co | Elektrolytsystem für Lithiumbatterien und dessen Verwendung sowie Verfahren zur Erhöhung |
JP4951933B2 (ja) * | 2005-02-18 | 2012-06-13 | ソニー株式会社 | リチウムイオン二次電池用電解質およびリチウムイオン二次電池 |
DE102005048802A1 (de) | 2005-10-10 | 2007-04-12 | Solvay Fluor Gmbh | Fluorierte Additive für Lithiumionenbatterien |
CN103078137B (zh) * | 2008-02-29 | 2015-09-16 | 三菱化学株式会社 | 非水电解液及非水电解质电池 |
JP5589287B2 (ja) * | 2008-02-29 | 2014-09-17 | 三菱化学株式会社 | 非水系電解液及び非水系電解液電池 |
JP5262266B2 (ja) * | 2008-04-22 | 2013-08-14 | 株式会社Gsユアサ | 非水電解質電池 |
US8208285B2 (en) * | 2009-07-13 | 2012-06-26 | Seagate Technology Llc | Vertical non-volatile switch with punchthrough access and method of fabrication therefor |
JP5714578B2 (ja) * | 2009-07-16 | 2015-05-07 | ゾルファイ フルーオル ゲゼルシャフト ミット ベシュレンクテル ハフツングSolvay Fluor GmbH | フルオロアルキル(フルオロ)アルキルカーボネートおよびカルバメートの調製方法 |
TW201121938A (en) * | 2009-09-28 | 2011-07-01 | Solvay Fluor Gmbh | Manufacture of difluoroethylene carbonate, trifluoroethylene carbonate and tetrafluoroethylene carbonate |
KR101532847B1 (ko) * | 2010-09-02 | 2015-06-30 | 닛본 덴끼 가부시끼가이샤 | 이차 전지 및 그것에 사용되는 이차 전지용 전해액 |
-
2013
- 2013-07-09 EP EP13175668.6A patent/EP2824096A1/en not_active Ceased
-
2014
- 2014-07-09 EP EP14739120.5A patent/EP3019464A1/en not_active Withdrawn
- 2014-07-09 CN CN201480039304.7A patent/CN105377807A/zh active Pending
- 2014-07-09 US US14/903,357 patent/US20160145190A1/en not_active Abandoned
- 2014-07-09 JP JP2016524814A patent/JP6498668B2/ja not_active Expired - Fee Related
- 2014-07-09 CA CA2916831A patent/CA2916831A1/en not_active Abandoned
- 2014-07-09 WO PCT/EP2014/064734 patent/WO2015004195A1/en active Application Filing
- 2014-07-09 MY MYPI2015704465A patent/MY174116A/en unknown
- 2014-07-09 KR KR1020167000271A patent/KR20160029065A/ko not_active Application Discontinuation
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CA2916831A1 (en) | 2015-01-15 |
US20160145190A1 (en) | 2016-05-26 |
WO2015004195A1 (en) | 2015-01-15 |
CN105377807A (zh) | 2016-03-02 |
KR20160029065A (ko) | 2016-03-14 |
JP2016531093A (ja) | 2016-10-06 |
EP2824096A1 (en) | 2015-01-14 |
MY174116A (en) | 2020-03-10 |
US20190177264A1 (en) | 2019-06-13 |
EP3019464A1 (en) | 2016-05-18 |
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