JP2000508678A - 過フッ化アミド塩及びイオン伝導物質としてのその使用方法 - Google Patents
過フッ化アミド塩及びイオン伝導物質としてのその使用方法Info
- Publication number
- JP2000508678A JP2000508678A JP52951898A JP52951898A JP2000508678A JP 2000508678 A JP2000508678 A JP 2000508678A JP 52951898 A JP52951898 A JP 52951898A JP 52951898 A JP52951898 A JP 52951898A JP 2000508678 A JP2000508678 A JP 2000508678A
- Authority
- JP
- Japan
- Prior art keywords
- group
- compound
- cation
- polymer
- alkyl
- 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.)
- Granted
Links
- -1 amide salts Chemical class 0.000 title claims abstract description 232
- 239000000126 substance Substances 0.000 title claims description 29
- 150000001875 compounds Chemical class 0.000 claims abstract description 213
- 150000003839 salts Chemical class 0.000 claims abstract description 139
- 238000006243 chemical reaction Methods 0.000 claims abstract description 96
- 150000001768 cations Chemical group 0.000 claims abstract description 95
- 239000004020 conductor Substances 0.000 claims abstract description 64
- 150000002500 ions Chemical class 0.000 claims abstract description 59
- 239000000203 mixture Substances 0.000 claims abstract description 53
- 150000008040 ionic compounds Chemical class 0.000 claims abstract description 41
- 150000001408 amides Chemical class 0.000 claims abstract description 28
- 239000003054 catalyst Substances 0.000 claims abstract description 28
- 150000001450 anions Chemical group 0.000 claims abstract description 26
- 229910052751 metal Inorganic materials 0.000 claims abstract description 24
- 239000002184 metal Substances 0.000 claims abstract description 24
- 239000003086 colorant Substances 0.000 claims abstract description 22
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 8
- KEJOCWOXCDWNID-UHFFFAOYSA-N Nitrilooxonium Chemical compound [O+]#N KEJOCWOXCDWNID-UHFFFAOYSA-N 0.000 claims abstract description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 164
- 229920000642 polymer Polymers 0.000 claims description 144
- 150000003254 radicals Chemical class 0.000 claims description 121
- 239000002904 solvent Substances 0.000 claims description 104
- 238000000034 method Methods 0.000 claims description 96
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 83
- 230000008569 process Effects 0.000 claims description 77
- 229910052731 fluorine Inorganic materials 0.000 claims description 66
- 239000011737 fluorine Substances 0.000 claims description 60
- 239000011541 reaction mixture Substances 0.000 claims description 57
- 239000000178 monomer Substances 0.000 claims description 56
- 229910052757 nitrogen Inorganic materials 0.000 claims description 54
- 125000001424 substituent group Chemical group 0.000 claims description 48
- 125000000217 alkyl group Chemical group 0.000 claims description 43
- 125000003118 aryl group Chemical group 0.000 claims description 42
- 239000003792 electrolyte Substances 0.000 claims description 39
- 229910052744 lithium Inorganic materials 0.000 claims description 39
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 37
- 239000002253 acid Substances 0.000 claims description 35
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 35
- 238000006116 polymerization reaction Methods 0.000 claims description 33
- 239000007788 liquid Substances 0.000 claims description 29
- 125000002091 cationic group Chemical group 0.000 claims description 27
- 239000003999 initiator Substances 0.000 claims description 26
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 25
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 24
- 229920001577 copolymer Polymers 0.000 claims description 24
- 229910052760 oxygen Inorganic materials 0.000 claims description 24
- 229910052799 carbon Inorganic materials 0.000 claims description 23
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
- 229910052717 sulfur Inorganic materials 0.000 claims description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 20
- 230000005855 radiation Effects 0.000 claims description 20
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 20
- 239000001301 oxygen Chemical group 0.000 claims description 18
- 125000005842 heteroatom Chemical group 0.000 claims description 17
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 16
- 239000011593 sulfur Chemical group 0.000 claims description 16
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 15
- 125000003710 aryl alkyl group Chemical class 0.000 claims description 15
- 229920001519 homopolymer Polymers 0.000 claims description 15
- 125000003342 alkenyl group Chemical group 0.000 claims description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 14
- 238000004132 cross linking Methods 0.000 claims description 14
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 13
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 13
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 12
- 238000010494 dissociation reaction Methods 0.000 claims description 12
- 150000002148 esters Chemical class 0.000 claims description 12
- 229920006112 polar polymer Polymers 0.000 claims description 12
- 230000005593 dissociations Effects 0.000 claims description 11
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 10
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 10
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 claims description 10
- 150000002825 nitriles Chemical class 0.000 claims description 10
- 239000000843 powder Substances 0.000 claims description 10
- 238000010248 power generation Methods 0.000 claims description 10
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- 125000001153 fluoro group Chemical group F* 0.000 claims description 9
- 125000003010 ionic group Chemical group 0.000 claims description 9
- 125000001425 triazolyl group Chemical group 0.000 claims description 9
- 229910052782 aluminium Inorganic materials 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 8
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- 230000000536 complexating effect Effects 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- 238000002844 melting Methods 0.000 claims description 8
- 230000008018 melting Effects 0.000 claims description 8
- 230000003287 optical effect Effects 0.000 claims description 8
- 229920001223 polyethylene glycol Polymers 0.000 claims description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 claims description 8
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims description 8
- 229910052723 transition metal Inorganic materials 0.000 claims description 8
- 229960000834 vinyl ether Drugs 0.000 claims description 8
- 229920002554 vinyl polymer Polymers 0.000 claims description 8
- 238000010538 cationic polymerization reaction Methods 0.000 claims description 7
- 239000000835 fiber Substances 0.000 claims description 7
- 125000000524 functional group Chemical group 0.000 claims description 7
- 125000000623 heterocyclic group Chemical group 0.000 claims description 7
- MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical compound [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 claims description 7
- 239000012948 isocyanate Substances 0.000 claims description 7
- 239000003446 ligand Substances 0.000 claims description 7
- 239000011777 magnesium Substances 0.000 claims description 7
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 7
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 7
- 238000010526 radical polymerization reaction Methods 0.000 claims description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- 229920001940 conductive polymer Polymers 0.000 claims description 6
- 229910052742 iron Inorganic materials 0.000 claims description 6
- 150000002513 isocyanates Chemical class 0.000 claims description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- 150000002892 organic cations Chemical class 0.000 claims description 6
- 150000003568 thioethers Chemical class 0.000 claims description 6
- 150000003624 transition metals Chemical class 0.000 claims description 6
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 claims description 6
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- 125000005024 alkenyl aryl group Chemical group 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 230000000977 initiatory effect Effects 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000004437 phosphorous atom Chemical group 0.000 claims description 5
- 229910052698 phosphorus Chemical group 0.000 claims description 5
- 239000003504 photosensitizing agent Substances 0.000 claims description 5
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 5
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 5
- 229910052718 tin Inorganic materials 0.000 claims description 5
- 239000011135 tin Substances 0.000 claims description 5
- 239000010936 titanium Substances 0.000 claims description 5
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims description 4
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 claims description 4
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 4
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- 239000005977 Ethylene Substances 0.000 claims description 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 4
- 125000000909 amidinium group Chemical group 0.000 claims description 4
- 150000001413 amino acids Chemical class 0.000 claims description 4
- 125000005626 carbonium group Chemical group 0.000 claims description 4
- 150000004292 cyclic ethers Chemical class 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical group I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 4
- 150000002466 imines Chemical class 0.000 claims description 4
- 239000011572 manganese Substances 0.000 claims description 4
- 150000002739 metals Chemical class 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- 229950000688 phenothiazine Drugs 0.000 claims description 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims description 4
- 125000005499 phosphonyl group Chemical group 0.000 claims description 4
- 229920001184 polypeptide Polymers 0.000 claims description 4
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 4
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 4
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 4
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 4
- NONOKGVFTBWRLD-UHFFFAOYSA-N thioisocyanate group Chemical group S(N=C=O)N=C=O NONOKGVFTBWRLD-UHFFFAOYSA-N 0.000 claims description 4
- 229910052725 zinc Inorganic materials 0.000 claims description 4
- 239000011701 zinc Substances 0.000 claims description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Natural products C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 3
- 150000001721 carbon Chemical group 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical group 0.000 claims description 3
- 239000008139 complexing agent Substances 0.000 claims description 3
- 229920000547 conjugated polymer Polymers 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- 229940052303 ethers for general anesthesia Drugs 0.000 claims description 3
- ZRALSGWEFCBTJO-UHFFFAOYSA-O guanidinium Chemical compound NC(N)=[NH2+] ZRALSGWEFCBTJO-UHFFFAOYSA-O 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 239000004973 liquid crystal related substance Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- VHYFNPMBLIVWCW-UHFFFAOYSA-O n,n-dimethylpyridin-1-ium-4-amine Chemical compound CN(C)C1=CC=[NH+]C=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-O 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-O oxonium Chemical compound [OH3+] XLYOFNOQVPJJNP-UHFFFAOYSA-O 0.000 claims description 3
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- 239000001294 propane Substances 0.000 claims description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- 230000002468 redox effect Effects 0.000 claims description 3
- 238000006467 substitution reaction Methods 0.000 claims description 3
- 125000000565 sulfonamide group Chemical group 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- YIKSHDNOAYSSPX-UHFFFAOYSA-N 1-propan-2-ylthioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C(C)C YIKSHDNOAYSSPX-UHFFFAOYSA-N 0.000 claims description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 238000006845 Michael addition reaction Methods 0.000 claims description 2
- 229910015468 Ni1-xCox Inorganic materials 0.000 claims description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 2
- XBDYBAVJXHJMNQ-UHFFFAOYSA-N Tetrahydroanthracene Natural products C1=CC=C2C=C(CCCC3)C3=CC2=C1 XBDYBAVJXHJMNQ-UHFFFAOYSA-N 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 125000002723 alicyclic group Chemical group 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 238000005937 allylation reaction Methods 0.000 claims description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 2
- 239000012965 benzophenone Substances 0.000 claims description 2
- 238000009739 binding Methods 0.000 claims description 2
- 229920001400 block copolymer Polymers 0.000 claims description 2
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical group C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 150000004294 cyclic thioethers Chemical group 0.000 claims description 2
- IDASTKMEQGPVRR-UHFFFAOYSA-N cyclopenta-1,3-diene;zirconium(2+) Chemical compound [Zr+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 IDASTKMEQGPVRR-UHFFFAOYSA-N 0.000 claims description 2
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 2
- 150000008282 halocarbons Chemical class 0.000 claims description 2
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 claims description 2
- 239000012442 inert solvent Substances 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 150000003951 lactams Chemical class 0.000 claims description 2
- 150000002596 lactones Chemical class 0.000 claims description 2
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 claims description 2
- 150000002828 nitro derivatives Chemical class 0.000 claims description 2
- 239000010450 olivine Substances 0.000 claims description 2
- 229910052609 olivine Inorganic materials 0.000 claims description 2
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims description 2
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 claims description 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims description 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 claims description 2
- 229920002120 photoresistant polymer Polymers 0.000 claims description 2
- 150000002910 rare earth metals Chemical class 0.000 claims description 2
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims description 2
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 claims description 2
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical group OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 claims description 2
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 2
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims description 2
- 125000004862 thiobutyl group Chemical group 0.000 claims description 2
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- LUYQYZLEHLTPBH-UHFFFAOYSA-N perfluorobutanesulfonyl fluoride Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)S(F)(=O)=O LUYQYZLEHLTPBH-UHFFFAOYSA-N 0.000 description 1
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- WRIKHQLVHPKCJU-UHFFFAOYSA-N sodium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([Na])[Si](C)(C)C WRIKHQLVHPKCJU-UHFFFAOYSA-N 0.000 description 1
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- SZHIIIPPJJXYRY-UHFFFAOYSA-M sodium;2-methylprop-2-ene-1-sulfonate Chemical compound [Na+].CC(=C)CS([O-])(=O)=O SZHIIIPPJJXYRY-UHFFFAOYSA-M 0.000 description 1
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- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
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- 125000004434 sulfur atom Chemical group 0.000 description 1
- IXPAAHZTOUOJJM-UHFFFAOYSA-N sulfuryl chloride fluoride Chemical compound FS(Cl)(=O)=O IXPAAHZTOUOJJM-UHFFFAOYSA-N 0.000 description 1
- YGIYXPDSUCRWCW-UHFFFAOYSA-N sulfuryl dichloride;4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical compound ClS(Cl)(=O)=O.C1CC2(C)C(=O)CC1C2(C)C YGIYXPDSUCRWCW-UHFFFAOYSA-N 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 125000001391 thioamide group Chemical group 0.000 description 1
- 150000003608 titanium Chemical class 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
- 125000005147 toluenesulfonyl group Chemical group C=1(C(=CC=CC1)S(=O)(=O)*)C 0.000 description 1
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- 230000002588 toxic effect Effects 0.000 description 1
- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical compound C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 125000005409 triarylsulfonium group Chemical group 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- PPPHYGCRGMTZNA-UHFFFAOYSA-M trifluoromethyl sulfate Chemical compound [O-]S(=O)(=O)OC(F)(F)F PPPHYGCRGMTZNA-UHFFFAOYSA-M 0.000 description 1
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 description 1
- MDCWDBMBZLORER-UHFFFAOYSA-N triphenyl borate Chemical compound C=1C=CC=CC=1OB(OC=1C=CC=CC=1)OC1=CC=CC=C1 MDCWDBMBZLORER-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- 239000010981 turquoise Substances 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- GRUMUEUJTSXQOI-UHFFFAOYSA-N vanadium dioxide Chemical compound O=[V]=O GRUMUEUJTSXQOI-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 229910003454 ytterbium oxide Inorganic materials 0.000 description 1
- 229940075624 ytterbium oxide Drugs 0.000 description 1
- XASAPYQVQBKMIN-UHFFFAOYSA-K ytterbium(iii) fluoride Chemical class F[Yb](F)F XASAPYQVQBKMIN-UHFFFAOYSA-K 0.000 description 1
- JRPGMCRJPQJYPE-UHFFFAOYSA-N zinc;carbanide Chemical compound [CH3-].[CH3-].[Zn+2] JRPGMCRJPQJYPE-UHFFFAOYSA-N 0.000 description 1
Classifications
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1. アミド又はその塩から成るイオン化合物であって、電子的な中性を与え るに十分な数の少なくとも1つのカチオン部分M+mに関連するアニオン部分を含 み、Mは、ヒドロキソニウム(hydroxonium)、ニトロソニウムNO+ 、アンモニウム−NH4 +、イオン価mを有する金属カチオン、イオン化mを有 する有機カチオン、又は、イオン価mを有する有機金属カチオンであり、前記ア ニオン部分は、組成式RF−SOx−N-−Zに対応し、 前記基−S(O)xは、スルホン酸基−SO2−又はスルフィニル基−SO−を 表しており、 RFは、ハロゲン又は過ハロゲン化アルキル、アルキルアリール、オキサ−ア ルキル、アザ−アルキル又はチア−アルキルの遊離基、あるいは、組成式RAC F2−、RACF2CF2−、RACF2CF(CF3)−、又は、CF3C(RA)F −の中の一つに相当する遊離基であり、 Zは、フェニル遊離基のハメット(Hammett)パラメータに少なくとも 等しいハメットパラメータを有する電子吸引遊離基を表しており、 前記電子吸引遊離基は、以下の遊離基から選択され、 j) −CN、−NO2、−SCN、−N3、−CF3、R’FCH2−(R’Fは 、過フッ化遊離基である)、フルオロアルキルオキシ遊離基、フルオロアルキル チオキシ遊離基、 jj) 水素、酸素、硫黄又はリンの原子を少なくとも一つ含む1又はそれ以 上の芳香核を含む遊離基(前記核は、縮合核であるか及び/又は前記核は、少な くとも1つの置換基を有し、該置換基は、ハロゲン、−CN、−NO2、−SC N、−N3、−CF3、CF3CH2−、CF2=CF−O−、CF2=CF−S−、 過フルオロアルキル基、フルオロアルキルオキシ基、フルオロアルキルチオキシ 基、アルキル、アルケニル、オキサ−アルキル、オキサ−アルケニル、アザ−ア ルキル、アザ−アルケニル、チア−アルキル、チア−アルケニル遊離基、ポリマ ー遊離基、少なくとも1つのカチオン選択性基及び/又は少なくとも1つのアニ オン選択性基から成る群から選択される)、 置換基Zは、−価遊離基、複数の基RF−S(O)x−N−を有する多価遊離基 、あるいは、ポリマーセグメントとすることができ、 Zは、遊離基RD−Yであり、Yは、スルホニル、スルフィニル又はホスホニ ル基であり、また、RDは、以下の群から選択され、 (a) アルキル又はアルケニル遊離基、アリール、アリールアルキル、アル キルアリール又はアルケニルアリール遊離基、脂環式又は多環式遊離基を含む複 素環式遊離基、 (b) エーテル、チオエーテル、アミン、イミン、カルボキシル、カルボニ ル、ヒドロキシ、シリル、イソシアネート又はチオイソシアネート基の少なくと も1つの官能基を含む、アルキル又はアルケニル遊離基、 (c) アリール、アリールアルキル、アリールアルケニル、アルキルアリー ル又はアルケニルアリール遊離基(芳香核及び/又は核の少なくとも1つの置換 基は、窒素、酸素、硫黄の如きヘテロ原子を含む)、 (d) 窒素、酸素、硫黄から選択された少なくとも1つのヘテロ原子を含む 縮合型芳香族サイクルを含む遊離基、 (e) ハロゲン化されたアルキル、アルケニル、アリール、アリールアルキ ル、アルキルアリール又はアルケニルアリール遊離基(少なくとも1つのハロゲ ンを有する炭素原子の数は、ハロゲン化されていない炭素原子の数に少なくとも 等しく、基Yのα位置の炭素は、Yが−SO2−である場合にはハロゲン化され ておらず、前記遊離基は、エーテル、チオエーテル、アミン、イミン、カルボキ シル、カルボニル、ヒドロキシ、シリル、イソシアネート又はチオイソシアネー トの官能基を含む)、 (f) 遊離基RCC(R’)(R’’)−O−(RCは、過フッ化アルキル遊 離基であり、R’及びR’’は、互いに独立している)、水素原子又は前記(a )、(b)、(c)、又は(d)に規定した遊離基、 (g) 遊離基(RB)2N−(同一又は異なるRBは、(a)、(b)、(c )、(d)及び(e)に規定したようなものであり、一方のRBは、水素原子と することができ、あるいは、2つの遊離基RBは一緒に、Nを有するサイクルを 形成する二価遊離基を形成する)、 (h) ポリマー鎖から成る遊離基、 (i) 1又はそれ以上のカチオン選択性基及び/又は1又はそれ以上のアニ オン選択性基を有する遊離基、 置換基RDは、一価遊離基、複数の基RFS(O)x−N−Y−を有する多価遊 離基の一部、又は、ポリマーのセグメントとすることができ、 Yがスルホニル又はカルボニルの場合には、RDは、(a)に規定したような 遊離基であり、RFは、RACF2−、RACF2CF2−、RACF2CF(CF3) −、CF3C(RA)F−、あるいは、1乃至2の炭素原子を有する過ハロゲンア ルキル遊離基である。 2. 請求項1に記載の化合物において、前記有機カチオンは、R3 +(オキソ ニム)、NR4 +(アンモニウム)、RC(NHR2)2 +(アミジニウム)、C(N HR2)3 +(グアニジニウム)、C5R6N+(ピリジニウム)、C3R5N2 +(イミ ダゾリウム)、C2R4N3 +(トリアゾリウム)、C3R7N2 +(イミダゾリニウム )、SR3 +(スルホニウム)、PR4 +(ホスホニウム)、IR2 +(ヨードニウム )、(C6R5)3C+(カルボニウム)から成る群から選択されたオニウムであり 、前記遊離基Rは、Hあるいは以下の遊離基から成る群から選択された遊離基を それぞれ表し、 − アルキル、アルケニル、オキサ−アルキル、オキサ−アルケニル、アザ− アルキル、アザ−アルケニル、チア−アルキル、チア−アルケニル、シラ−アル キル、シラ−アルケニル、アリール、アリールアルキル、アルキルアリール、ア ルケニルアリール遊離基、ジアルキルアミノ遊離基、及び、ジアルキルアゾ遊離 基、 − 窒素、酸素、硫黄の如きヘテロ原子を含む少なくとも1つの側鎖を有する 環式又は複素環式遊離基、 芳香核にヘテロ原子を含む環式又は複素環式遊離基、 − 窒素、酸素、硫黄又はリンの原子を少なくとも一つ含む、縮合型又は非縮 合型の複数の芳香族又は複素環式の核から成る基、 複数の遊離基Rは一緒になって、カチオン電荷を有する中心を包囲する脂肪族 又は芳香族のサイクル(環)を形成することができる 該化合物。 3. 請求項2に記載の化合物において、前記カチオン性オニウムは、遊離基 Z又は遊離基RDの一部であること、を特徴とする化合物。 4. 請求項2に記載の化合物において、前記オニウムカチオンは、ポリマー の反復単量体の一部であること、を特徴とする化合物。 5. 請求項2に記載の化合物において、M+よ、少なくとも1つのアルキル 化された窒素原子を環に含む芳香族の性質を有するカチオン性複素環であること 、を特徴とする化合物。 6. 請求項5に記載の化合物において、前記カチオンは、イミダゾリウム、 トリアゾリウム、ピリジニウム、4−ジメチル−アミノ−ピリジニウムであり、 前記カチオンは、環の炭素原子に置換基を有していること、を特徴とする化合物 。 7. 請求項2に記載の化合物において、前記カチオンMは、−N=N−,− N=N+結合を有する基、スルホニウム基、ヨードニウム基、あるいは、置換型 又は非置換型のポリマーの網目構造に含まれるアレーン−フェロセンカチオンで あること、を特徴とする化合物。 8. 請求項2に記載の化合物において、前記カチオンは、ジアリールヨード ニウムカチオン、ジアルキルアリールヨードニウムカチオン、トリアリールスル ホニウムカチオン、トリアルキルスルホニウムカチオン、あるいは、置換型又は 非置換型のフエナシル−ジアルキルスルホニウムカチオンであること、を特徴と する化合物。 9. 請求項8に記載の化合物において、前記カチオンは、ポリマー鎖の一部 であること、を特徴とする化合物。 10. 請求項2に記載の化合物において、Mは、2,2’[アゾビス(2,2 ’−イミダゾリニオ−2−イル]プロパン2+又は2,2’−アゾビス(2−ア ミジニオプロパン)2+を含む有機カチオンであること、を特徴とする化合物。 11. 請求項1に記載の化合物において、前記カチオンMは、ある金属のカチ オン、アルカリ土類金属のカチオン、遷移金属のカチオン、三価金属のカチオン 、稀土類金属のカチオン、及び、有機金属のカチオンから成る群から選択された 金属カチオンであること、を特徴とする化合物。 12. 請求項1に記載の化合物において、前記カチオンは、フェロセン、チタ ノセン、ジルコノセンから誘導されたカチオン、、インデノセンカチオン、アレ ーンメタロセニウムカチオン、キラリティーを有するリン化水素のタイプの配位 子と錯合された遷移金属のカチオン、原子又は原子団に共有結合された1又はそ れ以上のアルキル基又はアリール基を有する有機金属カチオンから成る群から選 択されたメタロセニウムであり、前記カチオンは、ポリマー鎖の一部とすること ができること、を特徴とする化合物。 13. 請求項1に記載の化合物において、RFは、フッ素原子、あるいは、1 から12の炭素原子を有する過ハロゲン化されたアルキル遊離基、あるいは、6 から9の炭素原子を有する過ハロゲン化されたアルキルアリール遊離基であるこ と、を特徴とする化合物。 14. 請求項1に記載の化合物において、RFは、RACF2−、RACF2CF2 −、RACF2CF(CF)−、あるいは、CF3C(RA)F−の遊離基から選択 され、RAは、アルキル基、アリール基、アルキルアリール基又はアリールアル キル基、あるいは、少なくとも1つのエチレン不飽和物及び/又は縮合可能な基 及び/又は解離可能な基、液晶性基、発色性基、自己ドープ型の電子伝導性のポ リマー、加水分解可能なアルコキシシラン、カルボニル基、スルホニル基、チオ ニル基又はホスホニル基を含むグラフトを担持するポリマー鎖、フリー・ラジカ ルトラップ(trap)を含む基、解離する双極子、レドックスカップル、配位 子錯合剤、両性イオン、アミノ酸又は光学的又は生物学的に活性なポリペプチド 、キラル基を表していること、を特徴とする化合物。 15. 請求項1に記載の化合物において、Zは、RD−SO2−基であること、 を特徴とする化合物。 16. 請求項1に記載の化合物において、RDは、1から24の炭素原子を有 する、アルキル、アルケニル、オキサ−アルキル、オキサ−アルケニル、アザ− アルキル、アザ−アルケニル、チア−アルキル又はチア−アルケニルの遊離基、 あるいは、5から24の炭素原子を有する、アリール、アリールアルキル、アル キルアリール又はアルケニルアリールの遊離基から選択されること、を特徴とす る化合物。 17. 請求項1に記載の化合物において、RDは、1から12の炭素原子を有 していて、主鎖又は側鎖にO、N又はSの少なくとも1つのヘテロ原子を有して いるか、及び/又は、ヒドロキシ基、カルボニル基、アミン基、カルボキシル基 を有している、アルキル又はアルケニルの遊離基から選択されること、を特徴と する化合物。 18. 請求項1に記載の化合物において、RDは、ポリ(オキシアルキレン) 遊離基あるいはポリスチレン遊離基の一部であること、を特徴とする化合物。 19. 請求項1に記載の化合物において、RDは、ヨードニウム、スルホニウ ム、オキソニウム、アンモニウム、アミジニウム、トリアゾリウム、グアニジニ ウム、ピリジニウム、イミダゾリウム、ホスホニウム又はカルボニウムの基を有 する遊離基であり、前記イオン基は、全体として又は部分的に、カチオンM+と して作用すること、を特徴とする化合物。 20. 請求項1に記載の化合物において、RDは、カルボキシル酸官能基(− CO2 -)、スルホン酸官能基(−SO3 -)、スルホンイミド官能基(−SO2N SO2 -)又はスルホンアミド官能基(−SO2N-)から成る1又はそれ以上のア ニオン選択性基であること、を特徴とする化合物。 21. 請求項1に記載の化合物において、RDは、エチレン不飽和物及び/又 は縮合可能な基、及び/又は、熱的手段、光化学手段又はイオン解離によって解 離可能な基を少なくとも1つ有していること、を特徴とする化合物。 22. 請求項1に記載の化合物において、RDは、液晶性基又は発色性基ある いは自己ドープ型の電子伝導性ポリマー又は加水分解可能なアルコキシシランを 表すこと、を特徴とする化合物。 23. 請求項1に記載の化合物において、Zは、ポリマー鎖の反復単量体を表 すこと、を特徴とする化合物。 24. 請求項1に記載の化合物において、RDは、フリー・ラジカルを捕捉す ることのできる基を含むこと、を特徴とする化合物。 25. 請求項1に記載の化合物において、RDは、解離する双極子を含むこと 、を特徴とする化合物。 26. 請求項1に記載の化合物において、RDは、レドックスカップルを含む こ と、を特徴とする化合物。 27. 請求項1に記載の化合物において、RDは、錯化配位子を含むこと、を 特徴とする化合物。 28. 請求項1に記載の化合物において、RD−Yは、光学的に活性であるこ と、を特徴とする化合物。 29. 請求項1に記載の化合物において、RD−Yは、アミノ酸、又は、光学 的に又は生物学的に活性なポリペプチドを表すこと、を特徴とする化合物。 30. 請求項1に記載の化合物において、RDは、2よりも大きな原子価vを 有していてその各々の自由端にRF−S(O)x−N−の基を有している遊離基を 表すこと、を特徴とする化合物。 31. 請求項1に記載の化合物において、前記置換基Zは、−OCnF2n+1、 −OC2F4H、−SCnF2n+1、及び、−SC2F4H、−OCF=CF2、−SC F=CF2、及び、CnF2n+1CH2ー(nは、1から8の整数である)から成る 群から選択されること、を特徴とする化合物。 32. 請求項1に記載の化合物において、Zは、ピリジン、ピラジン、ピリミ ジン、オキサジアゾール又はチアジアゾールから誘導されたフッ化された又はフ ッ化されていない複素環を含むこと、を特徴とする化合物。 33. 溶媒中の溶液の中のイオン化合物を含むイオン伝導物質であって、前記 イオン化合物は、請求項1の化合物であること、を特徴とするイオン伝導物質。 34. 請求項33に記載のイオン伝導物質において、前記イオン化合物の置換 基RF又はRDの少なくとも一方は、アルキル基、アリール基、アルキルアリール 基又はアリールアルキル基;液晶性基、又は、少なくとも1つのエチレン不飽和 物を含む基及び/又は縮合可能な基、及び/又は、熱的手段、光化学手段又はイ オン解離によって解離可能な基;自己ドープ型の電子伝導性ポリマー;加水分解 可能なアルコキシシラン;フリー・ラジカルトラップ;解離性双極子;レドック スカップル;錯化配位子を含むこと、を特徴とするイオン伝導物質。 35. 請求項33に記載のイオン伝導物質において、前記イオン化合物の置換 基RDは、O、N及びSから選択された少なくとも1つのヘテロ原子を含むアル キル又はアルケニル;ヒドロキシ基、カルボニル基、アミン基、カルボキシル基 を 有するアルキル又はアルケニル;側鎖及び/又は芳香核がヘテロ原子を含んでい る、アリール、アリールアルキル、アルキルアリール又はアルケンアリールであ ること、を特徴とするイオン伝導物質。 36. 請求項33に記載のイオン伝導物質において、前記置換基RDは、ポリ マーの反復単量体であること、を特徴とするイオン伝導物質。 37. 請求項33に記載のイオン伝導物質において、前記イオン化合物の置換 基Zは、−OCnF2n+1、−OC2F4H、−SCnF2n+1、及び、−SC2F4H、 −OCF=CF2、−SCF=CF2から成る群から選択されること、を特徴とす るイオン伝導物質。 38. 請求項33に記載のイオン伝導物質において、前記溶媒は、直鎖エーテ ル、及び、環式のエーテル、エステル、ニトリル、ニトロ誘導体、アミド、スル ホン、スルホラン、スルファミド、並びに、部分的ハロゲン化された炭化水素、 又は、極性ポリマー、あるいは、これらの混合物から選択された非プロトン性液 体溶媒であること、を特徴とするイオン伝導物質。 39. 請求項38に記載のイオン伝導物質において、前記溶媒は、移植された イオン基を有することのできる架橋型又は非架橋型のポリマーであること、を特 徴とするイオン伝導物質。 40. 請求項39に記載のイオン伝導物質において、前記溶媒和ポリマーは、 直鎖構造、櫛歯又はブロックのポリエステルから選択され、該ポリエステルは、 ポリ(エチレンオキシド)、エチレンオキシド、プロピレンオキシド又はアリル グリシジルエーテル単量体、ポリホスファジンに基づく網目構造、イソシアネー トと架橋されたポリエチレングリコールに基づく架橋網目構造、重縮合によって 得られ、架橋可能な基、及び、幾つかのブロックがレドックス特性を有する官能 基を担持しているブロックコポリマーを含むことを可能にする基を有しているポ リマー網目構造を形成することができること、を特徴とするイオン伝導物質。 41. 請求項33に記載のイオン伝導物質において、前記溶媒は、非プロトン 性液体溶媒と、硫黄、酸素、窒素及びフッ素から選択された少なくとも1つのヘ テロ原子を含む単量体から成る極性ポリマー溶媒とから構成されること、を特徴 とするイオン伝導物質。 42. 請求項41に記載のイオン伝導物質において、前記極性ポリマーは、主 として、アクリロニトリル、フッ化ビニリデン、N−ビニルピロリドン又はメタ クリル酸メチルから誘導された単量体を含むこと、を特徴とするイオン伝導物質 。 43. 請求項33に記載のイオン伝導物質において、少なくとも1つの第2の 塩を含むこと、を特徴とするイオン伝導物質。 44. 請求項33に記載のイオン伝導物質において、粉末又は繊維の形態の鉱 物又は有機装填物を含むこと、を特徴とするイオン伝導物質。 45. 負極と正極とを備え、これら負極及び正極が共に電解質によって分離さ れている、電気化学的な発電装置であって、前記電解質が、請求項33乃至44 のいずれかの物質であること、を特徴とする電気化学的な発電装置。 46. 請求項45に記載の電気化学的な発電装置において、前記負極は、金属 リチウム又はその合金、場合によっては酸化リチウムの中のナノメートル単位の 分散体の形態としてのリチウム、あるいは、二窒化リチウム及び遷移金属、ある いは、一般式Li1+y+x/3Ti2-x/3O4(0≦x≦1,0≦y≦1)を有する低 電位酸化物、若しくは、炭素及び有機物質の熱分解から生ずる炭素生成物から構 成されること、を特徴とする電気化学的な発電装置。 47. 請求項45に記載の電気化学的な発電装置において、前記正極は、酸化 バナジウムVOx(2≦x≦2.5)、LiV308、LiyNi1-xCoxO2(0 ≦x≦1;0≦y≦1)、マンガンのスピネルLiyMn1-xMxO2(M=Cr、 Al、V、Ni、0≦x≦0;0≦y≦2)、有機ポリジスルフィドFeS、F eS2、硫酸鉄Fe2(SO4)3、オリビン構造を有する鉄及びリチウムのリン酸 塩及びリン珪酸塩、又は、鉄がマンガンによって置換された単独又は混合して使 用される置換型の生成物から選択されること、を特徴とする電気化学的な発電装 置。 48. 請求項45に記載の電気化学的な発電装置において、前記カソードの集 電子がアルミニウムから形成されていること、を特徴とする電気化学的な発電装 置。 49. 大きな表面積を有する少なくとも1つの炭素電極、あるいは、レドック スポリマーを含む電極を用いたスーパーキャパシタンスであって、前記電解質が 、請求項33乃至44のいずれかの物質であること、を特徴とするスーパーキャ パ シタンス。 50. 請求項33乃至44のいずれか一の物質を用いて、電子伝導ポリマーの p形又はn形のドーピングを行うこと、を特徴とする方法。 51. 前記電解質が請求項33乃至44のいずれか一の物質であること、を特 徴とするエレクトロクローム装置。 52. カチオン反応が可能なプレポリマーのモノマーの重合又は架橋を行うプ ロセスであって、請求項1の化合物をその反応の触媒作用を行う酸の供給源とし て作用するフォトイニシエータとして使用すること、を特徴とするプロセス。 53. 請求項52に記載のプロセスであって、前記イオン化合物のカチオンが 、−N=N+,−N=N−の結合を有する基、スルホニウム基、ヨードニウム基 、あるいは、置換型又は非置換型のアレーン−フェロセンのカチオンであり、前 記基は、選択に応じて、ポリマー網目構造に含まれること、を特徴とするプロセ ス。 54. 請求項52に記載のプロセスにおいて、前記置換基RF又はZの少なく とも一方が、非置換型のアルコキシルラジカル、あるいは、オキサ、スルホキシ ド、スルホン、酸化リン又はホスホン酸の基を含む遊離基であること、を特徴と するプロセス。 55. 請求項52に記載のプロセスにおいて、前記モノマーは、環式エーテル 官能基、環式チオエーテル官能基、又は、環式アミノ官能基、ビニル化合物、ビ ニルエーテル、オキサゾリン、ラクトン及びラクタムを含む化合物から成る群か ら選択されること、を特徴とするプロセス。 56. 請求項52に記載のプロセスにおいて、前記ポリマーは、エポキシ基が 脂肪鎖、芳香鎖、又は、複素環鎖によって担持されている化合物から成る群から 選択されること、を特徴とするプロセス。 57. 請求項52に記載のプロセスにおいて、カチオン重合を行うことのでき る少なくとも1つのモノマー又はプレポリマーとフォトイニシエータとを混合す る工程と、得られた混合物をβ放射線を含む光化学放射線に曝す工程とを備える こと、を特徴とするプロセス。 58. 請求項57に記載のプロセスにおいて、反応混合物を薄層に整形された 後に放射線で処理すること、を特徴とするプロセス。 59. 請求項52に記載のプロセスにおいて、前記フォトイニシエータは、重 合反応に対して不活性な溶媒の中の溶液の形態で使用されること、を特徴とする プロセス。 60. 請求項59に記載のプロセスにおいて、前記不活性な溶媒は、アセトン 、メチルエチル、アセトニトリル、炭酸プロピレン、γ−ブチロラクトン、モノ 、ジ、トリのエチレン又はプロピレンのグリコールのエーテル/エステル、モノ 、ジ、トリのエチレン又はプロピレンのグリコールのエステル/アルコール、フ タル酸又はクエン酸のエステルから成る群から選択されること、を特徴とするプ ロセス。 61. 請求項52に記載のプロセスにおいて、重合反応に対して活性を有する 化合物から成る溶媒又は希釈剤の存在下で前記反応を行うこと、を特徴とするプ ロセス。 62. 請求項61に記載のプロセスにおいて、前記活性を有する化合物は、モ ノ、ジ、トリ、テトラのエチレン又はプロピレングリコールのモノ及びジビニル エステル、トリビニルエーテルトリメチロールプロパン、及び、ジメタノールシ クロヘキサンのジビニルエーテル、N−ビニルピロリドン、炭酸プロピレンの2 −プロペニルエーテルから成る群から選択されること、を特徴とするプロセス。 63. 請求項52に記載のプロセスにおいて、感光剤が、前記反応混合物に添 加されること、を特徴とするプロセス。 64. 請求項64に記載のプロセスにおいて、前記感光剤は、アントラセン、 ジフェニル−9,10−アントラセン、ペリレン、フェノチアジン、テトラセン 、キサントン、チオキサントン、イソプロピルチオキサントン、アセトフェノン 、ベンゾフェノン、1,3,5−トリアリール−2−ピラゾリン、及び、これら の誘導体、特に、アルキル、オキサ、又は、アザアルキルラジカルによって芳香 核上に置換された誘導体から成る群から選択されること、を特徴とするプロセス 。 65. 請求項52に記載のプロセスにおいて、前記反応混合物は、更に、フリ ー・ラジカル重合を行うことのできる少なくとも1つのモノマー又はプレポリマ ーと、光化学放射線又はβ放射線あるいは熱の影響によってフリー・ラジカル開 始剤を解放することのできる化合物を含むこと、を特徴とするプロセス。 66. 酸に対して感受性を有する基を含むポリマーの溶解性を変更するプロセ スであって、前記ポリマーを請求項1の化合物が存在する状態で光化学放射線又 はβ放射線に曝す工程を含むこと、を特徴とするプロセス。 67. 請求項65に記載のプロセスにおいて、前記ポリマーは、第三アルコー ルから誘導されたエステル又はアリールエステルを含むこと、を特徴とするプロ セス。 68. 請求項67に記載のプロセスにおいて、前記ポリマーは、第三ブチル又 は第三アミンのアクリル酸、第三チオブチル又は第三チオアミルのイタコン酸、 (第三チオブトキシカルボニルオキシスチレン)又は(第三チオアミルオキシス チレン)のホモポリマー又はコポリマーから成る群から選択されること、を特徴 とするプロセス。 69. 請求項66に記載のプロセスにおいて、フォトレジストの化学的な増幅 を行うために使用されること、を特徴とするプロセス。 70. ビニルモノマーを重合するためのプロセスであって、請求項10の化合 物をフリー・ラジカル開始剤として使用すること、を特徴とするプロセス。 71. カチオン性着色剤の組成であって、請求項1の化合物を含むこと、を特 徴とする組成。 72. 請求項71に記載のカチオン性着色剤の組成において、イオン基RF− SOx−N-−Zの負の電荷が、着色剤の分子に定着されるか、あるいは、着色剤 の正の電荷の対イオンを構成すること、を特徴とする組成。 73. 請求項1に記載の化合物をフリーデル/クラフト反応、ディールス/ア ルダー反応、ミハエルの添加、アリル化反応、ピナコリン結合反応、グリコース 化反応、オキセタンの開始サイクル反応、アルドール化反応、アルケンの複分解 反応、チーグラ/ナッタ型の重合反応、サイクル開始による複分解型の重合反応 、及び、非環式ジエンの複分解型の重合反応における触媒として使用する方法。 74. 請求項73に記載の方法において、前記化合物は、請求項1の化合物で あり、前記カチオンは、リチウム、マグネシウム、銅、亜鉛、錫、稀土類元素、 白金族を含む三価金属、及び、有機金属のカチオンから成る群から選択されるこ と、を特徴とする方法。 75. 請求項6に記載の化合物を、化学的、光化学的、電気化学的、光電気化 学的な反応を行うための溶媒として使用し、前記化合物は、その融点よりも高い 温度で使用されること、を特徴とする方法。 76. 請求項1のイオン化合物を含むこと、を特徴とする電子伝導物質。 77. 請求項76に記載の電子伝導物質において、前記イオン化合物のカチオ ン部分が、ドープされた共役ポリマー”p”から成る多価カチオンであること、 を特徴とする電子伝導物質。 78. 請求項76に記載の電子伝導物質において、前記イオン化合物の置換基 Zが、6から20の炭素原子を有するアルキル鎖を含むこと、を特徴とする電子 伝導物質。
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CA002199231A CA2199231A1 (fr) | 1997-03-05 | 1997-03-05 | Nouveaux materiaux ioniques |
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PCT/CA1997/001013 WO1998029388A1 (fr) | 1996-12-30 | 1997-12-30 | Sels d'amides perfluores, et leurs utilisations comme materiaux a conduction ionique |
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JP2009010733A Expired - Lifetime JP4927108B2 (ja) | 1996-12-30 | 2009-01-21 | 複素環式芳香族アニオン塩及びイオン性導電材料としてのその使用 |
JP2009120239A Expired - Lifetime JP5629061B2 (ja) | 1996-12-30 | 2009-05-18 | 過フッ化アミド塩及びイオン伝導物質としてのその使用方法 |
JP2010006864A Expired - Lifetime JP5209649B2 (ja) | 1996-12-30 | 2010-01-15 | マロン酸ニトリル誘導体アニオン塩、及びイオン伝導性材料としてのそれらの使用 |
JP2013033109A Pending JP2013173740A (ja) | 1996-12-30 | 2013-02-22 | 過フッ化アミド塩及びイオン伝導物質としてのその使用方法 |
JP2014001687A Withdrawn JP2014169271A (ja) | 1996-12-30 | 2014-01-08 | 過フッ化アミド塩及びイオン伝導物質としてのその使用方法 |
JP2015234934A Pending JP2016104739A (ja) | 1996-12-30 | 2015-12-01 | 過フッ化アミド塩及びイオン伝導物質としてのその使用方法 |
Family Applications After (13)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP52951398A Expired - Lifetime JP4070244B2 (ja) | 1996-12-30 | 1997-12-30 | 表面変性された炭化物質 |
JP52951498A Expired - Lifetime JP4124487B2 (ja) | 1996-12-30 | 1997-12-30 | 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 |
JP52951798A Expired - Lifetime JP4361137B2 (ja) | 1996-12-30 | 1997-12-30 | 液体形態のプロトン伝導体 |
JP52951598A Pending JP2000508677A (ja) | 1996-12-30 | 1997-12-30 | マロン酸ニトリル誘導体アニオン塩、及びイオン伝導性材料としてのそれらの使用 |
JP52951698A Expired - Lifetime JP4683675B2 (ja) | 1996-12-30 | 1997-12-30 | 複素環式芳香族アニオン塩及びイオン性導電材料としてのその使用 |
JP2007193021A Pending JP2008007781A (ja) | 1996-12-30 | 2007-07-25 | 表面変性された炭化物質 |
JP2008143090A Pending JP2009004374A (ja) | 1996-12-30 | 2008-05-30 | 液体形態のプロトン伝導体 |
JP2009010733A Expired - Lifetime JP4927108B2 (ja) | 1996-12-30 | 2009-01-21 | 複素環式芳香族アニオン塩及びイオン性導電材料としてのその使用 |
JP2009120239A Expired - Lifetime JP5629061B2 (ja) | 1996-12-30 | 2009-05-18 | 過フッ化アミド塩及びイオン伝導物質としてのその使用方法 |
JP2010006864A Expired - Lifetime JP5209649B2 (ja) | 1996-12-30 | 2010-01-15 | マロン酸ニトリル誘導体アニオン塩、及びイオン伝導性材料としてのそれらの使用 |
JP2013033109A Pending JP2013173740A (ja) | 1996-12-30 | 2013-02-22 | 過フッ化アミド塩及びイオン伝導物質としてのその使用方法 |
JP2014001687A Withdrawn JP2014169271A (ja) | 1996-12-30 | 2014-01-08 | 過フッ化アミド塩及びイオン伝導物質としてのその使用方法 |
JP2015234934A Pending JP2016104739A (ja) | 1996-12-30 | 2015-12-01 | 過フッ化アミド塩及びイオン伝導物質としてのその使用方法 |
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EP (9) | EP0890176B1 (ja) |
JP (14) | JP4823401B2 (ja) |
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Families Citing this family (299)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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US6852809B2 (en) * | 1999-12-27 | 2005-02-08 | Sumitomo Chemical Company, Limited | Catalyst component for addition polymerization, catalyst for addition polymerization, and process for producing addition polymer |
AU2000253140A1 (en) * | 2000-01-11 | 2001-07-24 | 3M Innovative Properties Company | Perfluoroalkanesulfonate salts in electrochemical systems |
WO2001053368A1 (en) | 2000-01-19 | 2001-07-26 | E.I. Dupont De Nemours And Company | Process for making graft copolymers |
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US7220914B2 (en) * | 2003-12-01 | 2007-05-22 | Konarka Technologies, Inc. | Zwitterionic compounds and photovoltaic cells containing same |
JP4682395B2 (ja) * | 2000-04-28 | 2011-05-11 | 日産自動車株式会社 | 非水電池 |
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JP2002134113A (ja) * | 2000-10-30 | 2002-05-10 | Matsushita Electric Ind Co Ltd | 非水系二次電池 |
US6841303B2 (en) * | 2001-01-17 | 2005-01-11 | Skc Co., Ltd. | High ionic conductivity gel polymer electrolyte for rechargeable polymer batteries |
WO2002094883A2 (en) * | 2001-01-22 | 2002-11-28 | Covalent Associates, Inc. | One-step process for the preparation of halide-free hydrophobic salts |
WO2002072260A2 (en) * | 2001-03-12 | 2002-09-19 | The Queen's University Of Belfast | Metal bis-triflimide compounds, their synthesis and their uses |
JP3969077B2 (ja) * | 2001-04-04 | 2007-08-29 | 住友化学株式会社 | 高分子電解質及びその製造方法 |
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JP4752135B2 (ja) * | 2001-05-25 | 2011-08-17 | 株式会社Gsユアサ | リチウム電池 |
JP4222466B2 (ja) * | 2001-06-14 | 2009-02-12 | 富士フイルム株式会社 | 電荷輸送材料、それを用いた光電変換素子及び光電池、並びにピリジン化合物 |
EP1402319B1 (en) * | 2001-06-22 | 2008-08-27 | Agfa-Gevaert | Material having a conductive pattern; and a material and method for making a conductive pattern |
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US7241535B2 (en) * | 2001-10-15 | 2007-07-10 | Samsung Sdi Co., Ltd. | Electrolyte for lithium-sulfur batteries and lithium-sulfur batteries comprising the same |
JP4004769B2 (ja) * | 2001-10-17 | 2007-11-07 | Necトーキン株式会社 | 電解液、並びにこれを用いた電気化学セル |
DE10155281A1 (de) * | 2001-11-08 | 2003-06-05 | Solvent Innovation Gmbh | Verfahren zur Entfernung polarisierbarer Verunreinigungen aus Kohlenwasserstoffen und Kohlenwasserstoffgemischen durch Extraktion mit ionischen Flüssigkeiten |
US7303852B2 (en) * | 2001-12-27 | 2007-12-04 | Shin-Etsu Chemical Co., Ltd. | Photoacid generating compounds, chemically amplified positive resist materials, and pattern forming method |
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US6803152B2 (en) * | 2002-04-19 | 2004-10-12 | Ener1 Battery Company | Nonaqueous electrolytes based on organosilicon ammonium derivatives for high-energy power sources |
US7709158B1 (en) | 2002-05-09 | 2010-05-04 | Electrochem Solutions, Inc. | Guanidine derivatives as cations for ambient temperature molten sales in electrochemical power sources |
US20030211389A1 (en) * | 2002-05-09 | 2003-11-13 | Schlaikjer Carl R. | Guanidine derivatives as cations for ambient temperature molten salts in electrochemical power sources |
US7042615B2 (en) | 2002-05-17 | 2006-05-09 | The Regents Of The University Of California | Electrochromic devices based on lithium insertion |
US7459103B2 (en) * | 2002-05-23 | 2008-12-02 | Columbian Chemicals Company | Conducting polymer-grafted carbon material for fuel cell applications |
US7241334B2 (en) * | 2002-05-23 | 2007-07-10 | Columbian Chemicals Company | Sulfonated carbonaceous materials |
US7390441B2 (en) * | 2002-05-23 | 2008-06-24 | Columbian Chemicals Company | Sulfonated conducting polymer-grafted carbon material for fuel cell applications |
BR0311226A (pt) * | 2002-05-23 | 2008-01-29 | Columbian Chem | material de carbono enxertado com polìmero condutor sulfonado para aplicações em células de combustìvel |
AU2003233656A1 (en) * | 2002-05-23 | 2003-12-12 | Columbian Chemicals Company | Conducting polymer-grafted carbon material for fuel cell applications |
US7763186B2 (en) * | 2002-06-21 | 2010-07-27 | Los Alamos National Security, Llc | Preparation and purification of ionic liquids and precursors |
AU2003256281A1 (en) * | 2002-06-21 | 2004-01-06 | The Regents Of The University Of California | Electrolytes for electrooptic devices comprising ionic liquids |
KR100463181B1 (ko) * | 2002-07-12 | 2004-12-23 | 삼성에스디아이 주식회사 | 리튬-설퍼 전지용 전해액 및 이를 포함하는 리튬-설퍼 전지 |
US20040038127A1 (en) * | 2002-08-20 | 2004-02-26 | Schlaikjer Carl Roger | Small cation/delocalizing anion as an ambient temperature molten salt in electrochemical power sources |
JP2004082365A (ja) * | 2002-08-23 | 2004-03-18 | Fuji Photo Film Co Ltd | 感熱記録材料 |
AU2003275203A1 (en) | 2002-09-24 | 2004-04-19 | E.I. Du Pont De Nemours And Company | Water dispersible polythiophenes made with polymeric acid colloids |
JP4464277B2 (ja) | 2002-09-24 | 2010-05-19 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 導電性有機ポリマー/ナノ粒子複合材料およびその使用方法 |
US7317047B2 (en) | 2002-09-24 | 2008-01-08 | E.I. Du Pont De Nemours And Company | Electrically conducting organic polymer/nanoparticle composites and methods for use thereof |
KR101148285B1 (ko) | 2002-09-24 | 2012-05-21 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 전기적 응용을 위한 중합체성 산 콜로이드로 제조된수분산성 폴리아닐린 |
EP1406336A1 (en) * | 2002-10-01 | 2004-04-07 | Xoliox SA | Electrolyte composition having improved aluminium anticorrosive properties |
TWI331626B (en) * | 2002-11-22 | 2010-10-11 | Japan Carlit Co Ltd | Near-infrared absorptive dye and near-infrared blocking filter |
US8124869B2 (en) | 2003-01-15 | 2012-02-28 | Nippon Shokubai Co., Ltd. | Dye-sensitized type solar cell |
US20040149472A1 (en) * | 2003-02-03 | 2004-08-05 | Warner Benjamin P. | Radiofrequency attenuator and method |
JP2004265638A (ja) * | 2003-02-25 | 2004-09-24 | Ebara Corp | 混合伝導カーボンおよび電極 |
US7390438B2 (en) | 2003-04-22 | 2008-06-24 | E.I. Du Pont De Nemours And Company | Water dispersible substituted polydioxythiophenes made with fluorinated polymeric sulfonic acid colloids |
US7312100B2 (en) * | 2003-05-27 | 2007-12-25 | The North Carolina State University | In situ patterning of electrolyte for molecular information storage devices |
DE112004001158T5 (de) * | 2003-06-27 | 2007-01-11 | E.I. Du Pont De Nemours And Co., Wilmington | Fluorierte Sulfonamidverbindungen und daraus hergestellte Polymer-Elektrolytmembranen zur Verwendung in elektrochemischen Zellen |
WO2005006352A1 (ja) * | 2003-07-11 | 2005-01-20 | Ube Industries, Ltd. | 酸・塩基混合物および該混合物からなるイオン伝導体 |
US7001936B2 (en) * | 2003-07-16 | 2006-02-21 | Lexmark International, Inc. | Pigmented inkjet ink |
JP4916882B2 (ja) * | 2003-09-30 | 2012-04-18 | ハネウェル・インターナショナル・インコーポレーテッド | 指示薬を伴う電解液 |
US7074491B2 (en) * | 2003-11-04 | 2006-07-11 | Dionex Corporation | Polar silanes for binding to substrates and use of the bound substrates |
US8828610B2 (en) * | 2004-01-06 | 2014-09-09 | Sion Power Corporation | Electrolytes for lithium sulfur cells |
US7358012B2 (en) * | 2004-01-06 | 2008-04-15 | Sion Power Corporation | Electrolytes for lithium sulfur cells |
US10297827B2 (en) | 2004-01-06 | 2019-05-21 | Sion Power Corporation | Electrochemical cell, components thereof, and methods of making and using same |
US10629947B2 (en) | 2008-08-05 | 2020-04-21 | Sion Power Corporation | Electrochemical cell |
TWI302760B (en) | 2004-01-15 | 2008-11-01 | Lg Chemical Ltd | Electrochemical device comprising aliphatic nitrile compound |
JP4433165B2 (ja) | 2004-02-16 | 2010-03-17 | ソニー株式会社 | カチオン伝導体およびこれを用いた電気化学デバイス |
JP4507629B2 (ja) * | 2004-02-20 | 2010-07-21 | 東洋インキ製造株式会社 | 樹脂グラフトカーボンブラック組成物 |
WO2005083159A2 (en) * | 2004-02-23 | 2005-09-09 | E.I. Dupont De Nemours & Company | Apparatus adapted for membrane mediated electropolishing |
US7351358B2 (en) | 2004-03-17 | 2008-04-01 | E.I. Du Pont De Nemours And Company | Water dispersible polypyrroles made with polymeric acid colloids for electronics applications |
US7785740B2 (en) * | 2004-04-09 | 2010-08-31 | Air Products And Chemicals, Inc. | Overcharge protection for electrochemical cells |
US8147962B2 (en) | 2004-04-13 | 2012-04-03 | E. I. Du Pont De Nemours And Company | Conductive polymer composites |
WO2005109562A1 (en) | 2004-05-10 | 2005-11-17 | Nippon Shokubai Co., Ltd. | Material for electrolytic solution, ionic material-containing composition and use thereof |
US7960057B2 (en) * | 2004-05-17 | 2011-06-14 | Toyota Motor Engineering & Manufacturing North America, Inc. | Battery with molten salt electrolyte and phosphorus-containing cathode |
US20050287441A1 (en) * | 2004-06-23 | 2005-12-29 | Stefano Passerini | Lithium polymer electrolyte batteries and methods of making |
JP2006008454A (ja) * | 2004-06-25 | 2006-01-12 | Fuji Xerox Co Ltd | 炭素微粒子構造体とその製造方法、およびこれを製造するための炭素微粒子転写体と炭素微粒子構造体製造用溶液、並びに炭素微粒子構造体を用いた炭素微粒子構造体電子素子とその製造方法、そして集積回路 |
JP4731132B2 (ja) * | 2004-06-29 | 2011-07-20 | 株式会社Adeka | 非水電解液及び該電解液を用いた非水電解液二次電池 |
JP4412598B2 (ja) * | 2004-07-20 | 2010-02-10 | 第一工業製薬株式会社 | イオンポリマーゲル電解質およびその前駆体組成物 |
AU2004240178A1 (en) * | 2004-08-20 | 2006-03-09 | Commonwealth Scientific And Industrial Research Organisation | Zwitterionic additives for electrochemical devices |
EP1634867A1 (de) * | 2004-08-25 | 2006-03-15 | Lonza AG | Tricyanomethansalze organischer Kationen |
EP1796193B1 (en) * | 2004-09-03 | 2011-12-14 | Nissan Motor Co., Ltd. | Proton conductor and fuel cell using the same |
KR100663032B1 (ko) * | 2004-09-21 | 2006-12-28 | 주식회사 엘지화학 | 공융혼합물을 포함하는 전해질 및 이를 이용한 전기 변색소자 |
US20060068987A1 (en) * | 2004-09-24 | 2006-03-30 | Srinivas Bollepalli | Carbon supported catalyst having reduced water retention |
JP4709518B2 (ja) * | 2004-09-29 | 2011-06-22 | 株式会社東芝 | プロトン伝導膜及び燃料電池 |
CN101090952A (zh) * | 2004-12-13 | 2007-12-19 | 特拉斯福特普拉斯公司 | 组合物,氧化还原对及其应用 |
FR2879458B1 (fr) * | 2004-12-21 | 2007-07-20 | Centre Nat Rech Scient Cnrse | Sulfamides et sulfinimides fluores |
KR20070104389A (ko) | 2005-01-10 | 2007-10-25 | 애버리 데니슨 코포레이션 | 제거 가능한 커얼 라벨들 |
KR100616666B1 (ko) | 2005-01-27 | 2006-08-28 | 삼성전기주식회사 | 카본나노튜브에 구아니딘기를 형성하는 방법,구아니딘기가 형성된 카본나노튜브를 기판에 부착하는방법 및 이에 따라 제조된 카본나노튜브 및 기판 |
JP2006257288A (ja) * | 2005-03-17 | 2006-09-28 | Kaneka Corp | 金属表面コーティング用組成物、導電性高分子の製造方法、金属表面のコーティング方法、ならびに電解コンデンサおよびその製造方法 |
WO2006088033A1 (ja) * | 2005-02-17 | 2006-08-24 | Kaneka Corporation | 金属表面コーティング用組成物、導電性高分子の製造方法、金属表面のコーティング方法、ならびに電解コンデンサおよびその製造方法 |
JP4856883B2 (ja) * | 2005-03-03 | 2012-01-18 | 富士フイルム株式会社 | 機能性素子、エレクトロクロミック素子、光学デバイス及び撮影ユニット |
DE102005013790B4 (de) * | 2005-03-24 | 2007-03-29 | Polymaterials Ag | Polymerelektrolyt, Verwendung des Polymerelektrolyten und elektrochemische Vorrichtung, die den Polymerelektrolyten umfasst |
CA2506104A1 (en) | 2005-05-06 | 2006-11-06 | Michel Gauthier | Surface modified redox compounds and composite electrode obtain from them |
US7619803B2 (en) * | 2005-05-31 | 2009-11-17 | Konica Minolta Holdings, Inc. | Electrochromic display element and full-color electrochromic display element |
US7579184B2 (en) * | 2005-06-02 | 2009-08-25 | Board Of Trustees Of Michigan State University | Methods to increase dynamic range and improve quantitative analysis in rapid biosensors |
CN101595532B (zh) | 2005-06-28 | 2013-07-31 | E.I.内穆尔杜邦公司 | 缓冲组合物 |
WO2007002737A2 (en) * | 2005-06-28 | 2007-01-04 | E. I. Du Pont De Nemours And Company | High work function transparent conductors |
EP1931626A1 (en) * | 2005-08-22 | 2008-06-18 | Transfert Plus S.E.C. | Process for preparing sulfonylimides and derivatives thereof |
EP1952477B1 (en) * | 2005-10-27 | 2010-09-15 | LG Chem. Ltd. | Secondary battery comprising eutectic mixture and preparation method thereof |
WO2007055392A1 (en) * | 2005-11-11 | 2007-05-18 | Nippon Shokubai Co., Ltd. | Ionic compound |
US7919629B2 (en) | 2005-12-12 | 2011-04-05 | Phostech Lithium Inc. | Sulphonyl-1,2,4-triazole salts |
WO2007117332A2 (en) * | 2005-12-29 | 2007-10-18 | The Board Of Trustees Of The University Of Illinois | Titanium oxide base photocatalysts |
US7521394B2 (en) * | 2005-12-29 | 2009-04-21 | The Board Of Trustees Of The University Of Illinois | Nanoparticles containing titanium oxide |
US8216680B2 (en) | 2006-02-03 | 2012-07-10 | E I Du Pont De Nemours And Company | Transparent composite conductors having high work function |
JP4682057B2 (ja) * | 2006-02-20 | 2011-05-11 | 富士フイルム株式会社 | 感光性組成物、該感光性組成物を用いたパターン形成方法及び該感光性組成物に用いられる化合物 |
WO2007104144A1 (en) * | 2006-03-10 | 2007-09-20 | Transfert Plus, S.E.C. | Compounds, ionic liquids, molten salts and uses thereof |
DE102007014048B4 (de) * | 2006-03-21 | 2013-02-21 | Novaled Ag | Mischung aus Matrixmaterial und Dotierungsmaterial, sowie Verfahren zum Herstellen einer Schicht aus dotiertem organischen Material |
WO2007115540A1 (de) * | 2006-03-30 | 2007-10-18 | Novaled Ag | Verwendung von bora-tetraazapentalenen |
US8268197B2 (en) * | 2006-04-04 | 2012-09-18 | Seeo, Inc. | Solid electrolyte material manufacturable by polymer processing methods |
WO2007142731A2 (en) | 2006-04-04 | 2007-12-13 | The Regents Of The University Of California | High elastic modulus polymer electrolytes |
US7696122B2 (en) * | 2006-07-05 | 2010-04-13 | Cabot Corporation | Electrocatalyst inks for fuel cell applications |
US20080214814A1 (en) * | 2006-07-18 | 2008-09-04 | Zaiwei Li | Stable ionic liquid complexes and methods for determining stability thereof |
KR101375675B1 (ko) * | 2006-07-27 | 2014-03-19 | 니치콘 가부시키가이샤 | 이온성 화합물 |
EP1903029A1 (de) * | 2006-08-16 | 2008-03-26 | Lonza Ag | Verfahren zur Herstellung von Alkali- oder Erdalkalimetalltricyanomethaniden |
EP2056380B1 (en) * | 2006-08-17 | 2018-02-28 | Mitsubishi Chemical Corporation | Negative electrode active material for lithium ion secondary battery, process for producing the same, and negative electrode for lithium ion secondary battery and lithium ion secondary battery both employing the same. |
US7833660B1 (en) | 2006-09-07 | 2010-11-16 | The United States Of America As Represented By The Secretary Of The Army | Fluorohaloborate salts, synthesis and use thereof |
US7820323B1 (en) | 2006-09-07 | 2010-10-26 | The United States Of America As Represented By The Secretary Of The Army | Metal borate synthesis process |
BRPI0717895B1 (pt) | 2006-11-02 | 2017-03-21 | Avery Dennison Corp | composição adesiva sensível à pressão baseada em emulsão, rótulos removíveis e método para desprender um rótulo em relação a um artigo |
EP2081082A4 (en) * | 2006-11-08 | 2010-12-08 | Konica Minolta Holdings Inc | DISPLAY ELEMENT |
US7864397B2 (en) * | 2006-12-04 | 2011-01-04 | 3M Innovative Properties Company | Curable electrolyte |
US8043418B2 (en) * | 2006-12-08 | 2011-10-25 | General Electric Company | Gas separator apparatus |
KR100767427B1 (ko) * | 2006-12-21 | 2007-10-17 | 제일모직주식회사 | 리튬 2차전지용 비수성 전해액 및 이를 포함하는 리튬2차전지 |
US20080191172A1 (en) | 2006-12-29 | 2008-08-14 | Che-Hsiung Hsu | High work-function and high conductivity compositions of electrically conducting polymers |
JP5110625B2 (ja) * | 2007-02-02 | 2012-12-26 | パナソニック株式会社 | 蓄電デバイス |
KR20090109570A (ko) * | 2007-02-06 | 2009-10-20 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 신규한 결합제를 포함하는 전극과, 그의 제조 방법 및 사용 방법 |
US7875388B2 (en) | 2007-02-06 | 2011-01-25 | 3M Innovative Properties Company | Electrodes including polyacrylate binders and methods of making and using the same |
US7820347B1 (en) * | 2007-02-06 | 2010-10-26 | The United States Of America As Represented By The Secretary Of The Air Force | Conversion of salt halides to nitrate salts |
US8540899B2 (en) * | 2007-02-07 | 2013-09-24 | Esionic Es, Inc. | Liquid composite compositions using non-volatile liquids and nanoparticles and uses thereof |
TW200909549A (en) * | 2007-04-13 | 2009-03-01 | 3M Innovative Properties Co | Antistatic optically clear pressure sensitive adhesive |
US8012277B2 (en) * | 2007-04-13 | 2011-09-06 | Alliant Techsystems Inc. | Ionic liquid and a method of synthesizing an ionic liquid |
WO2008134190A2 (en) | 2007-04-24 | 2008-11-06 | Sun Chemical Corporation | Pigments for non-aqueous inks and coatings |
US8241526B2 (en) * | 2007-05-18 | 2012-08-14 | E I Du Pont De Nemours And Company | Aqueous dispersions of electrically conducting polymers containing high boiling solvent and additives |
US8936946B2 (en) * | 2007-06-20 | 2015-01-20 | Board Of Trustees Of Michigan State University | Biologically enhanced electrically-active magnetic nanoparticles for concentration, separation, and detection applications |
KR101451802B1 (ko) * | 2007-07-31 | 2014-10-16 | 삼성에스디아이 주식회사 | 글리시딜 에테르계 화합물을 채용한 유기전해액 및 리튬전지 |
US8222445B2 (en) | 2007-08-16 | 2012-07-17 | Lonza Ltd | Process for preparing and method of purifying alkali metal and alkaline earth metal tricyanomethanides |
JP4936069B2 (ja) * | 2007-10-31 | 2012-05-23 | 株式会社デンソー | モータ制御装置 |
US20090122389A1 (en) | 2007-11-14 | 2009-05-14 | E Ink Corporation | Electro-optic assemblies, and adhesives and binders for use therein |
US20090181441A1 (en) * | 2007-11-27 | 2009-07-16 | Board Of Trustees Of Michigan State University | Porous silicon-polymer composites for biosensor applications |
EP2219260B1 (en) * | 2007-11-30 | 2015-11-04 | Fujikura, Ltd. | Electrolytic composition and photoelectric conversion element using the same |
FR2925181B1 (fr) * | 2007-12-12 | 2010-09-10 | Hydro Quebec | Lentille optique electrochrome |
KR101509278B1 (ko) * | 2007-12-27 | 2015-04-06 | 도까이 카본 가부시끼가이샤 | 표면 처리 카본 블랙 수성 분산체와 그 제조 방법 |
CN101939862B (zh) * | 2008-01-08 | 2014-03-12 | 赛昂能源有限公司 | 多孔电极以及相关联的方法 |
JP5694780B2 (ja) * | 2008-01-16 | 2015-04-01 | シーオゥ インコーポレイテッド | バッテリー用のポリマー電解質 |
KR101013328B1 (ko) * | 2008-01-18 | 2011-02-09 | 주식회사 엘지화학 | 공융혼합물을 포함하는 전해질 및 이를 구비한전기화학소자 |
US8034485B2 (en) | 2008-05-29 | 2011-10-11 | 3M Innovative Properties Company | Metal oxide negative electrodes for lithium-ion electrochemical cells and batteries |
US9782949B2 (en) | 2008-05-30 | 2017-10-10 | Corning Incorporated | Glass laminated articles and layered articles |
JP5471036B2 (ja) * | 2008-06-05 | 2014-04-16 | ソニー株式会社 | マグネシウムイオン含有非水電解液及びこれを用いた電気化学デバイス |
US7715082B2 (en) * | 2008-06-30 | 2010-05-11 | Soladigm, Inc. | Electrochromic devices based on lithium insertion |
JP2010047751A (ja) * | 2008-07-24 | 2010-03-04 | Sumitomo Chemical Co Ltd | イオン交換ポリマー |
FR2935382B1 (fr) * | 2008-08-29 | 2010-10-08 | Centre Nat Rech Scient | Sel d'anion pentacylique et son utilisation comme electrolyte |
JP4444355B2 (ja) * | 2008-09-03 | 2010-03-31 | 株式会社東芝 | 燃料電池 |
US7951525B2 (en) * | 2008-09-08 | 2011-05-31 | International Business Machines Corporation | Low outgassing photoresist compositions |
US8129448B2 (en) * | 2008-12-18 | 2012-03-06 | Cabot Corporation | Method of preparing polymer modified pigments |
US20100193449A1 (en) * | 2009-02-02 | 2010-08-05 | Jian-Ku Shang | Materials and methods for removing arsenic from water |
JP2012520381A (ja) | 2009-03-12 | 2012-09-06 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | コーティング用途向け導電性ポリマー組成物 |
US20120034402A1 (en) | 2009-03-30 | 2012-02-09 | Avery Dennison Corporation | Removable Adhesive Label Containing Polymeric Film Layer Having Water Affinity |
MX339260B (es) | 2009-03-30 | 2016-05-18 | Avery Dennison Corp | Etiqueta adhesiva desprendible que contiene una capa de película polimérica de alto módulo de tracción. |
CN107610582B (zh) | 2009-03-30 | 2020-07-31 | 艾利丹尼森公司 | 含有固有地可收缩高分子膜的可移除粘合标签 |
US8432603B2 (en) | 2009-03-31 | 2013-04-30 | View, Inc. | Electrochromic devices |
FR2944149B1 (fr) * | 2009-04-06 | 2011-04-29 | Centre Nat Rech Scient | Electrode composite. |
WO2010123962A2 (en) | 2009-04-21 | 2010-10-28 | E. I. Du Pont De Nemours And Company | Electrically conductive polymer compositions and films made therefrom |
EP2421919A4 (en) | 2009-04-24 | 2014-01-22 | Du Pont | ELECTRICALLY CONDUCTIVE POLYMER COMPOSITIONS AND FILMS MANUFACTURED THEREFROM |
WO2011031297A2 (en) | 2009-08-28 | 2011-03-17 | Sion Power Corporation | Electrochemical cells comprising porous structures comprising sulfur |
EP2314572A1 (de) | 2009-10-20 | 2011-04-27 | Philipps-Universität Marburg | Lithiumsalze von Pentafluorphenylamid-Anionen, ihre Herstellung und ihre Verwendung |
WO2011056895A1 (en) | 2009-11-03 | 2011-05-12 | University Of Notre Dame Du Lac | Ionic liquids comprising heteraromatic anions |
TW201117245A (en) | 2009-11-11 | 2011-05-16 | Taiwan Textile Res Inst | Water-based electrolyte for electric double layer capacitor and electric double layer capacitor having the same |
JP5629510B2 (ja) * | 2009-11-30 | 2014-11-19 | 大日本印刷株式会社 | トリアリールメタン系染料 |
KR101311933B1 (ko) * | 2009-12-29 | 2013-09-27 | 제일모직주식회사 | 전도성 고분자 중합체, 전도성 고분자 조성물, 전도성 고분자 조성물막 및 이를 이용한 유기광전소자 |
US8730649B2 (en) | 2010-03-12 | 2014-05-20 | Taiwan Textile Research Institute | Aqueous electrolyte solution for electric double-layer capacitor and electric double-layer capacitor having the same |
JP2011198508A (ja) * | 2010-03-17 | 2011-10-06 | Sony Corp | リチウム二次電池、リチウム二次電池用電解液、電動工具、電気自動車および電力貯蔵システム |
KR101346977B1 (ko) | 2010-06-04 | 2014-01-02 | 주식회사 엘지화학 | 하이드로포르밀화 반응 부산물 제거용 장치 및 방법 |
JP2013537699A (ja) | 2010-08-24 | 2013-10-03 | ビーエイエスエフ・ソシエタス・エウロパエア | 電気化学セルでの使用のための電解質材料 |
US8828346B2 (en) | 2011-03-08 | 2014-09-09 | Trinapco, Inc. | Method of making fluorosulfonylamine |
JP5673258B2 (ja) * | 2011-03-17 | 2015-02-18 | 大日本印刷株式会社 | カラーフィルター用着色組成物及びそれを用いたカラーフィルター、並びに表示装置 |
US8859297B2 (en) | 2011-05-23 | 2014-10-14 | Board Of Trustees Of Michigan State University | Detection of conductive polymer-labeled analytes |
US8735002B2 (en) | 2011-09-07 | 2014-05-27 | Sion Power Corporation | Lithium sulfur electrochemical cell including insoluble nitrogen-containing compound |
WO2012174393A1 (en) | 2011-06-17 | 2012-12-20 | Sion Power Corporation | Plating technique for electrode |
JP5268123B2 (ja) * | 2011-08-26 | 2013-08-21 | 株式会社 東北テクノアーチ | リチウム電池 |
US10739337B2 (en) | 2011-08-30 | 2020-08-11 | Board Of Trustees Of Michigan State University | Extraction and detection of pathogens using carbohydrate-functionalized biosensors |
JP2013053208A (ja) * | 2011-09-02 | 2013-03-21 | Dic Corp | 活性エネルギー線硬化型インクジェット記録用インク組成物及び画像形成方法 |
FR2979630B1 (fr) * | 2011-09-05 | 2013-10-04 | Univ Provence Aix Marseille 1 | Copolymeres a blocs dont un polyanionique base sur un monomere anion de type tfsili comme electrolyte de batterie. |
US9660294B2 (en) | 2011-09-13 | 2017-05-23 | Wildcat Discovery Technologies, Inc. | Electrolyte materials for batteries and methods for use |
US20140340729A1 (en) * | 2011-09-16 | 2014-11-20 | National Institute Of Advanced Industrial Science And Technology | Reflective dimming electrochromic element with non-water based hydrogen ion conductive electrolyte layer inserted therein, and dimming element using the same |
EP2760074B1 (en) * | 2011-09-19 | 2017-11-15 | LG Chem, Ltd. | Cable-type secondary cell |
WO2013055573A1 (en) | 2011-10-13 | 2013-04-18 | Sion Power Corporation | Electrode structure and method for making the same |
DE102011055028A1 (de) * | 2011-11-04 | 2013-05-08 | Jacobs University Bremen Ggmbh | Elektrolyt-Zusatz für Lithium-basierte Energiespeicher |
US9269987B2 (en) | 2011-11-17 | 2016-02-23 | Erlendur Jónsson | Anions and derived salts with high dissociation in non-protogenic solvents |
JP2013114934A (ja) * | 2011-11-29 | 2013-06-10 | Nippon Synthetic Chem Ind Co Ltd:The | 金属塩、電極保護膜形成剤、それを用いた二次電池用電解質、及び二次電池 |
KR20140106602A (ko) * | 2011-11-30 | 2014-09-03 | 솔베이(소시에떼아노님) | 멜드럼산의 플루오르화 유도체, 그 제조 방법, 및 용매 첨가제로서의 그의 용도 |
CN113359364A (zh) | 2011-12-12 | 2021-09-07 | 唯景公司 | 薄膜装置和制造 |
TWI447993B (zh) * | 2011-12-30 | 2014-08-01 | Ind Tech Res Inst | 負極材料與負極極板 |
DE102012201942B8 (de) * | 2012-02-09 | 2015-02-26 | Ewe-Forschungszentrum Für Energietechnologie E. V. | Verwendung eines aktivierten kohlenstoffhaltigen Materials, Verfahren zur Herstellung einer kohlenstoffhaltigen Elektrode, kohlestoffhaltige Elektrode, deren Verwendung sowie Vanadium-Redox-Flow-Zelle |
US9077041B2 (en) | 2012-02-14 | 2015-07-07 | Sion Power Corporation | Electrode structure for electrochemical cell |
DE102012102162A1 (de) * | 2012-03-14 | 2013-09-19 | Westfälische Wilhelms-Universität Münster Körperschaft des öffentlichen Rechts | Ionenleitende polymere Verbindung für elektrochemische Zellen |
KR101704889B1 (ko) * | 2012-03-28 | 2017-02-08 | 캐보트 코포레이션 | 폴리에테르아민으로 처리된 산화된 카본 블랙 및 그를 포함하는 코팅 조성물 |
WO2013142994A1 (en) * | 2012-03-30 | 2013-10-03 | Valorisation-Recherche, Limited Partnership | Redox-active ionic liquids |
CA2776178A1 (en) | 2012-04-05 | 2013-10-05 | Hydro-Quebec | Ionic compounds |
JP5660112B2 (ja) * | 2012-04-27 | 2015-01-28 | 株式会社豊田自動織機 | リチウムイオン二次電池用正極及びリチウムイオン二次電池 |
KR102115384B1 (ko) | 2012-11-16 | 2020-05-26 | 트리나프코 인크. | 테트라부틸암모늄 비스(플루오로술포닐)이미드 및 관련 염의 합성 |
JP6268833B2 (ja) * | 2012-12-17 | 2018-01-31 | 株式会社豊田中央研究所 | 非水電解液二次電池及び非水電解液二次電池の製造方法 |
US9577289B2 (en) | 2012-12-17 | 2017-02-21 | Sion Power Corporation | Lithium-ion electrochemical cell, components thereof, and methods of making and using same |
KR101991149B1 (ko) | 2012-12-19 | 2019-06-19 | 시온 파워 코퍼레이션 | 전극 구조물 및 그의 제조 방법 |
EP2936607B1 (en) | 2012-12-20 | 2017-02-22 | Solvay SA | Salts of n-containing heterocyclic anions as components in electrolytes |
CN102993196B (zh) * | 2012-12-20 | 2015-01-28 | 北京科技大学 | 三唑类衍生物、其制备方法及其纳米粒子和纳米粒子的应用 |
JP6201363B2 (ja) * | 2013-03-25 | 2017-09-27 | 三菱ケミカル株式会社 | 非水系電解液及びそれを用いた非水系電解液電池 |
US10385251B2 (en) | 2013-09-30 | 2019-08-20 | University Of Notre Dame Du Lac | Compounds, complexes, compositions, methods and systems for heating and cooling |
FR3011683A1 (fr) * | 2013-10-03 | 2015-04-10 | Arkema France | Sel d'anion pentacyclique : composition pour batteries |
FR3012462B1 (fr) * | 2013-10-31 | 2016-01-01 | Arkema France | Compositions stables de poly (3,4-ethylenedioxythiophene) et de stabilisants anioniques a acidite limitee |
WO2015069799A1 (en) | 2013-11-05 | 2015-05-14 | University Of Notre Dame Du Lac | Carbon dioxide capture using phase change ionic liquids |
WO2015166030A1 (en) | 2014-05-01 | 2015-11-05 | Basf Se | Electrode fabrication methods and associated articles |
CA2948001C (en) | 2014-05-12 | 2023-03-14 | Johna Leddy | Lanthanide electrochemistry |
JP2017518625A (ja) * | 2014-06-06 | 2017-07-06 | ローベルト ボツシユ ゲゼルシヤフト ミツト ベシユレンクテル ハフツングRobert Bosch Gmbh | リチウム硫黄電池用ポリマー電解質 |
JP6541508B2 (ja) * | 2014-08-25 | 2019-07-10 | 住友化学株式会社 | 塩、樹脂、レジスト組成物及びレジストパターンの製造方法 |
CN104600357B (zh) * | 2014-12-08 | 2017-05-31 | 上海大学 | 聚合物复合材料固态电解质及其制备方法 |
US10068715B2 (en) | 2014-12-12 | 2018-09-04 | Corning Incorporated | Activated carbon and electric double layer capacitor thereof |
US10826113B2 (en) * | 2015-04-13 | 2020-11-03 | Global Graphene Group, Inc. | Zinc ion-exchanging energy storage device |
DE102015210388A1 (de) * | 2015-06-05 | 2016-12-08 | Siemens Aktiengesellschaft | Organische Heterozyklische Alkalimetallsalze als n-Dotierstoffe in der Organischen Elektronik |
EP3113275B1 (de) * | 2015-06-29 | 2021-06-09 | VARTA Micro Innovation GmbH | Sekundäre magnesiumbatterie und elektrolytsystem sowie elektrode für eine sekundäre magnesiumbatterie |
US20180198167A1 (en) * | 2015-07-15 | 2018-07-12 | The Trustees Of Boston University | Ionic liquid electrolytes and electrochemical devices comprising same |
JP2017066377A (ja) * | 2015-09-29 | 2017-04-06 | Jsr株式会社 | 着色組成物、着色硬化膜、並びに表示素子及び固体撮像素子 |
GB2544495B (en) | 2015-11-17 | 2018-12-05 | Nexeon Ltd | Surface modified electrochemically active material |
US10847790B2 (en) | 2015-11-17 | 2020-11-24 | Nexeon Limited | Functionalised electrochemically active material and method of functionalisation |
KR102056591B1 (ko) * | 2015-12-07 | 2019-12-17 | 주식회사 엘지화학 | 점착제 조성물 |
TWI656111B (zh) | 2015-12-31 | 2019-04-11 | Rohm And Haas Electronic Materials Llc | 光酸產生劑 |
TWI662364B (zh) | 2015-12-31 | 2019-06-11 | Rohm And Haas Electronic Materials Llc | 光致抗蝕劑組合物、包含光致抗蝕劑組合物的經塗佈基板及形成電子裝置的方法 |
JP6744848B2 (ja) * | 2016-09-13 | 2020-08-19 | 信越化学工業株式会社 | 粘着剤組成物、生体電極、及び生体電極の製造方法 |
JP6761384B2 (ja) * | 2016-09-29 | 2020-09-23 | 信越化学工業株式会社 | 粘着剤組成物、生体電極、及び生体電極の製造方法 |
JP6761386B2 (ja) * | 2016-09-29 | 2020-09-23 | 信越化学工業株式会社 | 粘着剤組成物、生体電極、生体電極の製造方法、及び塩 |
KR102141267B1 (ko) * | 2016-11-04 | 2020-08-04 | 주식회사 엘지화학 | 방향족 고리를 포함하는 화합물 및 이를 포함하는 중합체 |
JP6919993B2 (ja) | 2017-01-06 | 2021-08-18 | 信越化学工業株式会社 | 生体電極組成物、生体電極及び生体電極の製造方法 |
JP6966310B2 (ja) * | 2017-02-06 | 2021-11-10 | 信越化学工業株式会社 | 生体電極組成物、生体電極、生体電極の製造方法、及び高分子化合物 |
JP6892376B2 (ja) | 2017-02-14 | 2021-06-23 | 信越化学工業株式会社 | 生体電極組成物、生体電極、生体電極の製造方法、及び高分子化合物 |
JP6765988B2 (ja) | 2017-02-22 | 2020-10-07 | 信越化学工業株式会社 | 導電性ポリマー用高分子化合物及びその製造方法 |
JP6661212B2 (ja) * | 2017-02-22 | 2020-03-11 | 信越化学工業株式会社 | 導電性ポリマー複合体及び基板 |
EP3601233B1 (en) * | 2017-03-27 | 2024-08-14 | Hydro-Québec | Salts for use in electrolyte compositions or as electrode additives |
ES2693587A1 (es) * | 2017-06-09 | 2018-12-12 | Universidad Carlos Iii De Madrid | Sales a base de aniones orgánicos de sulfonamidas y sus usos |
WO2019009300A1 (ja) * | 2017-07-06 | 2019-01-10 | 公立大学法人大阪府立大学 | 生体組織透明化法及びその試薬 |
EP3665528B1 (en) * | 2017-08-08 | 2023-04-05 | Gentex Corporation | Electro-optical device having a transparent ion exchange membrane |
US10245583B1 (en) * | 2017-09-12 | 2019-04-02 | Chevron Phillips Chemical Company, Lp | Use of charge-containing molecules linked with covalent bonds to enhance acetylene hydrogenation catalysts |
US10232360B1 (en) | 2017-09-12 | 2019-03-19 | Chevron Phillips Chemical Company, Lp | Use of organic dopants to enhance acetylene hydrogenation catalysts |
JP6845191B2 (ja) * | 2017-10-19 | 2021-03-17 | 信越化学工業株式会社 | 生体電極組成物、生体電極、及び生体電極の製造方法 |
JP6920000B2 (ja) | 2017-10-26 | 2021-08-18 | 信越化学工業株式会社 | 生体電極組成物、生体電極、及び生体電極の製造方法 |
KR102228070B1 (ko) | 2017-11-01 | 2021-03-12 | 주식회사 엘지화학 | 화학 증폭형 포토레지스트 조성물 및 이를 이용한 포토레지스트 필름 |
JP6850279B2 (ja) * | 2017-11-21 | 2021-03-31 | 信越化学工業株式会社 | 生体電極組成物、生体電極、及び生体電極の製造方法 |
CN107706463B (zh) * | 2017-11-23 | 2018-11-06 | 林宝领 | 一种锂电池的亚硝基接枝碳酸酯电解液及制备方法 |
CN109851703B (zh) * | 2017-11-30 | 2020-10-23 | 比亚迪股份有限公司 | 适用于粘结剂的偏二氟乙烯类共聚物及其制备方法和应用 |
CN109851704B (zh) * | 2017-11-30 | 2020-06-19 | 比亚迪股份有限公司 | 聚合物隔膜及其制备方法和应用及锂电池 |
CN109860471B (zh) * | 2017-11-30 | 2020-12-25 | 比亚迪股份有限公司 | 聚合物隔膜及其制备方法和应用及锂电池 |
CN109935902B (zh) * | 2017-12-19 | 2021-10-19 | 成都大超科技有限公司 | 固态电解质及其锂电池电芯、锂电池 |
JP6839125B2 (ja) * | 2018-04-02 | 2021-03-03 | 信越化学工業株式会社 | 生体電極組成物、生体電極、及び生体電極の製造方法 |
JP7080732B2 (ja) * | 2018-06-01 | 2022-06-06 | 三菱マテリアル電子化成株式会社 | 含フッ素スルホニルイミド塩基含有シリコーン化合物とそれを含有する導電性シリコーン組成物 |
US11394056B2 (en) * | 2018-06-08 | 2022-07-19 | Solid State Battery Incorporated | Composite solid polymer electrolytes for energy storage devices |
JP7111653B2 (ja) | 2018-06-25 | 2022-08-02 | 信越化学工業株式会社 | 生体電極組成物、生体電極、及び生体電極の製造方法 |
JP7099990B2 (ja) * | 2018-06-26 | 2022-07-12 | 信越化学工業株式会社 | 生体電極組成物、生体電極、及び生体電極の製造方法 |
CN112424685A (zh) | 2018-07-20 | 2021-02-26 | 株式会社尼康 | 相机附件及信息发送方法 |
EP3605700A1 (en) | 2018-07-31 | 2020-02-05 | Solvay Sa | New components for electrolyte compositions |
WO2020025502A1 (en) | 2018-07-31 | 2020-02-06 | Solvay Sa | New components for electrolyte compositions |
WO2020025501A1 (en) | 2018-07-31 | 2020-02-06 | Solvay Sa | New components for electrolyte compositions |
EP3604276A1 (en) | 2018-07-31 | 2020-02-05 | Solvay Sa | New components for electrolyte compositions |
EP3605699A1 (en) | 2018-07-31 | 2020-02-05 | Solvay Sa | New components for electrolyte compositions |
WO2020025499A1 (en) | 2018-07-31 | 2020-02-06 | Solvay Sa | New components for electrolyte compositions |
EP3605698A1 (en) | 2018-07-31 | 2020-02-05 | Solvay Sa | New components for electrolyte compositions |
KR102650658B1 (ko) * | 2018-11-15 | 2024-03-25 | 삼성전자주식회사 | 헤테로고리 방향족 구조의 음이온을 포함하는 금속염 및 그 제조방법, 그리고 상기 금속염을 포함하는 전해질 및 전기화학소자 |
CN109776709B (zh) * | 2018-12-25 | 2021-09-07 | 广东工业大学 | 一种聚对苯乙烯磺酰(三氟甲基磺酰)亚胺锂-聚碳酸亚乙烯基酯共聚物及其应用 |
ES2941245T3 (es) * | 2019-01-17 | 2023-05-19 | Lg Energy Solution Ltd | Electrolito para batería secundaria de litio y batería secundaria de litio que comprende el mismo |
DE102019208914A1 (de) * | 2019-06-19 | 2020-12-24 | Robert Bosch Gmbh | Salz mit Anion mit unfluorierter Dialkylamid-Sulfonyl- und/oder -Sulfoximid-Gruppe und mit Perfluoralkyl-Sulfonyl-Gruppe |
CN110305172B (zh) * | 2019-06-26 | 2020-09-01 | 武汉大学 | 一种钴膦酸盐及其制备方法和作为宽温域质子传导材料的应用 |
CN110368899A (zh) * | 2019-07-16 | 2019-10-25 | 邱越 | 一种活性炭复合材料及其制备方法和应用 |
CN110721745B (zh) * | 2019-09-25 | 2020-09-08 | 中山大学 | 一种抗中毒的水溶性过氧化物分解催化剂及其制备方法和应用 |
KR20210070609A (ko) * | 2019-12-05 | 2021-06-15 | 주식회사 엘지에너지솔루션 | 리튬 이차전지용 비수전해액 및 이를 포함하는 리튬 이차전지 |
KR20210094491A (ko) * | 2020-01-21 | 2021-07-29 | 하이드로메이트 코팅스, 인크. | 비닐 아미노 비방향족고리 화합물로 표면개질된 기질 및 그의 표면개질 방법 |
WO2021158581A1 (en) * | 2020-02-05 | 2021-08-12 | Gentex Corporation | Electrochromic compounds |
CN111477962B (zh) * | 2020-05-29 | 2021-07-20 | 珠海市赛纬电子材料股份有限公司 | 一种锂离子电池非水电解液及含该非水电解液的锂离子电池 |
CN111883834B (zh) * | 2020-07-24 | 2022-12-13 | 香河昆仑新能源材料股份有限公司 | 一种非水锂离子电池电解液添加剂、包含其的电解液以及锂离子电池 |
CN111883836A (zh) * | 2020-07-24 | 2020-11-03 | 香河昆仑化学制品有限公司 | 一种锂离子电池非水电解液和锂离子电池 |
CN111934015B (zh) * | 2020-08-28 | 2022-08-19 | 珠海市赛纬电子材料股份有限公司 | 一种锂离子电池非水电解液及含该非水电解液的锂离子电池 |
CN117280504A (zh) | 2021-05-12 | 2023-12-22 | 利特罗尼克电池技术有限公司 | 具有偕二腈添加剂的碱金属原电池 |
KR20230071246A (ko) * | 2021-11-16 | 2023-05-23 | 주식회사 엘지에너지솔루션 | 신규한 비수계 전해액용 첨가제 및 이를 포함하는 리튬 이차전지 |
CN115286587B (zh) * | 2022-07-06 | 2024-02-23 | 珠海中科先进技术研究院有限公司 | 一种高离域的碱金属化合物及其制备方法和应用 |
WO2024115088A1 (en) | 2022-11-29 | 2024-06-06 | Litronik Batterietechnologie Gmbh | Primary alkali metal cells with cyano-cycloalkanes additives |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53149938A (en) * | 1970-04-13 | 1978-12-27 | Minnesota Mining & Mfg | Process for fluoroalkyll sulfonamidearyl compound |
JPS58225045A (ja) * | 1982-06-01 | 1983-12-27 | アジエンス・ナチオナレ・ドウ・バロリザチオン・ドウ・ラ・レシエルシエ(アンバ−ル) | イオン性化合物 |
JPH01501822A (ja) * | 1986-10-30 | 1989-06-22 | サントル・ナシオナル・ドウ・ラ・ルシエルシユ・シアンテイフイク | 液体電解質中に溶解した塩を含む新規のイオン伝導材料 |
JPH05503808A (ja) * | 1990-08-01 | 1993-06-17 | コーバレント・アソシエィツ・インコーポレイテッド | メチド塩、処方、電解液、およびそれによって形成されるバッテリー |
JPH05506540A (ja) * | 1991-03-07 | 1993-09-22 | サントル・ナシオナル・ドウ・ラ・ルシエルシユ・シアンテイフイク | イオン伝導性ポリマー材料 |
JPH06503842A (ja) * | 1991-11-08 | 1994-04-28 | サントル・ナシオナル・ドウ・ラ・ルシエルシユ・シアンテイフイク | ビス(ペルフルオロスルホニル)メタン誘導体、それらの製造方法及びそれらの利用 |
JPH06128216A (ja) * | 1990-07-12 | 1994-05-10 | Ausimont Spa | ペルフルオロアルコキシスルホン酸化合物の製造法 |
JPH06509811A (ja) * | 1992-02-21 | 1994-11-02 | サントル・ナショナル・ドゥ・ラ・ルシェルシュ・シャンティフィク | 過ハロゲン化スルトン誘導単量体および当該単量体から得られる重合体 |
JPH0881436A (ja) * | 1994-09-12 | 1996-03-26 | Central Glass Co Ltd | スルホンイミドの製造方法 |
JPH08268998A (ja) * | 1995-03-06 | 1996-10-15 | Minnesota Mining & Mfg Co <3M> | フッ素化合物系電解質塩及びこれを含む電解質組成物並びにこれらを含んで成るバッテリー |
JPH08511274A (ja) * | 1994-03-21 | 1996-11-26 | サントル・ナショナル・ドゥ・ラ・ルシェルシュ・シャンティフィク | 良好な耐食性を示すイオン性伝導材料 |
JPH09231833A (ja) * | 1995-12-14 | 1997-09-05 | Electricite De France | ビス(フェニルスルホニル)イミド、それらの製造法およびそれらを含んでいるイオン伝導性材料 |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3054800A (en) * | 1949-09-17 | 1962-09-18 | Harry P Burchfield | 3, 5-dinitro-1, 2, 4-triazoles and process for preparing same |
US2959475A (en) * | 1957-02-19 | 1960-11-08 | Du Pont | Method for the control of weeds |
CH694566A4 (en) * | 1966-05-13 | 1970-03-13 | Electronic display unit is for incorporation in aviation instruments and uses liquid crystal display | |
NL174644C (nl) * | 1970-04-13 | 1984-07-16 | Minnesota Mining & Mfg | Werkwijze ter bereiding van een herbicide verbinding; tevens werkwijze voor de bereiding van een preparaat met herbicide werking. |
BE791595A (fr) | 1971-11-18 | 1973-05-17 | Omf California Inc | Electrolyte pour accumulateur |
JPS5148516B2 (ja) * | 1973-02-07 | 1976-12-21 | ||
DD118433A1 (ja) * | 1975-03-17 | 1976-03-05 | ||
US4226873A (en) * | 1977-02-23 | 1980-10-07 | Gulf Oil Corporation | 5-Substituted-3-fluorosulfonyl-4H-1,2,4-triazoles and use as insecticides and miticides |
JPS53117094A (en) * | 1977-03-23 | 1978-10-13 | Mitsubishi Gas Chem Co Inc | Preparation of composition and high polymer |
US4105525A (en) * | 1978-01-23 | 1978-08-08 | Orion Research Incorporated | Internal standard electrolyte for ammonia sensor |
EP0010396A1 (en) * | 1978-10-24 | 1980-04-30 | Fbc Limited | Fungicidal and herbicidal compositions, certain cyanomethane and cyanoethene derivatives being active agents thereof, the preparation of these derivatives and methods for combating fungi and weeds |
DE3230923A1 (de) * | 1982-08-20 | 1984-02-23 | Basf Ag, 6700 Ludwigshafen | Thiadiazinone, verfahren zu ihrer herstellung und diese enthaltende fungizide |
JPS6020950A (ja) * | 1983-07-13 | 1985-02-02 | Nippon Zeon Co Ltd | 硬質用塩化ビニル樹脂組成物 |
US5232940A (en) * | 1985-12-20 | 1993-08-03 | Hatton Leslie R | Derivatives of N-phenylpyrazoles |
US4664757A (en) * | 1985-12-27 | 1987-05-12 | Uop Inc. | Method and apparatus for gas detection using proton-conducting polymers |
US4664761A (en) * | 1985-12-27 | 1987-05-12 | Uop Inc. | Electrochemical method and apparatus using proton-conducting polymers |
JPH0654686B2 (ja) * | 1986-01-14 | 1994-07-20 | 三洋電機株式会社 | 二次電池 |
JPS62219908A (ja) * | 1986-03-20 | 1987-09-28 | 日本ケミコン株式会社 | 電解コンデンサ用電解液 |
US4714569A (en) * | 1986-07-22 | 1987-12-22 | Toska Co., Ltd. | Process for preparing conductive coating composition |
FR2606216A1 (fr) | 1986-10-30 | 1988-05-06 | Elf Aquitaine | Materiau a conduction ionique |
KR930011308B1 (ko) * | 1986-11-10 | 1993-11-30 | 닛뽕쇼꾸바이가가꾸고오교 가부시끼가이샤 | 착색구상 미립자, 그 제조방법 및 그 용도 |
US4966954A (en) * | 1987-03-04 | 1990-10-30 | Rensselaer Polytechnic Institute | Production and processing of thermally stable polyenaminonitriles and polyaminoquinolines therefrom |
US4882244A (en) * | 1987-04-02 | 1989-11-21 | The University Of Michigan-Ann Arbor | Battery containing a metal anode and an electrolyte providing high rates of metal electrolysis at near ambient temperatures |
US4835074A (en) * | 1987-09-25 | 1989-05-30 | The Electrosynthesis Company, Inc. | Modified carbons and electrochemical cells containing the same |
JPH01152165A (ja) * | 1987-12-09 | 1989-06-14 | Nippon Shokubai Kagaku Kogyo Co Ltd | 表面処理されたカーボンブラツクの製造方法 |
JP2724377B2 (ja) * | 1988-05-12 | 1998-03-09 | 汪芳 白井 | イオン伝導性組成物 |
FR2645533B1 (fr) | 1989-04-06 | 1991-07-12 | Centre Nat Rech Scient | Procede de synthese de sulfonylimidures |
NL9001075A (ja) * | 1990-05-04 | 1991-12-02 | Duphar Int Res | |
US5281261A (en) * | 1990-08-31 | 1994-01-25 | Xerox Corporation | Ink compositions containing modified pigment particles |
EP0532408A1 (fr) * | 1991-09-13 | 1993-03-17 | Saint-Gobain Vitrage International | Polymère conducteur protonique, application en tant qu'électrolyte dans des dispositifs électrochimiques |
JP2845389B2 (ja) * | 1992-03-10 | 1999-01-13 | 大日精化工業株式会社 | 熱転写記録用着色組成物 |
DE4217366A1 (de) | 1992-05-26 | 1993-12-02 | Bayer Ag | Imide und deren Salze sowie deren Verwendung |
US5354784A (en) * | 1992-08-10 | 1994-10-11 | Arakawa Kagaku Kogyo Kabushiki Kaisha | Cyclopentadienyliron complex salt, process for preparing the same and photopolymerizable composition containing the same |
US5518841A (en) * | 1993-02-12 | 1996-05-21 | Matsushita Electric Industrial Co., Ltd. | Composite cathode |
US5538812A (en) * | 1994-02-04 | 1996-07-23 | Moltech Corporation | Electrolyte materials containing highly dissociated metal ion salts |
JP3499916B2 (ja) | 1994-05-30 | 2004-02-23 | 三洋電機株式会社 | 高分子固体電解質電池とその製造方法 |
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 |
US5525436A (en) * | 1994-11-01 | 1996-06-11 | Case Western Reserve University | Proton conducting polymers used as membranes |
US5609990A (en) | 1995-02-08 | 1997-03-11 | Imation Corp. | Optical recording disk having a sealcoat layer |
DE69600572T2 (de) | 1995-02-08 | 1999-04-29 | Imation Corp (N.D.Ges.D. Staates Delaware), Oakdale, Minn. | Antistatikhartschicht |
US5874616A (en) | 1995-03-06 | 1999-02-23 | Minnesota Mining And Manufacturing Company | Preparation of bis (fluoroalkylenesulfonyl) imides and (fluoroalkysulfony) (fluorosulfonyl) imides |
US5748439A (en) * | 1995-06-06 | 1998-05-05 | Telectronics Pacing Systems, Inc. | Capacitors having high strength electrolytic capacitor separators |
JPH0912920A (ja) * | 1995-06-28 | 1997-01-14 | Nippon Oil Co Ltd | 炭素材料の製造方法 |
US5831108A (en) * | 1995-08-03 | 1998-11-03 | California Institute Of Technology | High metathesis activity ruthenium and osmium metal carbene complexes |
US5691081A (en) | 1995-09-21 | 1997-11-25 | Minnesota Mining And Manufacturing Company | Battery containing bis(perfluoroalkylsulfonyl)imide and cyclic perfluoroalkylene disulfonylimide salts |
US5795496A (en) * | 1995-11-22 | 1998-08-18 | California Institute Of Technology | Polymer material for electrolytic membranes in fuel cells |
US5962546A (en) | 1996-03-26 | 1999-10-05 | 3M Innovative Properties Company | Cationically polymerizable compositions capable of being coated by electrostatic assistance |
AU6485196A (en) | 1996-03-26 | 1997-10-17 | Minnesota Mining And Manufacturing Company | Cationically polymerizable compositions capable of being applied by electrostatic assistance |
US5817376A (en) | 1996-03-26 | 1998-10-06 | Minnesota Mining And Manufacturing Company | Free-radically polymerizable compositions capable of being coated by electrostatic assistance |
US5688613A (en) * | 1996-04-08 | 1997-11-18 | Motorola, Inc. | Electrochemical cell having a polymer electrolyte |
DE19632285A1 (de) * | 1996-08-09 | 1998-02-19 | Hoechst Ag | Protonenleiter mit einer Temperaturbeständigkeit in einem weiten Bereich und guten Protonenleitfähigkeiten |
WO1998029388A1 (fr) * | 1996-12-30 | 1998-07-09 | Hydro-Quebec | Sels d'amides perfluores, et leurs utilisations comme materiaux a conduction ionique |
US6063522A (en) | 1998-03-24 | 2000-05-16 | 3M Innovative Properties Company | Electrolytes containing mixed fluorochemical/hydrocarbon imide and methide salts |
US5874606A (en) | 1998-03-31 | 1999-02-23 | Occidental Chemical Corporation | Process for making o-arylbenzonitriles |
US6294289B1 (en) | 1998-08-25 | 2001-09-25 | 3M Innovative Properties Company | Cyano-substituted methide and amide salts |
US6350545B2 (en) | 1998-08-25 | 2002-02-26 | 3M Innovative Properties Company | Sulfonylimide compounds |
-
1997
- 1997-12-30 WO PCT/CA1997/001013 patent/WO1998029388A1/fr active Application Filing
- 1997-12-30 CA CA2248242A patent/CA2248242C/fr not_active Expired - Lifetime
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Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53149938A (en) * | 1970-04-13 | 1978-12-27 | Minnesota Mining & Mfg | Process for fluoroalkyll sulfonamidearyl compound |
JPS58225045A (ja) * | 1982-06-01 | 1983-12-27 | アジエンス・ナチオナレ・ドウ・バロリザチオン・ドウ・ラ・レシエルシエ(アンバ−ル) | イオン性化合物 |
JPH01501822A (ja) * | 1986-10-30 | 1989-06-22 | サントル・ナシオナル・ドウ・ラ・ルシエルシユ・シアンテイフイク | 液体電解質中に溶解した塩を含む新規のイオン伝導材料 |
JPH06128216A (ja) * | 1990-07-12 | 1994-05-10 | Ausimont Spa | ペルフルオロアルコキシスルホン酸化合物の製造法 |
JPH05503808A (ja) * | 1990-08-01 | 1993-06-17 | コーバレント・アソシエィツ・インコーポレイテッド | メチド塩、処方、電解液、およびそれによって形成されるバッテリー |
JPH05506540A (ja) * | 1991-03-07 | 1993-09-22 | サントル・ナシオナル・ドウ・ラ・ルシエルシユ・シアンテイフイク | イオン伝導性ポリマー材料 |
JPH06503842A (ja) * | 1991-11-08 | 1994-04-28 | サントル・ナシオナル・ドウ・ラ・ルシエルシユ・シアンテイフイク | ビス(ペルフルオロスルホニル)メタン誘導体、それらの製造方法及びそれらの利用 |
JPH06509811A (ja) * | 1992-02-21 | 1994-11-02 | サントル・ナショナル・ドゥ・ラ・ルシェルシュ・シャンティフィク | 過ハロゲン化スルトン誘導単量体および当該単量体から得られる重合体 |
JPH08511274A (ja) * | 1994-03-21 | 1996-11-26 | サントル・ナショナル・ドゥ・ラ・ルシェルシュ・シャンティフィク | 良好な耐食性を示すイオン性伝導材料 |
JPH0881436A (ja) * | 1994-09-12 | 1996-03-26 | Central Glass Co Ltd | スルホンイミドの製造方法 |
JPH08268998A (ja) * | 1995-03-06 | 1996-10-15 | Minnesota Mining & Mfg Co <3M> | フッ素化合物系電解質塩及びこれを含む電解質組成物並びにこれらを含んで成るバッテリー |
JPH09231833A (ja) * | 1995-12-14 | 1997-09-05 | Electricite De France | ビス(フェニルスルホニル)イミド、それらの製造法およびそれらを含んでいるイオン伝導性材料 |
Non-Patent Citations (5)
Title |
---|
INORGANIC AND NUCLEAR CHEMISTRY LETTERS, vol. 7(2), JPN6008058295, 1971, pages 171 - 175, ISSN: 0001182514 * |
JOURNAL OF FLUORINE CHEMISTRY, vol. 46(2), JPN6008058288, 1990, pages 297 - 305, ISSN: 0001182511 * |
JOURNAL OF FLUORINE CHEMISTRY, vol. 68(3), JPN6008058290, 1994, pages 277 - 286, ISSN: 0001182512 * |
JOURNAL OF MEDICINAL CHEMISTRY, vol. 30(4), JPN6008058292, 1987, pages 696 - 704, ISSN: 0001182513 * |
TETRAHEDRON, vol. 50(23), JPN6009049184, 1994, pages 6891 - 6906, ISSN: 0001423780 * |
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