DE60010936T2 - Sulfonierte perfluorvinylfunktionalisierte monomere - Google Patents
Sulfonierte perfluorvinylfunktionalisierte monomere Download PDFInfo
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- DE60010936T2 DE60010936T2 DE60010936T DE60010936T DE60010936T2 DE 60010936 T2 DE60010936 T2 DE 60010936T2 DE 60010936 T DE60010936 T DE 60010936T DE 60010936 T DE60010936 T DE 60010936T DE 60010936 T2 DE60010936 T2 DE 60010936T2
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- 239000000178 monomer Substances 0.000 title abstract description 54
- -1 trifluorovinyloxy group Chemical group 0.000 abstract description 24
- 150000001768 cations Chemical class 0.000 abstract description 7
- 125000001033 ether group Chemical group 0.000 abstract description 7
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052801 chlorine Inorganic materials 0.000 abstract description 3
- 229910052731 fluorine Inorganic materials 0.000 abstract description 3
- 229910005948 SO2Cl Inorganic materials 0.000 abstract 1
- 229910006095 SO2F Inorganic materials 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 48
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 36
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 33
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 33
- 239000000203 mixture Substances 0.000 description 31
- 239000000047 product Substances 0.000 description 26
- 238000002360 preparation method Methods 0.000 description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 20
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 19
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 18
- 239000012043 crude product Substances 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 17
- 239000002904 solvent Substances 0.000 description 17
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 15
- 239000012044 organic layer Substances 0.000 description 15
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 13
- 229910001873 dinitrogen Inorganic materials 0.000 description 13
- 238000001914 filtration Methods 0.000 description 13
- 229910052938 sodium sulfate Inorganic materials 0.000 description 13
- 235000011152 sodium sulphate Nutrition 0.000 description 13
- 239000011343 solid material Substances 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 238000005481 NMR spectroscopy Methods 0.000 description 12
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 12
- 238000003756 stirring Methods 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
- 150000003839 salts Chemical class 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
- 238000001816 cooling Methods 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 9
- 239000001257 hydrogen Substances 0.000 description 9
- 229920006395 saturated elastomer Polymers 0.000 description 9
- 239000011780 sodium chloride Substances 0.000 description 9
- 239000006227 byproduct Substances 0.000 description 8
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- 239000003610 charcoal Substances 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- 239000000706 filtrate Substances 0.000 description 7
- 238000001228 spectrum Methods 0.000 description 7
- 125000001424 substituent group Chemical group 0.000 description 7
- 238000001035 drying Methods 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 6
- 0 C*c(c(*)c1)ccc1-c1cc(C)c(*)cc1 Chemical compound C*c(c(*)c1)ccc1-c1cc(C)c(*)cc1 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000011698 potassium fluoride Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- CIOIIHKLWDETIM-UHFFFAOYSA-N 1,3-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)benzene Chemical compound FC(F)(Br)C(F)(F)OC1=CC=CC(OC(F)(F)C(F)(F)Br)=C1 CIOIIHKLWDETIM-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 4
- 239000002274 desiccant Substances 0.000 description 4
- KVBKAPANDHPRDG-UHFFFAOYSA-N dibromotetrafluoroethane Chemical compound FC(F)(Br)C(F)(F)Br KVBKAPANDHPRDG-UHFFFAOYSA-N 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 4
- BTODFFZJCAQNGZ-UHFFFAOYSA-M potassium;2,5-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)benzenesulfonate Chemical compound [K+].[O-]S(=O)(=O)C1=CC(OC(F)(F)C(F)(F)Br)=CC=C1OC(F)(F)C(F)(F)Br BTODFFZJCAQNGZ-UHFFFAOYSA-M 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- WVPMEUKFKQYZIS-UHFFFAOYSA-M sodium;3,5-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(OC(F)(F)C(F)(F)Br)=CC(OC(F)(F)C(F)(F)Br)=C1 WVPMEUKFKQYZIS-UHFFFAOYSA-M 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- YMNPQUYDHSINRN-UHFFFAOYSA-N 2,4-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)benzenesulfonyl chloride Chemical compound FC(F)(Br)C(F)(F)OC1=CC=C(S(Cl)(=O)=O)C(OC(F)(F)C(F)(F)Br)=C1 YMNPQUYDHSINRN-UHFFFAOYSA-N 0.000 description 3
- HRYSVRCQGVSQMO-UHFFFAOYSA-N 2,4-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)benzenesulfonyl fluoride Chemical compound FC(F)(Br)C(F)(F)OC1=CC=C(S(F)(=O)=O)C(OC(F)(F)C(F)(F)Br)=C1 HRYSVRCQGVSQMO-UHFFFAOYSA-N 0.000 description 3
- XAEBTHLVBMKSGN-UHFFFAOYSA-N 2,5-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)benzenesulfonyl chloride Chemical compound FC(F)(Br)C(F)(F)OC1=CC=C(OC(F)(F)C(F)(F)Br)C(S(Cl)(=O)=O)=C1 XAEBTHLVBMKSGN-UHFFFAOYSA-N 0.000 description 3
- BBZPKFXFQICBAU-UHFFFAOYSA-N 2-(2-bromo-1,1,2,2-tetrafluoroethoxy)-5-[4-(2-bromo-1,1,2,2-tetrafluoroethoxy)-3-chlorosulfonylphenyl]benzenesulfonyl chloride Chemical compound C1=C(S(Cl)(=O)=O)C(OC(F)(F)C(F)(Br)F)=CC=C1C1=CC=C(OC(F)(F)C(F)(F)Br)C(S(Cl)(=O)=O)=C1 BBZPKFXFQICBAU-UHFFFAOYSA-N 0.000 description 3
- BFSIVRMOZWREKZ-UHFFFAOYSA-N 3,5-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)benzenesulfonyl fluoride Chemical compound FC(F)(Br)C(F)(F)OC1=CC(OC(F)(F)C(F)(F)Br)=CC(S(F)(=O)=O)=C1 BFSIVRMOZWREKZ-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 238000005660 chlorination reaction Methods 0.000 description 3
- 238000004440 column chromatography Methods 0.000 description 3
- 238000005695 dehalogenation reaction Methods 0.000 description 3
- 238000003682 fluorination reaction Methods 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical group 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 238000000859 sublimation Methods 0.000 description 3
- 230000008022 sublimation Effects 0.000 description 3
- SUTQSIHGGHVXFK-UHFFFAOYSA-N 1,2,2-trifluoroethenylbenzene Chemical compound FC(F)=C(F)C1=CC=CC=C1 SUTQSIHGGHVXFK-UHFFFAOYSA-N 0.000 description 2
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 2
- VYJVUJGDOORPCC-UHFFFAOYSA-N 1-(2-bromo-1,1,2,2-tetrafluoroethoxy)-4-[4-(2-bromo-1,1,2,2-tetrafluoroethoxy)phenyl]benzene Chemical group C1=CC(OC(F)(F)C(F)(Br)F)=CC=C1C1=CC=C(OC(F)(F)C(F)(F)Br)C=C1 VYJVUJGDOORPCC-UHFFFAOYSA-N 0.000 description 2
- UWKQWQJTSNYCJC-UHFFFAOYSA-N 2,4-bis(1,2,2-trifluoroethenoxy)benzenesulfonyl fluoride Chemical compound FC(F)=C(F)OC1=CC=C(S(F)(=O)=O)C(OC(F)=C(F)F)=C1 UWKQWQJTSNYCJC-UHFFFAOYSA-N 0.000 description 2
- NCSYNDIZCWIRHM-UHFFFAOYSA-N 2,5-bis(1,2,2-trifluoroethenoxy)benzenesulfonyl fluoride Chemical compound FC(F)=C(F)OC1=CC=C(OC(F)=C(F)F)C(S(F)(=O)=O)=C1 NCSYNDIZCWIRHM-UHFFFAOYSA-N 0.000 description 2
- GMPPRNLSSVMSDS-UHFFFAOYSA-N 2-(2-bromo-1,1,2,2-tetrafluoroethoxy)-5-[4-(2-bromo-1,1,2,2-tetrafluoroethoxy)-3-fluorosulfonylphenyl]benzenesulfonyl fluoride Chemical compound C1=C(S(F)(=O)=O)C(OC(F)(F)C(F)(Br)F)=CC=C1C1=CC=C(OC(F)(F)C(F)(F)Br)C(S(F)(=O)=O)=C1 GMPPRNLSSVMSDS-UHFFFAOYSA-N 0.000 description 2
- YACFUVICKHFOEU-UHFFFAOYSA-N 3,5-bis(1,2,2-trifluoroethenoxy)benzenesulfonyl fluoride Chemical compound FC(F)=C(F)OC1=CC(OC(F)=C(F)F)=CC(S(F)(=O)=O)=C1 YACFUVICKHFOEU-UHFFFAOYSA-N 0.000 description 2
- SFCFSPBTKLATJQ-UHFFFAOYSA-N 3,5-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)benzenesulfonyl chloride Chemical class FC(F)(Br)C(F)(F)OC1=CC(OC(F)(F)C(F)(F)Br)=CC(S(Cl)(=O)=O)=C1 SFCFSPBTKLATJQ-UHFFFAOYSA-N 0.000 description 2
- AXRPVKUFLXBWEB-UHFFFAOYSA-N 5,5-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)-2-phenylcyclohexa-1,3-diene Chemical group C1=CC(OC(F)(F)C(F)(Br)F)(OC(F)(F)C(F)(F)Br)CC=C1C1=CC=CC=C1 AXRPVKUFLXBWEB-UHFFFAOYSA-N 0.000 description 2
- NPJNQVNBEFMYMD-UHFFFAOYSA-N 5-[3-fluorosulfonyl-4-(1,2,2-trifluoroethenoxy)phenyl]-2-(1,2,2-trifluoroethenoxy)benzenesulfonyl fluoride Chemical compound C1=C(S(F)(=O)=O)C(OC(F)=C(F)F)=CC=C1C1=CC=C(OC(F)=C(F)F)C(S(F)(=O)=O)=C1 NPJNQVNBEFMYMD-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 235000003270 potassium fluoride Nutrition 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 2
- 150000003457 sulfones Chemical class 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
- RRZIJNVZMJUGTK-UHFFFAOYSA-N 1,1,2-trifluoro-2-(1,2,2-trifluoroethenoxy)ethene Chemical compound FC(F)=C(F)OC(F)=C(F)F RRZIJNVZMJUGTK-UHFFFAOYSA-N 0.000 description 1
- XAUHHCMRFFGRMF-UHFFFAOYSA-N 1-[1,1-bis[4-(1,2,2-trifluoroethenoxy)phenyl]ethyl]-4-(1,2,2-trifluoroethenoxy)benzene Chemical compound C=1C=C(OC(F)=C(F)F)C=CC=1C(C=1C=CC(OC(F)=C(F)F)=CC=1)(C)C1=CC=C(OC(F)=C(F)F)C=C1 XAUHHCMRFFGRMF-UHFFFAOYSA-N 0.000 description 1
- HTSYFXSERPRMJH-UHFFFAOYSA-N 2,5-bis(2-bromo-1,1,2,2-tetrafluoroethoxy)benzenesulfonyl fluoride Chemical compound FC(F)(Br)C(F)(F)OC1=CC=C(OC(F)(F)C(F)(F)Br)C(S(F)(=O)=O)=C1 HTSYFXSERPRMJH-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- JAPZWILHNSWLIX-UHFFFAOYSA-N 4-(1,2,2-trifluoroethenoxy)benzenesulfonyl chloride Chemical compound FC(F)=C(F)OC1=CC=C(S(Cl)(=O)=O)C=C1 JAPZWILHNSWLIX-UHFFFAOYSA-N 0.000 description 1
- JEANJQNBNNSHDQ-UHFFFAOYSA-N 4-(1,2,2-trifluoroethenoxy)benzenesulfonyl fluoride Chemical compound FC(F)=C(F)OC1=CC=C(S(F)(=O)=O)C=C1 JEANJQNBNNSHDQ-UHFFFAOYSA-N 0.000 description 1
- SYMIEKVHCXHXBV-UHFFFAOYSA-N 4-(2-bromo-1,1,2,2-tetrafluoroethoxy)benzenesulfonyl chloride Chemical compound FC(F)(Br)C(F)(F)OC1=CC=C(S(Cl)(=O)=O)C=C1 SYMIEKVHCXHXBV-UHFFFAOYSA-N 0.000 description 1
- RTCUMEXIFIDLFL-UHFFFAOYSA-N C1(=C(C(=C(C(=C1S(=O)(=O)F)F)F)F)F)C(=C(F)F)F Chemical compound C1(=C(C(=C(C(=C1S(=O)(=O)F)F)F)F)F)C(=C(F)F)F RTCUMEXIFIDLFL-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical compound C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 1
- ODWXUNBKCRECNW-UHFFFAOYSA-M bromocopper(1+) Chemical compound Br[Cu+] ODWXUNBKCRECNW-UHFFFAOYSA-M 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000013058 crude material Substances 0.000 description 1
- 229940045803 cuprous chloride Drugs 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 238000007256 debromination reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 238000000806 fluorine-19 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000003014 ion exchange membrane Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 1
- 238000003760 magnetic stirring Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical group FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 1
- 125000006170 pentacyclic group Chemical group 0.000 description 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- VKDSBABHIXQFKH-UHFFFAOYSA-M potassium;4-hydroxy-3-sulfophenolate Chemical compound [K+].OC1=CC=C(O)C(S([O-])(=O)=O)=C1 VKDSBABHIXQFKH-UHFFFAOYSA-M 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- AEDSRGFUYHHZPW-UHFFFAOYSA-M sodium;3,5-dihydroxybenzenesulfonate Chemical compound [Na+].OC1=CC(O)=CC(S([O-])(=O)=O)=C1 AEDSRGFUYHHZPW-UHFFFAOYSA-M 0.000 description 1
- SXONATFNYJWFNK-UHFFFAOYSA-M sodium;4-hydroxybenzenesulfonate;dihydrate Chemical compound O.O.[Na+].OC1=CC=C(S([O-])(=O)=O)C=C1 SXONATFNYJWFNK-UHFFFAOYSA-M 0.000 description 1
- WZWGGYFEOBVNLA-UHFFFAOYSA-N sodium;dihydrate Chemical compound O.O.[Na] WZWGGYFEOBVNLA-UHFFFAOYSA-N 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F16/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F16/12—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
- C08F16/32—Monomers containing two or more unsaturated aliphatic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/78—Halides of sulfonic acids
- C07C309/86—Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/87—Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/48—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/04—Systems containing only non-condensed rings with a four-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/586,844 US6268532B1 (en) | 2000-06-05 | 2000-06-05 | Sulfonated perfluorovinyl functional monomers |
| US586844 | 2000-06-05 | ||
| PCT/US2000/025589 WO2001094305A1 (en) | 2000-06-05 | 2000-09-18 | Sulfonated perfluorovinyl functional monomers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60010936D1 DE60010936D1 (de) | 2004-06-24 |
| DE60010936T2 true DE60010936T2 (de) | 2005-06-16 |
Family
ID=24347317
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60010936T Expired - Fee Related DE60010936T2 (de) | 2000-06-05 | 2000-09-18 | Sulfonierte perfluorvinylfunktionalisierte monomere |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US6268532B1 (enExample) |
| EP (1) | EP1286961B1 (enExample) |
| JP (1) | JP4414135B2 (enExample) |
| KR (1) | KR100719414B1 (enExample) |
| AT (1) | ATE267165T1 (enExample) |
| AU (1) | AU2000277040A1 (enExample) |
| CA (1) | CA2407644A1 (enExample) |
| DE (1) | DE60010936T2 (enExample) |
| WO (1) | WO2001094305A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9370750B2 (en) | 2012-08-30 | 2016-06-21 | GM Global Technology Operations LLC | Polyolefin-PFCB ionomer |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6649715B1 (en) | 2000-06-27 | 2003-11-18 | Clemson University | Fluoropolymers and methods of applying fluoropolymers in molding processes |
| US7265174B2 (en) * | 2001-03-22 | 2007-09-04 | Clemson University | Halogen containing-polymer nanocomposite compositions, methods, and products employing such compositions |
| US6953653B2 (en) | 2001-08-30 | 2005-10-11 | Clemson University | Fluoropolymer compositions, optical devices, and methods for fabricating optical devices |
| US7632916B2 (en) * | 2002-08-02 | 2009-12-15 | 3M Innovative Properties Company | Process to modify polymeric materials and resulting compositions |
| US6903173B2 (en) * | 2002-08-02 | 2005-06-07 | 3M Innovative Properties Co. | Fluorinated polymers |
| US7534836B2 (en) * | 2005-07-01 | 2009-05-19 | Bausch & Lomb Incorporated | Biomedical devices |
| US7582704B2 (en) * | 2005-07-01 | 2009-09-01 | Bausch & Lomb Incorporated | Biomedical devices |
| US7538160B2 (en) * | 2005-07-01 | 2009-05-26 | Bausch & Lomb Incorporated | Trifluorovinyl aromatic containing poly(alkyl ether) prepolymers |
| US7425600B2 (en) * | 2005-07-01 | 2008-09-16 | Bausch & Lomb Incorporated | Polymerization products and biomedical devices containing same |
| US7402634B2 (en) * | 2005-07-01 | 2008-07-22 | Bausch And Lamb Incorporated | Perfluorocyclobutane copolymers |
| US20070099054A1 (en) * | 2005-11-01 | 2007-05-03 | Fuller Timothy J | Sulfonated-perfluorocyclobutane polyelectrolyte membranes for fuel cells |
| US7635744B2 (en) * | 2006-04-05 | 2009-12-22 | General Electric Company | Trifluorovinyloxy monomers and polymers |
| US8492460B2 (en) * | 2006-07-28 | 2013-07-23 | GM Global Technology Operations LLC | Fluorinated polymer blocks for PEM applications |
| US8030405B2 (en) * | 2008-05-09 | 2011-10-04 | GM Global Technology Operations LLC | Blended PEM's with elastomers for improved mechanical durability |
| US7897693B2 (en) * | 2008-05-09 | 2011-03-01 | Gm Global Technology Operations, Inc. | Proton conductive polymer electrolytes and fuel cells |
| US7897692B2 (en) | 2008-05-09 | 2011-03-01 | Gm Global Technology Operations, Inc. | Sulfonated perfluorocyclobutane block copolymers and proton conductive polymer membranes |
| US7888433B2 (en) * | 2008-05-09 | 2011-02-15 | Gm Global Technology Operations, Inc. | Sulfonated-polyperfluoro-cyclobutane-polyphenylene polymers for PEM fuel cell applications |
| US7897691B2 (en) * | 2008-05-09 | 2011-03-01 | Gm Global Technology Operations, Inc. | Proton exchange membranes for fuel cell applications |
| US7985805B2 (en) * | 2008-05-09 | 2011-07-26 | GM Global Technology Operations LLC | Polyelectrolyte membranes comprised of blends of PFSA and sulfonated PFCB polymers |
| US7976730B2 (en) * | 2008-08-25 | 2011-07-12 | GM Global Technology Operations LLC | Blends of low equivalent molecular weight PFSA ionomers with Kynar 2751 |
| US7989568B2 (en) * | 2008-11-13 | 2011-08-02 | E.I. Du Pont De Nemours And Company | Fluorosulfonates |
| US9539568B2 (en) | 2011-04-07 | 2017-01-10 | Solvay Specialty Polymers Italy S.P.A. | Process for the preparation of cross-linked fluorinated polymers |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4358412A (en) | 1980-06-11 | 1982-11-09 | The Dow Chemical Company | Preparation of vinyl ethers |
| US4337211A (en) | 1980-06-11 | 1982-06-29 | The Dow Chemical Company | Fluorocarbon ethers having substituted halogen site(s) and process to prepare |
| US5039561A (en) | 1986-08-25 | 1991-08-13 | Minnesota Mining And Manufacturing Company | Method for preparing an article having surface layer of uniformly oriented, crystalline, organic microstructures |
| US4812352A (en) | 1986-08-25 | 1989-03-14 | Minnesota Mining And Manufacturing Company | Article having surface layer of uniformly oriented, crystalline, organic microstructures |
| US5066746A (en) | 1989-06-09 | 1991-11-19 | The Dow Chemical Company | Perfluorocyclobutane ring-containing polymers |
| US5159038A (en) | 1989-06-09 | 1992-10-27 | Dow Chemical Company | Perfluorocyclobutane ring-containing polymers |
| US5162468A (en) | 1989-06-09 | 1992-11-10 | The Dow Chemical Company | Perfluorovinyl compounds |
| US5037917A (en) | 1989-06-09 | 1991-08-06 | The Dow Chemical Company | Perfluorocyclobutane ring-containing polymers |
| US5023380A (en) | 1989-06-09 | 1991-06-11 | The Dow Chemical Company | Perfluorovinyl compounds |
| US5210265A (en) | 1989-06-09 | 1993-05-11 | The Dow Chemical Company | Reactive compounds containing perfluorocyclobutane rings |
| US5159037A (en) | 1989-06-09 | 1992-10-27 | The Dow Chemical Company | Perfluorocyclobutane ring-containing polymers |
| US5364547A (en) | 1989-06-09 | 1994-11-15 | The Dow Chemical Company | Lubricants containing perfluorocyclobutane rings |
| US5364917A (en) | 1989-06-09 | 1994-11-15 | The Dow Chemical Company | Perfluorocyclobutane ring-containing polymers |
| US5037918A (en) | 1989-12-15 | 1991-08-06 | The Dow Chemical Company | Perfluorocyclobutane ring-containing polymers with crosslinking |
| US5198513A (en) | 1989-06-09 | 1993-03-30 | The Dow Chemical Company | Reactive compounds containing perfluorovinyl groups |
| US5037919A (en) | 1989-06-09 | 1991-08-06 | The Dow Chemical Company | Reactive compounds containing perfluorovinyl groups |
| US5246782A (en) | 1990-12-10 | 1993-09-21 | The Dow Chemical Company | Laminates of polymers having perfluorocyclobutane rings and polymers containing perfluorocyclobutane rings |
| US5021602A (en) | 1989-06-09 | 1991-06-04 | The Dow Chemical Company | Reactive compounds containing perfluorocyclobutane rings |
| US5159036A (en) | 1989-12-15 | 1992-10-27 | The Dow Chemical Company | Perfluorocyclobutane ring-containing polymers with crosslinking |
| US5264508A (en) | 1992-06-25 | 1993-11-23 | The Dow Chemical Company | Polymers of haloperfluoro and perfluoro ethers |
| US5449825A (en) | 1992-06-25 | 1995-09-12 | The Dow Chemical Company | Preparation of haloperfluoro and perfluoro ethers |
| US5338430A (en) | 1992-12-23 | 1994-08-16 | Minnesota Mining And Manufacturing Company | Nanostructured electrode membranes |
| US5426164A (en) | 1992-12-24 | 1995-06-20 | The Dow Chemical Company | Photodefinable polymers containing perfluorocyclobutane groups |
| US5834523A (en) | 1993-09-21 | 1998-11-10 | Ballard Power Systems, Inc. | Substituted α,β,β-trifluorostyrene-based composite membranes |
| US5620807A (en) | 1995-08-31 | 1997-04-15 | The Dow Chemical Company | Flow field assembly for electrochemical fuel cells |
| CA2266660C (fr) | 1997-07-25 | 2012-07-17 | Acep Inc. | Composes ioniques perfluorovinyliques, leurs utilisations comme composants de conducteurs ioniques du type polymere, de membranes selectives, de catalyseurs |
| US5879828A (en) | 1997-10-10 | 1999-03-09 | Minnesota Mining And Manufacturing Company | Membrane electrode assembly |
| US5910378A (en) | 1997-10-10 | 1999-06-08 | Minnesota Mining And Manufacturing Company | Membrane electrode assemblies |
| EP0973734B1 (fr) | 1998-01-30 | 2003-06-04 | Hydro-Quebec | Derives bis-sulfonyles polymerisables et leur utilisation dans la preparation de membranes echangeuses d'ions |
-
2000
- 2000-06-05 US US09/586,844 patent/US6268532B1/en not_active Expired - Lifetime
- 2000-09-18 AT AT00966743T patent/ATE267165T1/de not_active IP Right Cessation
- 2000-09-18 AU AU2000277040A patent/AU2000277040A1/en not_active Abandoned
- 2000-09-18 EP EP00966743A patent/EP1286961B1/en not_active Expired - Lifetime
- 2000-09-18 JP JP2002501821A patent/JP4414135B2/ja not_active Expired - Fee Related
- 2000-09-18 KR KR1020027016520A patent/KR100719414B1/ko not_active Expired - Fee Related
- 2000-09-18 DE DE60010936T patent/DE60010936T2/de not_active Expired - Fee Related
- 2000-09-18 CA CA002407644A patent/CA2407644A1/en not_active Abandoned
- 2000-09-18 WO PCT/US2000/025589 patent/WO2001094305A1/en not_active Ceased
-
2001
- 2001-04-06 US US09/827,990 patent/US6384167B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9370750B2 (en) | 2012-08-30 | 2016-06-21 | GM Global Technology Operations LLC | Polyolefin-PFCB ionomer |
| DE102013216706B4 (de) * | 2012-08-30 | 2017-01-12 | GM Global Technology Operations, LLC (n.d. Ges. d. Staates Delaware) | Verfahren zur Herstellung einer ionenleitenden Membran für Brennstoffzellen |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2000277040A1 (en) | 2001-12-17 |
| EP1286961B1 (en) | 2004-05-19 |
| US20020007083A1 (en) | 2002-01-17 |
| KR100719414B1 (ko) | 2007-05-22 |
| KR20030007863A (ko) | 2003-01-23 |
| EP1286961A1 (en) | 2003-03-05 |
| JP4414135B2 (ja) | 2010-02-10 |
| US6268532B1 (en) | 2001-07-31 |
| DE60010936D1 (de) | 2004-06-24 |
| ATE267165T1 (de) | 2004-06-15 |
| WO2001094305A1 (en) | 2001-12-13 |
| US6384167B2 (en) | 2002-05-07 |
| CA2407644A1 (en) | 2001-12-13 |
| JP2003535924A (ja) | 2003-12-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |