RU2373229C2 - Фторполиэфирное соединение - Google Patents
Фторполиэфирное соединение Download PDFInfo
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- RU2373229C2 RU2373229C2 RU2006129281/04A RU2006129281A RU2373229C2 RU 2373229 C2 RU2373229 C2 RU 2373229C2 RU 2006129281/04 A RU2006129281/04 A RU 2006129281/04A RU 2006129281 A RU2006129281 A RU 2006129281A RU 2373229 C2 RU2373229 C2 RU 2373229C2
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 293
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- IUHFWCGCSVTMPG-UHFFFAOYSA-N [C].[C] Chemical group [C].[C] IUHFWCGCSVTMPG-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229930195734 saturated hydrocarbon Natural products 0.000 claims abstract description 6
- 239000012634 fragment Substances 0.000 claims description 46
- 239000000203 mixture Substances 0.000 claims description 27
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- 238000009826 distribution Methods 0.000 claims description 6
- 238000005227 gel permeation chromatography Methods 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
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- 239000000126 substance Substances 0.000 abstract description 9
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- 230000006866 deterioration Effects 0.000 abstract description 4
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- 238000005481 NMR spectroscopy Methods 0.000 description 44
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- 238000005160 1H NMR spectroscopy Methods 0.000 description 34
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- 239000012528 membrane Substances 0.000 description 7
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- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 4
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- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
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- 238000000354 decomposition reaction Methods 0.000 description 4
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- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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- FYELSNVLZVIGTI-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-5-ethylpyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C=NN(C=1CC)CC(=O)N1CC2=C(CC1)NN=N2 FYELSNVLZVIGTI-UHFFFAOYSA-N 0.000 description 3
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- 238000007654 immersion Methods 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
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- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 239000010702 perfluoropolyether Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
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- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 3
- OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 2
- YSIGVPOSKQLNTO-UHFFFAOYSA-N 2,3,3,3-tetrafluoro-2-[1,1,2,3,3,3-hexafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy)propoxy]propanoyl fluoride Chemical compound FC(=O)C(F)(C(F)(F)F)OC(F)(F)C(F)(C(F)(F)F)OC(F)(F)C(F)(F)C(F)(F)F YSIGVPOSKQLNTO-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
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- 239000003795 chemical substances by application Substances 0.000 description 2
- LBJNMUFDOHXDFG-UHFFFAOYSA-N copper;hydrate Chemical compound O.[Cu].[Cu] LBJNMUFDOHXDFG-UHFFFAOYSA-N 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000006266 etherification reaction Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
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- 239000012454 non-polar solvent Substances 0.000 description 2
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- 238000005191 phase separation Methods 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
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- 229910002027 silica gel Inorganic materials 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NSWMDPVPXIVLMW-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-amine Chemical compound FC(F)(F)C(N)(C(F)(F)F)C(F)(F)F NSWMDPVPXIVLMW-UHFFFAOYSA-N 0.000 description 1
- CMVFABYKWZDQMC-UHFFFAOYSA-N 1,1,3,4-tetrachloro-1,2,2,3,4,4-hexafluorobutane Chemical compound FC(F)(Cl)C(F)(Cl)C(F)(F)C(F)(Cl)Cl CMVFABYKWZDQMC-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- COAUHYBSXMIJDK-UHFFFAOYSA-N 3,3-dichloro-1,1,1,2,2-pentafluoropropane Chemical compound FC(F)(F)C(F)(F)C(Cl)Cl COAUHYBSXMIJDK-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-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
- 230000005526 G1 to G0 transition Effects 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical class [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000005360 alkyl sulfoxide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
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- 238000005260 corrosion Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
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- 238000000105 evaporative light scattering detection Methods 0.000 description 1
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- 239000005357 flat glass Substances 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
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- 229910000856 hastalloy Inorganic materials 0.000 description 1
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- 239000003112 inhibitor Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 150000005217 methyl ethers Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000006011 modification reaction Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- GVGCUCJTUSOZKP-UHFFFAOYSA-N nitrogen trifluoride Chemical group FN(F)F GVGCUCJTUSOZKP-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 229950008618 perfluamine Drugs 0.000 description 1
- 125000005459 perfluorocyclohexyl group Chemical group 0.000 description 1
- JAJLKEVKNDUJBG-UHFFFAOYSA-N perfluorotripropylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)F JAJLKEVKNDUJBG-UHFFFAOYSA-N 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 238000011085 pressure filtration Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
- 238000000194 supercritical-fluid extraction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- JLQFVGYYVXALAG-CFEVTAHFSA-N yasmin 28 Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1.C([C@]12[C@H]3C[C@H]3[C@H]3[C@H]4[C@@H]([C@]5(CCC(=O)C=C5[C@@H]5C[C@@H]54)C)CC[C@@]31C)CC(=O)O2 JLQFVGYYVXALAG-CFEVTAHFSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/004—Surface-active compounds containing F
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/321—Polymers modified by chemical after-treatment with inorganic compounds
- C08G65/323—Polymers modified by chemical after-treatment with inorganic compounds containing halogens
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/337—Polymers modified by chemical after-treatment with organic compounds containing other elements
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/50—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing halogen
- C10M105/54—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing halogen containing carbon, hydrogen, halogen and oxygen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/38—Lubricating compositions characterised by the base-material being a macromolecular compound containing halogen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/0406—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2213/00—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2213/04—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen, halogen and oxygen
- C10M2213/043—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen, halogen and oxygen used as base material
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyethers (AREA)
- Lubricants (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004005586 | 2004-01-13 | ||
| JP2004-005586 | 2004-01-13 |
Publications (2)
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| RU2006129281A RU2006129281A (ru) | 2008-02-20 |
| RU2373229C2 true RU2373229C2 (ru) | 2009-11-20 |
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| RU2006129281/04A RU2373229C2 (ru) | 2004-01-13 | 2005-01-12 | Фторполиэфирное соединение |
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| EP (1) | EP1705203B1 (enExample) |
| JP (1) | JP5028801B2 (enExample) |
| KR (1) | KR101089078B1 (enExample) |
| CN (1) | CN100392000C (enExample) |
| AT (1) | ATE432954T1 (enExample) |
| DE (1) | DE602005014734D1 (enExample) |
| RU (1) | RU2373229C2 (enExample) |
| TW (1) | TW200538509A (enExample) |
| WO (1) | WO2005068534A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2522640C2 (ru) * | 2012-05-31 | 2014-07-20 | Общество с ограниченной ответственностью Научно Производственный Центр "Квадра" | Фторсодержащее пав и способ его получения |
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| TWI295299B (en) * | 2002-10-18 | 2008-04-01 | Asahi Glass Co Ltd | Perfluoropolyether derivatives |
| CN1989230B (zh) * | 2004-07-27 | 2010-05-05 | 旭硝子株式会社 | 以含氟聚醚化合物为润滑剂的磁记录媒体用润滑剂溶液 |
| WO2007013412A1 (ja) * | 2005-07-27 | 2007-02-01 | Asahi Glass Company, Limited | エーテル組成物および溶液組成物 |
| ITTO20060139A1 (it) * | 2006-02-27 | 2007-08-28 | Bridgestone Corp | Mescola di gomma vulcanizzabile contenente silice |
| JP2008034064A (ja) * | 2006-07-31 | 2008-02-14 | Toshiba Corp | 磁気記録媒体及び磁気記録再生装置 |
| US8338517B2 (en) | 2007-05-23 | 2012-12-25 | 3M Innovative Properties Company | Aqueous compositions of fluorinated surfactants and methods of using the same |
| WO2008154345A1 (en) | 2007-06-06 | 2008-12-18 | 3M Innovative Properties Company | Fluorinated ether compositions and methods of using the same |
| JPWO2009008380A1 (ja) * | 2007-07-06 | 2010-09-09 | 旭硝子株式会社 | 表面処理剤、物品、および新規含フッ素エーテル化合物 |
| JP5309622B2 (ja) * | 2007-11-28 | 2013-10-09 | 旭硝子株式会社 | 表面処理剤 |
| TW200948894A (en) * | 2007-12-19 | 2009-12-01 | Asahi Glass Co Ltd | Ether composition |
| JP4507263B2 (ja) * | 2008-01-16 | 2010-07-21 | 信越化学工業株式会社 | 含フッ素硬化性組成物 |
| JP5795457B2 (ja) * | 2008-01-24 | 2015-10-14 | 旭硝子株式会社 | エーテル化合物、潤滑剤、溶媒組成物および磁気ディスクの製造方法 |
| EP2236559B1 (en) * | 2008-01-24 | 2016-03-30 | Asahi Glass Company, Limited | Ether composition |
| WO2010009191A2 (en) | 2008-07-18 | 2010-01-21 | 3M Innovative Properties Company | Fluorinated ether compounds and methods of using the same |
| EP2325157B1 (en) | 2008-09-09 | 2014-11-05 | Asahi Glass Company, Limited | Method for producing a perfluoro compound having hydroxyl groups |
| US8629089B2 (en) | 2008-12-18 | 2014-01-14 | 3M Innovative Properties Company | Method of contacting hydrocarbon-bearing formations with fluorinated ether compositions |
| JP2010168512A (ja) * | 2009-01-26 | 2010-08-05 | Hitachi Ltd | 潤滑剤、および、それを用いた磁気ディスク装置 |
| US8697985B2 (en) | 2009-05-25 | 2014-04-15 | Solvay Solexis, S.PA. | Protective film for a solar cell module |
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| JPWO2011065312A1 (ja) | 2009-11-26 | 2013-04-11 | 旭硝子株式会社 | エーテル化合物、これを含む潤滑剤および潤滑剤用組成物 |
| JP6142915B2 (ja) * | 2013-02-13 | 2017-06-07 | 旭硝子株式会社 | 含フッ素エーテル組成物、表面改質剤、界面活性剤、液状組成物、物品 |
| SG11201601009VA (en) | 2013-08-13 | 2016-03-30 | Asahi Glass Co Ltd | Fluorinated polyether compound, lubricant, liquid composition and article |
| CN105518054B (zh) * | 2013-08-23 | 2018-02-16 | 大金工业株式会社 | 含全氟（聚）醚基的羧酸化合物的分离方法 |
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| CN107001611A (zh) | 2014-12-15 | 2017-08-01 | 索尔维特殊聚合物意大利有限公司 | 包含氟化聚合物的水基组合物 |
| KR101643364B1 (ko) | 2015-11-11 | 2016-08-26 | 상화시스템주식회사 | 얼터네이터 부품 해체 장치 및 해체 방법 |
| CN106832256B (zh) * | 2017-01-18 | 2020-07-28 | 济南齐氟新材料技术有限公司 | 一种含氟非离子表面活性剂的制备方法 |
| CN109022105B (zh) * | 2018-06-13 | 2021-09-17 | 权家（厦门）新材料有限公司 | 一种水溶性氟碳石墨烯机油及其制备方法 |
| WO2024038866A1 (ja) * | 2022-08-18 | 2024-02-22 | Ａｇｃ株式会社 | 化合物、組成物、表面処理剤、コーティング液、物品、及び物品の製造方法 |
| EP4516773A4 (en) * | 2023-03-03 | 2025-10-29 | Daikin Ind Ltd | COMPOUND CONTAINING FLUORIDE |
| WO2024225107A1 (ja) * | 2023-04-28 | 2024-10-31 | 株式会社レゾナック | 含フッ素エーテル化合物、磁気記録媒体用潤滑剤および磁気記録媒体 |
| CN119233961A (zh) * | 2023-04-28 | 2024-12-31 | 株式会社力森诺科 | 含氟醚化合物、磁记录介质用润滑剂及磁记录介质 |
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| JP2001208736A (ja) * | 2000-01-28 | 2001-08-03 | Asahi Glass Co Ltd | フッ素系有機化合物の分子量測定方法 |
| US9676603B1 (en) * | 2012-09-05 | 2017-06-13 | Dennis C. Oakley | Multipurpose handheld tool and associated method |
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| DE2403706A1 (de) | 1974-01-26 | 1975-08-14 | Hoechst Ag | Verfahren zur herstellung von chlorierten kupferphthalocyaninen |
| CA2098007A1 (en) * | 1991-01-11 | 1992-07-12 | Miguel A. Guerra | Curing fluorocarbon elastomers |
| EP0641460A1 (en) * | 1992-05-21 | 1995-03-08 | Minnesota Mining And Manufacturing Company | Organometallic monomers and polymers with improved adhesion |
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-
2005
- 2005-01-12 JP JP2005517045A patent/JP5028801B2/ja not_active Expired - Fee Related
- 2005-01-12 EP EP05703495A patent/EP1705203B1/en not_active Expired - Lifetime
- 2005-01-12 RU RU2006129281/04A patent/RU2373229C2/ru not_active IP Right Cessation
- 2005-01-12 KR KR1020067010575A patent/KR101089078B1/ko not_active Expired - Fee Related
- 2005-01-12 DE DE602005014734T patent/DE602005014734D1/de not_active Expired - Lifetime
- 2005-01-12 CN CNB2005800019115A patent/CN100392000C/zh not_active Expired - Fee Related
- 2005-01-12 WO PCT/JP2005/000256 patent/WO2005068534A1/ja not_active Ceased
- 2005-01-12 AT AT05703495T patent/ATE432954T1/de not_active IP Right Cessation
- 2005-01-13 TW TW094101015A patent/TW200538509A/zh not_active IP Right Cessation
-
2006
- 2006-07-11 US US11/483,566 patent/US7795375B2/en not_active Expired - Fee Related
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5508380A (en) * | 1993-04-19 | 1996-04-16 | Ausimont, S.P.A. | Fluorinated polymers containing perfluoropolyoxyalkylene sequences and having thermoplastic elastomeric properties |
| JP2001208736A (ja) * | 2000-01-28 | 2001-08-03 | Asahi Glass Co Ltd | フッ素系有機化合物の分子量測定方法 |
| US9676603B1 (en) * | 2012-09-05 | 2017-06-13 | Dennis C. Oakley | Multipurpose handheld tool and associated method |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2522640C2 (ru) * | 2012-05-31 | 2014-07-20 | Общество с ограниченной ответственностью Научно Производственный Центр "Квадра" | Фторсодержащее пав и способ его получения |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1705203B1 (en) | 2009-06-03 |
| TWI349023B (enExample) | 2011-09-21 |
| RU2006129281A (ru) | 2008-02-20 |
| TW200538509A (en) | 2005-12-01 |
| JP5028801B2 (ja) | 2012-09-19 |
| JPWO2005068534A1 (ja) | 2007-12-27 |
| US7795375B2 (en) | 2010-09-14 |
| US20060252910A1 (en) | 2006-11-09 |
| CN100392000C (zh) | 2008-06-04 |
| WO2005068534A1 (ja) | 2005-07-28 |
| KR101089078B1 (ko) | 2011-12-05 |
| EP1705203A1 (en) | 2006-09-27 |
| CN1906228A (zh) | 2007-01-31 |
| KR20060123221A (ko) | 2006-12-01 |
| ATE432954T1 (de) | 2009-06-15 |
| EP1705203A4 (en) | 2007-05-02 |
| DE602005014734D1 (de) | 2009-07-16 |
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| MM4A | The patent is invalid due to non-payment of fees |
Effective date: 20160113 |