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・ Perflenapent
・ Perflubron
・ Perfluorinated alkylated substances
・ Perfluorinated carboxylic acid
・ Perfluorinated compound
・ Perfluoro-1,3-dimethylcyclohexane
・ Perfluoroalkoxy alkane
・ Perfluorobutane
・ Perfluorobutanesulfonic acid
・ Perfluorobutanesulfonyl fluoride
・ Perfluorocarbon tracer
・ Perfluorocyclohexane
・ Perfluorodecalin
・ Perfluorodecyltrichlorosilane
・ Perfluoroethanamine
Perfluoroether
・ Perfluoroheptane
・ Perfluorohexane
・ Perfluoroisobutene
・ Perfluoromethylcyclohexane
・ Perfluoromethyldecalin
・ Perfluoromethyldiethylamine
・ Perfluorononanoic acid
・ Perfluorooctane
・ Perfluorooctanesulfonamide
・ Perfluorooctanesulfonic acid
・ Perfluorooctanesulfonyl fluoride
・ Perfluorooctanoic acid
・ Perfluoropentacene
・ Perfluorotoluene


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Perfluoroether : ウィキペディア英語版
Perfluoroether
Perfluoroethers are a class of organofluorine compound containing one or more ether functional group. In general these compounds are structural analogous to related hydrocarbon ethers, but they exhibit to the distinctive properties of fluorocarbons.〔Günter Siegemund, Werner Schwertfeger, Andrew Feiring, Bruce Smart, Fred Behr, Herward Vogel, Blaine McKusick “Fluorine Compounds, Organic” Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2002. 〕
==Low molecular weight fluorinated ethers==

Acyclic perfluoroethers are known, e.g. O(C2F5)2, the analogue of diethylether. More interesting and more useful are the cyclic ethers, especially, the epoxides. Thus tetrafluoroethyene oxide and hexafluoropropylene oxide are two of the simplest cyclic perfluoroethers. It is a precursor to perfluoro(methyl vinyl ether (CF2=CFOCF3) and perfluoro(propyl vinyl ether are used as a comonomers with tetrafluoroethylene.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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