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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Syntheses and characterization of bis(trifluoromethyl)phosphino naphthalenes and acenaphthenes
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Syntheses and characterization of bis(trifluoromethyl)phosphino naphthalenes and acenaphthenes

机译:双(三氟甲基)膦基萘和ena的合成与表征

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Syntheses of heteroleptic 1,8-bis(phosphino)naphthalenes and 5,6-bis(phosphino)acenaphthenes were attempted using several synthetic strategies. Reaction of aryllithium with triphenylphosphite gave ArP(OPh)(2) (Ar = substituted naphthalene or acenaphthene), which was transformed into ArP(CF3)(2), using a nucleophilic trifluoromethylation reaction with Me3SiCF3/CsF. The importance of the correct choice of solvent for the trifluoromethylation reactions is discussed. The incompatibility of ArP(CF3)(2) with organolithium hampered the attachment of the second phosphine functionality to the organic backbone. Tetraphenoxyethylene was obtained in a small amount as a side product in the trifluoromethylation reaction. Selected new compounds were characterized by single-crystal X-ray diffraction.
机译:尝试使用几种合成策略合成杂合的1,8-双(膦基)萘和5,6-双(膦基)ac啶。芳基锂与亚磷酸三苯酯反应生成ArP(OPh)(2)(Ar =取代的萘或ena),并通过与Me3SiCF3 / CsF的亲核三氟甲基化反应将其转化为ArP(CF3)(2)。讨论了正确选择溶剂对三氟甲基化反应的重要性。 ArP(CF3)(2)与有机锂的不相容性阻碍了第二膦官能团与有机骨架的连接。在三氟甲基化反应中作为副产物少量获得了四苯氧基乙烯。所选的新化合物通过单晶X射线衍射进行表征。

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