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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Ligating properties of anionic Fischer-type carbene complexes,[(CO)_5M=C(X)Y]-
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Ligating properties of anionic Fischer-type carbene complexes,[(CO)_5M=C(X)Y]-

机译:阴离子费歇尔型卡宾配合物的连接特性,[(CO)_5M = C(X)Y]-

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With the simplest of anionic Fischer-type carbene complexes acting as ligands,Cp_2Zr(Cl){OCMe}M(CO)_5compounds (M = Cr or W) promote a-olefin oligomerization andpolymerization in the presence of MAO. Attaching an N-heterocyclic ring to the carbene carbon atomin similar precursors, allows a variety of hard metal ions and fragments to be captured by externalbidentate coordination. The outcome of the attachment of a phosphorus or sulfur functionality to ana-carbon of an 0-anionic carbene is formation of a bidentate ligand and then internal four-memberedcarbene–heteroatom chelate formation. a-Deprotonated carbene complexes are also precursors forremote, one-N, six-membered carbene complexes of various metals whereas a-C-, a-N- ora-O-deprotonated as well as β-deprotonated Fischer-type carbene complexes display unique synthonproperties towards Ph_3PAu+ and partake in unusual ensuing coordination of liberated group 6 metalcarbonyl moieties to form dinuclear products.
机译:以最简单的阴离子费歇尔型卡宾配合物作为配体,Cp_2Zr(Cl){OCMe} M(CO)_5化合物(M = Cr或W)在存在MAO的情况下促进α-烯烃的低聚和聚合。在类似的前体中,将N杂环与卡宾碳原子相连,可以通过外部双配位捕获各种硬金属离子和碎片。磷或硫官能团与0阴离子卡宾的正碳相连的结果是形成双齿配体,然后形成内部四元卡宾-杂原子螯合物。 α-去质子化的卡宾配合物也是多种金属的远程,一-N,六元卡宾配合物的前体,而aC-,aN-或O-O-去质子化和β-去质子化的Fischer型卡宾配合物对Ph_3PAu +和Ph_3PAu +表现出独​​特的合成性质参与释放的第6族金属羰基部分的异常随后的配位以形成双核产物。

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