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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Preparing alpha,beta-unsaturated Fischer-type carbene complexes via an unforeseen route
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Preparing alpha,beta-unsaturated Fischer-type carbene complexes via an unforeseen route

机译:通过不可预见的途径制备α,β-不饱和费歇尔型卡宾配合物

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摘要

Four 4-(NH-amino)-1-metalla-1,3-diene carbene complexes, two of which contain novel 4-membered heterometallacycles, formed regioselectively from the reaction of a mixture of [(CH3)(2)(CH3S)S][BF4], the acetonitrilium electrophile, CH3CNCH3+, and the deprotonated alkoxycarbene complexes, (CO)(5)M=C(OCH3)CH2Li (M = Cr, W). The preferred Z-configurations of the alkoxy and amino groups are determined by strong H-bonding in the products. The metal-carbene bonds in the chelates are shorter by 0.08 angstrom than those in the acyclic compounds.
机译:四个4-(NH-氨基)-1-金属-1,3-二烯卡宾配合物,其中两个包含新颖的4-元杂金属杂环,它们是根据[(CH3)(2)(CH3S)的混合物的反应区域选择性地形成的S] [BF4],乙腈亲电子试剂CH3CNCH3 +和去质子化的烷氧基卡宾配合物(CO)(5)M = C(OCH3)CH2Li(M = Cr,W)。烷氧基和氨基的优选Z构型由产物中的强H键决定。螯合物中的金属碳烯键比无环化合物中的金属碳烯键短0.08埃。

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