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首页> 外文期刊>Doklady Chemistry >Complexes of Gold Clusters with the closo-Borate Anions B10H10~(2-) and B12H12~(2-)
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Complexes of Gold Clusters with the closo-Borate Anions B10H10~(2-) and B12H12~(2-)

机译:金簇与硼酸根阴离子B10H10〜(2-)和B12H12〜(2-)的配合物

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摘要

For closo-borane anions,only one gold(I) complex with a closo-hexaborate anion [Au2(mu-bis(eta3-B6H6))(PPh3)2] has been synthesized and characterized [1,2].The complex crystallizes either in the cubic (A) or in the orthorhombic (B) polymorphous modification,depending on the solvent used.In both polymorphs,gold atoms are in a severely distorted tetrahedral environment:each gold atom is bound to three boron atoms of a trigonal face of the closo-hexaborate anion and to the phosphorus atom of triphenylphosphine.The compound is a binuclear complex and contains the hexabo-rate anion as a binder coordinated to the central metal atoms through the opposite B3 faces.This compound was synthesized by the reaction of tetrabutylammo-nium closo-hexaborate with [Au(PPh3)Cl].Thus,it is evident that gold complexes with cluster boron anions are virtually unstudied.
机译:对于closo-borane阴离子,仅合成了一种与closo-hexaborate阴离子[Au2(mu-bis(eta3-B6H6))(PPh3)2]形成的金(I)配合物[1,2]。该配合物结晶取决于所使用的溶剂,在立方(A)或正交(B)多晶型变体中。在这两种多晶型物中,金原子都处于严重扭曲的四面体环境中:每个金原子都与一个三角形面的三个硼原子结合该化合物是双核络合物,包含六硼酸根阴离子作为粘合剂,通过相对的B3面与中心金属原子配位。含[Au(PPh3)Cl]的四丁基溴化六硼酸铵。因此,很明显未研究到带有簇状硼阴离子的金配合物。

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