Bi- and tridentate phosphanegold(I) chloride units linked by organosilane backbones

Peter Heinrichs, Beate Neumann, Hans-Georg Stammler, Norbert W. Mitzel
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Abstract

The tridentate ligand tris(dimethylphosphanyl-methyl)phenylsilane was prepared by the reaction of phenyltrichlorosilane with three equivalents of dimethylphosphanylmethyl lithium. This ligand and the bifunctional bis(dimethylphosphanylmethyl)dimethylsilane were converted into their corresponding gold(I) chloride complexes with three and two AuCl functions, respectively. The complexes were investigated for their ability to form intra- or intermolecular aurophilic interactions.
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由有机硅烷骨架连接的双叉和三叉磷金(I)氯化物单元
三叉配体三(二甲基膦酰甲基)苯基硅烷是通过苯基三氯硅烷与三当量的二甲基膦酰甲基锂反应制备的。这种配体和双官能双(二甲基膦酰甲基)二甲基硅烷分别被转化成相应的具有三个和两个 AuCl 官能的氯化金(I)络合物。研究人员对这些配合物形成分子内或分子间亲欧相互作用的能力进行了研究。
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