Constitution of the fully supported gold(I)alkynyl (dmpme)·bis[gold(I)ethynyldimethylsilyl]methane in solution

Peter Heinrichs, A. Mix, N. Mitzel
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Abstract

Abstract The dimetallacyclic complex H2C(Me2SiC≡CAuPMe2)2CH2 has been synthesized, in which the two gold centers are bridged by the diphosphine dmpme (= bis(dimethylphosphino)methane) and a diethynyl ligand providing “full support” for the possible transannular Au–Au contact (3). This compound and its “semi-” and “unsupported” analogues (2, 1) have been characterized by NMR spectroscopy and elemental analysis. The monomeric nature of complex 3 in solution has been established using diffusion coefficients measured by DOSY-NMR spectroscopy and comparing the data with those of complexes 1 and 2 as references.
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全负载金(I)炔基(dmpme)·二[金(I)乙基二甲基硅基]甲烷在溶液中的组成
已经合成了双金属环配合物H2C(Me2SiC≡CAuPMe2)2CH2,其中两个金中心由二膦dmpme(=双(二甲基膦)甲烷)和二乙基配体桥接,为可能的跨环Au-Au接触提供“完全支持”(3)。该化合物及其“半”和“非负载”类似物(2,1)已通过核磁共振波谱和元素分析进行了表征。利用DOSY-NMR测量的扩散系数,并与配合物1和2的数据进行比较,确定了配合物3在溶液中的单体性质。
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