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Synthesis and characterization of bis[(dimethylphosphanylethynyl)dimethylsilyl]methane-digold(I) dichloride
Zeitschrift für Naturforschung B ( IF 0.8 ) Pub Date : 2024-02-22 , DOI: 10.1515/znb-2024-0005
Peter Heinrichs 1 , Hans-Georg Stammler 1 , Norbert W. Mitzel 1
Affiliation  

The reaction of chlorodimethylphosphane with dilithiated bis(ethynyldimethylsilyl)methane leads to the corresponding bis[(dimethylphosphanylethynyl)dimethylsilyl]methane (1) which reacts readily with chloroauric acid in the presence of a reductant to form its dinuclear chlorogold(I) complex (2). The terminal chloride units of this compound can be substituted by reaction with nucleophiles. Furthermore, the metallophilic host functionality of the dinuclear complex 2 towards metallophilic atoms such as copper, silver, and thallium was tested. The crystal structure of bis[(dimethylphosphanylethynyl)dimethylsilyl]methane-digold(I) dichloride (2) is presented, which shows chains of the molecules aggregated by intermolecular aurophilic contacts.

中文翻译:

双[(二甲基膦基乙炔基)二甲基甲硅烷基]甲烷-二氯化二金(I)的合成与表征

氯二甲基膦与二锂化双(乙炔基二甲基甲硅烷基)甲烷反应生成相应的双[(二甲基膦基乙炔基)二甲基甲硅烷基]甲烷 (1),其在还原剂存在下很容易与氯金酸反应,形成其双核氯金 (I) 络合物 (2) 。该化合物的末端氯单元可以通过与亲核试剂反应而被取代。此外,还测试了双核配合物2对亲金属原子(例如铜、银和铊)的亲金属主体官能度。给出了双[(二甲基膦基乙炔基)二甲基甲硅烷基]甲烷-二氯化金(I) (2) 的晶体结构,其中显示了通过分子间亲金接触聚集的分子链。
更新日期:2024-02-22
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