化学
苯基硅烷
镁
酰胺
分子内力
氢化物
氢化镁
苯乙炔
重氮甲烷
晶体结构
两性离子
高分子化学
立体化学
药物化学
结晶学
有机化学
分子
氢
催化作用
作者
Philipp Rinke,Helmar Görls,Phil Liebing,Robert Kretschmer
出处
期刊:Organometallics
[American Chemical Society]
日期:2023-08-09
卷期号:42 (16): 2287-2292
被引量:7
标识
DOI:10.1021/acs.organomet.3c00278
摘要
Three magnesium-hydride complexes (3a–c) supported by alkylene-bridged bis(β-diketiminate) ligands have been synthesized by reacting the respective dinuclear magnesium bis(trimethylsilyl)amide complexes 1a–c with phenylsilane; 3a can alternatively be accessed by the same reaction but starting from the dinuclear magnesium n-butyl complex 2a. Single-crystal X-ray diffraction revealed a dimeric structure in the solid state, with inter- and intramolecular μ2-hydrides bridging the magnesium centers. The properties of the tetranuclear complexes are strongly impacted by the alkylene bridge. While 3b turned out to be virtually insoluble in common solvents, solutions of 3a and 3c are readily obtained, and NMR spectroscopic data indicate that the dimers persist in solution. 3a readily reacts with phenylacetylene, affording the tetranuclear magnesium complex 4a with bridging phenylacetylide groups.
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