高价分子
硅烯
卡宾
硅
结晶学
化学
双键
氧化态
粘结长度
金属
晶体结构
物理化学
有机化学
催化作用
试剂
作者
Yuzhong Wang,Yaoming Xie,Pingrong Wei,R. Bruce King,Henry F. Schaefer,Paul von Ragué Schleyer,Gregory H. Robinson
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2008-08-21
卷期号:321 (5892): 1069-1071
被引量:708
标识
DOI:10.1126/science.1160768
摘要
Dative, or nonoxidative, ligand coordination is common in transition metal complexes; however, this bonding motif is rare in compounds of main group elements in the formal oxidation state of zero. Here, we report that the potassium graphite reduction of the neutral hypervalent silicon-carbene complex L:SiCl4 {where L: is:C[N(2,6-Pri2-C6H3)CH]2 and Pri is isopropyl} produces L:(Cl)Si-Si(Cl):L, a carbene-stabilized bis-silylene, and L:Si=Si:L, a carbene-stabilized diatomic silicon molecule with the Si atoms in the formal oxidation state of zero. The Si-Si bond distance of 2.2294 +/- 0.0011 (standard deviation) angstroms in L:Si=Si:L is consistent with a Si=Si double bond. Complementary computational studies confirm the nature of the bonding in L:(Cl)Si-Si(Cl):L and L:Si=Si:L.
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