卡宾
化学
广场互动
配体(生物化学)
过渡金属卡宾配合物
酰胺
三角双锥分子几何
结晶学
立体化学
晶体结构
催化作用
有机化学
生物化学
受体
金属
作者
Wolfgang A. Herrmann,Florian C. Munck,Georg R. J. Artus,Oliver Runte,Reiner Anwander
出处
期刊:Organometallics
[American Chemical Society]
日期:1997-02-01
卷期号:16 (4): 682-688
被引量:122
摘要
The synthesis and X-ray crystal structures of Y[N(SiHMe2)2]3(carbene)x (carbene = 1,3-dimethylimidazolin-2-ylidene, x = 1, 2) are described. The donor capability of the strongly nucleophilic carbene ligand is expressed in both the displacement of two THF ligands by one carbene ligand in precursor compound Y[N(SiHMe2)2]3(THF)2 and by the addition of a second carbene ligand to yield the preferred (3 + 2) trigonal bipyramidal coordination geometry. In particular, the structural data reveal that the carbene ligands affect the coordination mode of the bis(dimethylsilyl)amide counterligands by forcing them to form close β-Si−H(silylamide)−yttrium agostic contacts. According to Pearson's terminology such carbene ligands have to be classified as hard donor ligands.
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