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首页> 外文期刊>Organometallics >Oxidative addition of hydrosilanes, hydrogermane, and hydrostannane to cyclopentadienylcobalt(I) bearing a pendant phosphane ligand: Cyclopentadienylhydridocobalt(III) chelate complexes with silyl, germyl, and stannyl ligands
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Oxidative addition of hydrosilanes, hydrogermane, and hydrostannane to cyclopentadienylcobalt(I) bearing a pendant phosphane ligand: Cyclopentadienylhydridocobalt(III) chelate complexes with silyl, germyl, and stannyl ligands

机译:将氢硅烷,氢锗烷和氢化锡烷氧化加成到一个侧基膦配体的环戊二烯基钴(I)中:环戊二烯基氢化钴(III)螯合物与甲硅烷基,十烷基和苯乙烯基配体

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摘要

Oxidative addition of hydrosilanes, a hydrogermane, and a hydrostannane to the ((cyclopentadienylalkyl)phosphane)cobalt(I) chelate 1 results in the formation of cyclopentadienylhydridocobalt(III) complexes having a tethered phosphorus ligand and silyl (rac4-rac-8), germyl (rac-10), and stannyl substituents (rac-11). The pseudo-four-coordinate complexes are chiral. The X-ray structures of 5 and 7 have been determined. Variable-temperature NMR spectra indicate racemization in solution due to reversible dissociation of the phosphorus ligand. The barrier of this process has been estimated to be in the range of 13-16 kcal/mol. [References: 22]
机译:在((环戊二烯基烷基)膦)钴(I)螯合物1中氧化加氢硅烷,氢锗烷和氢化锡烷,导致形成环戊二烯基氢化钴(III)配合物,该配合物具有束缚的磷配体和甲硅烷基(rac4-rac-8),胚芽(rac-10)和甲锡烷基取代基(rac-11)。伪四坐标配合物是手性的。已经确定了5和7的X射线结构。可变温度NMR光谱表明,由于磷配体的可逆解离,溶液中存在外消旋作用。据估计该方法的势垒在13-16kcal / mol的范围内。 [参考:22]

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