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首页> 外文期刊>Organometallics >Rhodium(I) Complexes of the Conformationally Rigid IBioxMe_4 Ligand: Isolation of a Stable Low-Coordinate T?Shaped Complex
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Rhodium(I) Complexes of the Conformationally Rigid IBioxMe_4 Ligand: Isolation of a Stable Low-Coordinate T?Shaped Complex

机译:构型刚性IBioxMe_4配体的铑(I)配合物:稳定的低坐标T型复合物的分离

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摘要

The isolation, characterization and reactivity of a T-shaped rhodium(I) complex containing Glorius’ bioxazoline derived N-heterocyclic carbene ligand IBioxMe_4 is described: [Rh(IBioxMe_4)_3][BAr~F_4] (1). 1 represents a rare example of a solution-stable “naked” 14-electron complex and is characterized in the solid state by highly distorted ligand geometries and Rh··· C distances >3.1 ? for the IBioxMe_4 alkyl substituents. Consistent with the bulky nature of the NHC ligand, no reaction was observed with excess IBioxMe_4, PCy_3, or norbornadiene. Reaction of 1 with CO, however, led to coordinatively saturated [Rh(IBioxMe_4)_3(CO)][BAr~F_4] (2).
机译:含有Glorius的生物恶唑啉衍生的N-杂环卡宾配体IBioxMe_4的T形铑(I)配合物的分离,表征和反应性描述为:[Rh(IBioxMe_4)_3] [BAr〜F_4](1)。图1表示溶液稳定的“裸” 14电子配合物的稀有实例,其特征在于固态的配体几何形状高度失真,Rh···C距离> 3.1? IBioxMe_4烷基取代基。与NHC配体的庞大性质一致,未观察到过量IBioxMe_4,PCy_3或降冰片二烯的反应。然而,1与CO的反应导致配位饱和[Rh(IBioxMe_4)_3(CO)] [BAr〜F_4](2)。

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