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Metal Activation of a Germylenoid, a New Approach to Metal–Germanium Triple Bonds: Synthesis and Reactions of the Germylidyne Complexes [Cp(CO)<sub>2</sub>M≡Ge–C(SiMe<sub>3</sub>)<sub>3</sub>] (M = Mo, W)
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2012
Year
Inorganic ChemistryChemical EngineeringEngineeringCoordination ComplexElectrophilic Germanium CenterGermylidyne ComplexesNew ApproachOrganometallic CatalysisMolecular ComplexGermylenoid LiChemistryMetal ActivationInorganic SynthesisMetal–germanium Triple BondsInorganic Compound
The reactions of the germylenoid Li(THF)3GeCl2C(SiMe3)3 with the carbonyl metalates Li[CpMo(CO)3] and K[CpW(CO)3] (Cp = η5-C5H5) in toluene afford selectively the germylidyne complexes [Cp(CO)2M≡Ge–C(SiMe3)3] (1-Mo, M = Mo; 1-W, M = W). The compounds 1-Mo and 1-W rapidly add 1,3,4,5-tetramethylimidazol-2-ylidene (Im-Me4) at the electrophilic germanium center to give the zwitterionic germylidene complexes [Cp(CO)2M═Ge(Im-Me4){C(SiMe3)3}] (2-Mo, M = Mo; 2-W, M = W). The molecular structures of 1-Mo/1-W and 2-Mo/2-W were determined by single-crystal X-ray diffraction studies, and the structural and spectroscopic features of all complexes are discussed.
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