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Synthesis and Structural Characterization of Metallogermylenes, Cp-Substituted Germylene, and a Germanium(II)-Borane Adduct from Pyridyl-1-azaallyl Germanium(II) Chloride

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Synthesis_and_Structural_Characterization_of_Metallogermylenes_Cp_Substituted_Germylene_and_a_Germanium_II_Borane_Adduct_from_Pyridyl_1_azaallyl_Germanium_II_Chloride/2480377
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The reaction of [{N­(SiMe3)­C­(Ph)­C­(SiMe3)­(C5H4N-2)}­GeCl] (1) with Na­[M­(η5-C5H5)­(CO)3]·2DME (M = Mo, W) afforded the metallogermylenes [{N­(SiMe3)­C­(Ph)­C­(SiMe3)­(C5H4N-2)}­Ge-M­(η5-C5H5)­(CO)3] (M = Mo (2), W (3)). Compounds 2 and 3 have been characterized by X-ray crystallography and NMR and IR spectroscopy. Structural analyses of compounds 2 and 3 are consistent with the presence of lone-pair electrons at the germanium­(II) center. The Ge–Mo and Ge–W bond distances of 2.875(1) and 2.852(1) Å are consistent with Ge–metal single bonds. The chlorogermylene 1 was also used in the synthesis of a substituted germylene, [{N­(SiMe3)­C­(Ph)­C­(SiMe3)­(C5H4N-2)}­Ge­(η1-C5H5)] (4), by reaction with sodium cyclopentadienylide. The reaction of compound 1 with tris­(pentafluorophenyl)­borane led to the formation of a Lewis acid–base adduct, [{N­(SiMe3)­C­(Ph)­C­(SiMe3)­(C5H4N-2)}­Ge­(Cl)→B­(C6F5)3] (5).
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2016-02-20
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