Synthesis, molecular and crystal structure, and stereochemical non-rigidity of (O→Ge)-Bischelate bis[1-(2-oxoperhydroazepinyl)methyl]bromogermanium iodide and triflate

VadV. Negrebetsky,A.A. Korlyukov,S. Yu Bylikin,E.P. Kramarova, YuI. Baukov

Journal of Organometallic Chemistry(2020)

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摘要
Reactions of (O→Ge)-bischelate dibromogermane (L7CH2)2GeBr2 (4c) with trimethyliodosilane and trimethylsilyl triflate proceed with the substitution of only one bromine atom and yield (O→Ge)-bischelate monobromogermanes (L7CH2)2Ge(Br)X (8c, X = I; 9c, X = OTf; LnCH2 = lactamomethyl C,O-chelate ligand; n = lactam ring size). According to X-ray crystal analysis data, triflate 9c is characterized by nearly ionic structure with the monodentate ligand and anion in trans-positions. The configuration of the germanium atom in the complex is intermediate between trigonal bipyramidal and square pyramidal. Quantum chemical calculations show the absence of additional coordinate bonding between the germanium atom and anion.
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关键词
Hypercoordinated germanium compounds,Synthesis,NMR spectroscopy,Dynamic NMR,X-ray crystal analysis,Quantum chemistry calculations
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