4.5 Article

Germa-closo-dodecaborate: An Ambident and Flexible Coordinating Ligand

期刊

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
卷 -, 期 2, 页码 235-240

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201000857

关键词

Germanium; Germylenes; Boranes; Coordination chemistry; Iron; Ruthenium

资金

  1. Deutsche Forschungsgemeinschaft (DFG)

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By following a simple one-pot procedure that starts with FeBr2 and triphos [MeC(CH2PPh2)(3)] or the dimer [Ru-2(mu-Cl)(3)(triphos)(2)]Cl in reaction with the nucleophile [Bu2MeN](2)-[GeB11R11] in acetonitrile, the zwitterionic acetonitrile adducts [M(GeB11H11)(triphos)(MeCN)(2)] [M = Fe (1), M = Ru (2)] were isolated in good yield. By means of a facile eta(1)(Ge) to eta(3)(B-H) rearrangement, 1 and 2 can he converted into [M(GeB11H11)(triphos)) [M = Fe (3), M = Ru (4)]. The nucleophilicity of the germanium cluster vertex in the iron derivative 3 is high enough to react with [Mo(CO)(5)(thf)] to give the bimetallic complex [(triphos)Fe(GeB11H11)(MoCO)(5)] (5), which contains an ambident coordinating germaborate moiety. The new compounds have been characterized by single-crystal X-ray diffraction and elemental analysis. Soluble complexes were also investigated by H-1, B-11 and P-31 NMR spectroscopy in solution. In the case of the insoluble complex 1, solid-state P-31 NMR spectroscopy was carried out.

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