| Literature DB >> 22522255 |
Liangchun Li1, Tomohide Fukawa, Tsukasa Matsuo, Daisuke Hashizume, Hiroyuki Fueno, Kazuyoshi Tanaka, Kohei Tamao.
Abstract
The carbon-oxygen double bond of ketones (R(2)C=O) makes them among the most important organic compounds, but their homologues, heavy ketones with an E=O double bond (E = Si, Ge, Sn or Pb), had not been isolated as stable compounds. Their unavailability as monomeric molecules is ascribed to their high tendency for intermolecular oligomerization or polymerization via opening of the E=O double bond. Can such an intermolecular process be inhibited by bulky protecting groups? We now report that it can, with the first isolation of a monomeric germanium ketone analogue (Eind)(2)Ge=O (Eind = 1,1,3,3,5,5,7,7-octaethyl-s-hydrindacen-4-yl), stabilized by appropriately designed bulky Eind groups, with a planar tricoordinate germanium atom. Computational studies and chemical reactions suggest the Ge=O double bond is highly polarized with a contribution of a charge-separated form (Eind)(2)Ge(+)-O(-). The germanone thus exhibits unique reactivities that are not observed with ordinary ketones, including the spontaneous trapping of CO(2) gas to provide a cyclic addition product.Entities:
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Year: 2012 PMID: 22522255 DOI: 10.1038/nchem.1305
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427