4.8 Article

Crystal Structure Determination of the Pentagonal-Pyramidal Hexamethylbenzene Dication C6(CH3)62+

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 56, 期 1, 页码 368-370

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201608795

关键词

carbocations; electron-deficient compounds; hypercoordination; oxidation; superacids

资金

  1. Free University Berlin
  2. Verband der Chemischen Industrie (VCI)
  3. Deutsche Forschungsgemeinschaft [GRK 1582]

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In contrast to the well-known 2-norbornyl cation, the structure of which was a matter of long debate until its pentacoordinated nature was recently proven by an X-ray structure, the pentagonal-pyramidal dication of hexamethylbenzene has received considerably less attention. This species was first prepared by Hogeveen in 1973 at low temperatures in magic acid (HSO3F/SbF5), for which he proposed a non-classical structure (containing a hexacoordinated carbon) based on NMR spectroscopy and reactivity studies, but no X-ray crystal structure has been reported. C-6(CH3)(6)(2+) can be obtained through the dissolution of hexamethyl Dewar benzene epoxide in HSO3F/SbF5 and crystallized as the SbF6- salt upon addition of excess anhydrous hydrogen fluoride. The crystal structure of C-6(CH3)(6)(2+) (SbF6-)(2)center dot HSO3F confirms the pentagonal pyramidal structure of the dication. The apical carbon is bound to one methyl group (distance 1.479(3) angstrom) and to the five basal carbon atoms (distances 1.694(2)-1.715(3) angstrom).

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