| Literature DB >> 27885766 |
Moritz Malischewski1, K Seppelt1.
Abstract
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 (HSO3 F/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. C6 (CH3 )62+ can be obtained through the dissolution of hexamethyl Dewar benzene epoxide in HSO3 F/SbF5 and crystallized as the SbF6- salt upon addition of excess anhydrous hydrogen fluoride. The crystal structure of C6 (CH3 )62+ (SbF6- )2 ⋅HSO3 F confirms the pentagonal pyramidal structure of the dication. The apical carbon is bound to one methyl group (distance 1.479(3) Å) and to the five basal carbon atoms (distances 1.694(2)-1.715(3) Å).Entities:
Keywords: carbocations; electron-deficient compounds; hypercoordination; oxidation; superacids
Year: 2016 PMID: 27885766 DOI: 10.1002/anie.201608795
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336