A recent report on the crystal structure of the pentagonal-pyramidal hexamethylbenzene dication C6 (CH3 )62+ by Malischewski and Seppelt [Angew. Chem. Int. Ed. 2017, 56, 368] confirmed the structural proposal made in the first report of this compound in 1973 by Hogeveen and Kwant [Tetrahedron Lett. 1973, 14, 1665]. The widespread attention that this compound quickly gained led us to reinvestigate its electronic structure. On the basis of intrinsic bond orbital analysis, effective oxidation state analysis, ring current analysis, and comparison with well-established coordination complexes, it is demonstrated that the central carbon atom behaves like a transition metal. The central (apical) carbon atom, although best described as a highly Lewis-acidic carbon atom coordinated with an anionic cyclopentadienyl ligand, is also capable of acting as an electron-pair donor to a formal CH3+ group. The different roles of coordination chemistry are discussed.
Keywords: bond theory; carbon; coordination modes; density functional calculations; donor-acceptor systems.
© 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.