Related Experiment Video
Updated: Mar 11, 2026

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
Crystal Structure Determination of the Pentagonal-Pyramidal Hexamethylbenzene Dication C6 (CH3 )62
Moritz Malischewski1, K Seppelt1
1Freie Universität Berlin, Institut für Chemie und Biochemie-Anorganische Chemie, Fabeckstraße 34-36, 14195, Berlin, Germany.
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).
More Related Videos
Related Concept Videos
Structure of Benzene: Molecular Orbital Model
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Radicals: Electronic Structure and Geometry
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...

