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In this work, the induced magnetic field is analyzed for a series of substituted benzenes dications with formula C6R62+ (R=I, At, SeH, SeCH3, TeH, TeCH3), presumably exhibiting concentric aromaticity. Previous studies concluded that in the carbon skeleton, just π‐electrons are delocalized. However, our results support that both the σ‐ and π‐electrons are delocalized in the carbon skeleton, combined with a σ‐delocalization in the external ring. The role of the relativistic effects in these dications is discussed in detail. [ABSTRACT FROM AUTHOR]

The authors discuss the role of the σ and π contributions to the induced magnetic field for simple hydrocarbons containing a double or a triple bond, as well as for benzene and cyclobutadiene. While the magnetic field induced by the σ electrons is short-ranged, the π system is responsible for the formation of long-range cones. These cones influence the chemical shift of atoms by additional shielding (for aromatic) or deshielding (for antiaromatic molecules) contributions. While the hydrogen atoms of benzene are found to lie within the deshielded region of the magnetic field induced by the π electrons, they are shielded by the total induced magnetic field. The induced magnetic field of the π electrons support Pople's model on the basis of first-principles calculations. © 2006 Wiley Periodicals, Inc. J Comput Chem 2007 [ABSTRACT FROM AUTHOR]