On a possible growth mechanism for polycyclic aromatic hydrocarbon di-cations: C(7)H(6)(2+) + C(2)H(2)

Chemistry. 2007;13(10):2893-902. doi: 10.1002/chem.200600913.

Abstract

The mechanism of the bond-forming reaction between C(7)H(6) (2+) and C(2)H(2) to yield C(9) entities has been investigated by density functional theory calculations with close comparison with experimental data. It is shown that the reaction produces the C(9)H(6) (2+) and C(9)H(7) (2+) di-cations with geometries most probably derived from the indene skeleton. In comparison, the formation of linear structures of di-cations is much more energy-demanding and therefore appears improbable.