New Channels in the Reaction Mechanism of the Atmospheric Oxidation of Toluene

Abstract

Two different theoretical approaches are used to study the OH radical attack on toluene: the Møller−Plesset perturbation theory and the B3LYP density functional method. The critical points of the potential energy surface for the OH addition to toluene are determined, and rate−equilibrium relationships are discussed. A stable structure corresponding to a prereactive complex which is formed when the OH radical is at about 2.5 Å from toluene is obtained. The existence of this loosely bound system is necessary to explain the experimentally observed negative activation energy. The geometry of transition states and products are determined for addition at different positions in the ring, including the ipso position, which has not been considered in previous works. Energy results at the MP4 and coupled cluster levels calculated at the optimized MP2 and B3LYP geometries confirm that the ipso adduct is more stable than the ortho adduct by about 0.5 kcal/mol. Several routes are proposed for the subsequent reactions of the ipso adduct, which could explain the very high yield of o-cresol with respect to the other cresol isomers.