Dissociative photodetachment of H3O2-: a full-dimensional quantum dynamics study.

Abstract

The transition state is a central concept of chemistry. Photoelectron-photofragment coincidence (PPC) spectroscopy has been proven as an attractive method to study the transition state dynamics. Within a state-of-the-art full-dimensional quantum mechanical model, the dissociative photodetachment dynamics of H3O2- is investigated on accurate anion and neutral potential energy surfaces. The calculated PPC spectrum of H3O2- agrees well with the experimental measurement. The dissociative product OH is exclusively populated on the ground vibrational state, implying the character of the spectator bond. In contrast, the product H2O is predominantly populated in the ground and fundamental states of the symmetric and antisymmetric stretching modes, which is caused by the strong coupling between the antisymmetric motion of the transferred H atom in the transient intermediate [H3O2]* and both stretching modes of the product H2O.