Vibrational mode-specificity in the dynamics of the OH− + CH3I multi-channel reaction

Abstract

We report a comprehensive characterization of the vibrational mode-specific dynamics of the OH− + CH3I reaction. Quasi-classical trajectory simulations are performed at four different collision energies on our previously-developed full-dimensional high-level ab initio potential energy surface in order to examine the impact of four different normal-mode excitations in the reactants. Considering the 11 possible pathways of OH− + CH3I, pronounced mode-specificity is observed in reactivity: In general, the excitations of the OH− stretching and CH stretching exert the greatest influence on the channels. For the SN2 and proton-abstraction products, the reactant initial attack angle and the product scattering angle distributions do not show major mode-specific features, except for SN2 at higher collision energies, where forward scattering is promoted by the CI stretching and CH stretching excitations. The post-reaction energy flow is also examined for SN2 and proton abstraction, and it is unveiled that the excess vibrational excitation energies rather transfer into the product vibrational energy because the translational and rotational energy distributions of the products do not represent significant mode-specificity. Moreover, in the course of proton abstraction, the surplus vibrational energy in the OH− reactant mostly remains in the H2O product owing to the prevailing dominance of the direct stripping mechanism.