Single Solvent Molecules Induce Dual Nucleophiles in Gas-Phase Ion–Molecule Nucleophilic Substitution Reactions
Chongyang Zhao, Xinyou Ma, Xiangyu Wu, Ditte Thomsen, Veronica M. Bierbaum, Jing Xie
Abstract
Direct dynamics simulation of singly hydrated peroxide ion reacting with CH3Cl reveals a new product channel that forms CH3OH + Cl– + HOOH, besides the traditional channel that forms CH3OOH + Cl– + H2O. This finding shows that singly hydrated peroxide ion behaves as a dual nucleophile through proton transfer between HOO–(H2O) and HO–(HOOH). Trajectory analysis attributes the occurrence of the thermodynamically and kinetically unfavored HO–-induced pathway to the entrance channel dynamics, where extensive proton transfer occurs within the deep well of the prereaction complex. This study represents the first example of a single solvent molecule altering the nucleophile in a gas-phase ion–molecule nucleophilic substitution reaction, in addition to reducing the reactivity and affecting the dynamics, signifying the importance of dynamical effects of solvent molecules.