Dynamics of the F− + CH3Cl → Cl− + CH3F SN2 reaction on a chemically accurate potential energy surface

Though bimolecular nucleophilic substitution (S N 2) reactions play a fundamental role in chemistry, chemically accurate full-dimensional global analytical potential energy surfaces (PESs) have not been developed for these systems. These PESs govern the motion of the atoms in a chemical reaction; thus, the knowledge of the PES is essential to study the dynamics and atomic-level mechanisms. Here, we report a full-dimensional ab initio PES for the F − + CH 3 Cl → Cl − + CH 3 F reaction, the PES has an estimated average accuracy of about 0.5 kcal mol −1 . Quasiclassical trajectories on this PES reveal that the direct rebound mechanism dominates at high collision energies, whereas the reaction is mainly indirect at low collision energies, where the formation of long-lived hydrogen-bonded and C 3v ion-dipole entrance-channel complexes play a major role in the dynamics. A direct stripping mechanism is also found at large impact parameters resulting in significant forward scattering, whereas the direct rebound mechanism scatters towards backward directions. At high collision energies the reaction can be controlled by orienting the reactants into a reactive F − + H 3 CCl orientation, whereas at low collision energies the initial orientation is not always maintained, because the long-range ion-dipole interactions efficiently steer the reactants into a reactive orientation even if F − initially approaches the non-reactive side of CH 3 Cl. Mode-specific vibrational distributions show that the reaction produces vibrationally hot CH 3 F molecules with excited CF stretching, especially at low collision energies. Quasiclassical trajectory calculations are performed for the F − + CH 3 Cl S N 2 reaction using a new full-dimensional ab initio analytical potential energy surface.