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Title: Mode specificity in the OH + CHD{sub 3} reaction: Reduced-dimensional quantum and quasi-classical studies on an ab initio based full-dimensional potential energy surface

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4947252· OSTI ID:22657934
;  [1];  [2];  [3];  [4]
  1. Key Laboratory of Magnetic Resonance in Biological Systems, National Center for Magnetic Resonance in Wuhan, State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences, Wuhan 430071 (China)
  2. Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371 (Singapore)
  3. School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China)
  4. Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, New Mexico 87131 (United States)

An initial state selected time-dependent wave packet method is applied to study the dynamics of the OH + CHD{sub 3} reaction with a six-dimensional model on a newly developed full-dimensional ab initio potential energy surface (PES). This quantum dynamical (QD) study is complemented by full-dimensional quasi-classical trajectory (QCT) calculations on the same PES. The QD results indicate that both translational energy and the excitation of the CH stretching mode significantly promote the reaction while the excitation of the umbrella mode has a negligible effect on the reactivity. For this early barrier reaction, interestingly, the CH stretching mode is more effective than translational energy in promoting the reaction except at very low collision energies. These QD observations are supported by QCT results. The higher efficacy of the CH stretching model in promoting this early barrier reaction is inconsistent with the prediction of the naively extended Polanyi’s rules, but can be rationalized by the recently proposed sudden vector projection model.

OSTI ID:
22657934
Journal Information:
Journal of Chemical Physics, Vol. 144, Issue 16; Other Information: (c) 2016 Author(s); Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-9606
Country of Publication:
United States
Language:
English

Cited By (5)

Thermal rate coefficients and kinetic isotope effects of the reaction HO + H2O → H2O + OH journal August 2019
Tracking the energy flow in the hydrogen exchange reaction OH + H 2 O → H 2 O + OH journal January 2018
A critical comparison of neural network potentials for molecular reaction dynamics with exact permutation symmetry journal January 2019
Mode-specific quantum dynamics and kinetics of the hydrogen abstraction reaction OH + H 2 O → H 2 O + OH journal January 2019
Potential energy surfaces from high fidelity fitting of ab initio points: the permutation invariant polynomial - neural network approach journal July 2016