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Variational transition‐state theory study of the atmospheric reaction OH + O 3 → HO 2 + O 2
Author(s) -
Ju LiPing,
Han KeLi,
Varandas António J. C.
Publication year - 2007
Publication title -
international journal of chemical kinetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.341
H-Index - 68
eISSN - 1097-4601
pISSN - 0538-8066
DOI - 10.1002/kin.20226
Subject(s) - chemistry , ab initio , transition state theory , reaction rate constant , potential energy surface , quantum tunnelling , ground state , thermodynamics , atomic physics , ab initio quantum chemistry methods , range (aeronautics) , atmospheric temperature range , computational chemistry , quantum mechanics , physics , molecule , kinetics , materials science , organic chemistry , composite material
Abstract We report variational transition‐state theory calculations for the OH + O 3 → HO 2 + O 2 reaction based on the recently reported double many‐body expansion potential energy surface for ground‐state HO 4 [Chem Phys Lett 2000, 331, 474]. The barrier height of 1.884 kcal mol −1 is comparable to the value of 1.77–2.0 kcal mol −1 suggested by experimental measurements, both much smaller than the value of 2.16–5.11 kcal mol −1 predicted by previous ab initio calculations. The calculated rate constant shows good agreement with available experimental results and a previous theoretical dynamics prediction, thus implying that the previous ab initio calculations will significantly underestimate the rate constant. Variational and tunneling effects are found to be negligible over the temperature range 100–2000 K. The O 1 O 2 bond is shown to be spectator like during the reactive process, which confirms a previous theoretical dynamics prediction. © 2007 Wiley Periodicals, Inc. 39: 148–153, 2007

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