Kinetics and mechanism of the OH + C6H6 reaction: A detailed analysis with first-principles calculations

I. V. Tokmakov, Ming-Chang Lin*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

85 Scopus citations

Abstract

The capability of various high-level DFT and ab initio MO methods to predict molecular and energetic parameters has been critically tested for the OH radical reaction with benzene. G3 theory proved to be the most accurate in estimating reaction barriers and enthalpies. For the first time, the molecular structure, stabilization energy and nature of the bonding interactions of the [C6H6⋯OH] prereaction complex have been characterized. Accurate thermochemistry for major reaction channels was established by making combined use of experimental and theoretical parameters. A multistep kinetic model for the OH-addition channel was proposed, and the effects of T, P, and reaction time on the apparent rate constants were evaluated by weak collision master equation/RRKM analysis. Available experimental kinetic data for all relevant reactions are critically analyzed and correlated with modeled effective rate constants.

Original languageEnglish
Pages (from-to)11309-11326
Number of pages18
JournalJournal of Physical Chemistry A
Volume106
Issue number46
DOIs
StatePublished - 21 Nov 2002

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