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M. Perakyla and T. A. Pakkanen, “Ab Initio Molecular Orbital Study on Reactivity of Phenol, Biphenyl, Benzoate and p-Hydroxybenzoate in the ·OH Addition Reaction and Stability of the Corresponding ·H and ·OH Cyclohexadienyl Adducts,” Journal of the Chemical Society-Perkin Transactions 2, No. 7, 1995, pp. 1405-1410. doi:10.1039/P29950001405

has been cited by the following article:

• TITLE: Density Functional Theory Studies on the Addition and Abstraction Reactions of OH Radical with Benzoate Anion

  AUTHORS: Nobuaki Tanaka, Shigeo Itoh

  KEYWORDS: DFT Calculation; Benzoate Anion; H-Atom Abstraction; OH Addition; Transition State Theory

  JOURNAL NAME: Open Journal of Physical Chemistry, Vol.3 No.1, February 19, 2013

  ABSTRACT: The addition and abstraction reactions of OH radical with benzoate anion are investigated by density functional theory calculations that include solvent effects using UB3LYP, UCAM-B3LYP, UmPW1PW91 and UM06-2X functionals with the 6-311++G(2d,2p) basis set. Geometry optimizations of the reactants, products and transition state species are performed for the possible reaction paths. For the addition reactions, those targeting the ipso-, ortho-, meta- and para-carbons are predicted to be exoergic. The H-atom abstraction reactions from ortho, meta and para positions are also predicted to be exoergic. On the basis of the rate constants calculated by means of the transition state theory, the H-atom abstraction reaction from the ortho position is determined to be the favored path followed by the ortho OH addition reaction.