Variational transition state theory rate constants and H/D kinetic isotope effects for CH3 + CH3OCOH reactions

The rate constants and H/D kinetic isotope effect for hydrogen abstraction reactions involving isotopomers of methyl formate by methyl radical are computed employing methods of the variational transition state theory (VTST) with multidimensional tunneling corrections. The energy paths were built with a dual-level method using the moller plesset second-order perturbation theory (MP2) method as the low-level and complete basis set (CBS) extrapolation as the high-level energy method. Benchmark calculations with the CBS_D-T approach give an enthalpy of reaction at 0 K for R1 (-4.5 kcal/mol) and R2 (-4.2 kcal/mol) which are in good agreement with the experiment, that is, -4.0 and - 4.8 kcal/mol. For the reactional paths involving the isotopomers CH₃ + CH₃ OCOH → CH₄ + CH₃ OCO and CH₃ + CH₃ OCOD → CH₃ D + CH₃ OCO, the value of k^H /k^D (T = 455 K) using the canonical VTST/small-curvature tunneling approximation method is 6.7 in close agreement with experimental value (6.2). © 2019 Wiley Periodicals, Inc.