On the Role of Hydrogen Atom Transfer (HAT) in Thermal Activation of Methane by MnO+: Entropy vs. Energy

Abstract

Abstract The temperature dependent kinetics and product branching fractions of first-row transition metal oxide cation MnO+ with CH4 and CD4 at temperatures between 200 and 600 K are measured using a selected-ion flow tube apparatus. Likely reaction mechanisms are determined by comparison of temperature dependent kinetics to statistical modeling along calculated reaction coordinates. The data is well-modeled with the reaction proceeding over a rate limiting four-centered transition state leading to an insertion intermediate, similar to reactions of NiO+ and FeO+, and showing characteristics of proton-coupled electron transfer (PCET). However, a more direct pathway traversing a transition state of hydrogen atom transfer (HAT) character to a hydroxyl intermediate is found to possibly be competitive, especially with increasing temperature. While uncertainties in calculated energetics limit quantitative assessment of the role of HAT at thermal energies, it is clear that this mechanism becomes increasingly prevalent in higher energy regimes.