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Thermal Activation of Methane by MgO$^+$: Temperature Dependent Kinetics, Reactive Molecular Dynamics Simulations and Statistical Modeling (2002.02151v1)

Published 6 Feb 2020 in physics.chem-ph

Abstract: The kinetics of MgO$+$ + CH$_4$ was studied experimentally using the variable ion source, temperature adjustable selected ion flow tube (VISTA-SIFT) apparatus from 300 $-$ 600 K and computationally by running and analyzing reactive atomistic simulations. Rates and product branching fractions were determined as a function of temperature. The reaction proceeded with a rate of $k = 5.9 \pm 1.5 10{-10}(T/300 $ K$){-0.5 \pm 0.2}$ cm$3$ s${-1}$. MgOH$+$ was the dominant product at all temperatures, but Mg$+$, the co-product of oxygen-atom transfer to form methanol, was observed with a product branching fraction of $0.08 \pm 0.03 (T / 300 $ K$){-0.8 \pm 0.7}$. Reactive molecular dynamics simulations using a reactive force field, as well as a neural network yield rate coefficients about one order of magnitude lower. This underestimation of the rates is traced back to the multireference character of the transition state [MgOCH$_4$]$+$. Statistical modeling of the temperature-dependent kinetics provides further insight into the reactive potential surface. The rate limiting step was found to be consistent with a four-centered activation of the C-H bond, consistent with previous calculations. The product branching was modeled as a competition between dissociation of an insertion intermediate directly after the rate-limiting transition state, and traversing a transition state corresponding to a methyl migration leading to a Mg-CH$_3$OH$+$ complex, though only if this transition state is stabilized significantly relative to the dissociated MgOH$+$ + CH$_3$ product channel. An alternative non-statistical mechanism is discussed, whereby a post-transition state bifurcation in the potential surface could allow the reaction to proceed directly from the four-centered TS to the Mg-CH$_3$OH$+$ complex thereby allowing a more robust competition between the product channels.

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