Ephemeral collision complexes mediate chemically termolecular transformations that affect system chemistry
Author(s) -
Michael P. Burke,
Stephen J. Klippenstein
Publication year - 2017
Publication title -
nature chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.996
H-Index - 232
eISSN - 1755-4349
pISSN - 1755-4330
DOI - 10.1038/nchem.2842
Subject(s) - chemistry , chemical reaction , radical , collision , chemical physics , ephemeral key , molecule , kinetic energy , collision theory , reactivity (psychology) , computational chemistry , reaction dynamics , photochemistry , organic chemistry , physics , medicine , alternative medicine , computer security , algorithm , quantum mechanics , pathology , computer science
Termolecular association reactions involve ephemeral collision complexes-formed from the collision of two molecules-that collide with a third and chemically inert 'bath gas' molecule that simply transfers energy to/from the complex. These collision complexes are generally not thought to react chemically on collision with a third molecule in the gas-phase systems of combustion and planetary atmospheres. Such 'chemically termolecular' reactions, in which all three molecules are involved in bond making and/or breaking, were hypothesized long ago in studies establishing radical chain branching mechanisms, but were later concluded to be unimportant. Here, with data from ab initio master equation and kinetic-transport simulations, we reveal that reactions of H + O 2 collision complexes with other radicals constitute major kinetic pathways under common combustion situations. These reactions are also found to influence flame propagation speeds, a common measure of global reactivity. Analogous chemically termolecular reactions mediated by ephemeral collision complexes are probably of significance in various combustion and planetary environments.
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