Selective deuteration illuminates the importance of tunneling in the unimolecular decay of Criegee intermediates to hydroxyl radical products

Abstract

Significance Ozonolysis of volatile biogenic and anthropogenic alkenes is a significant source of hydroxyl radicals, a key oxidant in the troposphere. A critical step in the generation of hydroxyl radicals is a hydrogen-atom transfer reaction involving a carbonyl oxide species, known as the Criegee intermediate. In this study, experiment and statistical theory reveal that selective deuteration of a Criegee intermediate results in deuterium atom transfer and slows the release of hydroxyl- d radicals. A large kinetic isotope effect is found at energies near the classical barrier to reaction and under thermal conditions relevant to the atmosphere. This demonstrates that quantum mechanical tunneling significantly enhances the rate of production of hydroxyl radicals in alkene ozonolysis reactions under atmospheric conditions.