Computational Investigation of the Formation of Peroxide (ROOR) Accretion Products in the OH- and NO-Initiated Oxidation of α-Pinene.

The formation of accretion products ("dimers") from recombination reactions of peroxyl radicals (RO) is a key step in the gas-phase generation of low-volatility vapors, leading to atmospheric aerosol particles. We have recently demonstrated that this recombination reaction very likely proceeds via an intermediate complex of two alkoxy radicals (RO···OR') and that the accretion product pathway involves an intersystem crossing (ISC) of this complex from the triplet to the singlet surface. However, ISC rates have hitherto not been computed for large and chemically complex RO···OR' systems actually relevant to atmospheric aerosol formation. Here, we carry out systematic conformational sampling and ISC rate calculations on (RO···OR') clusters formed in the recombination reactions of different diastereomers of the first-generation peroxyl radicals originating in both OH- and NO-initiated reactions of α-pinene, a key biogenic hydrocarbon for atmospheric aerosol formation. While we find large differences between the ISC rates of different diastereomer pairs, all systems have ISC rates of at least 10 s, and many have rates exceeding 10 s. Especially the latter value demonstrates that accretion product formation via the suggested pathway is a competitive process also for α-pinene-derived RO and likely explains the experimentally observed gas-phase formation of C compounds in α-pinene oxidation.