Computational Investigation of the Formation of Peroxide (ROOR) Accretion Products in the OH- and NO3-Initiated Oxidation of α-Pinene

Computational Investigation of the Formation of Peroxide (ROOR) Accretion Products in the OH- and NO3-Initiated Oxidation of α-Pinene

Detalhes bibliográficos
Parent link:Journal of Physical Chemistry A
Vol. 125, iss. 50.— 2021.— [P. 10632-10639]
Outros Autores: Galib H. Hasan, Valiev R. R. Rashid Rinatovich, Vili-Taneli S. Salo, Kurten T. Theo
Resumo:Title screen
The formation of accretion products (“dimers”) from recombination reactions of peroxyl radicals (RO2) 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 3(RO···OR′) clusters formed in the recombination reactions of different diastereomers of the first-generation peroxyl radicals originating in both OH- and NO3-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 106 s-1, and many have rates exceeding 1010 s-1. Especially the latter value demonstrates that accretion product formation via the suggested pathway is a competitive process also for α-pinene-derived RO2 and likely explains the experimentally observed gas-phase formation of C20 compounds in α-pinene oxidation.
Режим доступа: по договору с организацией-держателем ресурса
Idioma:inglês
Publicado em: 2021
Assuntos:
электронный ресурс
труды учёных ТПУ
Acesso em linha:https://doi.org/10.1021/acs.jpca.1c08969
Formato: Recurso Electrónico Capítulo de Livro
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=667867

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