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000889018 1001_ $$0P:(DE-Juel1)167140$$aVereecken, Luc$$b0$$eCorresponding author$$ufzj
000889018 1112_ $$aEGU General Assembly$$cvirtual$$d2020-05-04 - 2020-05-08$$wAustria
000889018 245__ $$aStructure-activity relationships for unimolecular reactions of peroxy radicals, RO2, at atmospheric temperatures
000889018 260__ $$c2020
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000889018 520__ $$aThe oxidation of most organic matter emitted to the atmosphere proceeds by radical reaction steps, where peroxy radicals, ROO•, are critical intermediates formed by addition of O2 molecules to carbon-based radicals. The chemistry of these RO2 radicals in high-NOx conditions is well-known, forming alkoxy radicals and NO2. In low-NOx and pristine conditions, the RO2 radicals react with HO2 and other R'O2 radicals, but can have a sufficiently long lifetime to also undergo unimolecular reactions. Hydrogen atom migration, forming a hydroperoxide (-OOH) and a new peroxy radical site after addition of an additional O2 on the newly formed radical site, has been studied extensively in some compounds, such as isoprene where it was shown to be the a critical step in OH radical regeneration. RO2 ring closure reactions have likewise been studied, where for β-pinene it has been shown to be a critical step governing the yield of the decomposition products such as acetone and nopinone.Despite the interest in RO2 unimolecular reactions, and the potential impact on atmospheric chemistry, no widely applicable structure-activity relationships (SARs) have been proposed to allow systematic incorporation of such unimolecular reactions in gas phase atmospheric kinetic models. In this work, we present a series of systematic theoretical predictions on the site-specific rate coefficients for such reactions for a wide range of molecular substitutions. Combined with extensive literature data this allows for the formulation of a SAR for RO2 unimolecular reactions, covering aliphatic, branched, and unsaturated RO2 with oxo, hydroxy, hydroperoxy, nitrate, carboxylic acid, and ether substitutions.The predictions are compared to experimental and theoretical data, including multi-functionalized species. Though some molecular classes are well represented in the training set (e.g. aliphatic RO2), other classes have little data available and additional work is needed to enhance and validate the reliability of the SAR. Direct experimental data is scarce for all RO2 classes. The fastest H-migrations are found to be for unsaturated RO2, with the double bond outside the H-migration TS ring. Ring closure of unsaturated RO2 are likewise fast if the product radical carbon is exocyclic to the newly formed peroxide ring.
000889018 536__ $$0G:(DE-HGF)POF3-243$$a243 - Tropospheric trace substances and their transformation processes (POF3-243)$$cPOF3-243$$fPOF III$$x0
000889018 7001_ $$0P:(DE-HGF)0$$aVu, G. H. T.$$b1
000889018 7001_ $$0P:(DE-HGF)0$$aNguyen, H. M. T.$$b2
000889018 8564_ $$uhttps://juser.fz-juelich.de/record/889018/files/Vereecken_EGU_2020_RO2_SARs.pdf$$yOpenAccess
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