Hydroxyl radical initiated oxidation of s-triazine: Hydrogen abstraction is faster than hydroxyl addition

Document Type

Article

Publication Date

7-30-2009

Abstract

Reaction with the hydroxyl radical (HȮ) is the primary removal mechanism for organic compounds in the atmosphere, and an important process in combustion. Molecules with unsaturated carbon sites are thought to react with HȮ via a rapid addition mechanism, with little or no barrier; this results in short lifetimes relative to the saturated alkanes, which undergo slower abstraction reactions. Computational chemistry and reaction rate theory are used in this study to investigate the s-triazine + HȮ reaction. We report that HȮ addition at a carbon ring site proceeds with the largest known barrier for addition to an unsaturated carbon (9.8 kcal mol -1 at the G3X level of theory). Abstraction of a hydrogen atom in s-triazine by HȮ, forming the s-triazinyl radical + H 2O, proceeds with a barrier of only 3.3 kcal mol -1, and this process dominates over HȮ addition. Our results are in contrast to those for the analogous reactions in benzene, where the abstraction reaction to phenyl + H 2O is slower than the HȮ addition, which forms a radical adduct that can further react with 02 or dissociate to phenol + Ḣ. The lifetime of s-triazine toward the hydroxyl radical in the troposphere is estimated at 6.4 years, potentially making it a long-lived pollutant. The aromatic s-triazine (1,3,5-triazine) molecule is a structural feature in herbicides such as atrazine and is a decomposition product of the common energetic material cyclotrimethylenetrinitramine (RDX). While the abstraction reaction dominates for the parent s-triazine, the addition mechanism may be of importance in the atmospheric degradation of substituted triazines, like atrazine, where ring H atoms are not available for abstraction. The high-barrier addition mechanism forms an activated hydroxy-triazinyl adduct which predominantly dissociates to 2-hydroxy-1,3,5-triazine (OST) + Ḣ. This OST species is a known intermediate of RDX decomposition. Results are also presented for isomerization of the less-stable 1,3,5-triazine-N-oxide OST species (which may form via unimolecular pathways in the liquid-phase decomposition of RDX) to 2-hydroxy-1,3,5-triazine. A reaction mechanism is proposed for further oxidation of the s-triazinyl radical, where an OST isomer is also a potential product. © 2009 American Chemical Society.

Identifier

67651176038 (Scopus)

Publication Title

Journal of Physical Chemistry A

External Full Text Location

https://doi.org/10.1021/jp904156r

ISSN

10895639

PubMed ID

19572687

First Page

8596

Last Page

8606

Issue

30

Volume

113

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