Journal
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS
Volume 49, Issue 5, Pages 339-353Publisher
WILEY
DOI: 10.1002/kin.21079
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Funding
- University Grants Commission (UGC), Government of India
- UGC
- Department of Science and Technology, India
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The reaction of nitrosodimethylamine, nitrosoazetidine, nitrosopyrrolidine, and nitrosopiperidine with the hydroxyl radical has been studied using electronic structure calculations in gas and aqueous phases. The rate constant was calculated using variational transition state theory. The reactions are initiated by H-atom abstraction from the alpha C -H group of nitrosamines and leads to the formation of alkyl radical intermediate. In the subsequent reactions, the initially formed alkyl radical intermediate reacts with O-2 forming a peroxy radical. The reaction of peroxy radical with other atmospheric oxidants, such as HO2 and NO radicals, is studied. The structures of the reactive species were optimized by using the density functional theory methods, such as M06-2X, MPW1K, and BHandHLYP, and hybrid methods G3B3. The single-point energy calculations were also performed at CCSD(T)/6-311+ G(d, p)//M062X/6-311+ G(d, p) level. The calculated thermodynamical parameters show that the reactions corresponding to the formation of intermediates and products are highly exothermic. We have calculated the rate constant for the initial H-atom abstraction and subsequent favorable secondary reactions using canonical variational transition state theory over the temperature range of 150-400 K. The calculated rate constant for initial H-atom abstraction reaction is similar to 3 x 10(-12) cm(3) molecule(-1) s(-1) and is in agreement with the previous experimental results. The calculated thermochemical data and rate constants show that the reaction profile and kinetics of the reactions are less dependent on the number of methyl groups present in the nitrosoamines. Furthermore, it has been found that the atmospheric lifetime of nitrosaminesis around 5 days in the normal atmospheric OH concentration. (C) 2017 Wiley Periodicals, Inc.
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