Computational Study of the Reactions of Chlorine Radicals with Atmospheric Organic Compounds Featuring NH-π-Bond (x = 1, 2) Structures.

Among 160 organic NH-containing compounds (x = 1, 2) detected in the atmosphere, there are about 80 species for which the molecules contain p-π conjugate substructures of NH-π-bonds. Here, chlorine radical (·Cl)-initiated reactions for formamide, N-methylformamide, ethenamine, and aniline, as their cases, were investigated by a quantum chemical method [CCSD(T)/aug-cc-pVTZ//MP2/6-31+G(3df,2p)] and kinetics modeling. The calculated overall rate constants are 5.5 × 10, 2.3 × 10, 2.7 × 10, and 1.7 × 10 cm molecule s for formamide, N-methylformamide, ethenamine, and aniline, respectively, and agree well with experimental values for available ones. Importantly, the results show that the reactions of two amides with ·Cl mainly lead to C-center radicals via ·Cl abstracting the -CHO hydrogen of amides. However, both ethenamine + ·Cl and aniline + ·Cl reactions mainly produce delocalized radicals with the radical center on the C-site and N-site via a ·Cl addition and the -NH hydrogen abstraction pathway, respectively. Therefore, this study reveals that reactions of organic NH-containing compounds with ·Cl have various reaction mechanisms, in contrast to our previous understanding that -NH hydrogen abstraction pathways, leading to N-center radicals, are the most favorable. The unveiled reaction mechanisms should be of significance for the risk assessment of atmospheric organic NH-containing compounds and enriching ·Cl chemistry.