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Theoretical study on the reaction mechanism of the methyl radical with nitrogen oxides
Author(s) -
Zhang JiaXu,
Liu JingYao,
Li ZeSheng,
Sun ChiaChung
Publication year - 2005
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.20217
Subject(s) - chemistry , isomerization , singlet state , transition state , adduct , potential energy surface , reaction mechanism , photochemistry , bond cleavage , computational chemistry , nitrogen , molecule , medicinal chemistry , catalysis , organic chemistry , excited state , atomic physics , physics
The radical‐molecule reaction mechanism of CH 3 with NO x ( x = 1, 2) has been explored theoretically at the B3LYP/6‐311G(d,p) and MC‐QCISD (single‐point) levels of theory. For the singlet potential energy surface (PES) of the CH 3 + NO 2 reaction, it is found that the carbon to middle nitrogen attack between CH 3 and NO 2 can form energy‐rich adduct a (H 3 CNO 2 ) with no barrier followed by isomerization to b 1 (CH 3 ONO‐ trans ), which can easily convert to b 2 (CH 3 ONO‐ cis ). Subsequently, starting from b (b 1 , b 2 ), the most feasible pathway is the direct NO bond cleavage of b (b 1 , b 2 ) leading to P 1 (CH 3 O + NO) or the 1,3‐H‐shift and NO bond rupture of b 1 to form P 2 (CH 2 O + HNO), both of which may have comparable contribution to the reaction CH 3 + NO 2 . Much less competitively, b 2 can take a concerted H‐shift and NO bond cleavage to form product P 3 (CH 2 O + HON). Because the intermediates and transition states involved in the above three channels are all lower than the reactants in energy, the CH 3 + NO 2 reaction is expected to be rapid, as is consistent with the experimental measurement in quality. For the singlet PES of the CH 3 + NO reaction, the major product is found to be P 1 (HCN + H 2 O), whereas the minor products are P 2 (HNCO + H 2 ) and P 3 (HNC +H 2 O). The CH 3 + NO reaction is predicted to be only of significance at high temperatures because the transition states involved in the most feasible pathways lie almost above the reactants. Compared with the singlet pathways, the triplet pathways may have less contributions to both reactions. The present study may be helpful for further experimental investigation of the title reactions. © 2005 Wiley Periodicals, Inc. J Comput Chem 26: 807–817, 2005