Theoretical Insight into the Reaction Mechanism and Kinetics for the Criegee Intermediate of -PhCHOO with SO.

In this study, the density functional theory (DFT) and CCSD(T) method have been performed to gain insight into the possible products and detailed reaction mechanism of the Criegee intermediate (CI) of -PhCHOO with SO for the first time. The potential energy surfaces (PESs) have been depicted at the UCCSD(T)/6-311++G(d,p)//UB3LYP/6-311++G(d,p) levels of theory with ZPE correction. Two different five-membered ring adducts, viz., PhCHOOS(O)O (IM1) and PhCHOOS(O)O (IM2) have been found in the entrance of reaction channels. Both direct and indirect reaction pathways from IM1 and IM2 have been considered for the title reaction. Our calculations show that the formation of PhCHO+SO (P1) via indirect reaction pathways from IM1 is predominant in all the pathways, and the production of P1 via direct dissociation pathway of IM1 and indirect reaction pathways of IM2 cannot be neglected. Moreover, PhCOOH+SO (P2) initiated from IM2 is identified as the minor product. According to the kinetic calculation, the total rate constant for the -PhCHOO+SO reaction is estimated to be 6.98 × 10 cm·molecule·s at 298 K.