Insertion and abstraction pathways in the reaction O(1D2)+H2→OH+H

Rigorous quantum dynamical calculations have been performed on the ground 1(1)A' and first ex cited 1(1)A electronic states of the title reaction, employing the most accurate potential energy surfaces available. Product rovibrational quantum start populations and rotational angular momentum alignment parameters are reported, and are compared with new experimental, and quasiclassical trajectory calculated results. The quantum calculations agree quantitatively with experiment. and reveal unequivocally that the 1(1)A excited state participates in the reaction.