摘要
Photodissociation of indole at 193 and 248 nm under collision-free conditions has been studied in separate experiments using multimass ion imaging techniques. H atom elimination was found to be the only dissociation channel at both wavelengths. The photofragment translational energy distribution obtained at 193 nm contains a fast and a slow component. Fifty-four percent of indole following the 193 nm photoexcitation dissociate from electronically excited state, resulting in the fast component. The rest of 46% indole dissociate through the ground electronic state, giving rise to the slow component. A dissociation rate of 6× 105 s-1, corresponding to the dissociation from the ground electronic state, was determined. Similar two-component translational energy distribution was observed at 248 nm. However, more than 80% of indole dissociate from electronically excited state after the absorption of 248 nm photons. A comparison with the potential energy surfaces from the ab initio calculation has been made. © 2005 American Institute of Physics.