Abstract
Tunable laser photodissociation spectroscopy and photofragment imaging experiments are employed to investigate the spectroscopy and dissociation dynamics of the Mg(+)(benzene) ion-molecule complex. When excited with ultraviolet radiation, Mg(+)(benzene) photodissociates efficiently, producing both Mg(+) and benzene(+) fragments, with branching ratios depending on the wavelength. The wavelength dependence of these processes are similar, with intense resonances at 330 and 241 nm and weaker features at 290 and 258 nm. Comparisons of the experimental spectra to those predicted by computational chemistry at the TD-DFT level allow assignment of these to metal ion-based (330 and 241 nm), charge-transfer (290 nm), and benzene-based (258 nm) transitions. However, the observation of the benzene cation fragment at all wavelengths, which can only result from charge-transfer, indicates unanticipated excited state dynamics. Spectroscopy experiments are complemented by photofragment imaging to investigate these dynamics. The high kinetic energy release indicates that multiphoton absorption based on the intense atomic resonances is responsible at least in part for the dissociation processes.