文摘
The ring-opening and ring-closure reactions of a photochromic indolylfulgimide are investigated withfemtosecond vibrational spectroscopy. Spectral signatures due to excited-state decay and vibrational coolingare seen in the mid-IR region. For the ring-opening reaction triggered with visible pulses, a lifetime of theexcited electronic state of 4 ps was obtained in polar solution. In a nonpolar solvent, this time constant isreduced to 2 ps. The ring-closure reaction induced with UV pulses displays an excited-state lifetime and thusa building of the photoproduct of roughly 0.5 ps. For all processes, the subsequent cooling occurs on a 15-pstime scale lasting up to ~50 ps. The time-resolved IR measurements do not support the existence of anylong-living intermediate states.