Effect of hydrogen bonding on the nonradiative properties of dibenzofuran.

Abstract

Femtosecond time-resolved transient absorption spectroscopy is employed to investigate the ultrafast excited-state dynamics from the S2 state of dibenzofuran and the hydrogen bonding effect in protic and aprotic solvents. Following the excitation with 266 nm, the initial population on the S2 state couples to the S1 state via internal conversion on tens of picoseconds. Afterwards, vibrational energy relaxation (VER) with dozens of picoseconds is determined in all solvents and strongly depended on the polarities of aprotic solvents. And the rising species related with the hydrogen-bonded intermediate S⁎ state are observed just in ethanol and methanol with the higher Kamlet parameter α. Subsequently, the intersystem crossing from the S1 state to the triplet manifold is a main deactivation pathway with the decay time of ≫ns. All the relaxation processes exhibit solvent dependence, indicating that hydrogen bonding interaction between solute and solvent enhances VER and significantly influences on the excited state dynamics of dibenzofuran.