| Abstract |
The microwave-assisted synthesis of tryptanthrin from indigo in mild oxidation conditions, and a comprehensive study of the excited state properties of this compound in a variety of solvents with different polarity and viscosity values at room and low temperatures are reported. In contrast with indigo, emission of the triplet state of tryptanthrin is observed with a very efficient singlet oxygen sensitization quantum yield, indicating that the triplet state is efficiently populated. From time-resolved fluorescence and femtosecond transient absorption data, further supported with time-dependent density functional theory (TDDFT) calculations, two species, with S-1 states with locally excited (LE) of pi,pi* nature and a charge transfer (CT) of Pi,pi* characteristics, originated from an initially populated Frank-Condon S-2 state (pi,pi*), are observed. The two electronically independent species are energetically nearly degenerate and inter-conversion is predicted (and rate constants determined) to occur between LE (S-1) and CT (S-1) species. Due to the low value of the fluorescence quantum yield (similar to 10(-3)) and high triplet state yield (phi(T)>=phi(Delta)), the high stability of this compound is associated to the high efficiency of the radiationless deactivation processes which involve the formation of the CT state which efficiently converts, through S-1 similar to similar to> T-n intersystem crossing, to the T-1 triplet state. |
