Abstract
The photophysics of aminoperylene (APe) in various solvents, including a room-temperature ionic liquid, has been investigated by steady-state and femtosecond transient absorption spectroscopies. The ultrafast excited-state dynamics originates from the solvation of the polar S-1 state and not from a transition from a locally-excited to a charge-transfer state, as found with perylene-dimethylaniline. Addition of acid yields the protonated form APeH(+), which exhibits similar photophysical properties than perylene, due to the suppression of the charge-transfer character of the S-0-S-1 transition. However, excited-state proton transfer, resulting to the formation of APe in the S-1 state, is observed in methanol. (C) 2010 Elsevier B.V. All rights reserved.