Triarylpyrylium cations bearing an electron donating group an studied
in solution by two pump-probe techniques with picosecond and nanosecon
d resolution. The transient spectra recorded on the picosecond time-sc
ale as a function of solvent viscosity are in agreement with the forma
tion of a TICT (twisted intramolecular charge transfer) state, predict
ed by quantum chemistry calculations. The ground state relaxation from
the twisted conformation is observed. It is shown that the tripler st
ate is formed only in solid matrices where the non-radiative decay of
the excited singlet to the ground state is slowed down. (C) 1997 Elsev
ier Science B.V.