The bi-exponential fluorescence decay of a rhodamine substituted with two 4
-(1-pyrenyl)-butyl moieties is attributed to a reversible intramolecular ph
oto-induced electron transfer. The additional decay channel is confirmed by
a decrease of the fluorescence quantum yield. Global compartmental analysi
s of fluorescence decays obtained at different scales allowed the determina
tion of the different rate constants of the excited state equilibrium. Tran
sient absorption indicates that the decay of the charge transfer state popu
lates the locally excited triplet state of the rhodamine. (C) 2000 Elsevier
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