Abstract

Abstract The possible role of photoinduced electron transfer is investigated in the fluorescence quenching of the donors metallo-octaethylporphyrins (zinc octaethylporphyrin and magnesium octaethylporphyrin) in presence of the acceptor 2-nitrofluorene in polar acetonitrile liquid medium by using steady state and time-resolved techniques at the ambient temperature (300 K). The donors are selectively excited at the Q band (S 1 state), where 2-nitrofluorene has negligible absorbance. The observed bimolecular fluorescence quenching rate constants for the present donor–acceptor systems from steady state as well as time-resolved fluorescence quenching data are of the order of 10 10 L/(mol s) (less than the diffusion-controlled limit of 1.9 × 10 10 L/(mol s)). The moderately negative values of Gibbs free energy change (Δ G °) indicate that photoinduced electron transfer from the metallo-porphyrins to 2-nitrofluorene in acetonitrile solvent is possible upon photoexcitation of the former molecules. Moreover, the fluorescence quenching rates for both the donor–acceptor systems obtained from Marcus theory agree quite well with the observed values from fluorescence quenching measurements (especially time-resolved measurements).

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