Abstract

Thermal relaxation process of a vibrational excess energy of ∼2800 cm −1 deposited on v ′=2 level of ring-breathing mode has been investigated on S 1 perylene and S 1 12-(3-perylenyl)dodecanoic acid in 2-methyltetrahydrofuran at room temperature. The Franck–Condon analysis of femtosecond time-resolved fluorescence spectra indicated that noticeable vibrational transients exist at v ′=2 level even a few picoseconds after photoexcitation. It was confirmed that the population distribution over v ′=0,1,2 levels is non-Boltzmann type at early time stage and converges into Boltzmann type with a few picoseconds time constant.

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