Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
29351 | Journal of Photochemistry and Photobiology A: Chemistry | 2006 | 7 Pages |
Abstract
We investigated vibrational energy relaxations of S1 perylene at an excess energy of ca. 2800 cm−1 in several ketone solvents by femtosecond time-resolved fluorescence measurements. Temporal evolution of fluorescence emissions occurs on the following distinct timescales: 70–330 fs, 0.6–1.1 ps and 1.8–4.9 ps. The latter two was assigned to the intramolecular vibrational redistribution (IVR), and to the solvent-assisted IVR (SA-IVR), respectively. In SA-IVR, intramolecular vibrational couplings are affected by elastic or quasi–elastic interactions between solute and solvents. Solvent dependence of the SA-IVR rates can be explained qualitatively by the tier V–V coupling mechanism.
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Authors
Takayuki Kiba, Shin-ichiro Sato, Seiji Akimoto, Tatsuya Kasajima, Iwao Yamazaki,