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Picosecond raman scattering study of electron localization in the charge-transfer excited state of tris(bipyridine)ruthenium(II)

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00259a005· OSTI ID:7076656

The picosecond time resolved resonance Raman spectra of the MLCT excited state have been observed in room temperature water, in isopropyl alcohol, in 4:1 ethanol/methanol above and below the glass transition temperature, and in anionic SDS micelles. In all cases the excited electron is localized on one bipyridine ligand. The vibrational relaxation-localization process appears to be complete within a few picoseconds. A broadening of MLCT Raman lines at high field intensities is attributed to nonlinear resonance scattering. Localization and subsequent electron hopping are discussed with use of the simple Franck-Condon electron transfer model for weakly coupled, mixed valence compounds.

Research Organization:
AT and T Bell Labs., Murray Hill, NJ (USA)
OSTI ID:
7076656
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 109:25; ISSN JACSA
Country of Publication:
United States
Language:
English