Resonance Raman Spectrum of the Phenanthroline Anion: Implications on Electron Delocalization in the MLCT Excited State of Ru(phen)32+
Author:
Affiliation:
1. Department of Chemistry and the LASER Laboratory, Michigan State University, East Lansing, Michigan 48824
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic9601091
Reference44 articles.
1. Time-resolved resonance Raman study of the lowest (d.pi.*,3CT) excited state of tris(2,2'-bipyridine)ruthenium(II)
2. Vibrational spectroscopy of the electronically excited state. 5. Time-resolved resonance Raman study of tris(bipyridine)ruthenium(II) and related complexes. Definitive evidence for the "localized" MLCT state
3. Molecular and electronic structure in the metal-to-ligand charge-transfer excited states of d6 transition-metal complexes in solution
4. Raman spectroscopy of electronic excited organometallic complexes: a comparison of the metal to 2,2'-bipyridine charge-transfer state of fac-(2,2'-bipyridine)tricarbonylhalorhenium and tris(2,2'-bipyridine)ruthenium(II)
5. Resonance Raman spectroscopy of the lowest excited state of derivatives of tris(2,2'-bipyridine)ruthenium(II): substituent effects on electron localization in mixed-ligand complexes
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