Time-resolved infrared spectra in the fingerprint region (1300-1700 cm(-)(1)) are reported for the metal-to-ligand charge-transfer (MLCT) excited state(s) of [Ru(phen)(3)](2+) and [Os(phen)(DAS)(2)](2+) (phen is 1,10-phenanthroline; DAS is 1,2-bis(diphenylarsino)ethane) in acetonitrile-d(3) at 298 K. The spectra are assigned by comparison to electrochemically generated [Ru(III)(phen)(3)](3+) and [Ru(II)(phen(*)(-)())(phen)(2)](+). The data provide clear evidence for the localized description [Ru(III)(phen(*)(-)())(phen)(2)](2+) on the approximately 100 ns time scale. They also give insight into electronic distribution in the excited state, aid in the interpretation of the time-resolved resonance Raman spectrum of [Ru(phen)(3)](2+), and suggest why measuring ground- and excited-state resonance Raman spectra of phen complexes is difficult.
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http://dx.doi.org/10.1021/ic971554e | DOI Listing |
JAMA Ophthalmol
January 2025
John A. Moran Eye Center, Department of Ophthalmology & Visual Sciences, Department of Neurology, University of Utah Health, Salt Lake City.
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State Key Labratory of Biocontrol, School of Life Sciences, Sun Yat-San University, Guangzhou, 510275, China.
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January 2025
School of Medicine, Faculty of Life Science & Medicine, Northwest University, Xi'an, China.
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View Article and Find Full Text PDFJ Sex Res
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School of Public Health, Indiana University.
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