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• W2031541718 abstract "A semi-empirical model of vibronic coupling was developed in the present work to provide a quantitative analysis of partially resolved vibronic structure in uranyl absorption spectra. The studied uranyl complexes share a similar structure but bear different electric charges in the equatorial ligands. Their optical absorption spectra exhibit the common characteristics of charge transfer vibronic transitions of uranyl complexes but fine structures arising from specific vibrational modes are obscured. Accordingly, in application of the Franck–Condon principle of vibronic coupling, our model takes a mode-degenerate approximation. The absorption spectra of uranyl in various ligand environments were calculated and fitted to the experimental data. The semi-empirical approach enabled quantitative evaluation of the electronic energy levels, vibrational frequencies, and vibronic coupling strength. Moreover, the expansion of the UO bond in the excited states was calculated from the values of the vibronic coupling parameters determined in simulation of the experimental spectra. The calculated results agree very well with the experimentally observed trends in thermodynamic binding constants and structural parameters. A theoretical interpretation is given to the dependence of the UO bond expansion on the charges carried by the uranyl ligand complexes." @default.
• W2031541718 created "2016-06-24" @default.
• W2031541718 creator A5034875662 @default.
• W2031541718 creator A5056571523 @default.
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• W2031541718 date "2013-01-01" @default.
• W2031541718 modified "2023-10-17" @default.
• W2031541718 title "Theoretical analysis and quantification of the absorption spectra of uranyl complexes with structurally-related tridentate ligands" @default.
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• W2031541718 doi "https://doi.org/10.1039/c3cp52900b" @default.
• W2031541718 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24026755" @default.
• W2031541718 hasPublicationYear "2013" @default.
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