Influence of non-Debye relaxation and of molecular shape on the time dependence of the stokes shift in polar media
β Scribed by Edward W. Castner Jr.; Graham R. Fleming; Biman Bagchi
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 599 KB
- Volume
- 143
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
We present theoretical analyses of two different aspects ofthe time dependence of the fluorescence Stokes shift in polar liquids. We show that a small deviation from the Debye form for the dielectric relaxation of the solvent can strongly influence the time evolution of the Stokes shift. Using the Davidson-Cole form for dielectric response we find a stretched exponential time dependence as observed in recent experiments. We also show that the shape of the fluorescing molecule can influence the dynamics of solvation.
' John Simon Guggenheim Fellow.
π SIMILAR VOLUMES
The non-coincidence 1n = n anison iso was investigated in the Raman spectra of OH and CO bands of methanol diluted with carbon tetrachloride. Dilution with carbon tetrachloride brings about an increase in the negative non-coincidence of the CO band from -5 to -12 cm -1 and leaves it almost constant