Femtosecond resolved solvation dynamics in polar solvents

Abstract

The transient solvation of a polar fluorescent probe has been studied by the time resolved Stokes shift technique with roughly five times shorter time resolution than previously reported. New shorter time components in the solvation relaxation function C(t) have been discovered for methanol, propionitrile, and propylene carbonate; the C(t) function for acetonitrile is singly exponential within the limitations of the instrument. The observed C(t) has been compared to theoretical calculations using the dielectric continuum (DC) model for each solvent, with non-Debye expressions for the solvent dielectric response. For methanol the DC model predictions agree closely with experiment. For the polar aprotic solvents propylene carbonate and propionitrile, the shape of the experimental decay is different from the DC predictions, but the average decay times 〈τs〉 are closer to the DC predictions than previously reported. The comparison of theory and experiment is clearly limited by the inconsistencies and limited frequency range of the dielectric relaxation data found in the literature. The dynamic solvation measurements have also been compared to predictions of the mean spherical approximation as applied to solvation dynamics, which appear to give slower solvation rates than are observed experimentally.

Isentropic Compressibility and Viscosity of Aqueous and Methanolic Calcium Chloride Solutions

“…In contrast, experimental 14 and theoretical 15,16 studies reveal that the solvation dynamics in methanol is strikingly different from that in water.…”

Electric Fields and Enzyme Catalysis

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Topical Review: Molecular reaction and solvation visualized by time-resolved X-ray solution scattering: Structure, dynamics, and their solvent dependence

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