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Dynamic Solvation in Room-Temperature Ionic Liquids
Author(s) -
Pramit K. Chowdhury,
Mintu Halder,
Lindsay Sanders,
Tessa R. Calhoun,
J. L. Anderson,
Daniel W. Armstrong,
Xueyu Song,
Jacob W. Petrich
Publication year - 2004
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/jp0376828
Subject(s) - solvation , excited state , photon upconversion , chemistry , polarizability , emission spectrum , fluorescence , ionic liquid , ionic bonding , analytical chemistry (journal) , wavelength , chemical physics , solvent , spectral line , materials science , ion , molecule , atomic physics , organic chemistry , optics , catalysis , physics , optoelectronics , astronomy
The dynamic solvation of the fluorescent probe, coumarin 153, is measured in five room-temperature ionic liquids using different experimental techniques and methods of data analysis. With time-resolved stimulated-emission and time-correlated single-photon counting techniques, it is found that the solvation is comprised of an initial rapid component of ∼55 ps. In all the solvents, half or more of the solvation is completed within 100 ps. The remainder of the solvation occurs on a much longer time scale. The emission spectra of coumarin 153 are nearly superimposable at all temperatures in a given solvent unless they are obtained using the supercooled liquid, suggesting that the solvents have an essentially glassy nature. The physical origin of the two components is discussed in terms of the polarizability of the organic cation for the faster one and the relative diffusional motion of the cations and the anions for the slower one. A comparison of the solvation response functions obtained from single-waveleng...

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