State-dependent solvation of pyrene in supercritical CO{sub 2}
- State Univ. of New York, Buffalo, NY (United States)
We experimentally address the issue of solute-fluid and solute-solute interactions in dilute supercritical solutions. Using the fluorescent probe pyrene, we carry out a detailed spectroscopic study of pyrene-pyrene and pyrene-fluid interactions as a function of CO{sub 2} density. UV-vis absorbance and steady-state fluorescence experiments confirm that the excimer-like emission seen for pyrene is not the result of soluble pyrene aggregates nor does it result from detectable, dissolved ground-state pyrene species. The extent of local density enhancement surrounding pyrene molecules is also independent (within experimental error) of pyrene concentration for the ground- and excited-state species, indicating that the pyrene molecules are solvated individually, not in pairs or higher aggregates. The magnitude of local density enhancement surrounding an excited-state pyrene molecule is, however, 1.5 times that of the ground-state pyrene species. This particular result is in excellent agreement with predictions based on the electrostatic interaction energy of ground- and excited-state pyrene with CO{sub 2}. Together these results provide strong evidence against dissolved ground-state solute-solute preassociation between pyrene molecules in CO{sub 2} and provides the first experimental evidence on state-dependent local density enhancements in dilute supercritical fluid solutions. 57 refs., 15 figs.
- Sponsoring Organization:
- USDOE
- OSTI ID:
- 62466
- Journal Information:
- Journal of the American Chemical Society, Journal Name: Journal of the American Chemical Society Journal Issue: 21 Vol. 117; ISSN JACSAT; ISSN 0002-7863
- Country of Publication:
- United States
- Language:
- English
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