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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 5474-5484 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Solvent density dependence of the absorption and fluorescence spectra of coumarin 153 in argon (Ar), ethane (C2H6), carbon dioxide (CO2), and trifluoromethane (CF3H) has been studied at 323.2 K over a wide density region up to ρr∼3, where ρr is the reduced density by the critical density (ρc) of the solvent (ρr≡ρ/ρc). By analyzing the line shape functions of the absorption and fluorescence spectra, the first moment and the full width of the half maximum (FWHM) have been determined. Both the free energy difference (ΔG) between the ground and the S1 states and the fluorescence Stokes shift (Δν), evaluated by the first moments of the absorption and fluorescence line shape functions, show larger shift to the values in vapor in the order of Ar, C2H6, CO2, and CF3H if compared at the same ρr. There are three characteristic density regions on the density dependence of ΔG and Δν; these values show larger dependence in the lower-density region (ρr〈0.5) and the higher-density region (ρr〉2), than that in the medium-density region. The solvent density and species dependence of the FWHM of the absorption spectrum is quite similar to that of Δν. The density dependence of Δν and FWHM in Ar and C2H6 indicates that the intramolecular reorganization energy decreases with increasing the solvent density, while the effect is small. We have estimated the solvent reorganization energy (λS) in CO2 and CF3H by assuming no contribution of λS in C2H6 and Ar. We have demonstrated that the dielectric continuum model makes a good prediction on the relation between ΔG and λS, while it is poor on their density dependence. The invariance of ΔG and λS in the medium-density region can be interpreted as the density saturation around the solute molecule. In the lower-density region (ρr〈∼0.5), the way of the solvation is suggested to be different from those in the medium- and high-density regions. The lifetime of S1 shows a large dependence on the solvent density and species in the very low-density region (ρr∼0.05). We have also found that slow solvation dynamics exists in the lower-density region of CF3H. The origin of the dynamics is discussed in relation with the static Stokes shift. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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