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Gaussian solvation

It should be noted, however, that the quantity AE, is not an experimental observable but it can be tested by molecular simulations this is done in section 18.5. We turn below to possible experimental evidences of the breakdown of Marcus Gaussian solvation theory, namely the study of reaction rate/free energy relationships. [Pg.472]

Mineva T, Russo N and Sicilia E 1998 Solvation effects on reaction profiles by the polarizable continuum model coupled with Gaussian density functional method J. Oomp. Ohem. 19 290-9... [Pg.864]

Hummer, G. Pratt, L. Garcia, A. E., Multistate Gaussian model for electrostatic solvation free energies, J. Am. Chem. Soc. 1997,119, 8523-8527... [Pg.74]

However, picosecond resolution is insufficient to fully describe solvation dynamics. In fact, computer simulations have shown that in small-molecule solvents (e.g. acetonitrile, water, methyl chloride), the ultrafast part of solvation dynamics (< 300 fs) can be assigned to inertial motion of solvent molecules belonging to the first solvation layer, and can be described by a Gaussian func-tiona) b). An exponential term (or a sum of exponentials) must be added to take into account the contribution of rotational and translational diffusion motions. Therefore, C(t) can be written in the following form ... [Pg.210]

A surprising aspect of SD is how rapidly C i) in highly polar solvents decays relative to other relaxation processes such as reorientation of solvent dipoles. This very rapid time scale cannot be ascribed to dynamical solvent-solvent correlations, which, as illustrated in Fig. 6, are modest even for the longest ranged A . Thus the key to imderstanding the reasons for the rapid decay of C i) is in examining how solvent-solvent correlations contribute to it and to what extent their contributions can be accounted for in terms of static correlations measured by ((5A ) ), Eq. (32). The initial cmvature of C(t), which characterizes its short-time Gaussian-like behavior is often characterized in terms of the solvation frequency co o/v... [Pg.220]

Most probable settling velocity from sedimentation data Particle-size determination from sedimentation equation Sedimentation in an ultracentrifuge Solvation and ellipticity from sedimentation data Diffusion and Gaussian distribution Temperature-dependence of diffusion coefficients... [Pg.638]

Range parameters, b (nm), for solvated electrons in various hydrocarbon solvents at room temperature, assuming a gaussian initial distribution of distances from the ionisation site to the thermalisation point... [Pg.181]


See other pages where Gaussian solvation is mentioned: [Pg.468]    [Pg.471]    [Pg.472]    [Pg.474]    [Pg.480]    [Pg.461]    [Pg.468]    [Pg.471]    [Pg.472]    [Pg.474]    [Pg.480]    [Pg.461]    [Pg.325]    [Pg.184]    [Pg.36]    [Pg.37]    [Pg.46]    [Pg.331]    [Pg.201]    [Pg.102]    [Pg.158]    [Pg.173]    [Pg.525]    [Pg.128]    [Pg.246]    [Pg.246]    [Pg.210]    [Pg.384]    [Pg.455]    [Pg.747]    [Pg.748]    [Pg.41]    [Pg.19]    [Pg.181]    [Pg.183]    [Pg.208]    [Pg.224]   


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