Pii: S0166-1280(98)00374-1
نویسندگان
چکیده
We examine the effects of frequency variation along the reaction path in intramolecular or lattice modes on the rate constant for light atom transfer in the condensed phase. Accurate quantum mechanical calculations using the quasi-adiabatic propagator path integral representation of the flux–flux auto-correlation function reveal significant variations in the reaction rate compared with the constant frequency case. The vibrationally adiabatic approximation captures these effects rather faithfully if the frequency of these modes is high, relative to that of the reaction coordinate. Significant deviations from the predictions of the adiabatic approximation are observed when low variable frequency modes are involved. In such cases, the competition between the decrease in the reactive flux accompanying a tightening or dilation of the reaction path valley and corner-cutting effects arising from sharp curvature of the reaction path leads to positive or negative corrections to the predictions of the adiabatic model. q 1999 Elsevier Science B.V. All rights reserved.
منابع مشابه
Pii: S0166-1280(98)00551-x
The Direct Reaction Field approach is briefly reviewed. Preliminary reports of the calculations on solvent induced shifts in the p* ← n transition of acetone in various solvents, and the dissociation of tert-butyl chloride in water are given. q 1999 Elsevier Science B.V. All rights reserved.
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s / Journal of Molecular Structure (Theochem) 463 (1999) 41–43 43 Potential energy surfaces and dynamics of chemical reactions
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Local exchange-correlation functionals are defined for different systems with spherical symmetry, by requiring that they reproduce the correct exchange-correlation energy and exchange-correlation potential (up to a constant). For comparison, the results with the uniform electron gas local density approximation and a generalized gradient approximation are also shown. q 2000 Elsevier Science B.V....
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The hydrogen bond interaction between acetone and water is investigated at the ab initio MBPT/CC levels using different approximations and basis sets. At the highest level the binding energy is obtained as 5.6 kcal mol. Analysis of the electron correlation effects shows only a very mild influence on the binding energy. Study of the blue shift of the n! p transition of acetone in water shows tha...
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