Adiabatic capture centrifugal sudden approximation

At low temperature the classical approximation fails, but a quantum generalization of the long-range-force-law collision theories has been provided by Clary (1984,1985,1990). His capture-rate approximation (called adiabatic capture centrifugal sudden approximation or ACCSA) is closely related to the statistical adiabatic channel model of Quack and Troe (1975). Both theories calculate the capture rate from vibrationally and rotationally adiabatic potentials, but these are obtained by interpolation in the earlier work (Quack and Troe 1975) and by quantum mechanical sudden approximations in the later work (Clary 1984, 1985). 

Figure 6. Temperature dependence of the reaction efficiency per collision for the reactions of OD + CH3Cl (open circles), 0D D20 + CH3Cl (filled circles and 0D (D20)2 + CH3Cl (half-filled circles). The reaction efficiency per collision is the experimental rate constant divided by the calculated collision rate constant, calculated by Clary using the adiabatic capture centrifugal sudden approximation (ACCSA) (28). For experimental reasons (29), the measurements were made with completely deuterated...

ABSTRACT. Calculation of the rate constant at several temperatures for the reaction +(2p) HCl X are presented. A quantum mechanical dynamical treatment of ion-dipole reactions which combines a rotationally adiabatic capture and centrifugal sudden approximation is used to obtain rotational state-selective cross sections and rate constants. Ah initio SCF (TZ2P) methods are employed to obtain the long- and short-range electronic potential energy surfaces. This study indicates the necessity to incorporate the multi-surface nature of open-shell systems. The spin-orbit interactions are treated within a semiquantitative model. Results fare better than previous calculations which used only classical electrostatic forces, and are in good agreement with CRESU and SIFT measurements at 27, 68, and 300 K. ... 

In the present study, we employ the ACCSA method which involves a combined rotationally adiabatic capture and centrifugal sudden approximation. The method enables the computation of cross-sections and rate constants which are state-selective in the initial rotational states of the reactant molecule. The ACCSA approach has been successful for ion-dipole reactions which involve proton transfer. Predicted rate constants for the reactions -f HCN H2CN + H2 and HCO + HCN - - CO are in... 

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