Strange kinetics of the C2H6+CNreaction explained

摘要

In this paper, we employ state of the art quantum chemical and transition state theory methods in making a priori kinetic predictions for the abstraction reaction of CN with ethane. This reaction, which has been studied experimentally over an exceptionally broad range of temperature (25-1140 K), exhibits an unusually strong minimum in the rate constant near 200 K. The present theoretical predictions, which are based on a careful consideration of the two distinct transition state regimes, quantitatively reproduce the measured rate constant over the full range of temperature, with no adjustable parameters. At low temperatures, the rate-determining step for such radical-molecule reactions involves the formation of a weakly bound van der Waals complex. At higher temperatures, the passage over a subthreshold saddle point on the potential energy surface, related to the formation and dissolution of chemical bonds, becomes the rate-determining step. The calculations illustrate the changing importance of the two transition states with increasing temperature and also clearly demonstrate the need for including accurate treatments of both transition states. The present two transition state model is an extension of that employed in our previous work on the C2H4 + OH reaction [J. Phys. Chem. A 2005, 109, 6031]. It incorporates direct ab initio evaluations of the potential in classical phase space integral based calculations of the fully coupled anharmonic transition state partition functions for both transition states. Comparisons with more standard rigid-rotor harmonic oscillator representations for the "inner" transition state illustrate the importance of variational, anharmonic, and nonrigid effects. The effects of tunneling through the "inner" saddle point and of dynamical correlations between the two transition states are also discussed. A study of the kinetic isotope effect provides a further test for the present two transition state model.