Rotational state dependence of rate constants for the reaction of ions with asymmetric top molecules at very low temperatures: Application to the N+/H2O system

The adiabatic rotational state method is applied to the study of reactions between ions and polar asymmetric top molecules at very low temperatures. Detailed results of the calculated rate coefficients for the reaction of N+ with H2O are presented. A strong dependence of the rate coefficients on the initial rotational state is observed at low temperatures. In the case of a thermal distribution of rotational states, where the rate constants are summed over a Boltzman distribution, the replacement of the asymmetric top by an average symmetric top, which leads to a considerable simplification of the calculations, appears to be satisfactory. On the other hand, for a non thermal distribution, no such simplifying assumption can be made. In particular, the rate coefficient for a specific initial rotational state is quite sensitive to the orientation of the dipole moment. (orig.)