Collisional energy transfer probabilities of highly excited molecules from kinetically controlled selective ionization (KCSI). II. The collisional relaxation of toluene: P(E[sup ′],E) and moments of energy transfer for energies up to 50 000 cm-1.

Complete and detailed experimental transition probability density functions P(E[sup ′],E) have been determined for the first time for collisions between a large, highly vibrationally excited molecule, toluene, and several bath gases. This was achieved by applying the method of kinetically controlled selective ionization (KCSI) (Paper I [J. Chem. Phys. 112, 4076 (2000), preceding article]). An optimum P(E[sup ′],E) representation is recommended (monoexponential with a parametric exponent in the argument) which uses only three parameters and features a smooth behavior of all parameters for the entire set of bath gases. In helium, argon, and CO[sub 2] the P(E[sup ′],E) show relatively increased amplitudes in the wings--large energy gaps |E[sup ′]-E|--which can also be represented by a biexponential form. The fractional contribution of the second exponent in these biexponentials, which is directly related to the fraction of the so-called "supercollisions," is found to be very small (<0.1%). For larger colliders the second term disappears completely and the wings of P(E[sup ′],E) have an even smaller amplitude than that provided by a monoexponential form. At such low levels, the second exponent is therefore of practically no relevance for the overall energy relaxation rate. All optimized P(E[sup ′],E) representations show a marked linear energetic dependence of the (weak) collision parameter α[sub 1](E), which also results in an (approximately) linear dependence of 〈ΔE〉 and of the square root of 〈ΔE[sup 2]〉. The energy transfer parameters presented in this study form a new benchmark class in certainty and accuracy, e.g., with only 2%-7% uncertainty for our 〈ΔE〉 data below 25 000 cm-1. They should also form a reliable testground for future trajectory calculations and theories describing collisional energy transfer of polyatomic molecules. © 2000 American Institute of Physics. [ABSTRACT FROM AUTHOR]