TITLE:

Indirect Information on Reactive Transition States from Conservation of Angular Momentum

AUTHORS:

Leach, C.A.; Tsekouras, A.A.; Vaccaro, P.H.; Zare, R.N.; Zhao, D.; Dept. of Chem., Stanford Univ., CA, USA

PUBLICATION:

Faraday Discussions of the Chemical Society vol. 91, p. 183-190, March 1991 9 Refs.

ABSTRACT:

By choosing a kinematically constrained bimolecular reaction of the type H + H' ® HH' + L, where H and H' are heavy atoms and L is a light atom, the orbital angular momentum, L, of the reagents appears almost exclusively as HH' product rotation, J. It follows that the magnitude of J is given by |L| = ìv_relb, where ì is the reduced mass of the reagent collision partners, v_rel is their relative velocity, and b is the impact parameter, i. e., the distance of closest approach if the reagents moved in undeflected straight-line paths. Hence, by measuring both the product rotational distribution and the relative velocity distribution of the reagents, it is possible to deduce the range of impact parameters resulting in specific vibrational levels of the HH' product. A prototype system is Ba + HI ® BaI + H. Experimental results for BaI (v=0) are presented for this kinematically constrained reaction showing that the range of b is restricted, peaking at or near the energetic cutoff.