Journal
JOURNAL OF CHEMICAL PHYSICS
Volume 123, Issue 20, Pages -Publisher
AMER INST PHYSICS
DOI: 10.1063/1.2128670
Keywords
-
Ask authors/readers for more resources
The effects of collision energy (E-col) and six different H2CO+ vibrational states on the title reaction have been studied over the center-of-mass E-col range from 0.1 to 2.6 eV, including measurements of product ion recoil velocity distributions. Ab initio and Rice-Ramsperger-Kassel-Marcus calculations were used to examine the properties of complexes and transition states that might be important in mediating the reaction. Reaction is largely direct, despite the presence of multiple deep wells on the potential surface. Five product channels are observed, with a total reaction cross section at the collision limit. The competition among the major H-2(+) transfer, hydrogen transfer, and proton transfer channels is strongly affected by E-col and H2CO+ vibrational excitation, providing insight into the factors that control competition and charge state unmixing during product separation. One of the more interesting results is that endoergic charge transfer appears to be controlled by Franck-Condon factors, implying that it occurs at large inter-reactant separations, contrary to the expectation that endoergic reactions should require intimate collisions to drive the necessary energy conversion. (c) 2005 American Institute of Physics.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available