
Journal of Chemical Physics p. 5781 - 5788 (1992)
Update date:2022-08-11
Topics:
Chiu, Yu-hui
Yang, Baorui
Fu, Hungshin
Anderson, Scott L.
Schweizer, Martin
Gerlich, Dieter
We report the effects of vibrational excitation and collision energy on the cross sections and branching ratios for reaction of acetylene cations with D2, using two different guided-ion-beam instruments.Two major reaction channels are observed, both of which are nearly thermoneutral.Hydrogen atom exchange is slightly exoergic due to zero point energy, and is inhibited by both collision and vibrational energy.Formation of the two isotopic C2H3+ products is enhanced by collision energy and C-C stretching vibration, but not by bending vibration.The branching ratios at low collision energies are consistent with reaction via an intermediate complex, and Rice-Ramsberger-Kassel-Marcus (RRKM) analysis is used to extract further information.At collision energies above 1 eV, D-atom transfer by a direct mechanism is also observed as a route to C2H2D+ production.Comparison of our results using both the Stony Brook and Freiburg instruments is made with the state-selected experiments of Honma, Kato, Tanaka, and Koyano
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