Looking for Reaction Complexes in Trapped Ion Reactions of Xe<sup>+</sup> and O<sub>2</sub><sup>+</sup> with C<sub>3</sub>H<sub>4</sub> Isomers
ORAL
Abstract
Ion-molecule reactions play an important role in a variety of environments such as the interstellar medium and the upper ionosphere. Significant progress has been made in understanding the mechanisms that control such reactions, but there is still much to discover. I will present recent work expanding on prior studies of the C3H4 isomers allene (H2C3H2) and propyne (H3C3H), which have shown isomeric dependence on their reactivities. Specifically, I will discuss our results from reactions of Xe+ and O2+ cations with these isomers in a cold ion-trap environment. These ions have nearly identical ionization potentials and thus offer nearly isoenergetic conditions for reactions due to the low level of kinetic energy available. Experimental measurements and theoretical calculations show that the propensity of forming a reaction complex depends not only on the isomeric structure of the neutral C3H4, but also on its ionic reaction partner. This expands on what was previously understood about reactions in these systems and offers a more thorough picture of ion-molecule reaction mechanisms.
*This work was supported by the NSF and AFOSR. T.P.S. would like to thank the Leverhulme Trust and the JILA Vising Fellow Program.
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Publication: C. Zagorec-Marks, et al. To form or not to form a reaction complex: Exploring ion-molecule reactions between C3H4 isomers and Xe+ and O2+. Faraday Discuss., 2024, Advance Article
Presenters
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Trevor A Kieft
- University of Colorado, Boulder