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Bimolecular reactions of S2+ with Ar, H2 and N2: reactivity and dynamics.
Armenta Butt, Sam; Price, Stephen D.
Afiliação
  • Armenta Butt S; Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK. sam.butt.16@ucl.ac.uk.
  • Price SD; Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK. sam.butt.16@ucl.ac.uk.
Phys Chem Chem Phys ; 24(14): 8113-8128, 2022 Apr 06.
Article em En | MEDLINE | ID: mdl-35322816
ABSTRACT
The reactivity, energetics and dynamics of bimolecular reactions between S2+ and three neutral species (Ar, H2 and N2) have been studied using a position-sensitive coincidence methodology at centre-of-mass collision energies below 6 eV. This is the first study of bimolecular reactions involving S2+, a species detected in planetary ionospheres, the interstellar medium, and in anthropogenic manufacturing processes. The reactant dication beam employed consists predominantly of S2+ in the ground 3P state, but some excited states are also present. Most of the observed reactions involve the ground state of S2+, but the dissociative electron transfer reactions appear to exclusively involve excited states of this atomic dication. We observe exclusively single electron-transfer between S2+ and Ar, a process which exhibits strong forward scatting typical of the Landau-Zener style dynamics observed for other dicationic electron transfer reactions. Following collisions between S2+ + H2, non-dissociative and dissociative single electron-transfer reactions were detected. The dynamics here show evidence for the formation of a long-lived collision complex, [SH2]2+, in the dissociative single electron-transfer channel. The formation of SH+ was not observed. In contrast, the collisions of S2+ + N2 result in the formation of SN+ + N+ in addition to the products of single electron-transfer reactions.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article