Dynamics of hydride anion and acetyloxyl radical production by electron attachment to acetic acid.


Journal

The Journal of chemical physics
ISSN: 1089-7690
Titre abrégé: J Chem Phys
Pays: United States
ID NLM: 0375360

Informations de publication

Date de publication:
28 Oct 2024
Historique:
received: 30 06 2024
accepted: 04 10 2024
medline: 22 10 2024
pubmed: 22 10 2024
entrez: 22 10 2024
Statut: ppublish

Résumé

We investigate the dynamics and site-selectivity in the dissociation of transient anions formed upon attachment of low energy electrons to acetic acid by anion fragment momentum imaging experiments. The resonances at 6.7 and 7.7 eV are confirmed to dissociate exclusively by the O-H bond, while a third resonance at 9.1 eV dissociates primarily by both C-H break and O-H break. A fourth resonance near 10 eV is found to dissociate by O-H break. For each resonance, the measured kinetic energy release indicates two-body dissociation produces a neutral radical in the ground electronic state, for all four resonances. The measured angular distributions are consistent with all four resonances having A' symmetry.

Identifiants

pubmed: 39435839
pii: 3317712
doi: 10.1063/5.0226252
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 Author(s). Published under an exclusive license by AIP Publishing.

Auteurs

M Hasan (M)

Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
Department of Physics and Astronomy, University of Nebraska-Lincoln, Lincoln, Nebraska 68588, USA.

Th Weber (T)

Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.

M Centurion (M)

Department of Physics and Astronomy, University of Nebraska-Lincoln, Lincoln, Nebraska 68588, USA.

D S Slaughter (DS)

Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.

Classifications MeSH