Selective formation and spectroscopic characterization of the H2CCS•+ radical cation via dissociative ionization of thiophene

The chemistry of sulfur-containing molecules is of significant interest to fields ranging from the combustion of petrochemicals to astrochemistry (with multiple S-containing species unambiguously detected in the interstellar medium or circumstellar shells). Here, infrared predissociation action spectroscopy and mass-analyzed ion kinetic energy spectroscopy measurements of the m/z 58 fragment from the dissociative ionization of thiophene are presented. Comparison is made between these experimental results and ab initio calculations (of both the spectral features and the fragmentation potential energy surface), which allows the fragment to be identified as the H2CCS•+ radical cation. This conclusive identification addresses long-standing questions about the dissociative ionization of thiophene. The findings will enable further spectroscopic measurements and reactivity studies to be conducted, allowing H2CCS•+ to be incorporated into models of astrochemical environments.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-04-22
DOI
https://doi.org/10.1063/5.0260839
Citations
1
Primary Topic
Advanced Chemical Physics Studies
Type
article
Field-Weighted Citation Impact
1.25

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article

Selective formation and spectroscopic characterization of the H2CCS•+ radical cation via dissociative ionization of thiophene

Daniela Ascenzi, Brianna R. Heazlewood, Vincent Richardson, Kim Steenbakkers et al.
1 citations
The Journal of Chemical Physics
Advanced Chemical Physics Studies
1.25
article

Selective formation and spectroscopic characterization of the H2CCS•+ radical cation via dissociative ionization of thiophene

Daniela Ascenzi, Brianna R. Heazlewood, Vincent Richardson, Kim Steenbakkers, Sandra Brünken, Miroslav Polášek, Jake A. Diprose, Matteo Michielan, Claire Romanzin
article en
1 citations

Abstract

The chemistry of sulfur-containing molecules is of significant interest to fields ranging from the combustion of petrochemicals to astrochemistry (with multiple S-containing species unambiguously detected in the interstellar medium or circumstellar shells). Here, infrared predissociation action spectroscopy and mass-analyzed ion kinetic energy spectroscopy measurements of the m/z 58 fragment from the dissociative ionization of thiophene are presented. Comparison is made between these experimental results and ab initio calculations (of both the spectral features and the fragmentation potential energy surface), which allows the fragment to be identified as the H2CCS•+ radical cation. This conclusive identification addresses long-standing questions about the dissociative ionization of thiophene. The findings will enable further spectroscopic measurements and reactivity studies to be conducted, allowing H2CCS•+ to be incorporated into models of astrochemical environments.

The Journal of Chemical PhysicsVol. 162(16)
Centre National de la Recherche Scientifique (FR), Radboud University Nijmegen (NL), University of Liverpool (GB), University of Trento (IT), Université Paris-Saclay (FR), Synchrotron soleil (FR), Czech Academy of Sciences, J. Heyrovský Institute of Physical Chemistry (CZ), Institut de Chimie (FR), HFML-FELIX (NL)
Laserlab-Europe, Leverhulme Trust, European Commission, University of Liverpool, Deutsche Forschungsgemeinschaft, Radboud Universiteit, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Università degli Studi di Trento, European Research Council, EU-CardioRNA
Affordable and clean energy
Openalex Percentile: Top 22%
Advanced Chemical Physics Studies
1.25
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