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Electronic state influence on selective bond breaking of core-excited nitrosyl chloride (ClNO)
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, FREIA.
IOM CNR Tasc, SS 14,Km 163-5 Area Sci Pk, I-34149 Trieste, Italy..ORCID iD: 0000-0001-8101-4022
Elettra Sincrotrone Trieste, Area Sci Pk, I-34149 Trieste, Italy..
IOM CNR Tasc, SS 14,Km 163-5 Area Sci Pk, I-34149 Trieste, Italy..ORCID iD: 0000-0002-8467-1842
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2022 (English)In: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 157, no 12, article id 124306Article in journal (Refereed) Published
Abstract [en]

The potential for selective bond breaking of a small molecule was investigated with electron spectroscopy and electron-ion coincidence experiments on ClNO. The electron spectra were measured upon direct valence photoionization and resonant core excitation at the N 1s- and O 1s-edges, followed by the emission of resonant-Auger (RA) electrons. The RA spectra were analyzed with particular emphasis on the assignment of the participator and spectator states. The states are of special relevance for investigating how distinct electronic configurations influence selective bond breaking. The electron-ion coincidence measurements provided branching fractions of the produced ion fragments as a function of electron binding energy. They explicitly demonstrate how the final electronic states created after photoionization and RA decay influence fragmentation. In particular, we observed a significantly different branching fraction for spectator states compared with participator states. In addition, it was also observed that the bonds broken for the spectator states correlate with the antibonding nature of the spectator-electron orbital.

Place, publisher, year, edition, pages
American Institute of Physics (AIP), 2022. Vol. 157, no 12, article id 124306
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Atom and Molecular Physics and Optics
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URN: urn:nbn:se:uu:diva-487630DOI: 10.1063/5.0106642ISI: 000862856000002PubMedID: 36182420OAI: oai:DiVA.org:uu-487630DiVA, id: diva2:1707499
Available from: 2022-10-31 Created: 2022-10-31 Last updated: 2022-10-31Bibliographically approved

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Salén, Peter

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