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Ground‐State Photoelectron Circular Dichroism of Methyl p‐Tolyl Sulfoxide by Single‐Photon Ionisation from a Table‐Top Source
Single‐photon ionisation of enantiopure methyl p‐tolyl sulfoxide by circularly polarised light at 133 nm shows remarkably strong photoelectron circular dichroism (PECD), which has been measured in a velocity‐map‐imaging spectrometer. Both enantiomers were measured, each showing a PECD of a similar m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087734/ https://www.ncbi.nlm.nih.gov/pubmed/35969023 http://dx.doi.org/10.1002/cphc.202200575 |
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author | Waters, Max D. J. Ladda, Nicolas Senftleben, Arne Svoboda, Vít Belozertsev, Mikhail Baumert, Thomas Wörner, Hans Jakob |
author_facet | Waters, Max D. J. Ladda, Nicolas Senftleben, Arne Svoboda, Vít Belozertsev, Mikhail Baumert, Thomas Wörner, Hans Jakob |
author_sort | Waters, Max D. J. |
collection | PubMed |
description | Single‐photon ionisation of enantiopure methyl p‐tolyl sulfoxide by circularly polarised light at 133 nm shows remarkably strong photoelectron circular dichroism (PECD), which has been measured in a velocity‐map‐imaging spectrometer. Both enantiomers were measured, each showing a PECD of a similar magnitude (ca. 25 %). These experiments were carried out with a tabletop high‐harmonic source with a photon energy of 9.3 eV, capable of ionising the electronic ground state of most organic and inorganic molecules. Ab‐initio scattering calculations provide a theoretical value of the expected chiral asymmetry parameter, and agree very well with the measured values once orbital mixing via configuration interaction in the cation is taken into account. This study demonstrates a simple photoionisation scheme that can be readily applied to study the time‐resolved PECD of photochemical reactions and suggests a pronounced sensitivity of PECD to electronic configuration interaction in the cation. |
format | Online Article Text |
id | pubmed-10087734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100877342023-04-12 Ground‐State Photoelectron Circular Dichroism of Methyl p‐Tolyl Sulfoxide by Single‐Photon Ionisation from a Table‐Top Source Waters, Max D. J. Ladda, Nicolas Senftleben, Arne Svoboda, Vít Belozertsev, Mikhail Baumert, Thomas Wörner, Hans Jakob Chemphyschem Research Articles Single‐photon ionisation of enantiopure methyl p‐tolyl sulfoxide by circularly polarised light at 133 nm shows remarkably strong photoelectron circular dichroism (PECD), which has been measured in a velocity‐map‐imaging spectrometer. Both enantiomers were measured, each showing a PECD of a similar magnitude (ca. 25 %). These experiments were carried out with a tabletop high‐harmonic source with a photon energy of 9.3 eV, capable of ionising the electronic ground state of most organic and inorganic molecules. Ab‐initio scattering calculations provide a theoretical value of the expected chiral asymmetry parameter, and agree very well with the measured values once orbital mixing via configuration interaction in the cation is taken into account. This study demonstrates a simple photoionisation scheme that can be readily applied to study the time‐resolved PECD of photochemical reactions and suggests a pronounced sensitivity of PECD to electronic configuration interaction in the cation. John Wiley and Sons Inc. 2022-09-19 2022-12-16 /pmc/articles/PMC10087734/ /pubmed/35969023 http://dx.doi.org/10.1002/cphc.202200575 Text en © 2022 The Authors. ChemPhysChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Waters, Max D. J. Ladda, Nicolas Senftleben, Arne Svoboda, Vít Belozertsev, Mikhail Baumert, Thomas Wörner, Hans Jakob Ground‐State Photoelectron Circular Dichroism of Methyl p‐Tolyl Sulfoxide by Single‐Photon Ionisation from a Table‐Top Source |
title | Ground‐State Photoelectron Circular Dichroism of Methyl p‐Tolyl Sulfoxide by Single‐Photon Ionisation from a Table‐Top Source |
title_full | Ground‐State Photoelectron Circular Dichroism of Methyl p‐Tolyl Sulfoxide by Single‐Photon Ionisation from a Table‐Top Source |
title_fullStr | Ground‐State Photoelectron Circular Dichroism of Methyl p‐Tolyl Sulfoxide by Single‐Photon Ionisation from a Table‐Top Source |
title_full_unstemmed | Ground‐State Photoelectron Circular Dichroism of Methyl p‐Tolyl Sulfoxide by Single‐Photon Ionisation from a Table‐Top Source |
title_short | Ground‐State Photoelectron Circular Dichroism of Methyl p‐Tolyl Sulfoxide by Single‐Photon Ionisation from a Table‐Top Source |
title_sort | ground‐state photoelectron circular dichroism of methyl p‐tolyl sulfoxide by single‐photon ionisation from a table‐top source |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087734/ https://www.ncbi.nlm.nih.gov/pubmed/35969023 http://dx.doi.org/10.1002/cphc.202200575 |
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