Photochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy

Sulfur-based thiyl radicals are known to be involved in a wide range of chemical and biological processes, but they are often highly reactive, which makes them difficult to observe directly. We report herein X-ray absorption spectra and analysis that support the direct observation of two different t...

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Main Authors: Sneeden, E., Hackett, Mark, Cotelesage, J., Prince, R., Barney, M., Goto, K., Block, E., Pickering, I., George, G.
Format: Journal Article
Published: American Chemical Society 2017
Online Access:http://hdl.handle.net/20.500.11937/57066
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author Sneeden, E.
Hackett, Mark
Cotelesage, J.
Prince, R.
Barney, M.
Goto, K.
Block, E.
Pickering, I.
George, G.
author_facet Sneeden, E.
Hackett, Mark
Cotelesage, J.
Prince, R.
Barney, M.
Goto, K.
Block, E.
Pickering, I.
George, G.
author_sort Sneeden, E.
building Curtin Institutional Repository
collection Online Access
description Sulfur-based thiyl radicals are known to be involved in a wide range of chemical and biological processes, but they are often highly reactive, which makes them difficult to observe directly. We report herein X-ray absorption spectra and analysis that support the direct observation of two different thiyl species generated photochemically by X-ray irradiation. The thiyl radical sulfur K-edge X-ray absorption spectra of both species are characterized by a uniquely low energy transition at about 2465 eV, which occurs at a lower energy than any previously observed feature at the sulfur K-edge and corresponds to a 1s?3p transition to the singly occupied molecular orbital of the free radical. Our results constitute the first observation of substantial levels of thiyl radicals generated by X-ray irradiation and detected by sulfur K-edge X-ray absorption spectroscopy.
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T10:08:55Z
publishDate 2017
publisher American Chemical Society
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spelling curtin-20.500.11937-570662018-01-09T07:09:33Z Photochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy Sneeden, E. Hackett, Mark Cotelesage, J. Prince, R. Barney, M. Goto, K. Block, E. Pickering, I. George, G. Sulfur-based thiyl radicals are known to be involved in a wide range of chemical and biological processes, but they are often highly reactive, which makes them difficult to observe directly. We report herein X-ray absorption spectra and analysis that support the direct observation of two different thiyl species generated photochemically by X-ray irradiation. The thiyl radical sulfur K-edge X-ray absorption spectra of both species are characterized by a uniquely low energy transition at about 2465 eV, which occurs at a lower energy than any previously observed feature at the sulfur K-edge and corresponds to a 1s?3p transition to the singly occupied molecular orbital of the free radical. Our results constitute the first observation of substantial levels of thiyl radicals generated by X-ray irradiation and detected by sulfur K-edge X-ray absorption spectroscopy. 2017 Journal Article http://hdl.handle.net/20.500.11937/57066 10.1021/jacs.7b05116 American Chemical Society restricted
spellingShingle Sneeden, E.
Hackett, Mark
Cotelesage, J.
Prince, R.
Barney, M.
Goto, K.
Block, E.
Pickering, I.
George, G.
Photochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy
title Photochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy
title_full Photochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy
title_fullStr Photochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy
title_full_unstemmed Photochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy
title_short Photochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy
title_sort photochemically generated thiyl free radicals observed by x-ray absorption spectroscopy
url http://hdl.handle.net/20.500.11937/57066