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dc.contributor.authorSneeden, E.
dc.contributor.authorHackett, Mark
dc.contributor.authorCotelesage, J.
dc.contributor.authorPrince, R.
dc.contributor.authorBarney, M.
dc.contributor.authorGoto, K.
dc.contributor.authorBlock, E.
dc.contributor.authorPickering, I.
dc.contributor.authorGeorge, G.
dc.date.accessioned2017-09-27T10:22:17Z
dc.date.available2017-09-27T10:22:17Z
dc.date.created2017-09-27T09:48:12Z
dc.date.issued2017
dc.identifier.citationSneeden, E. and Hackett, M. and Cotelesage, J. and Prince, R. and Barney, M. and Goto, K. and Block, E. et al. 2017. Photochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy. Journal of the American Chemical Society. 139 (33): pp. 11519-11526.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/57066
dc.identifier.doi10.1021/jacs.7b05116
dc.description.abstract

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.

dc.publisherAmerican Chemical Society
dc.titlePhotochemically Generated Thiyl Free Radicals Observed by X-ray Absorption Spectroscopy
dc.typeJournal Article
dcterms.source.volume139
dcterms.source.number33
dcterms.source.startPage11519
dcterms.source.endPage11526
dcterms.source.issn0002-7863
dcterms.source.titleJournal of the American Chemical Society
curtin.departmentDepartment of Chemistry
curtin.accessStatusFulltext not available


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