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hal.structure.identifierLaboratoire de Chimie et Biologie des Métaux [LCBM - UMR 5249]
dc.contributor.authorGUILLO, Pascal
hal.structure.identifierLaboratoire de Chimie et Biologie des Métaux [LCBM - UMR 5249]
dc.contributor.authorHAMELIN, Olivier
hal.structure.identifierLaboratoire Ondes et Matière d'Aquitaine [LOMA]
dc.contributor.authorBATAT, Pinar
hal.structure.identifierLaboratoire Ondes et Matière d'Aquitaine [LOMA]
dc.contributor.authorJONUSAUSKAS, Gediminas
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorMCCLENAGHAN, Nathan
hal.structure.identifierLaboratoire de Chimie et Biologie des Métaux [LCBM - UMR 5249]
dc.contributor.authorMENAGE, Stéphane
dc.date.created2011-10-12
dc.date.issued2012
dc.identifier.issn0020-1669
dc.description.abstractEnIn our research program aiming to develop new ruthenium-based polypyridine catalysts for oxidation we were interested in combining a photosensitizer and a catalytic fragment within the same complex to achieve catalytic light-driven oxidation. To respond to the lack of such conjugates, we report here a new catalytic system capable of using light to activate water molecules in order to perform selective sulfide oxygenation into sulfoxide via an oxygen atom transfer from H2O to the substrate with a TON of up to 197 ± 6. On the basis of electrochemical and photophysical studies, a proton-coupled electron-transfer process yielding to an oxidant Ru(IV)-oxo species was proposed. In particular, the synergistic effect between both partners in the dyad yielding a more efficient catalyst compared to the bimolecular system is highlighted.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/
dc.title.enPhotocatalyzed Sulfide Oxygenation with Water as the Unique Oxygen Atom Source
dc.typeArticle de revue
dc.identifier.doi10.1021/ic2022159
dc.subject.halChimie/Catalyse
bordeaux.journalInorganic Chemistry
bordeaux.page2222-2230
bordeaux.volume51
bordeaux.issue4
bordeaux.peerReviewedoui
hal.identifierhal-00676488
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00676488v1
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