Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/5102
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dc.contributor.authorSingh, Kirti-
dc.contributor.authorSingh, Rahul-
dc.contributor.authorAdhikari, Debashis-
dc.contributor.authorHazarib, Arijit Singha-
dc.date.accessioned2023-08-23T15:43:49Z-
dc.date.available2023-08-23T15:43:49Z-
dc.date.issued2022-
dc.identifier.citationChemical Communications, 58(27), 4384-4387.en_US
dc.identifier.uriDOI https://doi.org/10.1039/D2CC00397J-
dc.identifier.urihttp://hdl.handle.net/123456789/5102-
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractA photoactive zinc β-diketiminate complex spans a wide redox window of 3.97 V at its excited state. Having a highly reducing excited-state potential, it generates an electrophilic trifluoromethyl radical by the reductive cleavage of triflyl chloride. This leads to trifluoromethylation of a set of arenes and heteroarenes. During the oxidative quenching of the photocatalyst, a ligand-centered radical cation is formed, which has been detected by spectroelectrochemical EPR measurement.en_US
dc.language.isoen_USen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectBimodal photocatalytic behaviouren_US
dc.subjectzinc β-diketiminateen_US
dc.subjecttrifluoromethylation reactionsen_US
dc.titleBimodal photocatalytic behaviour of a zinc β-diketiminate: application to trifluoromethylation reactionsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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