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dc.contributor.authorKumar, Dalip-
dc.date.accessioned2021-10-27T04:19:05Z-
dc.date.available2021-10-27T04:19:05Z-
dc.date.issued2018-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob01818a-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3021-
dc.description.abstractCopper-catalysed N-arylation of fused triazoles using diaryliodonium salts as an aryl source is described. This scalable protocol displayed good compatibility towards diverse sensitive functional groups like ester, alkyl and nitro groups and halogens (F, Cl, Br). The synthetic usefulness of the prepared triazolium salts was proved by preparing α-hydroxyketone through benzoin condensation. Photophysical studies of these compounds showed promising Stokes-shifted fluorescence emission in aqueous medium, so this molecular framework could be a proficient probe for biological applications.en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectTriazoliumen_US
dc.subjectDiaryliodoniumen_US
dc.subjectPhotophysicalen_US
dc.titleAn efficient synthesis of triazolium ion based NHC precursors using diaryliodonium salts and their photophysical propertiesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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