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dc.contributor.authorDRAPER, SYLVIA
dc.contributor.authorWijesinghe, Lankani P.
dc.contributor.authorPerera, Sarath D.
dc.contributor.authorLarkin, Eugene
dc.contributor.authorÓ Máille, Gearóid M.
dc.contributor.authorConway-Kenny, Robert
dc.contributor.authorLankage, Buddhie S.
dc.contributor.authorWang, Longsheng
dc.date.accessioned2020-01-28T17:03:50Z
dc.date.available2020-01-28T17:03:50Z
dc.date.issued2017
dc.date.submitted2017en
dc.identifier.citationWijesinghe, L.P., Perera, S.D., Larkin, E., Ó Máille, G.M., Conway-Kenny, R., Lankage, B.S., Wang, L. & Draper, S.M., [2 + 2 + 2] cyclotrimerisation as a convenient route to 6N-doped nanographenes: A synthetic introduction to hexaazasuperbenzenes, 2017, RSC Advances, 7, 39en
dc.identifier.otherY
dc.descriptionPUBLISHEDen
dc.description.abstract6N-containing polyphenylene precursors were generated via [2 + 2 + 2] cyclotrimerisation. On methoxy substitution complete ring-closure can be achieved (via FeCl3-mediated oxidative cyclodehydrogenation) to give asymmetric and C3v symmetric hexaazasuperbenzenes. Investigations using DDQ/H+ mediated conditions reveal this to be a promising alternative and selective route to partial cyclodehydrogenation.en
dc.format.extent24163-24167en
dc.language.isoenen
dc.relation.ispartofseriesRSC Advances;
dc.relation.ispartofseries7;
dc.relation.ispartofseries39;
dc.rightsYen
dc.subjectcyclodehydrogenationen
dc.subject[2 + 2 + 2] cyclotrimerisationen
dc.title[2 + 2 + 2] cyclotrimerisation as a convenient route to 6N-doped nanographenes: A synthetic introduction to hexaazasuperbenzenesen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/smdraper
dc.identifier.rssinternalid184920
dc.identifier.doihttp://dx.doi.org/10.1039/C7RA02648J
dc.rights.ecaccessrightsopenAccess
dc.identifier.orcid_id0000-0003-1323-7245
dc.contributor.sponsorScience Foundation Irelanden
dc.contributor.sponsorGrantNumberSFI/IA/3046en
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2017/RA/C7RA02648J#!divAbstract
dc.identifier.urihttp://hdl.handle.net/2262/91406


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