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Synthesis and characterisation of the unsubstituted dipyrrin and 4,4-dichloro-4-bora-3a,4a-diaza-s-indacene: improved synthesis and functionalisation of the simplest BODIPY framework

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dc.contributor.authorGroves, Brandon R.en_US
dc.contributor.authorCrawford, Sarah M.en_US
dc.contributor.authorLundrigan, Travisen_US
dc.contributor.authorMatta, Cherif F.en_US
dc.contributor.authorSowlati-Hashjin, Shahinen_US
dc.contributor.authorThompson, Alisonen_US
dc.date.accessioned2013-08-12T17:55:00Z
dc.date.available2013-08-12T17:55:00Z
dc.date.issued2013en_US
dc.description.abstractAn improved and scalable synthesis of the unsubstituted 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene framework facilitates access to the previously unreported parent dipyrrin HCl salt, as well as 4,4-dichloro-4-bora-3a,4a-diaza-s-indacene.en_US
dc.identifier.citationGroves, Brandon R., Sarah M. Crawford, Travis Lundrigan, Cherif F. Matta, et al. 2013. "Synthesis and characterisation of the unsubstituted dipyrrin and 4,4-dichloro-4-bora-3a,4a-diaza-s-indacene: improved synthesis and functionalisation of the simplest BODIPY framework." Chemical Communications 49(8): 816-818.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issue8en_US
dc.identifier.startpage816en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c2cc37480cen_US
dc.identifier.urihttp://hdl.handle.net/10222/30708
dc.identifier.volume49en_US
dc.relation.ispartofChemical Communicationsen_US
dc.titleSynthesis and characterisation of the unsubstituted dipyrrin and 4,4-dichloro-4-bora-3a,4a-diaza-s-indacene: improved synthesis and functionalisation of the simplest BODIPY frameworken_US
dc.typearticleen_US

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