dc.contributor.author | Groves, Brandon R. | en_US |
dc.contributor.author | Crawford, Sarah M. | en_US |
dc.contributor.author | Lundrigan, Travis | en_US |
dc.contributor.author | Matta, Cherif F. | en_US |
dc.contributor.author | Sowlati-Hashjin, Shahin | en_US |
dc.contributor.author | Thompson, Alison | en_US |
dc.date.accessioned | 2013-08-12T17:55:00Z | |
dc.date.available | 2013-08-12T17:55:00Z | |
dc.date.issued | 2013 | en_US |
dc.identifier.citation | Groves, 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.issn | 1359-7345 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1039/c2cc37480c | en_US |
dc.identifier.uri | http://hdl.handle.net/10222/30708 | |
dc.description.abstract | An 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.relation.ispartof | Chemical Communications | en_US |
dc.title | 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 | en_US |
dc.type | article | en_US |
dc.identifier.volume | 49 | en_US |
dc.identifier.issue | 8 | en_US |
dc.identifier.startpage | 816 | en_US |