Facile "one pot" route to the novel benzazulene-type dye class: asymmetric, derivatizable, 5-7-6 fused ring puckered half BODIPY design

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dc.contributor.authorMurale, Dhiraj P.ko
dc.contributor.authorLee, Kang-Munko
dc.contributor.authorKim, Ki-Bongko
dc.contributor.authorChurchill, David Gko
dc.date.accessioned2013-03-09T06:33:01Z-
dc.date.available2013-03-09T06:33:01Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2011-10-
dc.identifier.citationCHEMICAL COMMUNICATIONS, v.47, no.46, pp.12512 - 12514-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/95601-
dc.description.abstractA novel fluorescent difluoroboroazaoxobenzazulene dye has been synthesized from commercially available substrates in "one pot"; it was characterized structurally and spectroscopically, derivatized and finally compared to a related BODIPY system that demonstrates "turn-on" H+ (42-fold) and F- (similar to 5-fold) responses.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectFLUORESCENT-
dc.subjectSYSTEMS-
dc.subjectBORON-
dc.titleFacile "one pot" route to the novel benzazulene-type dye class: asymmetric, derivatizable, 5-7-6 fused ring puckered half BODIPY design-
dc.typeArticle-
dc.identifier.wosid000296985100026-
dc.identifier.scopusid2-s2.0-81255197289-
dc.type.rimsART-
dc.citation.volume47-
dc.citation.issue46-
dc.citation.beginningpage12512-
dc.citation.endingpage12514-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.identifier.doi10.1039/c1cc15433h-
dc.contributor.localauthorChurchill, David G-
dc.contributor.nonIdAuthorMurale, Dhiraj P.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusFLUORESCENT-
dc.subject.keywordPlusSYSTEMS-
dc.subject.keywordPlusBORON-
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