Expanded bodipy dyes: anion sensing using a bodipy analog with an additional difluoroboron bridge

dc.citation.epage1531en_US
dc.citation.issueNumber6en_US
dc.citation.spage1528en_US
dc.citation.volumeNumber14en_US
dc.contributor.authorGuliyev, R.en_US
dc.contributor.authorOzturk, S.en_US
dc.contributor.authorSahin, E.en_US
dc.contributor.authorAkkaya, E. U.en_US
dc.date.accessioned2016-02-08T09:47:52Z
dc.date.available2016-02-08T09:47:52Z
dc.date.issued2012en_US
dc.departmentInstitute of Materials Science and Nanotechnology (UNAM)en_US
dc.departmentDepartment of Chemistryen_US
dc.description.abstractOxalyl-tethered pyrroles can be doubly bridged with two difluoroboron chelating units to yield bright orange dyes. Interestingly, in polar organic solvents, the addition of fluoride and cyanide result in reversible detachment of the otherwise stable difluoroboron bridges, resulting in sharp changes in color. Thus, this novel compound behaves as a highly selective chromogenic sensor for fluoride and cyanide ions.en_US
dc.identifier.doi10.1021/ol300260qen_US
dc.identifier.eissn1523-7052
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/11693/21548
dc.language.isoEnglishen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol300260qen_US
dc.source.titleOrganic Lettersen_US
dc.titleExpanded bodipy dyes: anion sensing using a bodipy analog with an additional difluoroboron bridgeen_US
dc.typeArticleen_US
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