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dc.contributor.authorDeniz, E.en_US
dc.contributor.authorIsbasar, G. C.en_US
dc.contributor.authorBozdemir, Ö. A.en_US
dc.contributor.authorYildirim, L. T.en_US
dc.contributor.authorSiemiarczuk, A.en_US
dc.contributor.authorAkkaya, E. U.en_US
dc.date.accessioned2016-02-08T10:06:58Z
dc.date.available2016-02-08T10:06:58Z
dc.date.issued2008en_US
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/11693/22955
dc.description.abstract(Graph Presented) Two novel distyryl-boradiazaindacene dyes with dimethylaminostyryl and pyridylethenyl substituents display opposite spectral shifts on protonation with TFA in organic solvents. This bidirectional switching of the dyes can be shown to be directly related to ICT donor and acceptor characteristics of the substituents attached to the BODIPY core. The observed spectral response of these dyes could be very useful in the design of novel NIR fluorescent ratiometric probes for pH. © 2008 American Chemical Society.en_US
dc.language.isoEnglishen_US
dc.source.titleOrganic Lettersen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol801062hen_US
dc.titleBidirectional switching of near IR emitting boradiazaindacene fluorophoresen_US
dc.typeArticleen_US
dc.departmentDepartment of Chemistryen_US
dc.departmentInstitute of Materials Science and Nanotechnology (UNAM)en_US
dc.citation.spage3401en_US
dc.citation.epage3403en_US
dc.citation.volumeNumber10en_US
dc.citation.issueNumber16en_US
dc.identifier.doi10.1021/ol801062hen_US


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