Atropisomeric dyes: axial chirality in orthogonal bodipy oligomers

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dc.citation.epage663en_US
dc.citation.issueNumber3en_US
dc.citation.spage660en_US
dc.citation.volumeNumber16en_US
dc.contributor.authorKolemen, S.en_US
dc.contributor.authorCakmak, Y.en_US
dc.contributor.authorKostereli, Z.en_US
dc.contributor.authorAkkaya, E. U.en_US
dc.date.accessioned2016-02-08T10:58:26Z
dc.date.available2016-02-08T10:58:26Z
dc.date.issued2014en_US
dc.departmentDepartment of Chemistryen_US
dc.departmentNanotechnology Research Center (NANOTAM)en_US
dc.description.abstractA dissymmetrically substituted orthogonal BODIPY dimer and an orthogonal BODIPY trimer exist as two stable conformers, which are in fact atropisomeric enantiomers. The racemic mixture can be separated by HPLC using a chiral stationary phase. These enantiomeric derivatives hold great potential as chiral agents in asymmetric synthesis, fluorogenic/chromogenic sensing, and biological applications.en_US
dc.identifier.doi10.1021/ol403193fen_US
dc.identifier.eissn1523-7052
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/11693/26334
dc.language.isoEnglishen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol403193fen_US
dc.source.titleOrganic Lettersen_US
dc.titleAtropisomeric dyes: axial chirality in orthogonal bodipy oligomersen_US
dc.typeArticleen_US
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