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dc.contributor.authorIsik, M.en_US
dc.contributor.authorOzdemir, T.en_US
dc.contributor.authorTuran, I. S.en_US
dc.contributor.authorKolemen, S.en_US
dc.contributor.authorAkkaya, E. U.en_US
dc.date.accessioned2015-07-28T11:59:22Z
dc.date.available2015-07-28T11:59:22Z
dc.date.issued2013en_US
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/11693/11939
dc.description.abstractJudicious design of BODIPY dyes carrying nitroethenyl substituents in conjugation with the BODIPY core yields dyes that respond to biological thiols by both absorbance and emission changes. Incorporation of solubilizing ethyleneglycol units ensures water solubility. The result is bright signaling of biologically relevant thiols in the longer wavelength region of the visible spectrum and in aqueous solutions.en_US
dc.language.isoEnglishen_US
dc.source.titleOrganic Lettersen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol303306sen_US
dc.subjectFluorescent-probeen_US
dc.subjectEnergy-transferen_US
dc.subjectEfficient Photosensitizersen_US
dc.subjectPhotodynamic Therapyen_US
dc.subjectHighly Efficienten_US
dc.subjectLogic Gatesen_US
dc.subjectDyesen_US
dc.subjectGlutathioneen_US
dc.subjectDerivativesen_US
dc.subjectEmissionen_US
dc.titleChromogenic and fluorogenic sensing of biological thiols in aqueous solutions using BODIPY-based reagentsen_US
dc.typeArticleen_US
dc.departmentDepartment of Chemistryen_US
dc.departmentInstitute of Materials Science and Nanotechnologyen_US
dc.citation.spage216en_US
dc.citation.epage219en_US
dc.citation.volumeNumber15en_US
dc.citation.issueNumber1en_US
dc.identifier.doi10.1021/ol303306sen_US
dc.publisherAmerican Chemical Societyen_US
dc.identifier.eissn1523-7052


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