Designing excited states: theory-guided access to efficient photosensitizers for photodynamic action

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dc.citation.epage11941en_US
dc.citation.issueNumber50en_US
dc.citation.spage11937en_US
dc.citation.volumeNumber50en_US
dc.contributor.authorCakmak, Y.en_US
dc.contributor.authorKolemen, S.en_US
dc.contributor.authorDuman, S.en_US
dc.contributor.authorDede, Y.en_US
dc.contributor.authorDolen, Y.en_US
dc.contributor.authorKilic, B.en_US
dc.contributor.authorKostereli, Z.en_US
dc.contributor.authorYildirim, L. T.en_US
dc.contributor.authorDogan, A. L.en_US
dc.contributor.authorGuc, D.en_US
dc.contributor.authorAkkaya, E. U.en_US
dc.date.accessioned2016-02-08T09:49:25Z
dc.date.available2016-02-08T09:49:25Z
dc.date.issued2011en_US
dc.departmentInstitute of Materials Science and Nanotechnology (UNAM)en_US
dc.departmentDepartment of Chemistryen_US
dc.description.abstractThe in silico design of tetraradical S 1 states was validated experimentally through synthesis, followed by characterization including phosphorescence measurements, use of trap molecules, and cell culture studies, leading to a series of orthogonal dimers of Bodipy chromophores with remarkable singlet oxygen efficiencies (see picture). A new path for the rational development of efficient photosensitizers is thus revealed.en_US
dc.identifier.doi10.1002/anie.201105736en_US
dc.identifier.eissn1521-3773
dc.identifier.issn1433-7851
dc.identifier.urihttp://hdl.handle.net/11693/21660
dc.language.isoEnglishen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/anie.201105736en_US
dc.source.titleAngewandte Chemie - International Editionen_US
dc.subjectBodipy dyesen_US
dc.subjectFluorescenceen_US
dc.subjectPhotodynamic therapyen_US
dc.subjectSensitizersen_US
dc.subjectSinglet oxygenen_US
dc.titleDesigning excited states: theory-guided access to efficient photosensitizers for photodynamic actionen_US
dc.typeArticleen_US

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Institute of Materials Science and Nanotechnology (UNAM)
Department of Chemistry