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dc.contributor.authorKilic, B.en_US
dc.contributor.authorYesilgul, N.en_US
dc.contributor.authorPolat, V.en_US
dc.contributor.authorGercek, Z.en_US
dc.contributor.authorAkkaya, E. U.en_US
dc.date.accessioned2018-04-12T10:52:36Z
dc.date.available2018-04-12T10:52:36Z
dc.date.issued2016en_US
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/11693/36767
dc.description.abstractBodipy dyes with n-decyloxyphenyl-(4, 5) and pentadecyl-(8) meso substituents can easily embed themselves into micellar structures formed from Cremophor-EL. In micelles of approximately 20 nm median size, heavy-atom substituted dyes show remarkable photosensitization properties as evidenced by the rate of reaction with an anthracene-based selective singlet oxygen trap in buffered aqueous solutions. Considering the ease of Bodipy derivatization and the advantages of Cremophor-EL carried therapeutic agents, these photosensitizing agents may offer novel targeting opportunities and enhanced chemical and photophysical stability.en_US
dc.language.isoEnglishen_US
dc.source.titleTetrahedron Lettersen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.tetlet.2016.02.033en_US
dc.subjectBodipyen_US
dc.subjectOrganic chromophoresen_US
dc.subjectOrganic photochemistryen_US
dc.subjectPhotosensitizersen_US
dc.subjectSinglet oxygenen_US
dc.titleBodipy-based photosensitizers with long alkyl tails at the meso position: efficient singlet oxygen generation in Cremophor-EL micellesen_US
dc.typeArticleen_US
dc.departmentDepartment of Chemistryen_US
dc.departmentInstitute of Materials Science and Nanotechnology (UNAM)en_US
dc.citation.spage1317en_US
dc.citation.epage1320en_US
dc.citation.volumeNumber57en_US
dc.citation.issueNumber12en_US
dc.identifier.doi10.1016/j.tetlet.2016.02.033en_US
dc.publisherElsevier Ltden_US
dc.identifier.eissn1873-3581


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