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dc.contributor.authorAdarsh, N-
dc.contributor.authorRekha, R A-
dc.contributor.authorRamaiah, D-
dc.date.accessioned2014-08-01T06:53:01Z-
dc.date.available2014-08-01T06:53:01Z-
dc.date.issued2010-
dc.identifier.citationOrganic Letters 12(24):5720-5723;17 Dec 2010en_US
dc.identifier.issn1523-7060-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1587-
dc.description.abstractNovel aza-BODIPY derivatives substituted with heavy atoms such as bromine and iodine were synthesized, and their triplet and singlet oxygen generation efficiencies have been investigated. These derivatives showed absorption in the NIR region with high molar extinction coefficients. The dye substituted with four iodine atoms showed yields of Phi(T) = 0.78 and Phi(O-1(2)) = 0.70, which are the highest values so far obtained for the aza-BODIPY derivatives.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectHalogenated squaraine dyesen_US
dc.subjectViologen-linked acridinesen_US
dc.subjectPhotodynamic therapyen_US
dc.titleTuning photosensitized singlet oxygen generation efficiency of novel aza-BODIPY dyesen_US
dc.typeArticleen_US
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