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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol202493c
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dc.titleAnthracene-fused BODIPYs as near-infrared dyes with high photostability
dc.contributor.authorZeng, L.
dc.contributor.authorJiao, C.
dc.contributor.authorHuang, X.
dc.contributor.authorHuang, K.-W.
dc.contributor.authorChin, W.-S.
dc.contributor.authorWu, J.
dc.date.accessioned2014-10-16T08:20:32Z
dc.date.available2014-10-16T08:20:32Z
dc.date.issued2011-11-18
dc.identifier.citationZeng, L., Jiao, C., Huang, X., Huang, K.-W., Chin, W.-S., Wu, J. (2011-11-18). Anthracene-fused BODIPYs as near-infrared dyes with high photostability. Organic Letters 13 (22) : 6026-6029. ScholarBank@NUS Repository. https://doi.org/10.1021/ol202493c
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93111
dc.description.abstractAn anthracene unit was successfully fused to the zigzag edge of a boron dipyrromethene (BODIPY) core by an FeCl 3-mediated oxidative cyclodehydrogenation reaction. Meanwhile, a dimer was also formed by both intramolecular cyclization and intermolecular coupling. The anthracene-fused BODIPY monomer 7a and dimer 7b showed small energy gaps (∼1.4 eV) and near-infrared absorption/emission. Moreover, they exhibited high photostability. © 2011 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol202493c
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol202493c
dc.description.sourcetitleOrganic Letters
dc.description.volume13
dc.description.issue22
dc.description.page6026-6029
dc.identifier.isiut000296756600024
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