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|Title:||Anthracene-fused BODIPYs as near-infrared dyes with high photostability||Authors:||Zeng, L.
|Issue Date:||18-Nov-2011||Citation:||Zeng, 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||Abstract:||An 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.||Source Title:||Organic Letters||URI:||http://scholarbank.nus.edu.sg/handle/10635/93111||ISSN:||15237060||DOI:||10.1021/ol202493c|
|Appears in Collections:||Staff Publications|
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