Anthracene-fused BODIPYs as near-infrared dyes with high photostability

Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol202493c

Title:	Anthracene-fused BODIPYs as near-infrared dyes with high photostability
Authors:	Zeng, L. Jiao, C. Huang, X. Huang, K.-W. Chin, W.-S. Wu, J.
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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