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|Title:||Soluble and stable zethrenebis(dicarboximide) and its quinone||Authors:||Sun, Z.
|Issue Date:||15-Oct-2010||Citation:||Sun, Z., Huang, K.-W., Wu, J. (2010-10-15). Soluble and stable zethrenebis(dicarboximide) and its quinone. Organic Letters 12 (20) : 4690-4693. ScholarBank@NUS Repository. https://doi.org/10.1021/ol102088j||Abstract:||Soluble and stable zethrenebis(dicarboximide) (1) was synthesized by an in situ Stille cross coupling/transannular cyclization reaction. 1 showed largely improved photostability and solubility compared with the very unstable zethrene and it also exhibited far-red absorption and emission with high photoluminescence quantum yield. Bromination of 1 with NBS/DMF gave its quinone form 2 via an unusual pathway. © 2010 American Chemical Society.||Source Title:||Organic Letters||URI:||http://scholarbank.nus.edu.sg/handle/10635/77019||ISSN:||15237060||DOI:||10.1021/ol102088j|
|Appears in Collections:||Staff Publications|
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