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.
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CITATION STYLE
APA
Sun, Z., Huang, K. W., & Wu, J. (2010). Soluble and stable zethrenebis(dicarboximide) and its quinone. Organic Letters, 12(20), 4690–4693. https://doi.org/10.1021/ol102088j
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