Soluble and stable zethrenebis(dicarboximide) and its quinone

Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol102088j

Title:	Soluble and stable zethrenebis(dicarboximide) and its quinone
Authors:	Sun, Z. Huang, K.-W. Wu, J.
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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