Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol102088j
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dc.titleSoluble and stable zethrenebis(dicarboximide) and its quinone
dc.contributor.authorSun, Z.
dc.contributor.authorHuang, K.-W.
dc.contributor.authorWu, J.
dc.date.accessioned2014-06-23T05:49:55Z
dc.date.available2014-06-23T05:49:55Z
dc.date.issued2010-10-15
dc.identifier.citationSun, 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
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77019
dc.description.abstractSoluble 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol102088j
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol102088j
dc.description.sourcetitleOrganic Letters
dc.description.volume12
dc.description.issue20
dc.description.page4690-4693
dc.identifier.isiut000282604700067
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