Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol102147f
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dc.titleTriptycene: No homoconjugation effect for extending optical properties of π-conjugated oligomers
dc.contributor.authorGu, X.
dc.contributor.authorLai, Y.-H.
dc.date.accessioned2014-10-16T08:46:48Z
dc.date.available2014-10-16T08:46:48Z
dc.date.issued2010-11-19
dc.identifier.citationGu, X., Lai, Y.-H. (2010-11-19). Triptycene: No homoconjugation effect for extending optical properties of π-conjugated oligomers. Organic Letters 12 (22) : 5200-5203. ScholarBank@NUS Repository. https://doi.org/10.1021/ol102147f
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95352
dc.description.abstract1,5- and 1,8-bis(bifluorenyl)anthracene were synthesized and converted to their corresponding bis(bifluorenyl)triptycenes and bis(bifluorenyl)-9,10- dihydroanthracenes. Analysis of their optical properties shows no feature of extended conjugation in the triptycene pair. The electronic spectra of the triptycene and dihydroanthracene pairs are in fact superimposable. There is definite evidence that triptycene displays zero homoconjugation effect. © 2010 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol102147f
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol102147f
dc.description.sourcetitleOrganic Letters
dc.description.volume12
dc.description.issue22
dc.description.page5200-5203
dc.identifier.isiut000284080400031
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