Please use this identifier to cite or link to this item:
https://doi.org/10.1021/ol102147f
DC Field | Value | |
---|---|---|
dc.title | Triptycene: No homoconjugation effect for extending optical properties of π-conjugated oligomers | |
dc.contributor.author | Gu, X. | |
dc.contributor.author | Lai, Y.-H. | |
dc.date.accessioned | 2014-10-16T08:46:48Z | |
dc.date.available | 2014-10-16T08:46:48Z | |
dc.date.issued | 2010-11-19 | |
dc.identifier.citation | Gu, 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.issn | 15237060 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/95352 | |
dc.description.abstract | 1,5- 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol102147f | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1021/ol102147f | |
dc.description.sourcetitle | Organic Letters | |
dc.description.volume | 12 | |
dc.description.issue | 22 | |
dc.description.page | 5200-5203 | |
dc.identifier.isiut | 000284080400031 | |
Appears in Collections: | Staff Publications |
Show simple item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.