Bridged triphenylamine-based dendrimers: Tuning enhanced two-photon absorption performance with locked molecular planarity

Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol801238n

Title:	Bridged triphenylamine-based dendrimers: Tuning enhanced two-photon absorption performance with locked molecular planarity
Authors:	Fang, Z. Teo, T.-L. Cai, L. Lal, Y.-H. Samoc, A. Samoc, M.
Issue Date:	1-Jan-2009
Citation:	Fang, Z., Teo, T.-L., Cai, L., Lal, Y.-H., Samoc, A., Samoc, M. (2009-01-01). Bridged triphenylamine-based dendrimers: Tuning enhanced two-photon absorption performance with locked molecular planarity. Organic Letters 11 (1) : 1-4. ScholarBank@NUS Repository. https://doi.org/10.1021/ol801238n
Abstract:	Triphenylamine derivatives bridged by methylene units afford a near planar molecular platform in a series of one dimer and two oligomers exhibiting increased structural rigidity compared to that of their parent triphenylamines. This series of dendrimers show significantly enhanced two-photon absorptions that are up to 3-fold that of triphenylamines with similar molecular size and structure. © 2009 American Chemical Society.
Source Title:	Organic Letters
URI:	http://scholarbank.nus.edu.sg/handle/10635/63552
ISSN:	15237060
DOI:	10.1021/ol801238n
Appears in Collections:	Staff Publications

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