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
Source: 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
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