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|Title:||Bridged triphenylamine-based dendrimers: Tuning enhanced two-photon absorption performance with locked molecular planarity|
|Authors:||Fang, Z. |
|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|
|Appears in Collections:||Staff Publications|
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