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| Content Provider | IEEE Xplore Digital Library |
|---|---|
| Author | Obliosca, J.M. Fan-Gang Tseng Ching-Mao Huang Leu-Wei Lo Pen-Cheng Wang |
| Copyright Year | 2012 |
| Description | Author affiliation: Division of Medical Engineering Research, National Health Research Institutes, Zhunan 35053, Taiwan (Ching-Mao Huang; Leu-Wei Lo) || Department of Engineering and System Science, National Tsing Hua University, 101, Section 2, Kuang-Fu Road, Hsinchu 30013, Taiwan (Obliosca, J.M.; Fan-Gang Tseng; Pen-Cheng Wang) |
| Abstract | A series of tertiary amine quinuclidine-capped cadmium selenide (Q-CdSe) quantum dots (QDs) of ∼4 nm in diameter was successfully synthesized via ligand exchange process in which the original hydrophobic trioctylphosphine oxide (TOPO) ligand bound to QDs was replaced with stronger quinuclidine derivatives, quinuclidine (Q1), 3-quinuclidinone (Q2) and 3-quinuclidinol (Q3). The ligand exchange of TOPO by Q probed using the combined fluorescence and absorption spectroscopy was achieved in just only a few minutes. Moreover, disappearance of prominent C-H aliphatic stretching (∼2900 $cm^{−1})$ and phosphate signal (35 ppm) of TOPO-capped CdSe after replacement with Q as revealed in FT-IR and solid state $^{31}P-NMR$ spectra was observed indicating efficient fast ligand exchange. |
| Starting Page | 343 |
| Ending Page | 346 |
| File Size | 585315 |
| Page Count | 4 |
| File Format | |
| ISBN | 9781467311229 |
| e-ISBN | 9781467311243 |
| DOI | 10.1109/NEMS.2012.6196789 |
| Language | English |
| Publisher | Institute of Electrical and Electronics Engineers, Inc. (IEEE) |
| Publisher Date | 2012-03-05 |
| Publisher Place | Japan |
| Access Restriction | Subscribed |
| Rights Holder | Institute of Electrical and Electronics Engineers, Inc. (IEEE) |
| Subject Keyword | Nuclear magnetic resonance Spectroscopy Heating Nanoelectromechanical systems Multiplexing Electronic mail Microscopy 31PNMR spectroscopy ligand-exchange CdSe quantum dots quinuclidines tertiary amines |
| Content Type | Text |
| Resource Type | Article |
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