Luminescent Quantum Dots Stabilized by N-Heterocyclic Carbene Polymer Ligands

被引:27
|
作者
Du, Liang [1 ]
Nosratabad, Neda Arabzadeh [1 ]
Jin, Zhicheng [1 ]
Zhang, Chengqi [1 ]
Wang, Sisi [1 ]
Chen, Banghao [1 ]
Mattoussi, Hedi [1 ]
机构
[1] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
基金
美国国家科学基金会;
关键词
POTENT IN-VITRO; GOLD NANOPARTICLES; ZWITTERIONIC LIGANDS; COLLOIDAL STABILITY; BIOCOMPATIBLE SEMICONDUCTOR; PLATINUM(II) COMPLEXES; IMIDAZOLIUM SALTS; GLYCOL) LIGANDS; COMPACT; ANTICANCER;
D O I
10.1021/jacs.0c10592
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have tested the ability of N-heterocyclic carbene (NHC)-modified ligands to coordinate and stabilize luminescent CdSe-ZnS core-shell quantum dot (QD) dispersions in hydrophilic media. In particular, we probed the effects of ligand structure and coordination number on the coating affinity to the nanocrystals. We find that such NHC-based ligands rapidly coordinate onto the QDs (requiring similar to 5-10 min of reaction time), which reflects the soft Lewis base nature of the NHC groups, with its two electrons sharing capacity. Removal of the hydrophobic cap and promotion of carbenedriven coordination on the nanocrystals have been verified by H-1 NMR spectroscopy, while C-13 NMR was used to identify the formation of carbene-Zn complexes. The newly coated QD dispersions exhibit great long-term colloidal stability over a wide range of conditions. Additionally, we find that coordination onto the QD surfaces affects the optical and spectroscopic properties of the nanocrystals. These include a size-dependent red-shift of the absorption and fluorescence spectra and a pronounced increase in the measured fluorescence intensity when the samples are stored under white light exposure compared to those stored in the dark.
引用
收藏
页码:1873 / 1884
页数:12
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