Chelating Ligands for nanocrystals' surface functionalization

被引:141
作者
Querner, C
Reiss, P
Bleuse, J
Pron, A
机构
[1] CEA Grenoble, Serv Interfaces Mat Mol & Macromol, Lab Phys Metaux Synth, F-38054 Grenoble 9, France
[2] CEA Grenoble, Serv Phys Mat & Microstruct, Lab Phys SemiConducteurs, Dept Rech Fondamentale Mat Condesee, F-38054 Grenoble 9, France
关键词
D O I
10.1021/ja047882c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new family of ligands for the surface functionalization of CdSe nanocrystals is proposed, namely alkyl or aryl derivatives of carbodithioic acids (R-C(S)SH). The main advantages of these new ligands are as follows: they nearly quantitatively exchange the initial surface ligands (TOPO) in very mild conditions; they significantly improve the resistance of nanocrystals against photooxidation because of their ability of strong chelate-type binding to metal atoms; their relatively simple preparation via Grignard intermediates facilitates the development of new bifunctional ligands containing, in addition to the anchoring carbodithioate group, a second function, which enables the grafting of molecules or macromolecules of interest on the nanocrystal surface. To give an example of this approach, we report, for the first time, the grafting of an electroactive oligomer from the polyaniline family-aniline tetramer-on CdSe nanocrystals after their functionalization with 4-formyldithiobenzoic acid. The grafting proceeds via a condensation reaction between the aldehyde group of the ligand and the terminal primary amine group of the tetramer. The resulting organic/ inorganic hybrid exhibits complete extinction of the fluorescence of its constituents, indicating efficient charge or energy transfer between the organic and the inorganic semiconductors.
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收藏
页码:11574 / 11582
页数:9
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