Electroless ultrasonic functional ization of diamond nanoparticles using aryl diazonium salts

被引:58
作者
Mangeney, Claire [1 ,2 ]
Qin, Zhengran [1 ,2 ]
Dahoumane, Si Amar [1 ,2 ]
Adenier, Alain [1 ,2 ]
Herbst, Frederic [1 ,2 ]
Boudou, Jean-Paul [3 ,4 ]
Pinson, Jean [5 ]
Chehimi, Mohamed M. [1 ,2 ]
机构
[1] Univ Paris Diderot, ITODYS, F-75005 Paris, France
[2] CNRS, UMR 7086, F-75005 Paris, France
[3] Univ Paris 06, BioEmCo, F-75252 Paris 05, France
[4] CNRS, UMR 7618, F-75252 Paris 05, France
[5] CNRS, Lab Environm & Chim Analyt, UMR 7121, F-75005 Paris, France
关键词
Nanodiamonds; Diazonium salts; Electroless grafting; Aqueous colloidal suspension;
D O I
10.1016/j.diamond.2008.04.003
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We report a novel and very handful strategy for the functionalization of diamond nanoparticles (NDs), based on the ultrasound-assisted grafting of aryl groups from the electroless reduction of diazonium salts. For this study, 4-nitrobenzenediazonium salt was used as a model molecule and the reaction was investigated in neutral and acidic aqueous media. Spectroscopic evidence for the successful attachment of aryl groups to nanodiamonds (NDs) was given by IR and XPS which clearly detect characteristic NO2 peaks. Moreover, the absence of any peaks from the N+ N- group in the IR spectra is a clear indication of the chemical reduction of the parent diazonium salt at the surface of NDs. This spontaneous chemical modification of NDs by aryl diazonium, salts was confined to the surface of the ND particles; indeed, XRD measurements have shown that the crystalline structure of the bulk of the particles was unaffected. It opens up new possibilities towards the control of the surface chemical composition of NDs using simple protocols operated in very soft conditions, i.e. in water at room temperature. It shows conclusively that the chemistry toolbox of experts interested in nanodiamonds should contain aryl diazonium salts. given their versatility in forming active platforms. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1881 / 1887
页数:7
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