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Covalent grafting nitrophenyl group on Au surface via click reaction: Assembling process and electrochemical behaviors

机译:通过点击反应在金表面上共价接枝硝基苯基:组装过程和电化学行为

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In this paper, we described a simple and facile method for the covalent functionalization of Au surface with nitrophenyl group via stepwise strategy. Structurally well-defined azide-terminated organic self-assembled monolayers; (SAMs) were formed on Au surface from a commercially available mixture solution of azidoundecanethiol and dilute thiol. Subsequent, derivatization of the azide-terminated monolayers was conducted in aqueous environments with ethynyl nitrobenzene via a selective, reliable, robust click reaction. By this way, the nitrophenyl group was covalently and quantitatively grafted on Au surface, which was confirmed by Raman Spectrometry and electrochemical methods. These results demonstrated the efficiency of using click chemistry in assembling covalently linked nanostructures. (C) 2008 Elsevier B.V. All rights reserved.
机译:在本文中,我们描述了一种通过分步策略将金表面与硝基苯基共价官能化的简便方法。结构清晰的叠氮化物末端有机自组装单层;由可商购的叠氮十一烷硫醇和稀硫醇的混合溶液在Au表面上形成(SAMs)。随后,通过乙炔基硝基苯通过选择性,可靠,稳健的点击反应在水性环境中进行叠氮化物封端的单分子膜的衍生。通过这种方式,通过拉曼光谱法和电化学方法证实了硝基苯基基团被共价且定量地接枝在Au表面上。这些结果证明了在组装共价连接的纳米结构中使用点击化学的效率。 (C)2008 Elsevier B.V.保留所有权利。

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