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Versatile Two‐Step Functionalization of Nanocarbons: Grafting of Propargylic Groups and Click Post‐Functionalization

机译:纳米碳的多功能两步功能化:丙炔基团的接枝和点击后功能化

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摘要

Chemical functionalization of nanocarbons is essential for further applications in various fields. We developed a facile, inexpensive, and gram‐scale one‐pot route towards alkynyl‐functionalized nanocarbons. Nucleophilic addition/propargylic capture places alkyne moieties at the surface of carbon nanotubes (CNTs) and graphene. Thermogravimetric analysis coupled with mass spectrometry and Raman analysis confirmed the efficiency of this process. Conductivity measurements demonstrated the maintenance of the CNT electrical properties. The attached alkynyl moieties were reacted with various azide derivatives through the click‐Huisgen [3+2] cycloaddition and characterized with XPS. The efficient addition of those derivatives enables the application of our finding in various fields. This route is a reliable and convenient alternative to the known diazonium functionalization and oxidation‐esterification reactions to graft alkyne groups.
机译:纳米碳的化学功能化对于在各个领域的进一步应用至关重要。我们开发了一种简便,便宜且克级的单罐路线,以实现炔基官能化的纳米碳。亲核加成/炔丙基捕获将炔烃部分置于碳纳米管(CNT)和石墨烯的表面。热重分析结合质谱和拉曼分析证实了该过程的效率。电导率测量表明保持了CNT的电性能。连接的炔基部分通过click-Huisgen [3 + 2]环加成反应与各种叠氮化物衍生物反应,并用XPS表征。那些衍生物的有效添加使得我们的发现可应用于各个领域。该方法是对接枝炔基的已知重氮官能化和氧化酯化反应的可靠便捷的替代方法。

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