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Repurposing of oxazolone chemistry: gaining access to functionalized graphene nanosheets in a top-down approach from graphite

机译:恶唑酮化学的再利用:以自上而下的方法从石墨中获得官能化的石墨烯纳米片

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摘要

Solvent-free 1,3-dipolar cycloaddition (1,3-DC) reactions between graphite flakes and mesoionic oxazolones were carried out by heating the resulting solid mixture at mild temperatures (70–120 °C). The direct functionalization and delamination of graphite flakes into few layers of graphene nanosheets was confirmed by micro-Raman and X-ray photoelectron spectroscopies, scanning transmission electron microscopy and thermogravimetric analysis. The 1,3-DC reactions of mesoionic dipoles have been investigated with density functional theory to model graphene, exploring three different pathways: center, corner and edge. These theoretical calculations highlighted that the 1,3-DC reaction can proceed both through a concerted mechanism competing with a stepwise one involving a zwitterionic intermediate. The irreversible decarboxylation inherent in the last step justifies the high degree of functionalization experimentally observed, representing the driving force of the process.
机译:通过在温和的温度(70–120°C)下加热生成的固体混合物,进行石墨薄片和中性离子唑酮之间的无溶剂1,3-偶极环加成(1,3-DC)反应。通过微拉曼和X射线光电子能谱,扫描透射电子显微镜和热重分析,证实了石墨薄片直接功能化和分层为几层石墨烯纳米片。已经使用密度泛函理论研究了介电偶极子的1,3-DC反应以建模石墨烯,探索了三种不同的途径:中心,拐角和边缘。这些理论计算突显了1,3-DC反应可以通过与涉及两性离子中间体的逐步反应竞争的协同机理进行。最后一步固有的不可逆脱羧证明了实验观察到的高度官能化是合理的,代表了该过程的驱动力。

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