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首页> 外文期刊>Angewandte Chemie >Flow-Assisted Synthesis of [10]Cycloparaphenylene through Serial Microreactions under Mild Conditions
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Flow-Assisted Synthesis of [10]Cycloparaphenylene through Serial Microreactions under Mild Conditions

机译:通过温和条件下通过连续微孔进行[10]环丙基的流动辅助合成

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摘要

Cycloparaphenylene (CPP) has been recognized as an attractive template for the bottom-up synthesis of carbon nanotubes with uniform diameter, and is important for the chemistry of graphitic as well as ring-shaped macromolecules. However, the reported routes from halogenated benzenes have suffered from low yields even under time-and labor-consuming multistep conditions. Herein we report a flow-assisted synthesis of [10]CPP in four steps under mild conditions. For the synthesis, a selective nucleophilic addition of the unprotected diketone without the double-added byproduct was achieved within 3 s in high yield. Subsequently, the obtained compound was reacted with dilithiated benzene at 25 degrees C to form a U-shaped precursor for CPP in a separate microreactor, which was finally dimerized and aromatized to obtain [10]CPP by a two-step in-flask reaction. Precise control of time and flow facilitated by the flow-assisted system enabled the development of an efficient synthetic route for [10]CPP.
机译:环丙烷(CPP)已被认为是具有均匀直径的碳纳米管的自下而上合成的有吸引力的模板,对于石墨和环形大分子的化学是重要的。然而,即使在耗时的多学期条件下,来自卤化苯的报道仍然受到低产率。在此,我们在温和条件下在四个步骤中报告了[10] CPP的流动合成。对于合成,在高产率高的3秒内实现了在没有双添加的副产物的情况下进行无保护的二酮的选择性亲核添加。随后,将所得化合物与碳酸苯,25℃反应,以在单独的微反应器中形成用于CPP的U形前体,最终将并芳香化以通过两步烧瓶反应获得[10] CPP。通过流动辅助系统促进的时间和流程的精确控制使得[10] CPP的高效合成路线的开发能够开发。

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