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Synthesis and Reactions of Carbon Nanohoop

机译:碳纳米的合成与反应

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摘要

Despite their intriguing structure and potential applications, the synthesis of structurally uniform carbon nanohoops has been a significant challenge until recently. The first synthesis of cycloparaphenylenes (CPPs), which are representative carbon nanohoops, nearly a decade ago considerably enhanced the availability of various carbon nanohoops, but the final products are usually only prepared on a mg scale. This review describes our endeavors to increase the availability of CPPs and their derivatives in large quantities. The three key reactions are1)the one-pot, stereoselective two-fold addition of aryllithium to1,4-benzoquinones to give U-shaped cyclization precursors, 2) subsequent nickel— or platinum-mediated selective cyclization, and 3) H2SnCl4-mediated reductive aromatization. This straightforward and high-yielding synthetic route provides gram quantities of various CPPs and their derivatives. Preliminary results on the applications of CPPs in electronic devices and the elucidation of CPP reactivity are also discussed.
机译:尽管其有趣的结构和潜在的应用,但在结构均匀的碳纳米植物的合成至最近直到最近的挑战是显着的挑战。第一次合成环丙烷基环氧(CPP),其是代表性的碳纳米,几乎十年前提高了各种碳纳米的可用性,但是最终产物通常仅在Mg刻度上制备。该审查描述了我们的努力,以提高CPPS及其衍生品大量的可用性。三个关键反应是1)单罐,立体选择性两倍加入芳基锂至1,4-苯醌,得到U形环化前体,2)随后的镍或铂介导的选择性环化,3)H2SNCL4介导的还原芳香化。这种直接和高收入的合成路线提供了克数量的各种CPP及其衍生物。还讨论了CPP在电子设备中的应用和CPP反应性阐明的初步结果。

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  • 来源
    《有機合成化学協会誌》 |2019年第11期|共12页
  • 作者单位

    Institute for Chemical Research Kyoto University Ujiy Kyoto 611-0011 Japan;

    Institute for Chemical Research Kyoto University Ujiy Kyoto 611-0011 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

  • 入库时间 2022-08-20 15:21:24

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