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One-Shot Multiple Borylation toward BN-Doped Nanographenes

机译:BN掺杂纳米石墨烯的一枪多硼基化。

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摘要

One-shot double, triple, and quadruple borylation reactions of triarylamines were developed through a judicious choice of boron source and Brønsted base. With the aid of borylation reactions, a variety of BN-doped nanographenes were synthesized in two steps from commercially available starting materials. An organic light-emitting diode device employing BN-doped nanographene as an emitter exhibited deep pure-blue emission at 460 nm, with CIE coordinates of (0.13, 0.11), and an external quantum efficiency of 18.3%.
机译:通过明智地选择硼源和布朗斯台德碱,开发了三芳基胺的单次双,三和四重硼化反应。借助于硼化反应,分两步从市售起始原料合成了各种BN掺杂的纳米石墨烯。使用掺杂了BN的纳米石墨烯作为发射器的有机发光二极管装置在460nm处显示深的纯蓝色发射,CIE坐标为(0.13,0.11),并且外部量子效率为18.3%。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2018年第4期|1195-1198|共4页
  • 作者单位

    Department of Chemistry, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyogo 669-1337, Japan;

    Department of Chemistry, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyogo 669-1337, Japan;

    Department of Chemistry, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyogo 669-1337, Japan;

    Department of Chemistry, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyogo 669-1337, Japan;

    Japan Synchrotron Radiation Research Institute (JASRI), 1-1-1, Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198, Japan;

    Department of Chemistry, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyogo 669-1337, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:07:17

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