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Synthesis and Structure of 2,5,8-Triazido-s-Heptazine: An Energetic and Luminescent Precursor to Nitrogen-Rich Carbon Nitrides

机译:2,5,8-Triazido-s-Heptazine的合成和结构:富氮碳氮化物的高能发光前体。

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摘要

Aromatic nitrogen heterocycles have a wide variety of uses in coordination chemistry and optical science. As one example, the 1,3,5-triazine ring motif (s-triazine, C_3N_3) has shown extensive utility in synthetic chemistry,1 coordination chemistry,2 and optical and magnetic studies.3 Over the past few years, s-triazine has played a key role in molecular routes to carbon nitride (CN_x) materials investigated by various groups,4 including ours.5 Several of our triazine ring precursors contrast with those of others in that they are energetically unstable and rapidly decompose to CN_x materials.
机译:芳香氮杂环在配位化学和光学科学中具有广泛的用途。例如,1,3,5-三嗪环基序(s-triazine,C_3N_3)在合成化学,1配位化学,2以及光学和磁学研究中显示出广泛的用途。3在过去的几年中,s-三嗪在包括我们在内的各种研究组[4]研究的碳氮化物(CN_x)材料的分子路线中起了关键作用。5我们的三嗪环前体与其他三嗪环前体相比,在能量上不稳定,并迅速分解为CN_x材料。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2004年第17期|p. 5372-5373|共2页
  • 作者单位

    Department of Chemistry and the Optical Science and Technology Center, University of Iowa, Iowa City, Iowa 52242;

    Department of Chemistry and the Optical Science and Technology Center, University of Iowa, Iowa City, Iowa 52242;

    Department of Chemistry and the Optical Science and Technology Center, University of Iowa, Iowa City, Iowa 52242;

  • 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
  • 中图分类 化学;
  • 关键词

  • 入库时间 2022-08-18 03:24:47

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