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Bi(Ⅰ)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane

机译:氨硼烷Bi(Ⅰ)催化转移加氢

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摘要

A catalytic transfer-hydrogenation utilizing a well-defined Bi(I) complex as catalyst and ammonia-borane as transfer agent has been developed. This transformation represents a unique example of low-valent pnictogen catalysis cycling between oxidation states I and III, and proved useful for the hydrogenation of azoarenes and the partial reduction of nitroarenes. Interestingly, the bismuthinidene catalyst performs well in the presence of low-valent transition-metal sensitive functional groups and presents orthogonal reactivity compared to analogous phosphorus-based catalysis. Mechanistic investigations suggest the intermediacy of an elusive bismuthine species, which is proposed to be responsible for the hydrogenation and the formation of hydrogen.
机译:已开发出一种以明确定义的Bi(I)配合物为催化剂,氨硼烷为转移剂的催化转移加氢方法。这种转变代表了氧化态I和III之间低价光催化反应循环的独特实例,并证明可用于偶氮芳烃的氢化和硝基芳烃的部分还原。有趣的是,与类似的基于磷的催化相比,双变亚丁基催化剂在低价过渡金属敏感官能团的存在下表现良好,并且具有正交的反应性。机理研究表明,存在一种难以捉摸的铋物种,该物种被认为负责氢化和氢的形成。

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  • 来源
    《Journal of the American Chemical Society》 |2019年第10期|4235-4240|共6页
  • 作者单位

    Max Planck Inst Kohlenforsch, Kaiser Wilhelm Pl 1, D-45470 Mulheim, Germany;

    Max Planck Inst Kohlenforsch, Kaiser Wilhelm Pl 1, D-45470 Mulheim, Germany;

    Max Planck Inst Kohlenforsch, Kaiser Wilhelm Pl 1, D-45470 Mulheim, Germany;

  • 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
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  • 入库时间 2022-08-18 04:12:48

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