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Metal-Organic Frameworks as Catalysts for Organic Synthesis: A Critical Perspective

机译:金属有机框架作为有机合成催化剂:批判性观点

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摘要

Recent advances in organic chemistry and materials chemistry have enabled the porosity of new materials to be accurately controlled on the nanometer scale. In this context, metal-organic frameworks (MOFs) have rapidly become one of the most attractive classes of solid supports currently under investigation in heterogeneous catalysis. Their unprecedented degree of tunability gives MOFs the chance to succeed where others have failed. The past decade has witnessed an exponential growth in the complexity of new structures. MOFs with a variety of topologies and pore sizes show excellent stability across wide ranges of pH and temperature. Even the controlled insertion of defects, to alter the MOF's properties in a predictable manner, has become commonplace. However, research on catalysis with MOFs has been sluggish in catching up with modern trends in organic chemistry. Relevant issues such as enantioselective processes, C-H activation, or olefin metathesis are still rarely discussed. In this Perspective, we highlight meritorious examples that tackle important issues from contemporary organic synthesis, and that provide a fair comparison with existing catalysts. Some of these MOF catalysts already outcompete state-of-the-art homogeneous solutions. For others, improvements may still be required, but they have merit in aiming for the bigger challenge. Furthermore, we also identify some important areas where MOFs are likely to make a difference, by addressing currently unmet needs in catalysis instead of trying to outcompete homogeneous catalysts in areas where they excel. Finally, we strongly advocate for rational design of MOF catalysts, founded on a deep mechanistic understanding of the events taking place inside the pore.
机译:有机化学和材料化学的最新进展使得能够在纳米级上精确控制的新材料的孔隙率。在这种情况下,金属 - 有机框架(MOF)迅速成为目前在异构催化下进行的最具吸引力的固体支持之一。他们前所未有的可调性,使MOF是成功的机会,别人失败了。过去十年目睹了新结构的复杂性的指数增长。具有各种拓扑和孔径的MOF在宽范围的pH和温度范围内具有出色的稳定性。即使是受到缺陷的控制插入,以以可预测的方式改变MOF的性质,已经变得普遍。然而,关于MOF的催化研究在赶上有机化学的现代趋势迟缓。仍然很少讨论映选择性过程,C-H激活或烯烃复分解等相关问题。在这种观点中,我们突出了具有当代有机合成的重要问题的功勋示例,并且提供了与现有催化剂的公平比较。其中一些MOF催化剂已经超越了最先进的均匀解决方案。对于其他人来说,可能仍然需要改进,但它们有旨在瞄准更大的挑战。此外,我们还确定了一些重要领域,通过解决催化中的目前未满足的需求而不是试图在他们擅长的区域中进行均匀的催化剂来判断MOF。最后,我们强烈倡导了MOF催化剂的合理设计,建立了对毛孔内部发生的事件的深刻机制理解。

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  • 来源
    《Journal of the American Chemical Society》 |2019年第18期|7223-7234|共12页
  • 作者单位

    Stockholm Univ Dept Organ Chem SE-10691 Stockholm Sweden|Univ Zurich Dept Chem CH-8057 Zurich Switzerland;

    Stockholm Univ Dept Organ Chem SE-10691 Stockholm Sweden|Nagoya Univ Inst Transformat Biomol WPI ITbM Chikusa Ku Nagoya Aichi 4648602 Japan|Nagoya Univ Grad Sch Sci Chikusa Ku Nagoya Aichi 4648602 Japan;

    Stockholm Univ Dept Mat & Environm Chem SE-10691 Stockholm Sweden;

    Stockholm Univ Dept Organ Chem SE-10691 Stockholm Sweden;

  • 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);
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  • 正文语种 eng
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