Pascanu Vlad, González Miera Greco, Inge A Ken, Martín-Matute Belén
Department of Organic Chemistry , Stockholm University , Stockholm SE-10691 , Sweden.
Department of Chemistry , University of Zurich , Zurich CH-8057 , Switzerland.
J Am Chem Soc. 2019 May 8;141(18):7223-7234. doi: 10.1021/jacs.9b00733. Epub 2019 Apr 23.
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.
有机化学和材料化学的最新进展使新型材料的孔隙率能够在纳米尺度上得到精确控制。在此背景下,金属有机框架(MOF)迅速成为目前多相催化研究中最具吸引力的固体载体类别之一。其前所未有的可调性使MOF有机会在其他材料失败的领域取得成功。在过去十年中,新结构的复杂性呈指数级增长。具有各种拓扑结构和孔径的MOF在很宽的pH值和温度范围内都表现出优异的稳定性。甚至通过可控地引入缺陷以可预测的方式改变MOF的性质也已变得很常见。然而,关于MOF催化的研究在跟上有机化学的现代趋势方面一直较为滞后。对映选择性过程、C-H活化或烯烃复分解等相关问题仍然很少被讨论。在这篇展望文章中,我们重点介绍了一些解决当代有机合成中重要问题的优秀实例,并与现有催化剂进行了合理比较。其中一些MOF催化剂已经超越了最先进的均相催化剂。对于其他一些催化剂,可能仍需要改进,但它们朝着更大的挑战努力是有价值的。此外,我们还确定了一些重要领域,MOF在这些领域可能会发挥作用,即满足目前催化领域未被满足的需求,而不是试图在均相催化剂擅长的领域与其竞争。最后,我们强烈主张基于对孔内发生的事件的深入机理理解,对MOF催化剂进行合理设计。