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分级金属有机框架中的酸酐后合成修饰

Anhydride Post-Synthetic Modification in a Hierarchical Metal-Organic Framework.

作者信息

Chen Shoushun, Song Zhongxin, Lyu Jinghui, Guo Ying, Lucier Bryan E G, Luo Wilson, Workentin Mark S, Sun Xueliang, Huang Yining

机构信息

Department of Chemistry, The University of Western Ontario, London, Ontario, Canada N6A 5B7.

Department of Mechanical and Materials Engineering, The University of Western Ontario, London, Ontario, Canada N6A 5B9.

出版信息

J Am Chem Soc. 2020 Mar 4;142(9):4419-4428. doi: 10.1021/jacs.9b13414. Epub 2020 Feb 20.

Abstract

Metal-organic frameworks (MOFs) are important porous materials. Post-synthetic modification (PSM) of MOFs via the pendant groups or secondary functional groups of organic linkers has been widely used to introduce new or enhance existing properties of MOFs for various practical applications. In this work, we have constructed, for the first time, a novel platform for PSM of MOFs by introducing an anhydride functional group into a hierarchically porous MOF (MIL-121) as an effective anchor. We have demonstrated that the combination of the high reactivity of anhydride and hierarchical porosity makes this protocol particularly novel and important, as it led to excellent opportunities of incorporating not only a wide variety of organic molecules with different sizes and chemical nature but also the noble metal complexes in MOFs. Specifically, we show that the anhydride group decorated in the MOF exhibits a high reactivity toward covalently binding 10 different guest molecules including alcohols, amines, thiols, and noble metal (Pt(II)/Pt(IV)) complexes, whereas the hierarchical pores created in the MOF allow the incorporation of guest species varying in size from methanol to larger molecules such as polyaromatic amines. This novel approach provides the community with a new avenue to prepare MOF-based materials for targeted applications. To illustrate this point, we furnish an example of using this new platform to prepare a Pt-based electrocatalyst which shows excellent catalytic activity toward the oxygen reduction reaction (ORR), a pivotal half-reaction in hydrogen-oxygen fuel cells and other energy storage and conversion devices.

摘要

金属有机框架材料(MOFs)是重要的多孔材料。通过有机连接体的侧基或二级官能团对MOFs进行后合成修饰(PSM)已被广泛用于引入新的或增强MOFs的现有性能,以实现各种实际应用。在这项工作中,我们首次构建了一个用于MOFs后合成修饰的新型平台,通过将酸酐官能团引入到分级多孔MOF(MIL-121)中作为有效锚定基团。我们已经证明,酸酐的高反应活性与分级孔隙率的结合使得该方案特别新颖且重要,因为它不仅为在MOFs中纳入各种不同尺寸和化学性质的有机分子,还为纳入贵金属配合物提供了绝佳机会。具体而言,我们表明在MOF中修饰的酸酐基团对包括醇、胺、硫醇和贵金属(Pt(II)/Pt(IV))配合物在内的10种不同客体分子具有高共价结合反应活性,而MOF中产生的分级孔隙允许纳入尺寸从甲醇到诸如多环芳烃等较大分子不等的客体物种。这种新方法为该领域提供了一条制备用于靶向应用的MOF基材料的新途径。为了说明这一点,我们提供了一个使用这个新平台制备基于Pt的电催化剂的例子,该催化剂对氧还原反应(ORR)表现出优异的催化活性,氧还原反应是氢氧燃料电池以及其他能量存储和转换装置中的关键半反应。

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