Wang Zhengyan, Babucci Melike, Zhang Yafeng, Wen Yujie, Peng Luming, Yang Bing, Gates Bruce C, Yang Dong
College of Chemical Engineering, State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing Tech University, Nanjing, Jiangsu 21000, China.
Department of Chemical Engineering, University of California at Davis, Davis, California 95616, United States.
ACS Appl Mater Interfaces. 2020 Nov 25;12(47):53537-53546. doi: 10.1021/acsami.0c16559. Epub 2020 Nov 12.
Many metal organic frameworks (MOFs) incorporate metal oxide clusters as nodes. Node sites where linkers are missing can be catalytic sites. We now show how to dial in the number and occupancy of such sites in MIL-53 and MIL-68, which incorporate aluminum-oxide-like nodes. The methods involve modulators used in synthesis and postsynthesis reactions to control the modulator-derived groups on these sites. We illustrate the methods using formic acid as a modulator, giving formate ligands on the sites, and these can be removed to leave μ-OH groups and open Lewis acid sites. Methanol dehydration was used as a catalytic reaction to probe these sites, with infrared spectra giving evidence of methoxide ligands as reaction intermediates. Control of node surface chemistry opens the door for placement of a variety of ligands on a wide range of metal oxide cluster nodes for dialing in reactivity and catalytic properties of a potentially immense class of structurally well-defined materials.
许多金属有机框架材料(MOF)都包含金属氧化物簇作为节点。缺少连接体的节点部位可能是催化位点。我们现在展示了如何调节MIL-53和MIL-68中此类位点的数量和占有率,这两种材料都包含类似氧化铝的节点。这些方法涉及合成过程中使用的调节剂以及后合成反应,以控制这些位点上源自调节剂的基团。我们以甲酸作为调节剂来说明这些方法,在这些位点上生成甲酸盐配体,并且可以将这些配体去除,留下μ-OH基团并形成开放的路易斯酸位点。甲醇脱水被用作催化反应来探测这些位点,红外光谱提供了甲醇盐配体作为反应中间体的证据。控制节点表面化学为在各种金属氧化物簇节点上放置多种配体打开了大门,从而调节一类潜在庞大的结构明确材料的反应性和催化性能。