Cleaving Carboxyls: Understanding Thermally Triggered Hierarchical Pores in the Metal–Organic Framework MIL-121

作者：Shoushun Chen, Soumya Mukherjee, Bryan E. G. Lucier, Ying Guo, Y. T. Angel Wong, Victor V. Terskikh, Michael J. Zaworotko, Yining Huang · 发表于：Journal of the American Chemical Society · 年份：2019 · DOI：10.1021/jacs.9b06194 · 被引用次数：90 · 研究领域：Metal-Organic Frameworks: Synthesis and Applications、Covalent Organic Framework Applications、X-ray Diffraction in Crystallography

Carboxylic acid linker ligands are known to form strong metal–carboxylate bonds to afford many different variations of permanently microporous metal–organic frameworks (MOFs). A controlled approach to decarboxylation of the ligands in carboxylate-based MOFs could result in structural modifications, offering scope to improve existing properties or to unlock entirely new properties. In this work, we demonstrate that the microporous MOF MIL-121 is transformed to a hierarchically porous MOF via thermally triggered decarboxylation of its linker. Decarboxylation and the introduction of hierarchical porosity increases the surface area of this material from 13 to 908 m 2 /g and enhances gas adsorption uptake for industrially relevant gases (i.e., CO 2, C 2 H 2, C 2 H 4, and CH 4 ). For example, CO 2 uptake in hierarchically porous MIL-121 is improved 8.5 times over MIL-121, reaching 215.7 cm 3 /g at 195 K and 1 bar; CH 4 uptake is 132.3 cm 3 /g at 298 K and 80 bar in hierarchically porous MIL-121 versus zero in unmodified MIL-121. The approach taken was validated using a related aluminum-based MOF, ISOMIL-53. However, many specifics of the decarboxylation procedure in MOFs have yet to be unraveled and demand prompt examination. Decarboxylation, the formation of heterogeneous hierarchical pores, gas uptakes, and host–guest interactions are comprehensively investigated using variable-temperature multinuclear solid-state NMR spectroscopy, X-ray diffraction, electron microscopy, and gas ...