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Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs
- Yuan, Shuai, Chen, Ying-Pin, Qin, Jun-Sheng, Lu, Weigang, Zou, Lanfang, Zhang, Qiang, Wang, Xuan, Sun, Xing, Zhou, Hong-Cai
- Journal of the American Chemical Society 2016 v.138 no.28 pp. 8912-8919
- adsorption, alcohols, engineering, hydrogen, oxidation, synergism, zirconium
- Precise placement of multiple functional groups in a highly ordered metal–organic framework (MOF) platform allows the tailoring of the pore environment, which is required for advanced applications. To realize this, we present a comprehensive study on the linker installation method, in which a stable MOF with coordinatively unsaturated Zr₆ clusters was employed and linkers bearing different functional groups were postsynthetically installed. A Zr-MOF with inherent missing linker sites, namely, PCN-700, was initially constructed under kinetic control. Twelve linkers with different substituents were then designed to study their effect on MOF formation kinetics and therefore resulting MOF structures. Guided by the geometrical analysis, linkers with different lengths were installed into a parent PCN-700, giving rise to 11 new MOFs and each bearing up to three different functional groups in predefined positions. Systematic variation of the pore volume and decoration of pore environment were realized by linker installation, which resulted in synergistic effects including an enhancement of H₂ adsorption capacities of up to 57%. In addition, a size-selective catalytic system for aerobic alcohol oxidation reaction is built in PCN-700 through linker installation, which shows high activity and tunable size selectivity. Altogether, these results exemplify the capability of the linker installation method in the pore environment engineering of stable MOFs with multiple functional groups, giving an unparalleled level of control.