Arraying Shape-Persistent Molecular Alkynyl Trap into Highly Porous and Robust Zirconium Metal–Organic Framework for Propyne Capture and Propyne/Propylene Separation

化学 吸附 多孔性 脱氢 金属有机骨架 分子筛 超分子化学 物理化学 丙炔 化学工程 结晶学 色谱分离 气体分离 原解 多孔介质 分子 选择性 微型多孔材料 吸附 无机化学
作者
Geng Yuan,Chengye Lou,Min Mao,Guangzu Xiong,Pengfu Gao,Junhua Zhang,Lingmei Liu,Yuanbin Zhang,Banglin Chen,Yong Cui,Wei Gong
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
标识
DOI:10.1021/jacs.6c05337
摘要

Adsorptive separation of propyne/propylene (C 3 H 4 /C 3 H 6 ) using porous adsorbents offers a promising route toward energy-efficient production of polymer-grade C 3 H 6 . Currently, the prevailing adsorbents are ultramicroporous metal–organic frameworks (MOFs) that feature narrow channels and/or consist of inorganic anion pillars, which often lead to limited C 3 H 4 uptake capacity and high isosteric enthalpy of adsorption. We report herein a highly porous and robust zirconium metal–organic framework, termed SJTU-520. This MOF incorporates shape-persistent molecular arrays in three-dimensional space derived from cyclotetrabenzoin, which function as selective sites for the preferential entrapment of C 3 H 4 over C 3 H 6, thus enabling high C 3 H 4 capture capacity, record high C 3 H 4 /C 3 H 6 uptake ratio at 1 bar and 298 K, and efficient C 3 H 4 /C 3 H 6 separation at ambient conditions. Compared with the cyclotetrabenzoin and tetraacetate cyclotetrabenzoin-based supramolecular organic crystals, SJTU-520 exhibits significantly higher surface area (3650 m 2 /g versus 42 and 570 m 2 /g), leading to a C 3 H 4 uptake boost by 6.1-fold and 3.7-fold at 298 K and 1 bar, without any compromise of the C 3 H 4 /C 3 H 6 selectivity. The efficient C 3 H 4 /C 3 H 6 separation was validated by extensive breakthrough experiments under various conditions with great recyclability and high productivity of polymer-grade C 3 H 6 from a 10/90 C 3 H 4 /C 3 H 6 mixture. Computational simulations revealed that the four benzene walls of the cyclotetrabenzoin macrocycle in SJTU-520 formed equidistant π–π interactions with the C≡C triple bond of encapsulated C 3 H 4 molecule. This work illustrates a general and powerful strategy─the reticulation of intrinsically functional organic scaffolds into highly porous frameworks─toward creating bespoke materials with precisely tailored functionalities and enhanced properties.
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