Metal−Organic Framework with Constrained Flexibility for Benchmark Separation of Hexane Isomers

Abstract

Flexible metal−organic frameworks (MOFs) are promising candidates for adsorptive separations, but achieving a balance among flexibility, adsorption capacity, and selectivity remains challenging. Herein, we report a novel flexible MOF, Ni(bhdc)(ted)_0.5 (ZUL−C6), incorporating hybrid three-dimensional alkane-bridged ligands, which realizes high-capacity molecular sieving for hexane isomer separation - a critical process in the petroleum industry. The alkyl-rich, confined pore system within the ZUL−C6 framework facilitated a strong affinity for n-hexane and 3-methylpentane. However, the narrow pore size and the constrained flexibility limited the uptake of 2,2-dimethylbutane (<4.0 mg/g), accompanied by a high gate-opening pressure. The gating behavior was elucidated by guest-loaded single-crystal (SC) X-ray diffraction and density functional theory (DFT) simulations, which revealed a unique SC to SC transformation driven by the non-centrosymmetric rotation of the 3D bhdc linker and distortion of the metal cluster and pillar units, along with a high deformation energy barrier. As a result, ZUL−C6 exhibited not only significantly higher uptake and selectivity than the industrially used 5 A molecular sieve, but also the record-high nHEX/3MP breakthrough uptake (92.8/73.9 mg/g) and unprecedented 22DMB producing time (309.2 min/g, corresponding to the productivity of 770 mmol/kg and yield of 92.8 %) among reported MOFs.