Guest-Controlled Incommensurate Modulation in a Meta-Rigid Metal–Organic Framework Material
Author(s) -
Jiangnan Li,
Zhengyang Zhou,
Xue Han,
Xinran Zhang,
Yong Yan,
Weiyao Li,
Gemma L. Smith,
Yongqiang Cheng,
Laura J. MCormick MPherson,
Simon J. Teat,
Mark D. Frogley,
Svemir Rudić,
Anibal J. RamirezCuesta,
Alexander J. Blake,
Junliang Sun,
Martin Schröder,
Sihai Yang⧫
Publication year - 2020
Publication title -
journal of the american chemical society
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.0c08794
Subject(s) - chemistry , aperiodic graph , crystal structure , lattice (music) , modulation (music) , crystallography , chemical physics , nanotechnology , physics , materials science , mathematics , combinatorics , acoustics
Structural transitions of host systems in response to guest binding dominate many chemical processes. We report an unprecedented type of structural flexibility within a meta-rigid material, MFM-520, which exhibits a reversible periodic-to-aperiodic structural transition resulting from a drastic distortion of a [ZnO 4 N] node controlled by the specific host-guest interactions. The aperiodic crystal structure of MFM-520 has no three-dimensional (3D) lattice periodicity but shows translational symmetry in higher-dimensional (3 + 2)D space. We have directly visualized the aperiodic state which is induced by incommensurate modulation of the periodic framework of MFM-520·H 2 O upon dehydration to give MFM-520. Filling MFM-520 with CO 2 and SO 2 reveals that, while CO 2 has a minimal structural influence, SO 2 can further modulate the structure incommensurately. MFM-520 shows exceptional selectivity for SO 2 under flue-gas desulfurization conditions, and the facile release of captured SO 2 from MFM-520 enabled the conversion to valuable sulfonamide products. MFM-520 can thus be used as a highly efficient capture and delivery system for SO 2 .
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