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Guest-Controlled Incommensurate Modulation in a Meta-Rigid Metal–Organic Framework Material

[Image: see text] 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 f...

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Detalles Bibliográficos
Autores principales: Li, Jiangnan, Zhou, Zhengyang, Han, Xue, Zhang, Xinran, Yan, Yong, Li, Weiyao, Smith, Gemma L., Cheng, Yongqiang, McCormick McPherson, Laura J., Teat, Simon J., Frogley, Mark D., Rudić, Svemir, Ramirez-Cuesta, Anibal J., Blake, Alexander J., Sun, Junliang, Schröder, Martin, Yang, Sihai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7668537/
https://www.ncbi.nlm.nih.gov/pubmed/33124803
http://dx.doi.org/10.1021/jacs.0c08794
Descripción
Sumario:[Image: see text] 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).