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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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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 |
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). |
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