4.8 Article

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

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 142, 期 45, 页码 19189-19197

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c08794

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资金

  1. EPSRC [EP/I011870]
  2. Royal Society
  3. University of Manchester
  4. National Basic Research Program [2013CB933402, 2016YFA0301004]
  5. National Natural Science Foundation of China [21527803, 21471009, 21621061, 21871009]
  6. European Research Council (ERC) under the European Union [742401]
  7. DOE Office of Science User Facility [DE-AC02-05CH11231]
  8. Laboratory Directed Research and Development Program
  9. Compute and Data Environment for Science (CADES) at ORNL
  10. China Scholarship Council (CSC)

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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 [ZnO4N] 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.H2O upon dehydration to give MFM-520. Filling MFM-520 with CO2 and SO2 reveals that, while CO2 has a minimal structural influence, SO2 can further modulate the structure incommensurately. MFM-520 shows exceptional selectivity for SO2 under flue-gas desulfurization conditions, and the facile release of captured SO2 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 SO2.

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