129Xe NMR Study of the Framework Flexibility of the Porous Hybrid MIL-53(Al)

• Published in: Journal of the American Chemical Society Vol. 132; no. 33; pp. 11599 - 11607
• Main Authors: Springuel-Huet, Marie-Anne, Nossov, Andrei, Adem, Ziad, Guenneau, Flavien, Volkringer, Christophe, Loiseau, Thierry, Férey, Gérard, Gédéon, Antoine
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 25.08.2010
• Subjects: Aluminum - chemistry; Magnetic Resonance Spectroscopy; Organometallic Compounds - chemistry; Porosity; Xenon Isotopes - chemistry
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/ja103105y

The metal−organic framework MIL-53 exhibits a structural transition between two possible porous structures, so-called large-pore (lp) and narrow-pore (np) forms, depending on the temperature or when guest molecules are adsorbed. 129Xe NMR has been used to study the lp → np transition induced by the adsorption of xenon as revealed by the adsorption isotherms. The NMR spectra show that the two structures, characterized by two distinct lines, coexist for xenon pressures above 5 × 104 Pa at room temperature, but a complete transformation is achieved when the temperature is decreased. An original interpretation of the NMR results allowed us to quantify the rate of the structural transformation. In particular, at room temperature, we have shown that 28% of the channels remain open. Two possible interpretations of the hysteresis observed in the chemical shift variation versus xenon pressure are proposed.