Understanding DABCO Nanorotor Dynamics in Isostructural Metal–Organic Frameworks

• Published in: The journal of physical chemistry letters Vol. 6; no. 5; pp. 812 - 816
• Main Authors: Burtch, Nicholas C, Torres-Knoop, Ariana, Foo, Guo Shiou, Leisen, Johannes, Sievers, Carsten, Ensing, Bernd, Dubbeldam, David, Walton, Krista S
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 05.03.2015
• Subjects: adsorption; framework flexibility; molecular dynamics; water; Porous materials
• ISSN: 1948-7185; 1948-7185
• DOI: 10.1021/jz502653y

Flexible framework dynamics present in the subset of metal–organic frameworks known as soft porous crystals give rise to interesting structural properties that are unique to this class of materials. In this work, we use experiments and molecular simulation to understand the highly dynamic nanorotor behavior of the 1,4-diazabicyclo[2.2.2]­octane (DABCO) ligand in the pillared Zn-DMOF and Zn-DMOF-TM (TM = tetramethyl) structures. While DABCO is known to be displaced in the presence of water in the parent Zn-DMOF structure, the Zn-DMOF-TM variation is highly stable even after adsorbing significant amounts of water vapor. The dynamics of DABCO in the presence of water guest molecules is therefore also explored in the Zn-DMOF-TM structure via in situ NMR and IR experiments. This analysis shows that the rotational motion of the DABCO linkers is dependent on water content, but not a likely source of water instability because the dynamics are fast and largely unaffected by the presence of methyl functional groups.