4.6 Article

Investigation of Guest-Induced Flexibility in Pyrazine Derivative of ALFFIVE MOF via Molecular Simulation

Journal

LANGMUIR
Volume 39, Issue 4, Pages 1373-1385

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.2c02027

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This study investigated the flexibility of a metal-organic framework (MOF) material and found that it undergoes structural changes when adsorbing gas molecules. The mechanism behind this flexibility is still unclear. Using molecular dynamics (MD) and Monte Carlo (MC) simulations, the ALFFIVE-Ni-pyr-TBP MOF was studied and changes were observed during the adsorption process, suggesting potential applications in future adsorption.
One of the important understandings of porous solids like metal-organic frameworks (MOFs) is their flexibility. Therefore, there are certain computational studies on flexible MOFs in the literature, primarily concentrating on MIL-53, UiO-66, and DUT-49. Here, investigation of another class of MOF, that is, [Ni(1,4-pyrazine)2(AlF5)]n, was shown to have guest-induced flexible characteristics; nevertheless, the mechanism for the emergence of flexibility is uncertain. We simulated the structural flexibility of [Ni(1,4-pyrazine)2(AlF5)]n, named ALFFIVE-Ni-pyr-TBP, upon adsorption of a guest molecule based on force fields using the molecular dynamics (MD) method and Monte Carlo (MC) simulations. As the first step towards understanding guest-induced flexibility, the MC simulations were performed by relaxing the framework and then further comparing it with the rigid framework. Subsequently, MD simulations were executed on the ALFFIVE-Ni-pyr-TBP framework with and without the guest molecules. In the case of moisture adsorption, the MOF system was identified to undergo a geometric transformation from trigonal bipyramidal to square bipyramidal geometry due to the strong interaction of oxygen of the water with the metal aluminum. However, some tilting in the pyrazine ligand was observed in the presence of all the guest molecules. Therefore, the detailed guest-induced flexibility described in this work could support the ALFFIVE series to be explored for future adsorption applications.

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