Kinetically Controlled Linker Binding in Rare Earth-2,5-Dihydroxyterepthalic Acid Metal–Organic Frameworks and Its Predicted Effects on Acid Gas Adsorption

Henkelis, Susan E.; Vogel, Dayton J.; Metz, Peter C.; Valdez, Nichole R.; Rodriguez, Mark A.; Rademacher, David X.; Purdy, Stephen; Percival, Stephen J.; Rimsza, Jessica M.; Page, Katharine; Nenoff, Tina M.

doi:10.1021/acsami.1c17670

Title: Kinetically Controlled Linker Binding in Rare Earth-2,5-Dihydroxyterepthalic Acid Metal–Organic Frameworks and Its Predicted Effects on Acid Gas Adsorption

Journal Article · Thu Nov 18 00:00:00 UTC 2021 · ACS Applied Materials and Interfaces

DOI: https://doi.org/10.1021/acsami.1c17670 · OSTI ID:1854451

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^[2]; Valdez, Nichole R. ^[1]; Rodriguez, Mark A. ^[1]; Rademacher, David X. ^[1];

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Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Univ. of Tennessee, Knoxville, TN (United States)

In the pursuit of highly stable and selective metal–organic frameworks (MOFs) for the adsorption of caustic acid gas species, an entire series of rare earth MOFs have been explored. Each of the MOFs in this series (RE-DOBDC; RE = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu; DOBDC = 2,5-dihydroxyterepthalic acid) was synthesized in the tetragonal space group I4/m. Crystallized MOF samples, specifically Eu-DOBDC, were seen to have a combination of monodentate and bidentate binding when synthesized under typical reaction conditions, resulting in a contortion of the structure. However, extended crystallization times determined that this binding is kinetically controlled and that the monodentate binding option was crystallographically eliminated by extended reaction times at higher temperatures. Furthermore, this series allows for the direct study of the effect of the metal center on the structure of the of the MOF; herein, the lanthanide metal ionic radii contraction across the periodic table results in a reduction of the MOF pore size and lattice parameters. Scanning electron microscopy–energy-dispersive spectroscopy was used to investigate the stages of crystal growth for these RE-DOBDC MOFs. All MOFs, except Er-DOBDC had a minimum of two stages of growth. These analogues were demonstrated by analysis of neutron diffraction (PND) to exhibit a cooperative rotational distortion of the secondary building unit, resulting in two crystallographically distinct linker sublattices. Computational modeling efforts were used to show distinct differences on acid gas (NO₂ and SO₂) binding energies for RE-DOBDC MOFs when comparing the monodentate/bidentate combined linker with the bidentate-only linker crystal structures.

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Research Organization:: Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States); Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States)

Sponsoring Organization:: USDOE Office of Science (SC), Basic Energy Sciences (BES)

Grant/Contract Number:: AC05-00OR22725; NA0003525; SC0012577

OSTI ID:: 1854451

Journal Information:: ACS Applied Materials and Interfaces, Journal Name: ACS Applied Materials and Interfaces Journal Issue: 47 Vol. 13; ISSN 1944-8244

Publisher:: American Chemical Society (ACS)Copyright Statement

Country of Publication:: United States

Language:: English

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CCDC 2045523: Experimental Crystal Structure Determination Susan, Henkelis,; Dayton, Vogel,; Peter, Metz, https://doi.org/10.5517/ccdc.csd.cc26njm1 The current record is supplemented by this dataset	dataset	January 2022
CCDC 2045642: Experimental Crystal Structure Determination Susan, Henkelis,; Dayton, Vogel,; Peter, Metz, https://doi.org/10.5517/ccdc.csd.cc26nng0 The current record is supplemented by this dataset	dataset	January 2022
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CCDC 2045857: Experimental Crystal Structure Determination Susan, Henkelis,; Dayton, Vogel,; Peter, Metz, https://doi.org/10.5517/ccdc.csd.cc26nwd5 The current record is supplemented by this dataset	dataset	January 2022
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Title: Kinetically Controlled Linker Binding in Rare Earth-2,5-Dihydroxyterepthalic Acid Metal–Organic Frameworks and Its Predicted Effects on Acid Gas Adsorption

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