Lattice-Imposed Geometry in Metal-Organic Frameworks: Lacunary Zn4O Clusters in MOF-5 Serve as Tripodal Chelating Ligands for Ni2+
Author(s)
Brozek, Carl Kavanaugh; Dinca, Mircea
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The inorganic clusters in metal–organic frameworks can be used to trap metal ions in coordination geometries that are difficult to achieve in molecular chemistry. We illustrate this concept by using the well-known basic carboxylate clusters in Zn[subscript 4]O(1,4-benzenedicarboxylate)3 (MOF-5) as tripodal chelating ligands that enforce an unusual pseudo-tetrahedral oxygen ligand field around Ni[superscript 2+]. The new Ni-based MOF-5 analogue is characterized by porosity measurements and a suite of electronic structure spectroscopies. Classical ligand field analysis of the Ni[superscript 2+] ion isolated in MOF-5 classifies the Zn3O(carboxylate)6 “tripodal ligand” as an unusual, stronger field ligand than halides and other oxygen donor ligands. These results may inspire the widespread usage of MOFs as chelating ligands for stabilizing site-isolated metal ions in future reactivity and electronic structure studies.
Date issued
2012-04Department
Massachusetts Institute of Technology. Department of ChemistryJournal
Chemical Science
Publisher
Royal Society of Chemistry, The
Citation
Brozek, Carl K., and Mircea Dincă. “Lattice-imposed Geometry in Metal–organic Frameworks: Lacunary Zn4O Clusters in MOF-5 Serve as Tripodal Chelating Ligands for Ni2+.” Chemical Science 3.6 (2012): 2110.
Version: Author's final manuscript
ISSN
2041-6520