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Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
Supramolecular Assembly of U(IV) Clusters and Superatoms with Unconventional Countercations
Ian Colliard1, Gregory Morrison2, Hans-Conrad Zur Loye2
1Department of Chemistry, Oregon State University, Corvallis, Oregon 97331, United States.
Abstract:
Superatoms are nanometer-sized molecules or particles that form ordered lattices, mimicking their atomic counterparts. Hierarchical assembly of superatoms gives rise to emergent properties in lattices of quantum dots, p-block clusters, and fullerenes. Here, we introduce a family of uranium-oxysulfate cluster anions whose hierarchical assembly in water is controlled by two parameters: acidity and the lanthanide or transition-metal countercation. In acid, larger LnIII (Ln = La-Ho) link hexamer (U6) oxoclusters into body-centered cubic frameworks, while smaller LnIII (Ln = Er-Lu and Y) promote linking of 14 U6 clusters into hollow superclusters (U84 superatoms). U84 assembles into superlattices including cubic-closest packed, body-centered cubic, and interpenetrating networks, bridged by interstitial countercations and U6 clusters. Divalent transition metals (TM = MnII and ZnII) charge-balance and promote the fusion of 10 U6 and 10 U monomers into a wheel-shaped cluster (U70). Dissolution of U70 in organic media reveals (by small-angle X-ray scattering) that differing supramolecular assemblies are accessed, controlled by TMII-linking of U70 clusters. Magnetic measurements of these assemblies reveal Curie-Weiss behavior at high temperatures, without pairing of the 5f2-electrons down to 2 K.
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