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Updated: May 16, 2026

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
Published on: February 6, 2020
Time-resolved assembly of chiral uranyl peroxo cage clusters containing belts of polyhedra
Jie Qiu1, Kevin Nguyen, Laurent Jouffret
1Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, Notre Dame, Indiana 46556, United States.
Abstract:
Two chiral cage clusters built from uranyl polyhedra and (HPO(3))(2-) groups have been synthesized in pure yield and characterized structurally and spectroscopically in the solid state and aqueous solution. Synthesis reactions under ambient conditions in mildly acidic aqueous solutions gave clusters U(22)PO(3) and U(28)PO(3) that contain belts of four uranyl peroxide pentagonal and hexagonal bipyramids, in contrast to earlier reported uranyl peroxide cage clusters that are built from four-, five-, and six-membered rings of uranyl hexagonal bipyramids. U(22)PO(3) and U(28)PO(3) are also the first chiral uranyl-based cage clusters, the first that contain uranyl pentagonal bipyramids that contain no peroxide ligands, and the first that incorporate (HPO(3))(2-) bridges between uranyl ions. They are built from 22 uranyl polyhedra and 20 (HPO(3))(2-) groups, or 28 uranyl polyhedra and 24 (HPO(3))(2-) groups, with the outer and inner surfaces of the cages passivated by the O atoms of uranyl ions. Small-angle X-ray scattering (SAXS) profiles demonstrated that U(22)PO(3) clusters formed in solution within 1 h after mixing of reactants, and remained in solution for 2 weeks prior to crystallization. Time-resolved electrospray ionization mass spectrometry and SAXS demonstrated that U(28)PO(3) clusters formed in solution within 1 h of mixing the reactants, and remained in solution 1 month before crystallization. Crystallization of U(22)PO(3) and U(28)PO(3) is accelerated by addition of KNO(3). Clusters of U(22)PO(3) with and without encapsulated cations exhibit markedly different aqueous solubility, reflecting the importance of cluster surface charge in fostering linkages through counterions to form a stable solid.
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