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• W2973193148 abstract "We report herein a general synthetic approach for designing uranyl coordination cages. Compounds 1 and 2 are constructed through a temperature-dependent and solvent-driven self-assembly. In both cases, the synthetic strategy involves in situ phosphonate ligand condensation into a flexible pyrophosphonate ligand. This pyrophosphonate ligand formation is essential for the introduction of curvature into these compounds. In the presence of PF6- ions that are derived from hydrofluoric acid, a macrocyclic uranyl-phosphonate discrete compound, 1, whose cavity contains PF6- ions, hydronium ions, and water molecules, is obtained. When Cs+ cations are used in the synthesis, a remarkable uranyl coordination nanocage, 2, resulted. The macrocycle (1) is approximately 10.9 × 10.9 Å2 in diameter while the nanocage (2) is approximately 15.0 × 11.3 Å2 in diameter, as measured from the outer oxygen atoms of the uranyl centers. Both compounds are constructed from a UO22+ moiety, coordinated by an additional four oxygen atoms from the phosphonate group to form pentagonal bipyramidal geometry. All the compounds fluoresce at room temperature, showing characteristic vibronically coupled charge-transfer based emission." @default.
• W2973193148 created "2019-09-19" @default.
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• W2973193148 date "2019-09-12" @default.
• W2973193148 modified "2023-09-26" @default.
• W2973193148 title "Hybrid Uranyl–Phosphonate Coordination Nanocage" @default.
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• W2973193148 doi "https://doi.org/10.1021/acs.inorgchem.9b01448" @default.
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