Title: Spectroscopic properties of uranyl crown ether complexes in non-aqueous solvents
Authors: Servaes, Kelly
De Houwer, Sandy
Görller-Walrand, Christiane
Binnemans, Koen # ×
Issue Date: 2004
Publisher: Royal soc chemistry
Series Title: Physical Chemistry Chemical Physics vol:6 issue:11 pages:2946-2950
Abstract: The spectroscopic properties of the complexes of uranyl with oxacrowns, azacrowns, thiacrowns of different ring size, polyethyleneglycols (PEG-200, PEG-300, PEG-400), and [2.2.1] and [2.2.2] cryptands were studied in acetonitrile and propylene carbonate solutions by absorption and luminescence spectroscopy. Depending on the ligand, marked differences in the fine structure of the spectra were observed. The crown ethers with six oxygen atoms (18-crown-6, dicyclohexano-18-crown-6, benzo-18-crown-6, dibenzo-18-crown-6 and [2,4]-dibenzo-18-crown-6) form inclusion complexes with the uranyl ion in the central cavity. In the case of 18-crown-6 and dibenzo-18-crown-6, a complex with a high coordination symmetry is formed. Outer-sphere complexes are formed with the crown ethers with small ring size (12-crown-4 and 15-crown-5) and with PEG-200. Only minor changes in the spectra were observed when changing the ligand. The spectra of the large crown ethers ([3,4]-dibenzo-21-crown-7, dibenzo-24-crown-8 and dibenzo-30-crown-10), together with those of PEG-300 and PEG-400 show that these ligands coordinate in the equatorial plane to the uranyl ion. In the presence of competing inorganic ligands like chloride and nitrate ions, the crown ether is replaced in the first coordination sphere. Azacrowns and cryptands coordinate externally to the uranyl ion, and the corresponding spectra do not show fine structure. In the case of the thiacrowns, no coordination of the ligand to the uranyl ion was observed.
ISSN: 1463-9076
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Molecular Design and Synthesis
Chemistry - miscellaneous
× corresponding author
# (joint) last author

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