Abstract
The cation influence on substitution reactions in aqua dioxalate uranyl complexes with the participation of a fluoride ion as an attacking ligand and two-charge cations of ethylene diammonium and propylene diammonium was considered. The structure of (C2H10N2)3[UO2(C2O4)2F]2 · 6H2O and (C3H12N2)[UO2(C2O4)2(H2O)] complexes was determined by X-ray crystallography.
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