Treatment of UO3 with pure triflic acid TfOH at 110 °C or with boiling triflic anhydride TfOTf afforded [UO2(OTf)2] (1) in high yields. The latter was also prepared by the reaction of UO3 with TfOH in water, or by dehydration of [UO2(OTf)2(H2O)n] in boiling TfOTf. Anhydrous [Ce(OTf)4] (2) was similarly obtained from the commercially hydrated compound. X-ray analysis revealed that in [UO2(OTf)2(py)3] (3), the triflate ligands are monodentate whereas they are dissociated in [{UO2(py)4}2(μ-O)][OTf]2 (4).
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Berthet et al. (2000) studied this question.
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