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Reactivity of Rare-Earth Oxides in Anhydrous Imidazolium Acetate Ionic Liquids

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Shah,  Sameera
Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Pietsch,  Tobias
Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Jach,  Franziska
Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Ruck,  Michael
Michael Ruck, Max Planck Fellow, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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引用

Shah, S., Pietsch, T., Herz, M. A., Jach, F., & Ruck, M. (2023). Reactivity of Rare-Earth Oxides in Anhydrous Imidazolium Acetate Ionic Liquids. Chemistry, 5(2), 1378 -1394. doi:10.3390/chemistry5020094.


引用: https://hdl.handle.net/21.11116/0000-000D-A1EE-1
要旨
Rare-earth metal sesquioxides (RE2O3) are stable compounds that require high activation energies in solid-state reactions or strong acids for dissolution in aqueous media. Alternatively, dissolution and downstream chemistry of RE2O3 have been achieved with ionic liquids (ILs), but typically with additional water. In contrast, the anhydrous IL 1-butyl-3-methylimidazolium acetate [BMIm][OAc] dissolves RE2O3 for RE = La–Ho and forms homoleptic dinuclear metal complexes that crystallize as [BMIm]2[RE2(OAc)8] salts. Chloride ions promote the dissolution without being included in the compounds. Since the lattice energy of RE2O3 increases with decreasing size of the RE3+ cation, Ho2O3 dissolves very slowly, while the sesquioxides with even smaller cations appear to be inert under the applied conditions. The Sm and Eu complex salts show blue and red photoluminescence and Van Vleck paramagnetism. The proton source for the dissolution is the imidazolium cation. Abstraction of the acidic proton at the C2-atom yields an N-heterocyclic carbene (imidazole-2-ylidene). The IL can be regenerated by subsequent reaction with acetic acid. In the overall process, RE2O3 is dissolved by anhydrous acetic acid, a reaction that does not proceed directly. © 2023 by the authors.