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Sulfate Separation by Selective Crystallization with a Bis-iminoguanidinium Ligand
Published on: September 8, 2016
Alkaline-Earth Metal Bis[bis(trimethylsilyl)amide] Complexes with Weakly Coordinating
Sven Krieck1, Philipp Schüler1, Helmar Görls1
1Institute of Inorganic and Analytical Chemistry , Friedrich Schiller University Jena , Humboldtstraße 8 , D-07743 Jena , Germany.
Abstract:
The reaction of [(Me3Si)2N-Ae{μ-N(SiMe3)2}]2 with 2,2,5,5-tetramethyltetrahydrofuran in pentane yields the mononuclear complexes [(Me4thf)Ae{N(SiMe3)2}2] (Ae = Mg (1), Ca (2), Sr (3), and Ba (4)) with three-coordinate alkaline-earth metal centers. With increasing radius of the alkaline-earth metal atoms, the N-Ae-N bond angles decrease. These ether adducts significantly enhance the solubility of the bis(trimethylsilyl)amides of the alkaline-earth metals in hydrocarbon solvents. Contrary to the magnesium derivative 1, the heavier congeners dissociate into mononuclear [Ae{N(SiMe3)2}2] and free Me4THF without formation of sparingly soluble dinuclear [(Me3Si)2N-Ae{μ-N(SiMe3)2}]2.
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