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Uranyl-tri-bis(silyl)amide Alkali Metal Contact and Separated Ion Pair Complexes
Author(s) -
Philip J. Cobb,
David J. Moulding,
Fabrizio Ortu,
Simon Randall,
Ashley J. Wooles,
Louise S. Natrajan,
Stephen T. Liddle
Publication year - 2018
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.8b00715
Subject(s) - chemistry , uranyl , alkali metal , crystallography , cryptand , crown ether , raman spectroscopy , amide , inorganic chemistry , x ray crystallography , metal , ion , diffraction , organic chemistry , physics , optics
We report the preparation of a range of alkali metal uranyl(VI) tri- bis(silyl)amide complexes [{M(THF) x }{(μ-O)U(O)(N″) 3 }] (1M) (N″ = {N(SiMe 3 ) 2 } - , M = Li, Na, x = 2; M = K, x = 3; M = K, Rb, Cs, x = 0) containing electrostatic alkali metal uranyl-oxo interactions. Reaction of 1M with 2,2,2-cryptand or 2 equiv of the appropriate crown ether resulted in the isolation of the separated ion pair species [U(O) 2 (N″) 3 ][M(2,2,2-cryptand)] (3M, M = Li-Cs) and [U(O) 2 (N″) 3 ][M(crown) 2 ] (4M, M = Li, crown = 12-crown-4 ether; M = Na-Cs, crown = 15-crown-5 ether). A combination of crystallographic studies and IR, Raman and UV-vis spectroscopies has revealed that the 1M series adopts contact ion pair motifs in the solid state where the alkali metal caps one of the uranyl-oxo groups. Upon dissolution in THF solution, this contact is lost, and instead, separated ion pair motifs are observed, which is confirmed by the isolation of [U(O) 2 (N″) 3 ][M(THF) n ] (2M) (M = Li, n = 4; M = Na, K, n = 6). The compounds have been characterized by single crystal X-ray diffraction, multinuclear NMR spectroscopy, IR, Raman, and UV-vis spectroscopies, and elemental analyses.

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