Resolving Confined 7Li Dynamics of Uranyl Peroxide Capsule U24
Author(s) -
Jing Xie,
Harrison A. Neal,
Jennifer E. S. Szymanowski,
Peter C. Burns,
Todd M. Alam,
May Nyman,
Laura Gagliardi
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.8b00474
Subject(s) - chemistry , uranyl , peroxide , capsule , hydrogen peroxide , dynamics (music) , radiochemistry , inorganic chemistry , nuclear chemistry , ion , organic chemistry , botany , physics , acoustics , biology
We obtained a kerosene-soluble form of the lithium salt [UO 2 (O 2 )(OH) 2 ] 24 phase (Li-U 24 ), by adding cetyltrimethylammonium bromide surfactant to aqueous Li-U 24 . Interestingly, its variable-temperature solution 7 Li NMR spectroscopy resolves two narrowly spaced resonances down to -10 °C, which shift upfield with increasing temperature, and finally coalesce at temperatures > 85 °C. Comparison with solid-state NMR demonstrates that the Li dynamics in the Li-U 24 -CTA phase involves only exchange between different local encapsulated environments. This behavior is distinct from the rapid Li exchange dynamics observed between encapsulated and external Li environments for Li-U 24 in both the aqueous and the solid-state phases. Density functional theory calculations suggest that the two experimental 7 Li NMR chemical shifts are due to Li cations coordinated within the square and hexagonal faces of the U 24 cage, and they can undergo exchange within the confined environment, as the solution is heated. Very different than U 24 in aqueous media, there is no evidence that the Li cations exit the cage, and therefore, this represents a truly confined space.
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