SUF<sub>4</sub>: A Terminal Monosulfido Complex ofUranium(VI) with a Linear SUF Moiety

Although there have been a few terminal sulfido complexes of uranium(VI) with either SUO or SUN moiety, it remains a question whether the terminal sulfido ligand can be stabilized in the absence of such multiply bound oxo or nitrido ligands. Herein, we report a terminal monosulfide complex of uranium(VI) in the form of SUF<sub>4</sub> bearing a linear SUF moiety that was prepared via the reaction of laser-ablated uranium atoms with SF<sub>4</sub> in cryogenic matrixes. On the basis of the results from infrared spectroscopy combined with density functional theory calculations at the B3LYP level, the SUF<sub>4</sub> complex possesses a trigonal bipyramid structure with singlet ground state and nonplanar <i>C</i><sub>3<i>v</i></sub> symmetry where the terminal sulfido ligand is stabilized by the monovalent fluoro ligand trans to sulfur. A triple U–S bond with a positively charged sulfur atom was identified according to the natural bond orbital analysis. Inverse trans influence is present in SUF<sub>4</sub> as revealed by the difference in bond length between U–F<sub>axial</sub> from the linear SUF moiety and U–F<sub>equatorial</sub> from the UF<sub>3</sub> equatorial plane, which is further supported by bonding analysis.

Publication Details

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Published
2025-03-27
DOI
https://doi.org/10.1021/acs.inorgchem.4c05157.s001
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Legal and Regulatory Analysis
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article

SUF4: A Terminal Monosulfido Complex ofUranium(VI) with a Linear SUF Moiety

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Legal and Regulatory Analysis
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SUF4: A Terminal Monosulfido Complex ofUranium(VI) with a Linear SUF Moiety

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Abstract

Although there have been a few terminal sulfido complexes of uranium(VI) with either SUO or SUN moiety, it remains a question whether the terminal sulfido ligand can be stabilized in the absence of such multiply bound oxo or nitrido ligands. Herein, we report a terminal monosulfide complex of uranium(VI) in the form of SUF<sub>4</sub> bearing a linear SUF moiety that was prepared via the reaction of laser-ablated uranium atoms with SF<sub>4</sub> in cryogenic matrixes. On the basis of the results from infrared spectroscopy combined with density functional theory calculations at the B3LYP level, the SUF<sub>4</sub> complex possesses a trigonal bipyramid structure with singlet ground state and nonplanar <i>C</i><sub>3<i>v</i></sub> symmetry where the terminal sulfido ligand is stabilized by the monovalent fluoro ligand trans to sulfur. A triple U–S bond with a positively charged sulfur atom was identified according to the natural bond orbital analysis. Inverse trans influence is present in SUF<sub>4</sub> as revealed by the difference in bond length between U–F<sub>axial</sub> from the linear SUF moiety and U–F<sub>equatorial</sub> from the UF<sub>3</sub> equatorial plane, which is further supported by bonding analysis.

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Legal and Regulatory Analysis
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