期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 -, 期 -, 页码 -出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c04947
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资金
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Heavy Element Chemistry program [DE-SC0016568]
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Separation Science program [DE-SC0017259]
- National Science Foundation [CHE 1625543]
- U.S. Department of Energy (DOE) [DE-SC0017259] Funding Source: U.S. Department of Energy (DOE)
This study presents the first synthesis of a non-uranyl, f-element oxo complex from dioxygen in dry air. The characterization of the complexes using various spectroscopic techniques confirmed their electronic structures.
The first non-uranyl, f-element oxo complex synthesized from dioxygen in dry air is presented in this work. The synthesis was accomplished by treating the redox-active thorium amidophenolate complex, [Th((dipp)ap)(3)] [K(15-c-5)(2)](2) (1-as crown), with dioxygen in dry air, forming a rare terminal thorium oxo, [O=Th((dipp)isq)(2)((d)(ipp)ap)][K(1S-c-5)(2)](2) (2-oxo). Compound 1-ap crown was regenerated by treating 2-oxo with potassium graphite. X-ray crystallography of 2-oxo revealed a comparatively longer bond length for the thorium-oxygen double bond when compared to other thorium oxos. As such, several thorium-oxygen single bonds were synthesized for comparison, including Th((dipp)isq)(2) (OSiMe3)(2) (THF) (4-OSiMe3)(4) Th(OSiMe3)(4) (bipy)(2) (5-OSiMe3), and [Th(OH)(2) ((dipp)Hap)(4)] [K(15-c-5)(2)](2) (6-OH). Full spectroscopic and structural characterization of the complexes was performed via H-1 NMR spectroscopy, X-ray crystallography, EPR spectroscopy, and electronic absorption spectroscopy as well as SQUID magnetometry, which all confirmed the electronic structure of these complexes.
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