期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 26, 页码 6696-6700出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201403892
关键词
carbene ligands; imido ligands; multiple bonding; oxo ligands; uranium
资金
- Royal Society
- Marie Curie International Incoming Fellowship Scheme
- European Research Council
- Engineering and Physical Sciences Research Council
- University of Nottingham
- National Nuclear Laboratories
- EPSRC [EP/F030517/1, EP/K038869/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/K038869/1, EP/F030517/1] Funding Source: researchfish
We report the uranium(VI) carbene imido oxo complex [U(BIPMTMS)(NMes)(O)(DMAP)(2)] (5, BIPMTMS = C(PPh2NSiMe3)(2); Mes=2,4,6-Me3C6H2; DMAP=4-(dimethylamino)pyridine) which exhibits the unprecedented arrangement of three formal multiply bonded ligands to one metal center where the coordinated heteroatoms derive from different element groups. This complex was prepared by incorporation of carbene, imido, and then oxo groups at the uranium center by salt elimination, protonolysis, and two-electron oxidation, respectively. The oxo and imido groups adopt axial positions in a T-shaped motif with respect to the carbene, which is consistent with an inverse trans-influence. Complex 5 reacts with tert-butylisocyanate at the imido rather than carbene group to afford the uranyl(VI) carbene complex [U(BIPMTMS)(O)(2)(DMAP)(2)] (6).
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