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Synthesis, characterization, and reactivity of a uranium(VI) carbene imido oxo complex.


ABSTRACT: We report the uranium(VI) carbene imido oxo complex [U(BIPM(TMS))(NMes)(O)(DMAP)2] (5, BIPM(TMS) = C(PPh2 NSiMe3)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(BIPM(TMS))(O)2(DMAP)2] (6).

SUBMITTER: Lu E 

PROVIDER: S-EPMC4464547 | biostudies-literature | 2014 Jun

REPOSITORIES: biostudies-literature

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Synthesis, characterization, and reactivity of a uranium(VI) carbene imido oxo complex.

Lu Erli E   Cooper Oliver J OJ   McMaster Jonathan J   Tuna Floriana F   McInnes Eric J L EJ   Lewis William W   Blake Alexander J AJ   Liddle Stephen T ST  

Angewandte Chemie (International ed. in English) 20140519 26


We report the uranium(VI) carbene imido oxo complex [U(BIPM(TMS))(NMes)(O)(DMAP)2] (5, BIPM(TMS) = C(PPh2 NSiMe3)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-elect  ...[more]

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