CO Cleavage and CO2 Functionalization under Mild Conditions by a Multimetallic CsU2 Nitride Complex

被引:6
|
作者
Falcone, Marta [1 ]
Chatelain, Lucile [1 ]
Scopelliti, Rosario [1 ]
Mazzanti, Marinella [1 ]
机构
[1] Ecole Polytech Fed Lausanne, PhD Program, Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
CO2; activation; CO cleavage; N-C bond formation; Nitrides; Uranium; TERMINAL URANIUM NITRIDE; MULTIPLE BOND FORMATION; CARBON-MONOXIDE; DINITROGEN CLEAVAGE; CRYSTAL-STRUCTURES; ACTIVATION; CHEMISTRY; REACTIVITY; LIGAND; DEOXYGENATION;
D O I
10.2533/chimia.2017.209
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novel efficient chemical processes involving cheap and widely accessible carbon dioxide or carbon monoxide under mild conditions for the production of valuable chemical products are highly desirable in the current energetic context. Uranium nitride materials act as high activity catalysts in the Haber-Bosch process but the reactivity of molecular nitride compounds remains unexplored. Here we review recent results obtained in our group showing that a multimetallic nitride complex [Cs{[U(OSi(OtBu)(3))(3)](2)(mu-N)}] (1) with a CsUIV-N-U-IV core, is able to promote N-C bond formation due to its strong nucleophile behaviour. In particular, complex 1, in the presence of excess CO2 leads to a remarkable dicarbamate product. The multimetallic CsUIV-N-U-IV nitride also readily cleaves the C O bond under mild conditions.
引用
收藏
页码:209 / 212
页数:4
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