Falcone Marta, Chatelain Lucile, Scopelliti Rosario, Mazzanti Marinella
Institut des Sciences et Ingénierie Chimiques Ecole Polytechnique Fédérale de Lausanne (EPFL) CH-1015 Lausanne.
Institut des Sciences et Ingénierie Chimiques Ecole Polytechnique Fédérale de Lausanne (EPFL) CH-1015 Lausanne;, Email:
Chimia (Aarau). 2017 Apr 26;71(4):209-212. doi: 10.2533/chimia.2017.209.
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(μ-N)}] (1) with a CsUIV-N-UIV 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-UIV nitride also readily cleaves the C≡O bond under mild conditions.
在当前能源背景下,非常需要新型高效的化学工艺,即在温和条件下使用廉价且易于获取的二氧化碳或一氧化碳来生产有价值的化学产品。氮化铀材料在哈伯-博施法中作为高活性催化剂,但分子氮化物化合物的反应活性仍未得到探索。在此,我们综述了我们小组最近获得的结果,结果表明具有CsUIV-N-UIV核心的多金属氮化物配合物[Cs{[U(OSi(OtBu)3)3]2(μ-N)}] (1),由于其强亲核行为,能够促进N-C键的形成。特别是,配合物1在过量二氧化碳存在下会生成一种显著的二氨基甲酸盐产物。多金属CsUIV-N-UIV氮化物在温和条件下也能轻易裂解C≡O键。