Oxidative Addition of E-H (E=C, N) Bonds to Transient Uranium(II) Centers.
Wei FangYafei LiTianze ZhangThayalan RajeshkumarIker Del RosalYue ZhaoTianwei WangShuao WangLaurent MaronCongqing ZhuPublished in: Angewandte Chemie (International ed. in English) (2024)
Two-electron oxidative addition is one of the most important elementary reactions for d-block transition metals but it is uncommon for f-block elements. Here, we report the first examples of intermolecular oxidative addition of E-H (E=C, N) bonds to uranium(II) centers. The transient U(II) species was formed in-situ by reducing a heterometallic cluster featuring U(IV)-Pd(0) bonds with potassium-graphite (KC 8 ). Oxidative addition of C-H or N-H bonds to the U(II) centers was observed when this transient U(II) species was treated with benzene, carbazole or 1-adamantylamine, respectively. The U(II) centers could also react with tetracene, biphenylene or N 2 O, leading to the formation of arene reduced U(IV) products and uranyl(VI) species via two- or four-electron processes. This study demonstrates that the intermolecular two-electron oxidative addition reactions are viable for actinide elements.