Valerio Leyla R, Roy Chowdhury Sabyasachi, Lewis Rob, Knowles Kathryn E, Vlaisavljevich Bess, Matson Ellen M
Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
Department of Chemistry, University of South Dakota, Vermillion, South Dakota 57069, United States.
JACS Au. 2024 Dec 12;5(1):332-342. doi: 10.1021/jacsau.4c01022. eCollection 2025 Jan 27.
In this report, we describe the photoluminescence of a homoleptic uranium(IV) alkoxide complex. Excitation of [Li(THF)][U(O Bu)] leads to the first example of photoluminescence from a well-defined actinide complex originating from an f-f excitation, supported by second order multiconfigurational electronic structure calculations including spin-orbit coupling. These calculations show strong spin-orbit coupling between the excited triplet and singlet states for the 5f-orbital manifold, which leads to a long-lived excited state lifetime of 0.85 s at low temperature. The photophysical properties of homoleptic uranium(V) and uranium(VI) tertbutoxide complexes are also presented; we find that oxidation of the uranium(IV) alkoxide results in quenching of luminescence in [Li(THF)][U(O Bu)] and [U(O Bu)]. This is attributed to competing ligand to metal charge transfer absorption processes shifted to lower energy upon oxidation of the actinide center, which mask the relevant f-f transitions in the visible region of the electronic absorption spectrum.
在本报告中,我们描述了一种均配型铀(IV)醇盐配合物的光致发光。[Li(THF)][U(O Bu)]的激发产生了首例源自明确定义的锕系配合物的光致发光,其源于f-f激发,并得到了包括自旋轨道耦合的二阶多组态电子结构计算的支持。这些计算表明,对于5f轨道集,激发三重态和单重态之间存在强自旋轨道耦合,这导致在低温下激发态寿命长达0.85秒。文中还介绍了均配型铀(V)和铀(VI)叔丁醇盐配合物的光物理性质;我们发现,铀(IV)醇盐的氧化导致[Li(THF)][U(O Bu)]和[U(O Bu)]中的发光猝灭。这归因于在锕系中心氧化后,竞争的配体到金属电荷转移吸收过程转移到更低能量,从而掩盖了电子吸收光谱可见区域中相关的f-f跃迁。