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一种铀(IV)醇盐配合物的光致发光

Photoluminescence of a Uranium(IV) Alkoxide Complex.

作者信息

Valerio Leyla R, Roy Chowdhury Sabyasachi, Lewis Rob, Knowles Kathryn E, Vlaisavljevich Bess, Matson Ellen M

机构信息

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.

出版信息

JACS Au. 2024 Dec 12;5(1):332-342. doi: 10.1021/jacsau.4c01022. eCollection 2025 Jan 27.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6e5/11775688/62a701e65829/au4c01022_0001.jpg

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