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含二氨基卡宾配体的线性卤化金(I)配合物:合成、反应性及磷光

Linear Gold(I) Halide Complexes with a Diamidocarbene Ligand: Synthesis, Reactivity, and Phosphorescence.

作者信息

Riley Charlotte, Phuoc Nguyen Le, Linnolahti Mikko, Romanov Alexander S

机构信息

Department of Chemistry, The University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.

Department of Chemistry University of Eastern Finland, FI-80101 Joensuu, Finland.

出版信息

Organometallics. 2023 Nov 20;43(16):1687-1697. doi: 10.1021/acs.organomet.3c00360. eCollection 2024 Aug 26.

Abstract

A series of halide and pseudohalide gold complexes (DAC)Au(I)X (DAC = ,'-diamidocarbene; X = Cl, Br, I, and SCN) were prepared in high yields. All complexes possess linear geometry around the gold atom with no aurophilic interactions between neighboring molecules. Reactivity studies for (DAC)Au(I)Cl revealed that the diamido backbone of the carbene ligand is vulnerable to nucleophilic attack by a strong base, potassium -butoxide, resulting in cleavage of the carbene backbone and formation of a neutral trigold cluster. Halide and pseudohalide complexes are bright phosphorescent emitters in the solid state, exhibiting photoluminescence quantum yields up to unity. Phosphorescence occurs in the range 480-520 nm with lifetimes as short as 1 μs, resulting in fast radiative rates up to 9.4 × 10 s which is on par with the most efficient heavy metal emitters. Photophysical properties are explained by the intrinsic π-accepting nature of the DAC carbene and are supported by TDDFT calculations.

摘要

一系列卤化物和拟卤化物金配合物(DAC)Au(I)X(DAC = ,'-二氨基卡宾;X = Cl、Br、I和SCN)以高产率制备。所有配合物在金原子周围具有线性几何结构,相邻分子之间不存在亲金相互作用。对(DAC)Au(I)Cl的反应性研究表明,卡宾配体的二氨基主链易受强碱叔丁醇钾的亲核攻击,导致卡宾主链断裂并形成中性三核簇。卤化物和拟卤化物配合物在固态下是明亮的磷光发射体,光致发光量子产率高达1。磷光发生在480 - 520 nm范围内,寿命短至1 μs,导致高达9.4×10 s的快速辐射速率,这与最有效的重金属发射体相当。光物理性质由DAC卡宾的固有π-接受性质解释,并得到TDDFT计算的支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3903/11351423/1f4f6b2100ca/om3c00360_0007.jpg

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