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作为推挽式磷光发射体的均配炔基鏻金(I)配合物

Homoleptic Alkynylphosphonium Au(I) Complexes as Push-Pull Phosphorescent Emitters.

作者信息

Petrovskii Stanislav, Paderina Aleksandra, Sizova Anastasia, Grachova Elena

机构信息

Institute of Chemistry, St Petersburg University, Universitetskii pr. 26, 198504 St. Petersburg, Russia.

出版信息

Inorg Chem. 2023 Apr 3;62(13):5123-5133. doi: 10.1021/acs.inorgchem.2c04360. Epub 2023 Mar 20.

Abstract

A series of compounds - bearing terminal alkynyl sites connected with a phosphonium group via different π-conjugated linkers have been synthesized. The compounds themselves are efficient push-pull emitters and exhibit bright fluorescence in blue and near-UV regions. - were used as alkynyl ligands to obtain a series of homoleptic bis-alkynyl Au(I) complexes -. The complexes demonstrate bright phosphorescence and dual emission with dominating phosphorescence (). Terphenyl derivative complex exhibits warm white emission in DMSO solution and pure white emission in PMMA films. Time-dependent density functional theory calculations have shown that the T excited state has a hybrid MLCT/ILCT nature with a dominant contribution of charge transfer across a ligand-centered "D-π-A" system. The variation of linker allows tuning the effect of intermolecular charge transfer and thus changing the electronic and photophysical properties of the organogold "D-π-A" system. The results presented unambiguously display the advances of the conception of organometallic "D-π-A" construction.

摘要

已经合成了一系列通过不同的π共轭连接基与鏻基团相连的带有末端炔基位点的化合物。这些化合物本身是高效的推拉型发光体,在蓝色和近紫外区域表现出明亮的荧光。——被用作炔基配体以获得一系列均配双炔基Au(I)配合物——。这些配合物表现出明亮的磷光和以磷光为主的双重发射()。三联苯衍生物配合物在二甲基亚砜溶液中呈现暖白色发射,在聚甲基丙烯酸甲酯薄膜中呈现纯白色发射。含时密度泛函理论计算表明,T激发态具有混合的MLCT/ILCT性质,电荷转移主要通过以配体为中心的“D-π-A”体系。连接基的变化允许调节分子间电荷转移的效应,从而改变有机金“D-π-A”体系的电子和光物理性质。所呈现的结果明确显示了有机金属“D-π-A”结构概念的进展。

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