Petrovskii Stanislav, Paderina Aleksandra, Sizova Anastasia, Grachova Elena
Institute of Chemistry, St Petersburg University, Universitetskii pr. 26, 198504 St. Petersburg, Russia.
Inorg Chem. 2023 Apr 3;62(13):5123-5133. doi: 10.1021/acs.inorgchem.2c04360. Epub 2023 Mar 20.
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.
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。