Institut de Physique et Chimie des Matériaux de Strasbourg UMR 7504, Université de Strasbourg & CNRS, 23 rue du Loess, 67034, Strasbourg, France.
Institut Parisien de Chimie Moléculaire UMR 8232, Sorbonne Université, 4 Place Jussieu, 75005, Paris, France.
Chempluschem. 2023 Nov;88(11):e202300303. doi: 10.1002/cplu.202300303. Epub 2023 Sep 13.
A series of four binuclear complexes of general formula [(C^C)Au(Cl)(L^L)(Cl)Au(C^C)], where C^C is 4,4'-diterbutylbiphenyl and L^L is either a bridging diphosphine or 4,4'-bipyridine, are synthetized with 52 to 72 % yield and structurally characterized by X-ray diffraction. The use of the chelating 1,2-diphenylphosphinoethane ligand in a 1 : 2 (P^P):Au stoichiometry leads to the near quantitative formation of a gold double-complex salt of general formula [(C^C)Au(P^P)][(C^C^)AuCl ]. The compounds display long-lived yellow-green phosphorescence with λ in the range of 525 to 585 nm in the solid state with photoluminescence quantum yields (PLQY) up to 10 %. These Au complexes are tested for their antiproliferative activity against lung adenocarcinoma cells A549 and results show that compounds 2 and 5 are the most promising candidates. The digold salt 5 shows anticancer activity between 66 and 200 nM on the tested cancer cell lines, whereas derivative 2 displays concentration values required to reduce by 50 % the cell viability (IC ) between 7 and 11 μM. Reactivity studies of compound 5 reveal that the [(C^C)Au(P^P)] cation is stable in the presence of relevant biomolecules including glutathione suggesting a structural mechanism of action.
一系列通式为[(C^C)Au(Cl)(L^L)(Cl)Au(C^C)]的四核配合物,其中 C^C 是 4,4'-二特丁基联苯,L^L 是桥联二膦或 4,4'-联吡啶,通过 X 射线衍射结构表征。在 1:2(P^P):Au 的化学计量比下使用螯合 1,2-二苯基膦乙烷配体,导致几乎定量地形成通式为[(C^C)Au(P^P)][(C^C^)AuCl ]的金双配合物盐。这些化合物在固态下具有长达寿命的黄色绿色磷光,λ 在 525 到 585nm 范围内,光致发光量子产率(PLQY)高达 10%。这些 Au 配合物被测试其对肺腺癌细胞 A549 的抗增殖活性,结果表明化合物 2 和 5 是最有前途的候选物。二金盐 5 在测试的癌细胞系中表现出 66 到 200nm 的抗癌活性,而衍生物 2 显示出降低细胞活力 50%所需的浓度值(IC)在 7 到 11μm 之间。化合物 5 的反应性研究表明,[(C^C)Au(P^P)]阳离子在存在包括谷胱甘肽在内的相关生物分子时是稳定的,这表明了一种结构作用机制。