Faculty of Pharmaceutical Sciences, Showa Pharmaceutical University, 3-3165 Higashi-tamagawagakuen, Machida, 194-8543, Japan.
Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan.
Sci Rep. 2019 Nov 27;9(1):17723. doi: 10.1038/s41598-019-53882-z.
Push-pull type fluorescent amino-quinoline derivatives (TFMAQ) bearing phenyl aromatic groups in the 8-position (TFMAQ-8Ar series) were synthesized via palladium-catalyzed C-H activation reaction in short steps. The N-arylation or C-H activation reactions were selectively controlled with high yield by combinations of palladium and phosphine ligands. The TFMAQ-8Ar analogues exhibited fluorescent solvatochromism in non-polar and polar solvents. In non-polar solvent, the absolute fluorescence quantum yield was high, wheareas the fluorescence was almost quenched in polar solvent. The TFMAQ-8Ar derivatives also showed high fluorescence emission at solid state owing to the planar structure between the quinoline ring and phenyl ring at the 7-amino group, as demonstrated by X-ray crystal structure analysis. The fluorescence imaging of 3T3-L1 cell using TFMAQ-8Ar derivatives was performed by confocal laser microscopy. Strong and specific emissions at lipid droplets were observed owing to the accumulation of TFMAQ-8Ar derivatives. Therefore, we propose that the TFMAQ-8Ar derivatives should become a versatile fluorescence probe for the live imaging of lipid droplets.
推挽式荧光氨基喹啉衍生物(TFMAQ)在 8 位带有苯芳基(TFMAQ-8Ar 系列),通过钯催化 C-H 活化反应短步骤合成。通过钯和膦配体的组合,可以选择性地控制 N-芳基化或 C-H 活化反应,以高产率进行。TFMAQ-8Ar 类似物在非极性和极性溶剂中表现出荧光溶剂化变色。在非极性溶剂中,绝对荧光量子产率很高,而在极性溶剂中荧光几乎被猝灭。TFMAQ-8Ar 衍生物也由于在 7-氨基处的喹啉环和苯环之间的平面结构,在固态下表现出高荧光发射,如 X 射线晶体结构分析所示。通过共聚焦激光显微镜对 3T3-L1 细胞进行 TFMAQ-8Ar 衍生物的荧光成像。由于 TFMAQ-8Ar 衍生物的积累,观察到在脂滴处的强且特异的发射。因此,我们提出 TFMAQ-8Ar 衍生物应该成为用于脂滴活细胞成像的通用荧光探针。