铱
阳离子聚合
喹啉
细胞毒性
化学
线粒体
红外线的
光化学
生物化学
高分子化学
体外
物理
有机化学
光学
催化作用
作者
Simin Liu,Pei‐Pei Zhang,Xiaoqiang Fang,Gongqing Wu,Shuting Chen,Zhina Zhang,Hui Chao,Wenying Tan,Li Xu
出处
期刊:Dalton Transactions
[The Royal Society of Chemistry]
日期:2017-01-01
卷期号:46 (14): 4777-4785
被引量:43
摘要
Biocompatible transition metal complexes dyes emitting in the near-infrared (NIR) region, are highly desirable in fluorescence imaging techniques. However, a high-performance mitochondria-specific labeling NIR probe with high photostability is still lacking. Herein we reported two NIR-emitting cationic iridium(iii) complexes [Ir(pbq-g)2(N^N)]+Cl- (pbq-g = phenylbenzo[g]-quinoline; N^N = 2-(1-benzyl-1H-pyrazol-3-yl) pyridine (Ir1) and 2-(1-(naphthalen-1-ylmethyl)-1H-pyrazol-3-yl) pyridine (Ir2)). These two novel Ir(iii) complexes with different N^N ligands exhibited similar NIR emission with λmax at 751 nm for Ir1 and 750 nm for Ir2 in PBS solution, with luminescence quantum yields of around 0.62 for Ir1 and 0.85 for Ir2. These two complexes showed high mitochondrial specificity, superior photostability, high resistance to the loss of the mitochondrial membrane potential and appreciable tolerance to environmental changes, allowing NIR imaging of mitochondrial morphological changes over long periods of time. These excellent photophysical and imaging properties made them promising NIR luminescent tags for applications in bioimaging.
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