荧光
化学
检出限
钯
光化学
肉眼
水溶液中的金属离子
水溶液
紧身衣
结合常数
乙腈
分子内力
分析化学(期刊)
离子
物理化学
立体化学
有机化学
色谱法
结合位点
催化作用
物理
量子力学
生物化学
作者
Xiaofei Chen,Qinhai Ma,Zhoulang Wang,Zeqiang Xie,Yu Song,Yanfang Ma,Zifeng Yang,Xin Zhao
标识
DOI:10.1002/asia.202001144
摘要
Abstract A novel boron dipyrromethene (BODIPY)‐based fluorescent probe BDP−Pd was designed and synthesized. Upon coordination with Pd 2+ , the emission of the probe at 508 nm significantly increased, showing an ‘OFF‐ON’ fluorescence response. The complexation of BDP−Pd with Pd 2+ in both acetonitrile and aqueous solution were then studied by absorption and fluorescence spectra. The binding stoichiometry between the probe and Pd 2+ was found to be 1 : 2, and the binding constant was determined to be 8.5×10 10 M −2 and 8.2×10 10 M −2 in acetonitrile and aqueous solution, respectively. The probe exhibited a detection limit as low as 0.72 ppb toward Pd 2+ with no obvious interference from up to 21 species of common metal ions, suggesting BDP−Pd as a sensitive and selective fluorescent probe for Pd 2+ detection. The fast fluorescence ‘OFF‐ON’ phenomenon of the probe upon coordination with Pd 2+ ions could be easily observed by a hand‐hold UV lamp under naked eye in solution as well as on homemade test trips. Density functional theory (DFT) calculations were carried out to give the optimized structure of complex BDP−Pd : 2Pd 2+ and rationalize the detection mechanism through a prohibited intramolecular photoinduced electron transfer (PET) process. The bio‐imaging application of the probe was investigated and it showed excellent cell permeability for fluorescent imaging of Pd 2+ ions in A549 human non‐small cell lung cancer cells.
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