检出限
硝基苯
荧光
化学
脱质子化
粉末衍射
配体(生物化学)
核化学
金属有机骨架
单晶
热稳定性
X射线光电子能谱
联苯
结晶学
分析化学(期刊)
物理化学
色谱法
吸附
有机化学
量子力学
核磁共振
催化作用
离子
生物化学
物理
受体
作者
Yu-Pei Fu,Hua Yang,Lulu Dong,Fang Wang,Xiaoli Chen,Ji‐Jiang Wang
标识
DOI:10.1016/j.saa.2023.123619
摘要
A novel metal–organic framework (MOF) with the formula of [Cd(CIA)(4,4′-BB)·H2O]·H2O (Cd-MOF) (H2CIA = 5-methoxyisophthalic acid, 4,4′-BB: 4,4′-bis((1H-imidazol-1-yl)methyl)-1,1′-biphenyl) has been designed and synthesized through solvothermal reaction. The structure was characterized by TG, IR, PXRD, elemental analysis, single-crystal X-ray diffraction and XPS. The coordination pattern of the fully deprotonated ligand (CIA) in Cd-MOF is μ2-к1: к0: к2. The complex is found to be a three-dimensional reticular material with good thermal stability. Further study revealed that Cd-MOF has good fluorescence performance and can be used as a fluorescent probe for sensitive detection of histidine (His), nitrobenzene (NB), tetracycline (TC) and pyrimethanil (PTH) in water. Four cycles experiments can be achieved with a low detection limit. The detection limits were 0.3 µM (His), 0.05 µM (NB), 0.2 µM (TC) and 0.01 µM (PTH), respectively. To verify the feasibility of detecting PTH in real samples, we further explored it in water samples and apple peels. The spiked recoveries were 95.3–99.4 % and 97.2–101.2 %, respectively. Finally, the fluorescence quenching mechanism of Cd-MOF in His, NB, TC and PTH detection is discussed in detail.
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