化学
对苯二酚
儿茶酚
席夫碱
间苯二酚
选择性
纳米片
荧光
苯醌
检出限
核化学
光化学
高分子化学
有机化学
催化作用
色谱法
物理
量子力学
作者
Jiayi Fan,Jinfan Li,Chunyan Liu,Mengyun Lu,Xinwen Jia,Wuduo Zhao,Ajuan Yu,Shusheng Zhang
标识
DOI:10.1021/acs.analchem.4c06359
摘要
A novel sensing platform was constructed for the recognition and identification of dihydroxybenzene isomers based on the MOF-0.02TEA fluorescence sensor with the morphology of nanosheet microspheres through coordination modulation. Based on the sensing principle that the amino group on the MOF-0.02TEA can make the Michael reaction with o -benzoquinone and p -benzoquinone, which were individually the oxidation intermediate of catechol and hydroquinone, the fluorescence intensity of MOF-0.02TEA could be quenched through the inner filter effect (IFE) without the interference from resorcinol. Besides, catechol and hydroquinone could be further distinguished with the assistance of the Schiff-base reaction by introducing o -phenylenediamine (OPD) to the detection system. The MOF-0.02TEA sensor exhibited good selectivity, and the detection limits for catechol and hydroquinone were 90.5 nmol/L and 0.52 μmol/L (S/N = 3), respectively. Moreover, the sensor could be used for the determination of dihydroxybenzene isomers in tap water and lake water.
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