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Tb-Metal Organic Frameworks-Referenced Bathocuproine Disulfonate Enable Fluorescence Distinguishing Cu+ from Cu2+
被引:8
|作者:
Zuo, Ya-Nan
[1
]
Liu, Shuyi
[1
]
Zhao, Xian-en
[1
,2
]
Zhu, Shuyun
[1
,2
]
Xu, Guobao
[3
]
机构:
[1] Qufu Normal Univ, Sch Chem & Chem Engn, Key Lab Catalyt Convers & Clean Energy Univ Shando, Qufu 273165, Shandong, Peoples R China
[2] Qufu Normal Univ, Institue Med Hlth & New Mat Appl Technol, Qufu City 273165, Shandong, Peoples R China
[3] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Ratiometric sensor;
Cuprous ion;
Fluorescence;
Metal-organic framework;
Static quenching;
LANTHANIDE COORDINATION POLYMERS;
CARBON DOTS;
RATIOMETRIC DETECTION;
COPPER;
CU(I);
SPECIATION;
PROBE;
ISOMERS;
LIQUID;
SENSOR;
D O I:
10.1016/j.snb.2023.134487
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
As the main existing form of copper, Cu+ plays vital roles in human health. It is highly significant to detect Cu+ selectively in biological matrixes especially in the coexistence of Cu2+. Herein, a ratiometric fluorescence sensor has been fabricated to discriminate Cu+ from Cu2+ and realize ratiometric detection of Cu+ by using Tb-MOFs and bathocuproine disulfonate (BCS). The sensor exhibits two fluorescence emissions at 400 nm from BCS as the response signal and 548 nm from Tb-MOFs as the reference signal. BCS can chelate with Cu+ selectively to form a stable adduct, inducing the fluorescence quenching of BCS through static quenching. When Cu+ is added, the intensity at 400 nm decreases significantly while that at 548 nm changes negligibly. Notably, the presence of Cu2+ exhibits no effect on the emissions both at 400 nm and 548 nm. Thus, Tb-MOFs-BCS system enable discrimination of Cu+ from Cu2+ and fast ratiometric detection of Cu+ within 1 min. The fluorescence ratio (F548/F440) shows a good linear relationship in Cu+ concentrations ranging from 1-200 nM with a low limit of detection of 0.3 nM, which is 1-3 orders magnitude lower than those of other methods. The high selectivity and sensitivity of this method enables the detection of Cu+ in human serum successfully.
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