A sensitive "on-off-on" fluorescent probe for sequential Cu2+/S2- detection in actual water samples and living cells

被引:8
|
作者
Qiao, Yi-Jie [1 ,2 ]
Xu, Fang-Zhou [1 ,2 ]
Chen, Yun [1 ,2 ]
Wang, Zhi-Qiang [3 ,4 ]
Gong, Xue-Qing [3 ,4 ]
Wang, Cheng-Yun [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Key Lab Adv Mat, 130 Meilong Rd, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Sch Chem & Mol Engn, Inst Fine Chem, 130 Meilong Rd, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Ctr Computat Chem, Key Lab Adv Mat, 130 Meilong Rd, Shanghai 200237, Peoples R China
[4] East China Univ Sci & Technol, Res Inst Ind Catalysis, Sch Chem & Mol Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China
基金
上海市自然科学基金;
关键词
Fluorescent probe; Copper ion (II); Sulfide ion (II); Sequential detection; HYDROGEN-SULFIDE; BASIS-SETS; COPPER; IONS;
D O I
10.1016/j.tet.2022.132791
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Aquatic organism is far less tolerant to Cu2+ than that of mammals, and the excessive Cu2+ can also be harmful to human by bioconcentration. Herein, a fluorescent probe (DPA-SAA) that can be easily synthesized was developed for detecting traces of Cu(2+ )in actual aqueous environment and cells. The experimental and theoretical results showed that the fluorescence of DPA-SAA could be evidently quenched by only 1% equivalent of Cu2+. The limit of detection (LOD) was calculated to be 0.66 nM, which is far below the Chinese standard of fishery water quality (157 nM). Simultaneously, the Cu2+ of complex DPA-SAA/Cu2+ could be captured by S2-, thus realizing sequential S(2- )detection with a low LOD of 13.93 nM. Moreover, DPA-SAA was proved qualified for Cu2+ detection in actual water samples with good recovery, and sequential Cu2+/S2- sensing in living cells. (C) 2022 Elsevier Ltd. All rights reserved.
引用
收藏
页数:8
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