A new near-infrared fluorescence sensor based on dicyanomethylene-4H-pyran for the detection of Al3+, Cr3+, Fe3+and Cu2+

被引:6
作者
Liu, Tiantian [1 ]
Huang, Qiushuo [1 ]
Tian, Mengna [1 ]
Lin, Zhangfei [1 ]
Wu, Wenpeng [1 ]
Ren, Tiegang [1 ]
Zhang, Jinglai [1 ]
机构
[1] Henan Univ, Inst Upconvers Nanoscale Mat, Coll Chem & Chem Engn, Henan Prov Engn Res Ctr Green Anticorros Technol M, Kaifeng 475004, Peoples R China
基金
中国国家自然科学基金;
关键词
Dicyanomethylene-4H-pyran; Near infrared; Chemical sensor; Density functional theory; Intramolecular charge transfer; TURN-ON PROBE; SELECTIVE DETECTION; ALZHEIMERS-DISEASE; WATER SAMPLES; LIVING CELLS; RHODAMINE; ALUMINUM; IONS; CHEMOSENSOR; RECOGNITION;
D O I
10.1016/j.jphotochem.2022.113991
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A novel near-infrared (NIR) fluorescence sensor DCM-PSI based on dicyanomethylene-4H-pyran(DCM) was designed and synthesized to selectively detect Al3+, Cr3+, Fe3+ and Cu2+. It had a large Stokes shift (lambda abs = 450 nm, lambda ex = 490 nm, lambda em = 690 nm), low detection limits and large binding constants. With the addition of Al3+, Cr3+, Fe3+ and Cu2+, the fluorescence quenched and the emission peaks blue shifted to different extent. Experimental analysis and quantum chemical calculations showed that the luminescence of DCM-PSI experienced an excited state intramolecular proton transfer (ESIPT) and partly intramolecular charge transfer (ICT) process, while the complexation of Al3+, Cr3+, Fe3+ and Cu2+ caused ligand-to-metal electron transfer, and altered the "push-pull" effect in DCM-PSI. Furthermore, the Al3+ and Fe3+ in drinking water was also measured with DCM-PSI to test the practical application of the sensor.
引用
收藏
页数:10
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