Fluorescence chemosensor for acetate ion and fluorine ion based on 1,2,4-triazolyl substituted pentaphenylpyridinium

被引:4
作者
Wang, Guangyao [1 ,2 ]
Zheng, Ting [1 ,2 ]
Zhang, Siqi [1 ,2 ]
Ye, Junwei [1 ,2 ]
Ning, Guiling [1 ,2 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116012, Peoples R China
[2] Dalian Univ Technol, Sch Chem Engn, 2 Linggong Rd, Dalian 116012, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescence sensor; Triazole-based pyridinium salt; Acetate ion and fluorine ion recognition; Hydrogen bond; AGGREGATION-INDUCED EMISSION; ANION-BINDING; RECEPTORS; PYRIDINIUM; TRIAZOLE; LOMEFLOXACIN; RECOGNITION; MECHANISMS; AFFINITY; BEHAVIOR;
D O I
10.1016/j.molstruc.2021.129918
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 pyridinium salt derivative, 2,3,4,5,6-pentaphenyl-1-(1H-1,2,4-triazol-3-yl)pyridinium perchlorate (1) has been designed and synthesized by using pyrylium perchlorate and 3-amino-1H-1,2,4-triazole as ingredients, which can be exploited for the binding and specific sensing of anion via hydrogen bonds. Compound 1 exhibits intense blue emission in solution with maximum emission at 469 nm with a red shift relative to that (426 nm) of solid state. The luminescence intensity of 1 could be selectively and sensitivity quenched with acetate ion and fluorine ion among various anions including F-, Cl-, Br-, I-, AcO- and NO3-. Furthermore, the possible detection mechanism was investigated. This work could contribute a credible potential sensing application of 1,2,4-triazolyl substituted pentaphenylpyridinium salts towards the specific anions in biological and environmental concerns. (C) 2021 Elsevier B.V. All rights reserved.
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页数:7
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