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Fluorescence chemosensor for acetate ion and fluorine ion based on 1,2,4-triazolyl substituted pentaphenylpyridinium
被引:5
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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