Ion recognition by 1,2,3-triazole moieties synthesized via "click chemistry"

被引:21
|
作者
Singh, Gurleen [1 ]
George, Nancy [1 ]
Singh, Riddima [1 ]
Singh, Gurjaspreet [2 ,3 ]
Sushma [2 ,3 ]
Kaur, Gurpreet [4 ]
Singh, Harminder [1 ]
Singh, Jandeep [1 ]
机构
[1] Lovely Profess Univ, Sch Chem Engn & Phys Sci, Phagwara 144411, Punjab, India
[2] Panjab Univ, Dept Chem, Chandigarh, India
[3] Panjab Univ, Ctr Adv Studies Chem, Chandigarh, India
[4] Gujranwala Guru Nanak Khalsa Coll, Dept Chem, Ludhiana, Punjab, India
关键词
alkyne-azide cycloaddition; chemosensor; fluorescence spectroscopy; ion sensing; UV-Vis spectroscopy; AZIDE-ALKYNE CYCLOADDITION; SELECTIVE FLUORESCENT CHEMOSENSOR; RESONANCE ENERGY-TRANSFER; PYRENYL-APPENDED TRIAZOLE; COPPER-CATALYZED HUISGEN; NAKED-EYE DETECTION; TURN-ON SENSOR; NMR-SPECTROSCOPY; COMPLEX STABILITY; RHODAMINE-BODIPY;
D O I
10.1002/aoc.6897
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
1,2,3-Triazole-based ligands obtained through copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) have been exploited in vast array of research domains owing to the stitching of simpler molecules through a needle of Cu(I) catalyst. The numerous reports on ion(s) detection capabilities of synthesized 1,4-disubstituted 1,2,3-triazole ligands using absorption and fluorescence spectroscopy are accessible. This review enlists substituted 1,2,3-triazole-based sensor probes, since 2010, synthesized selectively by CuAAC, having the ability to sense either a single ion or multiple ions under specific set of conditions along with their detection limits. The review also apprehends the different techniques and sensing mechanisms involved in the detection of ions by chemosensor probes.
引用
收藏
页数:62
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