4.6 Review

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

Journal

APPLIED ORGANOMETALLIC CHEMISTRY
Volume 37, Issue 1, Pages -

Publisher

WILEY
DOI: 10.1002/aoc.6897

Keywords

alkyne-azide cycloaddition; chemosensor; fluorescence spectroscopy; ion sensing; UV-Vis spectroscopy

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This review focuses on the 1,2,3-triazole-based sensor probes synthesized selectively by CuAAC, which have the ability to detect single or multiple ions under specific conditions. The review also discusses the techniques and sensing mechanisms involved in ion detection using chemosensor probes.
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.

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