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

来源：

APPLIED ORGANOMETALLIC CHEMISTRY | 2023年 / 37卷 / 01期

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

页数：62

共 50 条

[21] Preparation and Properties of Polyimides Containing 1,2,3-Triazole Moieties
Rukmanikrishnan, Balasubramanian
Muthusamy, Sarojadevi
ADVANCES IN POLYMER TECHNOLOGY, 2018, 37 (01) : 50 - 59
[22] Click generated o-Cresolphthalein linked 1,2,3-triazole derivative for selective Pb(II) ion recognition
Saini, Parveen
Singh, Gurjaspreet
Kaur, Gurpreet
Singh, Jandeep
Singh, Harminder
JOURNAL OF MOLECULAR STRUCTURE, 2022, 1251
[23] Corey lactone as key precursor for a facile synthesis of novel 1,2,3-triazole carbocyclic nucleosides via Click Chemistry
Gonzalez-Gonzalez, Carlos A.
Fuentes-Benitez, Aydee
Cuevas-Yanez, Erick
Corona-Becerril, David
Gonzalez-Romero, Carlos
Gonzalez-Calderon, Davir
TETRAHEDRON LETTERS, 2013, 54 (21) : 2726 - 2728
[24] Synthesis of N1 and N2 coumarin substituted 1,2,3-triazole isomers via click chemistry approach
Shamala, Devadas
Shivashankar, Kalegowda
Chandra
Mahendra, Madegowda
SYNTHETIC COMMUNICATIONS, 2016, 46 (05) : 433 - 441
[25] Versatile Synthetic Platform for 1,2,3-Triazole Chemistry
Vala, Disha P.
Vala, Ruturajsinh M.
Patel, Hitendra M.
ACS OMEGA, 2022, 7 (42): : 36945 - 36987
[26] The 1,2,3-triazole ring as a bioisostere in medicinal chemistry
Bonandi, Elisa
Christodoulou, Michael S.
Fumagalli, Gaia
Perdicchia, Dario
Rastelli, Giulio
Passarella, Daniele
DRUG DISCOVERY TODAY, 2017, 22 (10) : 1572 - 1581
[27] Synthesis and Characterization of Compounds Containing 1,2,3-Triazole via Click Reaction and Ag(Ⅰ) Complex
李文思
冯圣玉
ChineseJournalofStructuralChemistry, 2018, 37 (12) : 1932 - 1938
[28] Design and Synthesis of Novel 1,2,3-Triazole Levonorgestrel Derivatives via Click Chemistry. Anticancer Activity and Molecular Docking
Alshamari, A. K.
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2022, 58 (12) : 1878 - 1888
[29] Click Synthesis of 1,2,3-Triazole Nucleosides Based on Functionalized Nicotinonitriles
H. A. Morsy
S. M. Mohammed
A. M. Abdel Hamid
A. H. Moustafa
H. A. El-Sayed
Russian Journal of Organic Chemistry, 2020, 56 : 143 - 147
[30] 1,2,3-Triazole stabilized click radiopeptidomimetics for improved tumor targeting
Mindt, Thomas
Valverde, Ibai
Fischer, Christiane
Vomstein, Sandra
Bauman, Andreas
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 250

← 1 2 3 4 5 →