1,2,3-Triazolium macrocycles in supramolecular chemistry

In this short review, we describe different pathways for synthesizing 1,2,3-triazolium macrocycles and focus on their application in different areas of supramolecular chemistry. The synthesis is mostly relying on the well-known “click reaction” (CuAAC) leading to 1,4-disubstituted 1,2,3-triazoles th...

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Main Authors: Mastaneh Safarnejad Shad, Pulikkal Veettil Santhini, Wim Dehaen
Format: Article
Language:English
Published: Beilstein-Institut 2019-09-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.15.211
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spelling doaj-85f460a67e374a9299233f6f79c04f072021-02-02T03:46:36ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972019-09-011512142215510.3762/bjoc.15.2111860-5397-15-2111,2,3-Triazolium macrocycles in supramolecular chemistryMastaneh Safarnejad Shad0Pulikkal Veettil Santhini1Wim Dehaen2Molecular Design and Synthesis, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, BelgiumMolecular Design and Synthesis, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, BelgiumMolecular Design and Synthesis, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, BelgiumIn this short review, we describe different pathways for synthesizing 1,2,3-triazolium macrocycles and focus on their application in different areas of supramolecular chemistry. The synthesis is mostly relying on the well-known “click reaction” (CuAAC) leading to 1,4-disubstituted 1,2,3-triazoles that then can be quaternized. Applications of triazolium macrocycles thus prepared include receptors for molecular recognition of anionic species, pH sensors, mechanically interlocked molecules, molecular machines, and molecular reactors.https://doi.org/10.3762/bjoc.15.211anion recognitioncatenanechalcogen bondingclick reactionmolecular reactorhydrogen bondingph sensorrotaxanesupramolecular1,2,3-triazolium macrocycles
collection DOAJ
language English
format Article
sources DOAJ
author Mastaneh Safarnejad Shad
Pulikkal Veettil Santhini
Wim Dehaen
spellingShingle Mastaneh Safarnejad Shad
Pulikkal Veettil Santhini
Wim Dehaen
1,2,3-Triazolium macrocycles in supramolecular chemistry
Beilstein Journal of Organic Chemistry
anion recognition
catenane
chalcogen bonding
click reaction
molecular reactor
hydrogen bonding
ph sensor
rotaxane
supramolecular
1,2,3-triazolium macrocycles
author_facet Mastaneh Safarnejad Shad
Pulikkal Veettil Santhini
Wim Dehaen
author_sort Mastaneh Safarnejad Shad
title 1,2,3-Triazolium macrocycles in supramolecular chemistry
title_short 1,2,3-Triazolium macrocycles in supramolecular chemistry
title_full 1,2,3-Triazolium macrocycles in supramolecular chemistry
title_fullStr 1,2,3-Triazolium macrocycles in supramolecular chemistry
title_full_unstemmed 1,2,3-Triazolium macrocycles in supramolecular chemistry
title_sort 1,2,3-triazolium macrocycles in supramolecular chemistry
publisher Beilstein-Institut
series Beilstein Journal of Organic Chemistry
issn 1860-5397
publishDate 2019-09-01
description In this short review, we describe different pathways for synthesizing 1,2,3-triazolium macrocycles and focus on their application in different areas of supramolecular chemistry. The synthesis is mostly relying on the well-known “click reaction” (CuAAC) leading to 1,4-disubstituted 1,2,3-triazoles that then can be quaternized. Applications of triazolium macrocycles thus prepared include receptors for molecular recognition of anionic species, pH sensors, mechanically interlocked molecules, molecular machines, and molecular reactors.
topic anion recognition
catenane
chalcogen bonding
click reaction
molecular reactor
hydrogen bonding
ph sensor
rotaxane
supramolecular
1,2,3-triazolium macrocycles
url https://doi.org/10.3762/bjoc.15.211
work_keys_str_mv AT mastanehsafarnejadshad 123triazoliummacrocyclesinsupramolecularchemistry
AT pulikkalveettilsanthini 123triazoliummacrocyclesinsupramolecularchemistry
AT wimdehaen 123triazoliummacrocyclesinsupramolecularchemistry
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