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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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Autores principales: Safarnejad Shad, Mastaneh, Santhini, Pulikkal Veettil, Dehaen, Wim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753851/
https://www.ncbi.nlm.nih.gov/pubmed/31579083
http://dx.doi.org/10.3762/bjoc.15.211
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author Safarnejad Shad, Mastaneh
Santhini, Pulikkal Veettil
Dehaen, Wim
author_facet Safarnejad Shad, Mastaneh
Santhini, Pulikkal Veettil
Dehaen, Wim
author_sort Safarnejad Shad, Mastaneh
collection PubMed
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.
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spelling pubmed-67538512019-10-02 1,2,3-Triazolium macrocycles in supramolecular chemistry Safarnejad Shad, Mastaneh Santhini, Pulikkal Veettil Dehaen, Wim Beilstein J Org Chem Review 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. Beilstein-Institut 2019-09-12 /pmc/articles/PMC6753851/ /pubmed/31579083 http://dx.doi.org/10.3762/bjoc.15.211 Text en Copyright © 2019, Safarnejad Shad et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Safarnejad Shad, Mastaneh
Santhini, Pulikkal Veettil
Dehaen, Wim
1,2,3-Triazolium macrocycles in supramolecular chemistry
title 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_short 1,2,3-Triazolium macrocycles in supramolecular chemistry
title_sort 1,2,3-triazolium macrocycles in supramolecular chemistry
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753851/
https://www.ncbi.nlm.nih.gov/pubmed/31579083
http://dx.doi.org/10.3762/bjoc.15.211
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