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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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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. |
format | Online Article Text |
id | pubmed-6753851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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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