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Recent Advances in the Synthesis of Ammonium-Based Rotaxanes

The number of synthetic methods enabling the preparation of ammonium-based rotaxanes has increased very rapidly in the past ten years. The challenge in the synthesis of rotaxanes results from the rather weak interactions between the ammonium-containing rod and the crown ether macrocycle in the pseud...

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Detalles Bibliográficos
Autores principales: Thibeault, Dominic, Morin, Jean-François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263328/
https://www.ncbi.nlm.nih.gov/pubmed/20657509
http://dx.doi.org/10.3390/molecules15053709
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author Thibeault, Dominic
Morin, Jean-François
author_facet Thibeault, Dominic
Morin, Jean-François
author_sort Thibeault, Dominic
collection PubMed
description The number of synthetic methods enabling the preparation of ammonium-based rotaxanes has increased very rapidly in the past ten years. The challenge in the synthesis of rotaxanes results from the rather weak interactions between the ammonium-containing rod and the crown ether macrocycle in the pseudorotaxane structure that rely mostly on O·H hydrogen bonds. Indeed, no strong base or polar solvent that could break up H-bonding can be used during the formation of rotaxanes because the two components will separate as two distinct entities. Moreover, most of the reactions have to be performed at room temperature to favor the formation of pseudorotaxane in solution. These non-trivial prerequisites have been taken into account to develop efficient reaction conditions for the preparation of rotaxanes and those are described in detail along this review.
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spelling pubmed-62633282019-01-02 Recent Advances in the Synthesis of Ammonium-Based Rotaxanes Thibeault, Dominic Morin, Jean-François Molecules Review The number of synthetic methods enabling the preparation of ammonium-based rotaxanes has increased very rapidly in the past ten years. The challenge in the synthesis of rotaxanes results from the rather weak interactions between the ammonium-containing rod and the crown ether macrocycle in the pseudorotaxane structure that rely mostly on O·H hydrogen bonds. Indeed, no strong base or polar solvent that could break up H-bonding can be used during the formation of rotaxanes because the two components will separate as two distinct entities. Moreover, most of the reactions have to be performed at room temperature to favor the formation of pseudorotaxane in solution. These non-trivial prerequisites have been taken into account to develop efficient reaction conditions for the preparation of rotaxanes and those are described in detail along this review. MDPI 2010-05-25 /pmc/articles/PMC6263328/ /pubmed/20657509 http://dx.doi.org/10.3390/molecules15053709 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Thibeault, Dominic
Morin, Jean-François
Recent Advances in the Synthesis of Ammonium-Based Rotaxanes
title Recent Advances in the Synthesis of Ammonium-Based Rotaxanes
title_full Recent Advances in the Synthesis of Ammonium-Based Rotaxanes
title_fullStr Recent Advances in the Synthesis of Ammonium-Based Rotaxanes
title_full_unstemmed Recent Advances in the Synthesis of Ammonium-Based Rotaxanes
title_short Recent Advances in the Synthesis of Ammonium-Based Rotaxanes
title_sort recent advances in the synthesis of ammonium-based rotaxanes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263328/
https://www.ncbi.nlm.nih.gov/pubmed/20657509
http://dx.doi.org/10.3390/molecules15053709
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