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Creating molecular macrocycles for anion recognition

The creation and functionality of new classes of macrocycles that are shape persistent and can bind anions is described. The genesis of triazolophane macrocycles emerges out of activity surrounding 1,2,3-triazoles made using click chemistry; and the same triazoles are responsible for anion capture....

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Autor principal: Flood, Amar H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902025/
https://www.ncbi.nlm.nih.gov/pubmed/27340452
http://dx.doi.org/10.3762/bjoc.12.60
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author Flood, Amar H
author_facet Flood, Amar H
author_sort Flood, Amar H
collection PubMed
description The creation and functionality of new classes of macrocycles that are shape persistent and can bind anions is described. The genesis of triazolophane macrocycles emerges out of activity surrounding 1,2,3-triazoles made using click chemistry; and the same triazoles are responsible for anion capture. Mistakes made and lessons learnt in anion recognition provide deeper understanding that, together with theory, now provides for computer-aided receptor design. The lessons are acted upon in the creation of two new macrocycles. First, cyanostars are larger and like to capture large anions. Second is tricarb, which also favors large anions but shows a propensity to self-assemble in an orderly and stable manner, laying a foundation for future designs of hierarchical nanostructures.
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spelling pubmed-49020252016-06-23 Creating molecular macrocycles for anion recognition Flood, Amar H Beilstein J Org Chem Review The creation and functionality of new classes of macrocycles that are shape persistent and can bind anions is described. The genesis of triazolophane macrocycles emerges out of activity surrounding 1,2,3-triazoles made using click chemistry; and the same triazoles are responsible for anion capture. Mistakes made and lessons learnt in anion recognition provide deeper understanding that, together with theory, now provides for computer-aided receptor design. The lessons are acted upon in the creation of two new macrocycles. First, cyanostars are larger and like to capture large anions. Second is tricarb, which also favors large anions but shows a propensity to self-assemble in an orderly and stable manner, laying a foundation for future designs of hierarchical nanostructures. Beilstein-Institut 2016-03-31 /pmc/articles/PMC4902025/ /pubmed/27340452 http://dx.doi.org/10.3762/bjoc.12.60 Text en Copyright © 2016, Flood https://creativecommons.org/licenses/by/2.0https://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/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Flood, Amar H
Creating molecular macrocycles for anion recognition
title Creating molecular macrocycles for anion recognition
title_full Creating molecular macrocycles for anion recognition
title_fullStr Creating molecular macrocycles for anion recognition
title_full_unstemmed Creating molecular macrocycles for anion recognition
title_short Creating molecular macrocycles for anion recognition
title_sort creating molecular macrocycles for anion recognition
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902025/
https://www.ncbi.nlm.nih.gov/pubmed/27340452
http://dx.doi.org/10.3762/bjoc.12.60
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