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Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes

Some examples of atropoisomeric pseudorotaxanes in which the isomerism arises by the different conformations adopted by the wheel are reported here. Upon threading hexahexyloxycalix[6]arene 1 with ammonium axles 2(+) or 3(+), bearing biphenyl or trifluoromethylbenzyl moieties, respectively, two atro...

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Autores principales: Gaeta, Carmine, Talotta, Carmen, Neri, Placido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122310/
https://www.ncbi.nlm.nih.gov/pubmed/30202465
http://dx.doi.org/10.3762/bjoc.14.186
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author Gaeta, Carmine
Talotta, Carmen
Neri, Placido
author_facet Gaeta, Carmine
Talotta, Carmen
Neri, Placido
author_sort Gaeta, Carmine
collection PubMed
description Some examples of atropoisomeric pseudorotaxanes in which the isomerism arises by the different conformations adopted by the wheel are reported here. Upon threading hexahexyloxycalix[6]arene 1 with ammonium axles 2(+) or 3(+), bearing biphenyl or trifluoromethylbenzyl moieties, respectively, two atropoisomeric pseudorotaxanes were formed in which the calix[6]-wheel 1 adopts the 1,2,3-alternate and cone conformations. The interconversion between them cannot be obtained by simple rotation around the ArCH(2)Ar bonds of the calixarene wheel, which is blocked by the presence of the axle inside its cavity. Therefore, it can only be obtained through a mechanism of de-threading/re-threading of the axle. In all the examined cases, the 1,2,3-alternate and cone atropoisomers are, respectively, the kinetic and the thermodynamic ones.
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spelling pubmed-61223102018-09-10 Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes Gaeta, Carmine Talotta, Carmen Neri, Placido Beilstein J Org Chem Full Research Paper Some examples of atropoisomeric pseudorotaxanes in which the isomerism arises by the different conformations adopted by the wheel are reported here. Upon threading hexahexyloxycalix[6]arene 1 with ammonium axles 2(+) or 3(+), bearing biphenyl or trifluoromethylbenzyl moieties, respectively, two atropoisomeric pseudorotaxanes were formed in which the calix[6]-wheel 1 adopts the 1,2,3-alternate and cone conformations. The interconversion between them cannot be obtained by simple rotation around the ArCH(2)Ar bonds of the calixarene wheel, which is blocked by the presence of the axle inside its cavity. Therefore, it can only be obtained through a mechanism of de-threading/re-threading of the axle. In all the examined cases, the 1,2,3-alternate and cone atropoisomers are, respectively, the kinetic and the thermodynamic ones. Beilstein-Institut 2018-08-14 /pmc/articles/PMC6122310/ /pubmed/30202465 http://dx.doi.org/10.3762/bjoc.14.186 Text en Copyright © 2018, Gaeta 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 Full Research Paper
Gaeta, Carmine
Talotta, Carmen
Neri, Placido
Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes
title Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes
title_full Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes
title_fullStr Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes
title_full_unstemmed Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes
title_short Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes
title_sort calix[6]arene-based atropoisomeric pseudo[2]rotaxanes
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122310/
https://www.ncbi.nlm.nih.gov/pubmed/30202465
http://dx.doi.org/10.3762/bjoc.14.186
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