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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2018
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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. |
format | Online Article Text |
id | pubmed-6122310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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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