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Inducing Single-Handed Helicity in a Twisted Molecular Nanoribbon
[Image: see text] Molecular conformation has an important role in chemistry and materials science. Molecular nanoribbons can adopt chiral twisted helical conformations. However, the synthesis of single-handed helically twisted molecular nanoribbons still represents a considerable challenge. Herein,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855342/ https://www.ncbi.nlm.nih.gov/pubmed/35099195 http://dx.doi.org/10.1021/jacs.1c12385 |
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author | Dubey, Rajeev K. Melle-Franco, Manuel Mateo-Alonso, Aurelio |
author_facet | Dubey, Rajeev K. Melle-Franco, Manuel Mateo-Alonso, Aurelio |
author_sort | Dubey, Rajeev K. |
collection | PubMed |
description | [Image: see text] Molecular conformation has an important role in chemistry and materials science. Molecular nanoribbons can adopt chiral twisted helical conformations. However, the synthesis of single-handed helically twisted molecular nanoribbons still represents a considerable challenge. Herein, we describe an asymmetric approach to induce single-handed helicity with an excellent degree of conformational discrimination. The chiral induction is the result of the chiral strain generated by fusing two oversized chiral rings and of the propagation of that strain along the nanoribbon’s backbone. |
format | Online Article Text |
id | pubmed-8855342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-88553422022-02-18 Inducing Single-Handed Helicity in a Twisted Molecular Nanoribbon Dubey, Rajeev K. Melle-Franco, Manuel Mateo-Alonso, Aurelio J Am Chem Soc [Image: see text] Molecular conformation has an important role in chemistry and materials science. Molecular nanoribbons can adopt chiral twisted helical conformations. However, the synthesis of single-handed helically twisted molecular nanoribbons still represents a considerable challenge. Herein, we describe an asymmetric approach to induce single-handed helicity with an excellent degree of conformational discrimination. The chiral induction is the result of the chiral strain generated by fusing two oversized chiral rings and of the propagation of that strain along the nanoribbon’s backbone. American Chemical Society 2022-01-31 2022-02-16 /pmc/articles/PMC8855342/ /pubmed/35099195 http://dx.doi.org/10.1021/jacs.1c12385 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Dubey, Rajeev K. Melle-Franco, Manuel Mateo-Alonso, Aurelio Inducing Single-Handed Helicity in a Twisted Molecular Nanoribbon |
title | Inducing
Single-Handed Helicity in a Twisted Molecular
Nanoribbon |
title_full | Inducing
Single-Handed Helicity in a Twisted Molecular
Nanoribbon |
title_fullStr | Inducing
Single-Handed Helicity in a Twisted Molecular
Nanoribbon |
title_full_unstemmed | Inducing
Single-Handed Helicity in a Twisted Molecular
Nanoribbon |
title_short | Inducing
Single-Handed Helicity in a Twisted Molecular
Nanoribbon |
title_sort | inducing
single-handed helicity in a twisted molecular
nanoribbon |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855342/ https://www.ncbi.nlm.nih.gov/pubmed/35099195 http://dx.doi.org/10.1021/jacs.1c12385 |
work_keys_str_mv | AT dubeyrajeevk inducingsinglehandedhelicityinatwistedmolecularnanoribbon AT mellefrancomanuel inducingsinglehandedhelicityinatwistedmolecularnanoribbon AT mateoalonsoaurelio inducingsinglehandedhelicityinatwistedmolecularnanoribbon |