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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,...

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Autores principales: Dubey, Rajeev K., Melle-Franco, Manuel, Mateo-Alonso, Aurelio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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
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