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Diastereomeric multi‐chiral pendant groups: Their key role in stimuli‐responsive polymeric responses

Chiral information transmission in helical polymers bearing multi‐chiral pendant groups is usually determined by the absolute configuration of the first chiral center. The second chiral residue usually has low‐to‐null influence in the macromolecular handedness of the polymer, due to its remote posit...

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Autores principales: Rodríguez, Rafael, Rivadulla‐Cendal, Elena, Quiñoá, Emilio, Freire, Félix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107841/
https://www.ncbi.nlm.nih.gov/pubmed/36625726
http://dx.doi.org/10.1002/chir.23530
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author Rodríguez, Rafael
Rivadulla‐Cendal, Elena
Quiñoá, Emilio
Freire, Félix
author_facet Rodríguez, Rafael
Rivadulla‐Cendal, Elena
Quiñoá, Emilio
Freire, Félix
author_sort Rodríguez, Rafael
collection PubMed
description Chiral information transmission in helical polymers bearing multi‐chiral pendant groups is usually determined by the absolute configuration of the first chiral center. The second chiral residue usually has low‐to‐null influence in the macromolecular handedness of the polymer, due to its remote position respect to the polyene main chain. Here, we demonstrate how the stimuli responsive properties of diastereomeric polymers, obtained by changing the absolute configuration of the second chiral center, are different due to the unlike properties of diastereoisomers.
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spelling pubmed-101078412023-04-18 Diastereomeric multi‐chiral pendant groups: Their key role in stimuli‐responsive polymeric responses Rodríguez, Rafael Rivadulla‐Cendal, Elena Quiñoá, Emilio Freire, Félix Chirality Special Issue: Chiral Materials Chiral information transmission in helical polymers bearing multi‐chiral pendant groups is usually determined by the absolute configuration of the first chiral center. The second chiral residue usually has low‐to‐null influence in the macromolecular handedness of the polymer, due to its remote position respect to the polyene main chain. Here, we demonstrate how the stimuli responsive properties of diastereomeric polymers, obtained by changing the absolute configuration of the second chiral center, are different due to the unlike properties of diastereoisomers. John Wiley and Sons Inc. 2023-01-10 2023-03 /pmc/articles/PMC10107841/ /pubmed/36625726 http://dx.doi.org/10.1002/chir.23530 Text en © 2023 The Authors. Chirality published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Special Issue: Chiral Materials
Rodríguez, Rafael
Rivadulla‐Cendal, Elena
Quiñoá, Emilio
Freire, Félix
Diastereomeric multi‐chiral pendant groups: Their key role in stimuli‐responsive polymeric responses
title Diastereomeric multi‐chiral pendant groups: Their key role in stimuli‐responsive polymeric responses
title_full Diastereomeric multi‐chiral pendant groups: Their key role in stimuli‐responsive polymeric responses
title_fullStr Diastereomeric multi‐chiral pendant groups: Their key role in stimuli‐responsive polymeric responses
title_full_unstemmed Diastereomeric multi‐chiral pendant groups: Their key role in stimuli‐responsive polymeric responses
title_short Diastereomeric multi‐chiral pendant groups: Their key role in stimuli‐responsive polymeric responses
title_sort diastereomeric multi‐chiral pendant groups: their key role in stimuli‐responsive polymeric responses
topic Special Issue: Chiral Materials
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107841/
https://www.ncbi.nlm.nih.gov/pubmed/36625726
http://dx.doi.org/10.1002/chir.23530
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