Diastereomeric multi-chiral pendant groups: their key role in stimuli-responsive polymeric responses
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares | es_ES |
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Departamento de Química Orgánica | es_ES |
| dc.contributor.author | Rodríguez Riego, Rafael | |
| dc.contributor.author | Rivadulla Cendal, Elena | |
| dc.contributor.author | Quiñoá Cabana, Emilio | |
| dc.contributor.author | Freire Iribarne, Félix Manuel | |
| dc.date.accessioned | 2023-06-22T12:27:02Z | |
| dc.date.available | 2023-06-22T12:27:02Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Chiral information transmission in helical polymers bearing multi-chiral pen-dant groups is usually determined by the absolute configuration of the first chi-ral center. The second chiral residue usually has low-to-null influence in themacromolecular handedness of the polymer, due to its remote position respectto the polyene main chain. Here, we demonstrate how the stimuli responsiveproperties of diastereomeric polymers, obtained by changing the absolute con-figuration of the second chiral center, are different due to the unlike propertiesof diastereoisomers | es_ES |
| dc.description.peerreviewed | SI | es_ES |
| dc.description.sponsorship | We thank financial support from AEI (PID2019-109733GB-I00) and Juan de la Cierva Incorporación contract (IJC2020-042689-I) for R.R., Xunta de Galicia (ED431C 2022/21), Centro Singular de Investigación de Galicia acreditación 2019-2022 (ED431G 2019/03), and the European Regional Development Fund (ERDF) | es_ES |
| dc.identifier.citation | Rodríguez, R, Rivadulla-Cendal, E, Quiñoá, E, Freire, F. Diastereomeric multi-chiral pendant groups: Their key role in stimuli-responsive polymeric responses. Chirality. 2023; 35( 3): 172- 177. doi:10.1002/chir.23530 | es_ES |
| dc.identifier.doi | 10.1002/chir.23530 | |
| dc.identifier.essn | 1520-636X | |
| dc.identifier.issn | 0899-0042 | |
| dc.identifier.uri | http://hdl.handle.net/10347/30762 | |
| dc.language.iso | eng | es_ES |
| dc.publisher | Wiley | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-109733GB-I00/ES/MATERIALES QUIRALES CON PROPIEDADES-ESTIMULO RESPUESTA: DISEÑO, SINTESIS Y APLICACIONES | es_ES |
| dc.relation.publisherversion | https://doi.org/10.1002/chir.23530 | es_ES |
| dc.rights | © 2023 The Authors. Chirality published by Wiley Periodicals LLC. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | |
| dc.subject | Chiroptical switches | es_ES |
| dc.subject | Diastereomers | es_ES |
| dc.subject | Helical polymers | es_ES |
| dc.subject | Helical stretching | es_ES |
| dc.subject | Solvent polarity | es_ES |
| dc.title | Diastereomeric multi-chiral pendant groups: their key role in stimuli-responsive polymeric responses | es_ES |
| dc.type | journal article | es_ES |
| dc.type.hasVersion | VoR | es_ES |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | c9dfab78-68b6-4ae2-a4f5-c95d35443366 | |
| relation.isAuthorOfPublication | 20b69c32-3d11-4383-896f-e2c8a0beca15 | |
| relation.isAuthorOfPublication | 2943e14b-a7a1-4b71-9bd4-74c28b79e935 | |
| relation.isAuthorOfPublication.latestForDiscovery | c9dfab78-68b6-4ae2-a4f5-c95d35443366 |
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