Poly(O-Propargyl-N-Amino Carbamate), a Reactive Polymer to Underpin Biomedical Applications of Poly(Acetylene)S
| UDC.coleccion | Investigación | |
| UDC.departamento | Fisioterapia, Medicina e Ciencias Biomédicas | |
| UDC.departamento | Química | |
| UDC.grupoInv | Nanochemistry and Self-Assembly for Biological Sciences (NANOSELF4BIO) | |
| UDC.institutoCentro | CICA - Centro Interdisciplinar de Química e Bioloxía | |
| UDC.journalTitle | Macromolecular Rapid Communications | |
| UDC.startPage | e00566 | |
| dc.contributor.author | Leigh, Thomas | |
| dc.contributor.author | Bellio, Greta | |
| dc.contributor.author | Crisan, Daniel N. | |
| dc.contributor.author | Deb, Amit | |
| dc.contributor.author | Ramil-Bouzas, Alba | |
| dc.contributor.author | Romanyuk, Andrey | |
| dc.contributor.author | Torreiro-León, Iván | |
| dc.contributor.author | Rey-Rico, Ana | |
| dc.contributor.author | Fernández-Trillo, Paco | |
| dc.date.accessioned | 2026-05-12T11:29:36Z | |
| dc.date.available | 2026-05-12T11:29:36Z | |
| dc.date.issued | 2025-10-25 | |
| dc.description.abstract | [Abstract] Synthetic polymers are widely used in biomedical applications, yet most lack defined secondary structures common in nature,such as helices or β-sheets. In particular, dynamic helical polymers such as poly(acetylene)s have been rarely explored in thisfield. Here, we report the preparation of a new reactive poly(acetylene), poly(O-propargyl-N-amino carbamate) (P1), as a platformfor the preparation of functional poly(acetylene)s in water. P1 was prepared from readily available starting materials throughRh-catalyzed polymerization and acid-mediated deprotection. 1 H-NMR indicated that the formed polymer had a high content ofcis double bonds, while UV–vis and DSC suggested a predominant cis-cisoid conformation. This conformation was also observedvia CD for chiral derivatives of Boc-protected P1, while a partially deprotected chiral derivative of P1 could be adopting multipleconformations in solution, including cis-transoid and cis-cisoid conformations. P1 was functionalized under aqueous conditionswith a small set of aldehydes, including cationic, aliphatic, and aromatic derivatives, as well as a small set of carbohydrates. Finally,we demonstrate that P1, and a guanidinium derivative P1-mod-4, were well tolerated by cells, highlighting the potential of thispolymer to underpin the development of biomedical applications of poly(acetylene)s | |
| dc.description.sponsorship | The work is supported by the University of Birmingham (John Evans fellowship to P.F.-T., PhD studentship to D.C.), the Spanish Ministerio de Educación, Cultura y Deporte (Beatriz Galindo Award to P.F.-T., BG20/00213), the Engineering and Physical Sciences Research Council and the Centre for Doctoral Training in Physical Sciences for Health (PhD studentship to T.L., EP/L016346/1), the Leverhulme Trust (PhD studentship to A.D. under grant RPG-2019-382), the Ministerio de Ciencia, Innovación y Universidades (Ramon y Cajal Fellowship to A.R.-R., RYC2018-025617-I, and pre-doctoral fellowship toA.R.-B., PRE2022-104070), the European Union’s Horizon 2020 Research and Innovation Programme (Marie Sklodowska-Curie Grant Agreement No. 795082 toA.R.), the La Caixa Foundation (CI22-00167) and Xunta de Galicia (ED431F 2021/10 and ED431B 2023/60). This work is part of the project PID2021-128461OB-I00, funded by MCIN/AEI/10.13039/501100011033/FEDER, UE | |
| dc.description.sponsorship | Xunta de Galicia; ED431F 2021/10 | |
| dc.description.sponsorship | Xunta de Galicia; ED431B 2023/60 | |
| dc.description.sponsorship | Reino Unido. Engineering and Physical Sciences Research Council, UK; EP/L016346/1 | |
| dc.description.sponsorship | Reino Unido. The Leverhulme Trust; RPG-2019-382 | |
| dc.description.sponsorship | Fundación La Caixa; CI22-00167 | |
| dc.identifier.citation | T. Leigh, G. Bellio, D. Crisan, et al. “ Poly(O-Propargyl-N-Amino Carbamate), a Reactive Polymer to Underpin Biomedical Applications of Poly(acetylene)s.” Macromolecular Rapid Communications (2025): e00566. https://doi.org/10.1002/marc.202500566 | |
| dc.identifier.doi | 10.1002/marc.202500566 | |
| dc.identifier.issn | 1022-1336 | |
| dc.identifier.issn | 1521-3927 | |
| dc.identifier.uri | https://hdl.handle.net/2183/48221 | |
| dc.language.iso | eng | |
| dc.publisher | Wiley | |
| dc.relation.projectID | info:eu-repo/grantAgreement/MUNI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/BG20%2F00213/ES | |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RYC2018-025617-I/ES/Targeted and controlled delivery systems of bioactive molecules | |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PRE2022-104070/ES/ POLIMEROS HELICOIDALES PARA LA LIBERACION DE GENES EN CELULAS MADRE MESENQUIMALES | |
| dc.relation.projectID | info:eu-repo/grantAgreement/EC/HE/795082 | |
| dc.relation.uri | https://doi.org/10.1002/marc.202500566 | |
| dc.rights | © 2025 The Author(s). Macromolecular Rapid Communications published by Wiley-VCH GmbH | |
| dc.rights | Attribution 4.0 International | en |
| dc.rights.accessRights | open access | |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | Biocompatible polymers | |
| dc.subject | Poly(acetylene)s | |
| dc.subject | Post-polymerization modification | |
| dc.title | Poly(O-Propargyl-N-Amino Carbamate), a Reactive Polymer to Underpin Biomedical Applications of Poly(Acetylene)S | |
| dc.type | journal article | |
| dc.type.hasVersion | VoR | |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 937c8896-eba8-4bd7-9bb8-9d75244c46c9 | |
| relation.isAuthorOfPublication | 70a74a46-7cea-40e2-85ef-e99554e97bbe | |
| relation.isAuthorOfPublication.latestForDiscovery | 937c8896-eba8-4bd7-9bb8-9d75244c46c9 |
Files
Original bundle
1 - 1 of 1
Loading...
- Name:
- FernandezTrillo_Paco_2025_Poly(O-Propargyl-N-Amino Carbamate), a Reactive Polymer to Underpin Biomedical Applications of Poly(Acetylene)S.pdf
- Size:
- 1.3 MB
- Format:
- Adobe Portable Document Format

