Poly(O-Propargyl-N-Amino Carbamate), a Reactive Polymer to Underpin Biomedical Applications of Poly(Acetylene)S

UDC.coleccionInvestigación
UDC.departamentoFisioterapia, Medicina e Ciencias Biomédicas
UDC.departamentoQuímica
UDC.grupoInvNanochemistry and Self-Assembly for Biological Sciences (NANOSELF4BIO)
UDC.institutoCentroCICA - Centro Interdisciplinar de Química e Bioloxía
UDC.journalTitleMacromolecular Rapid Communications
UDC.startPagee00566
dc.contributor.authorLeigh, Thomas
dc.contributor.authorBellio, Greta
dc.contributor.authorCrisan, Daniel N.
dc.contributor.authorDeb, Amit
dc.contributor.authorRamil-Bouzas, Alba
dc.contributor.authorRomanyuk, Andrey
dc.contributor.authorTorreiro-León, Iván
dc.contributor.authorRey-Rico, Ana
dc.contributor.authorFernández-Trillo, Paco
dc.date.accessioned2026-05-12T11:29:36Z
dc.date.available2026-05-12T11:29:36Z
dc.date.issued2025-10-25
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.sponsorshipThe 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.sponsorshipXunta de Galicia; ED431F 2021/10
dc.description.sponsorshipXunta de Galicia; ED431B 2023/60
dc.description.sponsorshipReino Unido. Engineering and Physical Sciences Research Council, UK; EP/L016346/1
dc.description.sponsorshipReino Unido. The Leverhulme Trust; RPG-2019-382
dc.description.sponsorshipFundación La Caixa; CI22-00167
dc.identifier.citationT. 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.doi10.1002/marc.202500566
dc.identifier.issn1022-1336
dc.identifier.issn1521-3927
dc.identifier.urihttps://hdl.handle.net/2183/48221
dc.language.isoeng
dc.publisherWiley
dc.relation.projectIDinfo:eu-repo/grantAgreement/MUNI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/BG20%2F00213/ES
dc.relation.projectIDinfo: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.projectIDinfo: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.projectIDinfo:eu-repo/grantAgreement/EC/HE/795082
dc.relation.urihttps://doi.org/10.1002/marc.202500566
dc.rights© 2025 The Author(s). Macromolecular Rapid Communications published by Wiley-VCH GmbH
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBiocompatible polymers
dc.subjectPoly(acetylene)s
dc.subjectPost-polymerization modification
dc.titlePoly(O-Propargyl-N-Amino Carbamate), a Reactive Polymer to Underpin Biomedical Applications of Poly(Acetylene)S
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication937c8896-eba8-4bd7-9bb8-9d75244c46c9
relation.isAuthorOfPublication70a74a46-7cea-40e2-85ef-e99554e97bbe
relation.isAuthorOfPublication.latestForDiscovery937c8896-eba8-4bd7-9bb8-9d75244c46c9

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