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dc.contributor.authorBarnard, Elaine
dc.contributor.authorPfukwa, Rueben
dc.contributor.authorMaiz, Jon
dc.contributor.authorMüller Sánchez, Alejandro Jesús ORCID
dc.contributor.authorKlumperman, Bert
dc.date.accessioned2021-03-25T16:49:58Z
dc.date.available2021-03-25T16:49:58Z
dc.date.issued2020-02-24
dc.identifier.citationMacromolecules 53(5) : 1585-1595 (2020)es_ES
dc.identifier.issn0024-9297
dc.identifier.issn1520-5835
dc.identifier.urihttp://hdl.handle.net/10810/50779
dc.descriptionUnformatted post-print version of the accepted articlees_ES
dc.description.abstractA series of hetero-arm amphiphilic molecular brushes (AMBs) with poly(ethylene glycol) (PEG) and long chain n-alkyl side chains were synthesized via conventional free radical polymerization (FRP) of mainly 4-vinyl benzyl-PEG methyl ether and N-alkylmaleimide macromonomers. By varying PEG side chain degree of polymerization (D.P. = 12, 16 and 20) and n-alkyl chain lengths (C16 and C20), AMBs with varying combinations of side chain lengths were produced. This enabled the elucidation of the effect of side chain length on AMB phase behavior, semicrystalline morphologies and crystallization kinetics, via differential scanning calorimetry, polarized light optical microscopy and x-ray diffraction experiments. Calculations of segregation strength together with SAXS measurements indicate that all materials are probably phase segregated structure in the melt. Most of the AMB materials prepared were double crystalline, i.e., contained crystals from alkyl and PEG chains. AMB crystallization was constrained by AMB architecture, the frustration being most evident in AMBs with combinations of either low D.P.PEG, or short alkyl chain lengths. Large, well-developed spherulites, implying break-out crystallization from a weakly segregated melt, were only observed for the AMBs with the combination of the longest PEG chain (D.P. = 20) and longest alkyl chain length (C20). A peculiar behavior was found when spherulitic growth rates and overall crystallization rates of the PEG chains, within this particular AMB sample, were determined as a function of crystallization temperature. In both cases, a distinct minimum with decreasing temperature was observed, probably caused by the challenges encountered in crystal packing of the PEG side chains, tethered to an amorphous backbone, which also contained already crystallized C20 chains. This minimum is analogous to that observed in the crystallization of long chain n-alkanes, or high molar mass polyethylenes with bromine pendant groups that has been attributed to a self-poisoning effect; this is the first observation of this phenomenon in AMBs.es_ES
dc.description.sponsorshipThis work is based on the research supported by the South African Research Chairs Initiative of the Department of Science and Technology (DST) and National Research Foundation (NRF) of South Africa (Grant No 46855). J.M. acknowledges support from the Provincial Council of Gipuzkoa under the program Fellow Gipuzkoa and “Fomento San Sebastián” in the framework program “Retorno del Talento Local” Donostia up! 2016. This work has received funding from the European Union´s Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement No 778092, from MINECO, project: MAT2017-83014-C2-1-P and from the Basque Government through grant IT1309-19. We also thank ALBA Synchrotron facility for providing funding and beam time (proposal number: 2018082953).es_ES
dc.language.isoenges_ES
dc.publisherACSes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/778092es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/MAT2017-83014-C2-1-Pes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectamphiphilic molecular brusheses_ES
dc.subjectdouble crystalline materialses_ES
dc.subjectPEG self-poisoninges_ES
dc.subjectalkyl side chainses_ES
dc.subjectPEG side chainses_ES
dc.subjectscatteringes_ES
dc.subjectcrystallizationes_ES
dc.subjectalcoholses_ES
dc.subjectdifferential scanning calorimetryes_ES
dc.subjectalkylses_ES
dc.titleSynthesis, Structure and Crystallization Behavior of Amphiphilic Hetero-arm Molecular Brushes with Crystallizable Poly(ethylene oxide) and N-Alkyl Side Chainses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderCopyright © 2020 American Chemical Societyes_ES
dc.relation.publisherversionhttps://pubs.acs.org/doi/abs/10.1021/acs.macromol.9b02473es_ES
dc.identifier.doi10.1021/acs.macromol.9b02473
dc.contributor.funderEuropean Commission
dc.departamentoesCiencia y tecnología de polímeroses_ES
dc.departamentoeuPolimeroen zientzia eta teknologiaes_ES


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