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dc.contributor.authorTakano, Shin
dc.contributor.authorNishimura, Tomoki
dc.contributor.authorCheng, Yen Theng
dc.contributor.authorMuellner, Markus
dc.date.accessioned2026-03-18T04:45:17Z
dc.date.available2026-03-18T04:45:17Z
dc.date.issued2025en
dc.identifier.urihttps://hdl.handle.net/2123/35000
dc.description.abstractAmphiphilic diblock copolymers are widely studied for their ability to self-assemble into diverse nanostructures for various applications. Linear-linear diblock copolymers and linear-bottlebrush diblock copolymers exhibit distinct self-assembly due to differences in their molecular architecture. In this study, linear poly(ethylene glycol) (PEG) was used as the solvophilic block, and poly(2-(methylthio)ethyl methacrylate) (MTEMA, a thioether-containing polymer), was used as the solvophobic block to generate block copolymers where PMTEMA was either also a linear (LL) or a bottlebrush (LB) block. Comparing both architectures revealed differences in their self-assembly in aqueous environments. LL formed vesicles with broad size distributions while LB produced relatively uniform particles with ordered internal morphology, as confirmed by small-angle X-ray scattering (SAXS) and electron microscopy. The polymer particles could further be disassembled through an oxidizing agent which in turn allowed them to be used for oxidation-triggered release studies.en
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.relation.ispartofPolymer Chemistryen
dc.rightsCopyright All Rights Reserveden
dc.titleSelf-assembly of thioether-based diblock copolymers: a comparative study of linear and bottlebrush architecturesen
dc.typeArticleen
dc.identifier.doi10.1039/D5PY00153F
dc.type.pubtypeAuthor accepted manuscripten
dc.relation.arcFT200100185
dc.relation.arcDP220100452
dc.relation.otherGSTDS000001 – 6
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen
usyd.citation.volume16en
usyd.citation.issue19en
usyd.citation.spage2244en
usyd.citation.epage2253en
workflow.metadata.onlyNoen


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