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dc.contributor.authorHakobyan, Karen
dc.contributor.authorMcErlean, Christopher S.P.
dc.contributor.authorMuellner, Markus
dc.date.accessioned2021-10-14T01:41:19Z
dc.date.available2021-10-14T01:41:19Z
dc.date.issued2020en
dc.identifier.urihttps://hdl.handle.net/2123/26458
dc.description.abstractHeterogeneous photocatalysis is increasingly used in reversible deactivation radical polymerization (RDRP). In this study, we found that alkyl bromide redox chemistry typically found in atom transfer radical polymerization (ATRP) can be incorporated in concert with dithiocarbonyl disulfide chemistry into the reversible addition–fragmentation chain transfer (RAFT) process via bismuth oxide photocatalysis. This amalgamation of mechanisms introduces end-group modularity—a new layer of control—into RAFT polymers uniquely enabled by photoredox catalysis. We found that a diversity of functionality can be installed at the α-end group via alkyl bromides, while the molecular weight distribution can be tuned seamlessly at the ω-end group through the simultaneous addition of multiple disulfides.en
dc.language.isoenen
dc.publisherAmercian Chemical Societyen
dc.relation.ispartofMacromoleculesen
dc.rightsCopyright All Rights Reserveden
dc.subjectRAFT polymerizationen
dc.subjectpolymer-peptide hybridsen
dc.subjectphotocatalysisen
dc.subjectbismuth oxideen
dc.titleActivating ATRP Initiators to Incorporate End-Group Modularity into Photo-RAFT Polymerizationen
dc.typeArticleen
dc.subject.asrc0303 Macromolecular and Materials Chemistryen
dc.identifier.doi10.1021/acs.macromol.0c01697
dc.relation.arcDE180100007
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen
usyd.citation.volume53en
usyd.citation.issue23en
usyd.citation.spage10357en
usyd.citation.epage10365en
workflow.metadata.onlyNoen


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