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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_AU
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_AU
dc.language.isoenen_AU
dc.publisherAmercian Chemical Societyen_AU
dc.relation.ispartofMacromoleculesen_AU
dc.rightsCopyright All Rights Reserveden_AU
dc.subjectRAFT polymerizationen_AU
dc.subjectpolymer-peptide hybridsen_AU
dc.subjectphotocatalysisen_AU
dc.subjectbismuth oxideen_AU
dc.titleActivating ATRP Initiators to Incorporate End-Group Modularity into Photo-RAFT Polymerizationen_AU
dc.typeArticleen_AU
dc.subject.asrc0303 Macromolecular and Materials Chemistryen_AU
dc.identifier.doi10.1021/acs.macromol.0c01697
dc.relation.arcDE180100007
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.citation.volume53en_AU
usyd.citation.issue23en_AU
usyd.citation.spage10357en_AU
usyd.citation.epage10365en_AU
workflow.metadata.onlyNoen_AU


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