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dc.contributor.authorRoth, P.
dc.contributor.authorBoyer, C.
dc.contributor.authorLowe, Andrew
dc.contributor.authorDavis, T.
dc.date.accessioned2017-01-30T12:32:23Z
dc.date.available2017-01-30T12:32:23Z
dc.date.created2015-10-29T04:09:31Z
dc.date.issued2011
dc.identifier.citationRoth, P. and Boyer, C. and Lowe, A. and Davis, T. 2011. RAFT polymerization and thiol chemistry: A complementary pairing for implementing modern macromolecular design. Macromolecular Rapid Communications. 32 (15): pp. 1123-1143.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/22588
dc.identifier.doi10.1002/marc.201100127
dc.description.abstract

Reversible addition fragmentation chain transfer (RAFT) polymerization is one of the most extensively studied reversible deactivation radical polymerization methods for the production of well-defined polymers. After polymerization, the RAFT agent end-group can easily be converted into a thiol, opening manifold opportunities for thiol modification reactions. This review is focused both on the introduction of functional end-groups using well-established methods, such as thiol-ene chemistry, as well as on creating bio-cleavable disulfide linkages via disulfide exchange reactions. We demonstrate that thiol modification is a highly attractive and efficient chemistry for modifying RAFT polymers.

dc.titleRAFT polymerization and thiol chemistry: A complementary pairing for implementing modern macromolecular design
dc.typeJournal Article
dcterms.source.volume32
dcterms.source.number15
dcterms.source.startPage1123
dcterms.source.endPage1143
dcterms.source.issn1022-1336
dcterms.source.titleMacromolecular Rapid Communications
curtin.departmentNanochemistry Research Institute
curtin.accessStatusFulltext not available


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