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dc.contributorVirginia Tech. Department of Chemistryen
dc.contributorMacromolecules and Interfaces Institute at Virginia Techen
dc.contributor.authorRadzinski, Scott C.en
dc.contributor.authorFoster, Jeffrey C.en
dc.contributor.authorMatson, John B.en
dc.date.accessioned2015-04-20T18:49:33Zen
dc.date.available2015-04-20T18:49:33Zen
dc.date.issued2015-01-14en
dc.identifier.citationRadzinski, S. C., Foster, J. C., & Matson, J. B. (2015). Synthesis of bottlebrush polymers via transfer-to and grafting-through approaches using a RAFT chain transfer agent with a ROMP-active Z-group. Polymer Chemistry. doi: 10.1039/C4PY01567Cen
dc.identifier.issn1759-9954en
dc.identifier.urihttp://hdl.handle.net/10919/51696en
dc.description.abstractA novel dithiocarbamate chain transfer agent (CTA1) with a directly polymerizable Z-group was synthesized for use in reversible addition_fragmentation chain transfer polymerization (RAFT). This CTA effectively mediated RAFT polymerization of styrenic and acrylic monomers with dispersities (_) < 1.08. Utilizing the polymerizable Z-group on the _-chain end that is inherited from the RAFT process, bottlebrush polymers were synthesized via ring-opening metathesis polymerization (ROMP) in a grafting-through process. The effect of a number of parameters on the grafting process was studied, and optimized conditions yielded bottlebrush polymers of controllable molecular weights, narrow molecular weight distributions, and high conversions (>90%). Bottlebrush polymers made by a transfer-to strategy were also synthesized from CTA1. In this case, ROMP was first carried out to produce poly(CTA1) (PCTA1), then RAFT was performed from the PCTA1 backbone. This technique allows for the preparation of high molecular weight bottlebrush polymers without radical coupling between bottlebrush polymers. Lastly, regardless of the synthetic method, all bottlebrush polymers produced using CTA1 are composed of polymeric side chains that are attached to the bottlebrush backbone through a labile dithiocarbamate linkage that can be cleaved in the presence of nucleophiles such as amines. The unique combination of these capabilities allows for the study of bottlebrush polymer formation by both transfer-to and grafting-through strategies using a single agent.en
dc.description.sponsorshipVirginia Tech. Department of Chemistryen
dc.description.sponsorshipOak Ridge Associated Universities - Powe Junior Faculty Enhancement Awarden
dc.format.mimetypeapplication/pdfen
dc.format.mimetypeapplication/pdfen
dc.language.isoen_USen
dc.publisherThe Royal Society of Chemistryen
dc.rightsCreative Commons Attribution-NonCommercial 3.0 Unporteden
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/en
dc.subjectBottlebrush polymersen
dc.subjectReversible addition_fragmentation chain transfer polymerizationen
dc.subjectRing-opening metathesis polymerizationen
dc.titleSynthesis of Bottlebrush Polymers via Transfer-To and Grafting-Through Approaches Using a RAFT Chain Transfer Agent with a ROMP-Active Z-Groupen
dc.typeArticle - Refereeden
dc.typeDataseten
dc.contributor.departmentChemistryen
dc.description.notesSupplementary information is included in a separate fileen
dc.identifier.urlhttp://pubs.rsc.org/en/content/articlelanding/2015/py/c4py01567cen
dc.date.accessed2015-04-15en
dc.title.serialPolymer Chemistryen
dc.identifier.doihttps://doi.org/10.1039/C4PY01567Cen
dc.type.dcmitypeTexten
dc.type.dcmitypeDataseten


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