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dc.contributor.authorLeibfarth, Frank A.
dc.contributor.authorWicker, Amanda Catherine
dc.contributor.authorJamison, Timothy F
dc.date.accessioned2018-08-22T18:41:16Z
dc.date.available2018-08-22T18:41:16Z
dc.date.issued2017-09
dc.date.submitted2017-07
dc.identifier.issn1759-9954
dc.identifier.issn1759-9962
dc.identifier.urihttp://hdl.handle.net/1721.1/117484
dc.description.abstractMonodisperse oligomers are important intermediates for studying structure–property relationships in soft materials but are traditionally laborious to synthesize. A semi-automated synthetic system that combines the benefits of telescoped reactions in continuous flow with iterative exponential growth (IEG) greatly expedites this process and makes the rapid synthesis of structurally diverse oligomer libraries practical. Herein, the coupling chemistry in the Flow-IEG system has been upgraded and expanded to include both 1,4- and 1,5-triazole linkages between monomers through an improved copper-catalyzed azide–alkyne cycloaddition (CuAAC) and a newly-optimized ruthenium-catalyzed azide–alkyne cycloaddition (RuAAC), respectively. Improvements to the Flow-IEG framework enabled the library synthesis of monodisperse oligomers with variations in triazole connectivity. These discrete oligomers allowed the systematic evaluation of the consequences of triazole sequence on material properties. The crystallization properties of these macromolecules were highly dependent on both their monomer sequence and triazole substitution pattern.en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/C7PY01204Gen_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceProf. Jamison via Erja Kajosaloen_US
dc.titleFlow-IEG enables programmable thermodynamic properties in sequence-defined unimolecular macromoleculesen_US
dc.typeArticleen_US
dc.identifier.citationWicker, Amanda C. et al. “Flow-IEG Enables Programmable Thermodynamic Properties in Sequence-Defined Unimolecular Macromolecules.” Polymer Chemistry 8, 37 (2017): 5786–5794 © The Royal Society of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverJamison, Timothy F.en_US
dc.contributor.mitauthorWicker, Amanda Catherine
dc.contributor.mitauthorJamison, Timothy F
dc.relation.journalPolymer Chemistryen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsWicker, Amanda C.; Leibfarth, Frank A.; Jamison, Timothy F.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6366-4627
dc.identifier.orcidhttps://orcid.org/0000-0002-8601-7799
mit.licenseOPEN_ACCESS_POLICYen_US


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