Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/19823
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dc.contributor.authorVANDENBERGH, Joke-
dc.contributor.authorREEKMANS, Gunter-
dc.contributor.authorADRIAENSENS, Peter-
dc.contributor.authorJUNKERS, Tanja-
dc.date.accessioned2015-11-25T11:22:57Z-
dc.date.available2015-11-25T11:22:57Z-
dc.date.issued2015-
dc.identifier.citationCHEMICAL SCIENCE, 6 (10), p. 5753-5761-
dc.identifier.issn2041-6520-
dc.identifier.urihttp://hdl.handle.net/1942/19823-
dc.description.abstractPhoto-induced copper-mediated radical polymerization is used to synthesize monodisperse sequence defined acrylate oligomers via consecutive single unit monomer insertion reactions and intermediate purification of the compounds by column chromatography or preparative recycling size exclusion chromatography. Monomer conversions are followed during reaction by means of infrared spectroscopy. When reaction conditions are chosen carefully and any residues from chlorinated solvents are avoided, 100% pure Br end capped sequence defined oligomers are obtained, demonstrating the convenience and power of photo-induced copper mediated radical insertion for establishing sequence control. Within this work, a library of sequence defined oligomers containing polar and apolar ester groups have been obtained, and for the first time, perfectly monodisperse acrylate pentamers became accessible from radical insertion reactions.-
dc.description.sponsorshipThe authors are grateful for funding in the framework of the Odysseus scheme from the Fonds Wetenschappelijk Onderzoek (FWO) and for the postdoctoral mandate of J. V. Additionally, support from the European Science Foundation - "Precision Polymer Materials (P2M)" and the Hercules foundation for funding in the framework of the project "LC-MS@UHasselt: Linear Trap Quadrupool-Orbitrap mass spectrometer" is gratefully acknowledged. We further want to acknowledge the support of the Interuniversity Attraction Poles Programme (P7/05) initiated by the Belgian Science Policy Office.-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.rightsThis journal is © The Royal Society of Chemistry 2015-
dc.titleSynthesis of sequence-defined acrylate oligomers via photo-induced copper-mediated radical monomer insertions-
dc.typeJournal Contribution-
dc.identifier.epage5761-
dc.identifier.issue10-
dc.identifier.spage5753-
dc.identifier.volume6-
local.format.pages9-
local.bibliographicCitation.jcatA1-
dc.description.notes[Vandenbergh, Joke; Junkers, Thomas] Univ Hasselt, Inst Mat Res IMO IMOMEC, Polymer React Design Grp, B-3500 Hasselt, Belgium. [Reekmans, Gunter; Adriaensens, Peter] Univ Hasselt, Inst Mat Res IMO IMOMEC, Nucl Magnet Resonance Spect Grp, B-3590 Diepenbeek, Belgium. [Adriaensens, Peter; Junkers, Thomas] IMEC Associated Lab IMOMEC, B-3590 Diepenbeek, Belgium.-
local.publisher.placeCAMBRIDGE-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1039/c5sc02035b-
dc.identifier.isi000361212000050-
item.contributorVANDENBERGH, Joke-
item.contributorREEKMANS, Gunter-
item.contributorADRIAENSENS, Peter-
item.contributorJUNKERS, Tanja-
item.fulltextWith Fulltext-
item.validationecoom 2016-
item.fullcitationVANDENBERGH, Joke; REEKMANS, Gunter; ADRIAENSENS, Peter & JUNKERS, Tanja (2015) Synthesis of sequence-defined acrylate oligomers via photo-induced copper-mediated radical monomer insertions. In: CHEMICAL SCIENCE, 6 (10), p. 5753-5761.-
item.accessRightsRestricted Access-
crisitem.journal.issn2041-6520-
crisitem.journal.eissn2041-6539-
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