Title
Naked and Self-Clickable Propargylic-Decorated Single-Chain Nanoparticle Precursors via Redox-Initiated RAFT PolymerizationOther institutions
Universidad del País Vasco/Euskal Herriko Unibertsitatea (UPV/EHU)Ikerbasque
Version
Published version
Rights
© 2012 WILEY-VCH Verlag GmbH & Co. KGaA, WeinheimAccess
Embargoed accessPublisher’s version
https://doi.org/10.1002/marc.201200180Published at
Macromolecular Rapid Communications Vol. 33. Nº 15. August 14, 2012xmlui.dri2xhtml.METS-1.0.item-publicationfirstpage
1262xmlui.dri2xhtml.METS-1.0.item-publicationlastpage
1267Publisher
WileyKeywords
NanotechnologyAbstract
Protection of acetylenic monomers is a common practice to avoid parasitic side reactions during polymerization. Herein, we report that redox-initiated RAFT polymerization allows the direct, room tempe ... [+]
Protection of acetylenic monomers is a common practice to avoid parasitic side reactions during polymerization. Herein, we report that redox-initiated RAFT polymerization allows the direct, room temperature synthesis of a variety of single-chain nanoparticle precursors (displaying narrow molecular weight dispersity, equation image/equation image = 1.12 –1.37 up to equation image = 100 kDa) containing well-defined amounts of naked, unprotected acetylenic functional groups available for rapid and quantitative intrachain cross-linking via metal-catalyzed carbon–carbon coupling (i.e., C–C “click” chemistry). To illustrate the useful “self-clickable” character of the new unprotected acetylenic precursors, single-chain nanoparticles have been prepared for the first time in a facile and highly efficient manner by copper-catalyzed alkyne homocoupling (i.e., Glaser–Hay coupling) at room temperature under normal air atmosphere. [-]
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