<?xml version='1.0' encoding='UTF-8'?><?xml-stylesheet href='static/style.xsl' type='text/xsl'?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-10T12:39:16Z</responseDate><request verb="GetRecord" identifier="oai:ebiltegia.mondragon.edu:20.500.11984/6998" metadataPrefix="rdf">https://ebiltegia.mondragon.edu/oai/request</request><GetRecord><record><header><identifier>oai:ebiltegia.mondragon.edu:20.500.11984/6998</identifier><datestamp>2025-05-14T06:15:29Z</datestamp><setSpec>com_20.500.11984_473</setSpec><setSpec>col_20.500.11984_478</setSpec></header><metadata><rdf:RDF xmlns:rdf="http://www.openarchives.org/OAI/2.0/rdf/" xmlns:ow="http://www.ontoweb.org/ontology/1#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/rdf/ http://www.openarchives.org/OAI/2.0/rdf.xsd">
   <ow:Publication rdf:about="oai:ebiltegia.mondragon.edu:20.500.11984/6998">
      <dc:title>Naked and Self-Clickable Propargylic-Decorated Single-Chain Nanoparticle Precursors via Redox-Initiated RAFT Polymerization</dc:title>
      <dc:creator>Sánchez Sánchez, Ana</dc:creator>
      <dc:creator>Asenjo Sanz, Isabel</dc:creator>
      <dc:creator>Buruaga, Lorea</dc:creator>
      <dc:creator>Pomposo, José A.</dc:creator>
      <dc:subject>Nanotechnology</dc:subject>
      <dc:description>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.</dc:description>
      <dc:date>2025-05-13T15:41:15Z</dc:date>
      <dc:date>2025-05-13T15:41:15Z</dc:date>
      <dc:date>2012</dc:date>
      <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
      <dc:identifier>1521-3927</dc:identifier>
      <dc:identifier>https://katalogoa.mondragon.edu/janium-bin/janium_login_opac.pl?find&amp;ficha_no=128551</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.11984/6998</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>© 2012 WILEY-VCH Verlag GmbH &amp; Co. KGaA, Weinheim</dc:rights>
      <dc:publisher>Wiley</dc:publisher>
   </ow:Publication>
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