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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1021/acs.macromol.6b01112</dc:identifier><dc:language>eng</dc:language><dc:creator>Oriol Langa, Luis Teodoro</dc:creator><dc:creator>Piñol, Milagros</dc:creator><dc:creator>Nogales, A</dc:creator><dc:creator>Concellón, A.</dc:creator><dc:creator>Blasco, E.</dc:creator><dc:creator>Martínez-Felipe, A.</dc:creator><dc:creator>Martínez, J. C.</dc:creator><dc:creator>Šics, I.</dc:creator><dc:creator>Ezquerra, T. A.</dc:creator><dc:title>Light-Responsive Self-Assembled Materials by Supramolecular Post-Functionalization via Hydrogen Bonding of Amphiphilic Block Copolymers</dc:title><dc:identifier>ART-2016-97007</dc:identifier><dc:description>A new class of light-responsive supramolecular amphiphilic block copolymers (BCs) based on the association through multiple H-bonding between 4-isobutyloxyazobenzene motifs and 2, 6-diacylaminepyridine units is reported. Block copolymers containing 2, 6-diacylaminopyridine side units, as hydrophobic block, and poly(ethylene glycol), as a hydrophilic segment, were functionalized with either a carboxylic acid azodendron, via double H-bonding, or a thymine azobenzene, via triple H-bonding. The structural and thermal characterization of these supramolecular azo-copolymers in bulk and solution is presented. The work emphasizes the self-assembly of these supramolecular polymers in water and the study of their UV-light responsive properties by UV-vis spectroscopy, dynamic light scattering (DLS), transmission electron microscopy (TEM), and synchrotron small-angle X-ray (SAXS). The present noncovalent postpolymerization functionalization strategy has provided stable self-assemblies in water with light responsive properties that can be used to load and trigger the delivery of small fluorescent molecules.</dc:description><dc:date>2016</dc:date><dc:source>http://zaguan.unizar.es/record/130641</dc:source><dc:doi>10.1021/acs.macromol.6b01112</dc:doi><dc:identifier>http://zaguan.unizar.es/record/130641</dc:identifier><dc:identifier>oai:zaguan.unizar.es:130641</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/MAT2014-55205-P</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/MAT2014-59187-R</dc:relation><dc:identifier.citation>MACROMOLECULES 49, 20 (2016), 7825-7836</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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