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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:10.1039/d3ma00698k</dc:identifier><dc:language>eng</dc:language><dc:creator>Marín, Iván</dc:creator><dc:creator>Merino, Rosa I.</dc:creator><dc:creator>Barberá, Joaquín</dc:creator><dc:creator>Concellón, Alberto</dc:creator><dc:creator>Serrano, José L.</dc:creator><dc:title>Ionic self-assembly of pillar[5]arenes: proton-conductive liquid crystals and aqueous nanoobjects with encapsulation properties</dc:title><dc:identifier>ART-2023-135524</dc:identifier><dc:description>Liquid crystal (LC) pillar[n]arenes have been barely explored due to their time-consuming and complicated synthesis, despite their promising properties for metal-ion separation, drug delivery, or surface functionalization. Herein, we report an easy and reliable method to functionalize pillar[n]arene macrocycles through electrostatic interactions. These ionic materials were prepared by ionically functionalizing a pillar[n]arene containing ten amine terminal groups with six different carboxylic acids. This supramolecular approach results in ionic pillar[n]arenes which self-organize into LC phases with good proton-conducting properties. Moreover, ionic functionalization provides a new amphiphilic character to the pillar[n]arenes, which self-assemble in water to produce a variety of nanoobjects (i.e., spherical or cylindrical micelles, vesicles, solid nanospheres, or nanotubes) that are capable of encapsulating a model hydrophobic drug. Interestingly, the presence of coumarin moieties in the chemical structure of the ionic pillar[n]arenes results in self-organized materials with light-responsive properties due to the ability of coumarins to undergo photo-induced [2+2] cycloaddition. In particular, we demonstrate that coumarin pohotodimerization can be employed to fabricate mechanically stable proton-conductive LC materials, as well as to obtain photo-responsive nanocarriers with light-induced release of encapsulated molecules.</dc:description><dc:date>2023</dc:date><dc:source>http://zaguan.unizar.es/record/129397</dc:source><dc:doi>10.1039/d3ma00698k</dc:doi><dc:identifier>http://zaguan.unizar.es/record/129397</dc:identifier><dc:identifier>oai:zaguan.unizar.es:129397</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E47-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN-FEDER/PID2021-122882NB-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PGC2018-097583-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/RYC2021-031154-I</dc:relation><dc:identifier.citation>Materials Advances 4, 22 (2023), 5564-5572</dc:identifier.citation><dc:rights>by-nc</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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