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    <subfield code="a">10.1002/hlca.202300010</subfield>
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    <subfield code="a">Concellón, Alberto</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-8932-9085</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Ionic liquid crystalline calixarene with photo-switchable proton conduction</subfield>
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    <subfield code="c">2023</subfield>
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    <subfield code="a">We have developed a new strategy for the preparation of a light-responsive ionic liquid crystal (LC) that shows photo-switchable proton conduction. The ionic LC consists of a bowl-shaped calix[4]arene core ionically functionalized with azobenzene moieties. The non-covalent architectures were obtained by the formation of ionic salts between the carboxylic acid group of an azo-derivative and the terminal amine groups of a calixarene core. The presence of ionic salts results in a hierarchical self-assembly process that extends to the formation of a nanostructured lamellar LC arrangement (smectic A phase). In this LC phase, the ionic LC calixarene is able to display proton conductive properties, since the ionic nanosegregated areas (formed by the ionic pairs) generate the continuous channels that favor proton transport. The optical and photo-responsive properties were studied by UV-Vis spectroscopy, demonstrating that the azobenzene moieties of the ionic LC undergo reversible (E)-to-(Z) isomerization by irradiation with UV light. Interestingly, this (E)-to-(Z) photoisomerization results in a decrease of the proton conductivity values since the bent-shaped (Z)-isomer disrupts the lamellar LC phase. This isomerization process is totally reversible and leads to an ionic LC material with unique photo-switchable proton conductive properties.</subfield>
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    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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    <subfield code="b">155 / 231 = 0.671</subfield>
    <subfield code="c">2023</subfield>
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    <subfield code="a">Drug Discovery</subfield>
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    <subfield code="a">Organic Chemistry</subfield>
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    <subfield code="a">Physical and Theoretical Chemistry</subfield>
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    <subfield code="a">Inorganic Chemistry</subfield>
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    <subfield code="a">Catalysis</subfield>
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    <subfield code="a">Biochemistry</subfield>
    <subfield code="c">2023</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Marín, Iván</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="a">Barberá, Joaquín</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-5816-7960</subfield>
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    <subfield code="a">Marcos, Mercedes</subfield>
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    <subfield code="a">Serrano, José L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-9866-6633</subfield>
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    <subfield code="1">2013</subfield>
    <subfield code="2">765</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Orgánica</subfield>
    <subfield code="c">Área Química Orgánica</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">106, 5 (2023), e202300010 [8 pp.]</subfield>
    <subfield code="p">Helv. chim. acta</subfield>
    <subfield code="t">HELVETICA CHIMICA ACTA</subfield>
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