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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/D3QO01832F</dc:identifier><dc:language>eng</dc:language><dc:creator>González, Lucía</dc:creator><dc:creator>Marín, Iván</dc:creator><dc:creator>Tejedor, Rosa M.</dc:creator><dc:creator>Barberá, Joaquín</dc:creator><dc:creator>Romero, Pilar</dc:creator><dc:creator>Concellón, Alberto</dc:creator><dc:creator>Uriel, Santiago</dc:creator><dc:creator>Serrano, José L.</dc:creator><dc:title>Hydantoin hexameric rosettes: harnessing H-bonds for supergelation and liquid crystals</dc:title><dc:identifier>ART-2024-136611</dc:identifier><dc:description>We have synthesized two geometric isomers of a cyclohexane-5-spirohydantoin derivative (1,3-diazaspiro[4.5]decane-2,4-dione) incorporating a hydrophobic phenyl 3,4,5-tris(dodecyloxy)benzoate unit at position 8. Separation of these diastereomers was accomplished through silica gel flash chromatography. The interplay of intermolecular hydrogen bonding and micro-segregation between the polar hydantoin unit and nonpolar aliphatic chains within the molecule endows them with remarkable self-assembly capabilities, both in solution and in the solid state. These hydantoin derivatives spontaneously form rosette-shaped structures composed of six molecules. In the solid state, these compounds display hexagonal columnar liquid crystal phases, with hydrogen-bonded disks as their fundamental building blocks. Similarly, when exposed to apolar solvents such as cyclohexane or dodecane, they adopt a columnar arrangement, resulting in gel formation comprising nanoscale fibers that intricately interlace to form a network. Remarkably, the two isomers exhibit markedly different properties. The major isomer behaves as a glassy liquid crystalline material, while the minor one exhibits liquid crystalline behavior with a high propensity to crystallize. Our experimental findings, in combination with theoretical studies, underscore the fundamentally distinct supramolecular organizations present in these isomers, shedding light on their unique self-assembling properties.</dc:description><dc:date>2024</dc:date><dc:source>http://zaguan.unizar.es/record/132238</dc:source><dc:doi>10.1039/D3QO01832F</dc:doi><dc:identifier>http://zaguan.unizar.es/record/132238</dc:identifier><dc:identifier>oai:zaguan.unizar.es:132238</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E47-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/RYC2021-031154-I</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO-FEDER/PGC2018-097583-B-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/PID2021-122882NB-I00</dc:relation><dc:identifier.citation>ORGANIC CHEMISTRY FRONTIERS 11, 3 (2024), 735-745</dc:identifier.citation><dc:rights>by-nc</dc:rights><dc:rights>https://creativecommons.org/licenses/by-nc/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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