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Carbocycle-Based Organogelators : Influence of Chirality and Structural Features on Their Supramolecular Arrangements and Properties
Ortuño Mingarro, Rosa María (Universitat Autònoma de Barcelona. Departament de Química)

Fecha: 2021
Resumen: The rational design and engineer of organogel-based smart materials and stimuli-responsive materials with tuned properties requires the control of the non-covalent forces driving the hierarchical self-assembly. Chirality, as well as cis/trans relative configuration, also plays a crucial role promoting the morphology and characteristics of the aggregates. Cycloalkane derivatives can provide chiral chemical platforms allowing the incorporation of functional groups and hydrophobic structural units able for a convenient molecular stacking leading to gels. Restriction of the conformational freedom imposed by the ring strain is also a contributing issue that can be modulated by the inclusion of flexible segments. In addition, donor/acceptor moieties can also be incorporated favoring the interactions with light or with charged species. This review offers a perspective on the abilities and properties of carbocycle-based organogelators starting from simple cycloalkane derivatives, which were the key to establish the basis for an effective self-assembling, to sophisticated polycyclic compounds with manifold properties and applications.
Derechos: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Lengua: Anglès
Documento: Article ; recerca ; Versió publicada
Materia: Low-molecular-weight organogelators ; Cycloalkanes ; Cholesterol-based organogelators ; Chirality ; Stimuli-responsive materials ; Self-healing gels
Publicado en: Gels, Vol. 7, Num. 2 (June 2021) , art. 54, ISSN 2310-2861

DOI: 10.3390/gels7020054
PMID: 34062755


24 p, 11.3 MB

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 Registro creado el 2022-02-20, última modificación el 2023-10-01



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