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Título: Mechanical bonding of rigid MORFs using a tetratopic rotaxane
Fecha de publicación: 28-may-2024
Fecha de defensa / creación: 2024
Editorial: Royal Society of Chemistry
Cita bibliográfica: Chemical Communications, 2024, Vol. 60, pp. 6431-6434
ISSN: Print: 1359-7345
Electronic: 1364-548X
Materias relacionadas: CDU::5 - Ciencias puras y naturales::54 - Química::547 - Química orgánica
Palabras clave: Rotaxane
Metal-organic frameworks
Crystalline materials
Rigid materials
Resumen: The preparation of highly rigid cobalt(II)- and copper(II)–organic frameworks incorporating a tetralactam [2]rotaxane as a ligand is described. The interlocked ligand is functionalized with two pairs of carboxylate groups placed at each counterpart, thus limiting its dynamics within the crystal. The solid structure of the metal–organic rotaxane frameworks showed different, unprecedented polycatenation modes of grids, depending on the employed metal, providing great rigidity to the structures. This rigidity has been evaluated by using single crystal X-ray diffraction analyses of the cobalt(II)–organic frameworks embedded in different solvents, observing that the lattices remain unchanged. Thus, this research demonstrates that rigid and robust materials with permanent porosity can be achieved using dynamic ligands.
Autor/es principal/es: Saura Sanmartín, Adrián
Cutillas Font, Guillermo
Martinez-Cuezva, Alberto
Alajarín, Mateo
Esteban Betegón, Fátima
Pena Sánchez, Pilar
Gándara, Felipe
Berná Cánovas, José
Versión del editor: https://pubs.rsc.org/en/content/articlelanding/2024/cc/d4cc02065k
URI: http://hdl.handle.net/10201/142793
DOI: https://doi.org/10.1039/D4CC02065K
Tipo de documento: info:eu-repo/semantics/article
Número páginas / Extensión: 4
Derechos: info:eu-repo/semantics/openAccess
Atribución-NoComercial 4.0 Internacional
Descripción: © The Royal Society of Chemistry 2024. This manuscript version is made available under the CC-BY-NC 4.0 license http://creativecommons.org/licenses/by-nc/4.0/ This document is the Published version of a Published Work that appeared in final form in Chemical Communications. To access the final edited and published work see https://doi.org/10.1039/D4CC02065K
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