Lanthanide(III) Metal-Organic Frameworks (Ln=Gd, Tb, Dy)Based on a C3 Symmetrical Tricarboxylate Linker

Lanthanide-based metal-organic frameworks have attracted significant interest due to their ability to combine porosity with one or more additional properties, providing an alternative method for the development of multifunctional materials. With this in mind, we report the synthesis and characterisa...

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Detalles Bibliográficos
Autores: McHugh, Darragh, Tong, Wenming, Bezrukov, Andrey, Farras, Pau, Zaworotko, Michael J., Mayans Ayats, Júlia, Skelton, Jonathan M., Barnett. Sarah, Pallipurath, Anuradha R., Papatriantafyllopoulou, Constantina
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2025
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:dnet:ubarcelona__::8635e6972fd942b37e578dca8fb30003
Acceso en línea:https://hdl.handle.net/2445/228649
Access Level:acceso abierto
Palabra clave:Estructura química
Química organometàl·lica
Chemical structure
Organometallic chemistry
Descripción
Sumario:Lanthanide-based metal-organic frameworks have attracted significant interest due to their ability to combine porosity with one or more additional properties, providing an alternative method for the development of multifunctional materials. With this in mind, we report the synthesis and characterisation of the OnG5 family of MOFs with the formula [LnLH(DMF)3][(4-NH2Ph)3C](NO3)(CH3CO2H), where Ln=Gd (OnG5-Gd), Tb (OnG5-Tb), Dy (OnG5-Dy), and LH3−= the trianion of 4,4′,4′′-(1 E)-[4,4′,4′′-(methanetriyl)tris(benzene-4,1-diyl)tris(azan-1- yl-1-ylidene)]tris(methan-1-yl-1-ylidene)tribenzoic acid. OnG5 were synthesised in situ from the reaction of Ln(NO3)3.xH2O, pararosaniline base [(4-NH2Ph)3COH] and terephthalaldehydic acid in DMF. Their structure was studied through single crystal x-ray crystallography and confirmed with DFT calculations. OnG5 display a 2D, three-fold interpenetrated structure with a honeycomb lattice topology. They are the first examples bearing the ligand LHH3 and they display photoluminescence originating from an intraligand π-π* or n-π* transition. Dc and ac magnetic susceptibility studies conducted on the OnG5-Gd analogue revealed an absence of magnetic interaction between the metal centres.