Synthesis, structure, and magnetism of a family of heterometallic {Cu2Ln7} and {Cu4Ln12} (Ln = Gd, Tb, and Dy) complexes: The Gd analogues exhibiting a large magnetocaloric effect

The syntheses, structures, and magnetic properties of two heterometallic CuII-LnIII (LnIII = Gd, Tb, and Dy) families, utilizing triethanolamine and carboxylate ligands, are reported. The first structural motif displays a nonanuclear {CuII 2LnIII 7} metallic core, while the second reveals a hexadeca...

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Detalles Bibliográficos
Autores: Langley, S. K., Moubaraki, Boujemaa, Tomasi, Corrado, Evangelisti, Marco, Brechin, Euan K., Murray, Keith S.
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2014
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/120985
Acceso en línea:http://hdl.handle.net/10261/120985
Access Level:acceso abierto
Descripción
Sumario:The syntheses, structures, and magnetic properties of two heterometallic CuII-LnIII (LnIII = Gd, Tb, and Dy) families, utilizing triethanolamine and carboxylate ligands, are reported. The first structural motif displays a nonanuclear {CuII 2LnIII 7} metallic core, while the second reveals a hexadecanuclear {CuII 4LnIII 12} core. The differing nuclearities of the two families stem from the choice of carboxylic acid used in the synthesis. Magnetic studies show that the most impressive features are displayed by the {CuII 2GdIII 7} and {CuII 4GdIII 12} complexes, which display a large magnetocaloric effect, with entropy changes -ΔSm = 34.6 and 33.0 J kg-1 K-1 at T = 2.7 and 2.9 K, respectively, for a 9 T applied field change. It is also found that the {CuII 4DyIII 12} complex displays single-molecule magnet behavior, with an anisotropy barrier to magnetization reversal of 10.1 K.