Hexanuclear lanthanide clusters encapsulating a mu(6)-CO32- ion displaying an unusual binding mode

Reaction of hydrated lanthanum halides (Ln=La, Pr and Nd) with LH2 [1-(2-HydroxyPhenyl)-3-(2-thienyl)-1,3-Propanedione] in presence of excess triethylamine with methanol as a solvent resulted in the isolation and structural characterization of a series of novel hexanuclear lanthanide clusters templa...

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Detalles Bibliográficos
Autores: Rasamsetty, Amaleswari, Viswanathan, Baskar, Sañudo Zotes, Eva Carolina
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2016
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/154364
Acceso en línea:https://hdl.handle.net/2445/154364
Access Level:acceso abierto
Palabra clave:Terres rares
Imants
Rare earths
Magnets
Descripción
Sumario:Reaction of hydrated lanthanum halides (Ln=La, Pr and Nd) with LH2 [1-(2-HydroxyPhenyl)-3-(2-thienyl)-1,3-Propanedione] in presence of excess triethylamine with methanol as a solvent resulted in the isolation and structural characterization of a series of novel hexanuclear lanthanide clusters templated by mu(6)-CO32- introduced via spontaneous fixation of atmospheric carbon dioxide depicting a new coordination mode of binding. This particular mode of bridging is a first report of its kind in lanthanide clusters. Magnetic analysis of the praseodymium and neodymium analogue shows strong antiferromagnetic interactions in case of praseodymium and weak antiferromagnetic interactions in case of neodymium.