First crystal structures of lanthanide-hydrocinnamate complexes: Hydrothermal synthesis and photophysical studies
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2013-01-15
Autores
Marques, Lippy Faria
Cantaruti, Anderson A.B.
Correa, Charlane Cimini
Lahoud, Marcelo Galindo [UNESP]
Da Silva, Robson Rosa [UNESP]
Ribeiro, Sidney José Lima [UNESP]
MacHado, Flávia Cavalieri
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Five new lanthanide(III) complexes of hydrocinnamic acid (Hcin), [Ln(cin)3(H2O)3]·3Hcin (Ln = Tb(III) (1), Dy(III) (2), Er(III) (3), Eu(III) (4) and Gd(III) (5)) have been synthesized and characterized. The X-ray structures of 1-5 reveal that all compounds are isostructural and that each lanthanide ion is nine-coordinated by oxygen atoms in an overall distorted tricapped trigonal-prismatic geometry. Six oxygen atoms are provided by carboxylate moieties, and the other three by water molecules. The supramolecular architectures of 1-5 show the presence of uncoordinated hydrocinnamic acid molecules which induce the formation of numerous hydrogen bonds. The photophysical properties of these complexes in the solid state at room temperature were studied using diffuse reflectance (DR), fluorescence excitation and emission spectra. An energy level diagram was used to establish the most relevant channels involved in the ligand-to-metal energy transfer, indicating that cin- ligands can act as intramolecular energy donors for Tb(III), Dy(III) and Eu(III) ions. © 2012 Elsevier B.V.
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Hydrocinnamic acid, Lanthanides, Photophysical studies
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Journal of Photochemistry and Photobiology A: Chemistry, v. 252, p. 69-76.