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Immobilization of Lanthanide Ions in a Pillared Layered Double Hydroxide

2005; American Chemical Society; Volume: 17; Issue: 23 Linguagem: Inglês

10.1021/cm051431p

1520-5002

Sandra Gago, Martyn Pillinger, Rute A. S. Ferreira, Luís D. Carlos, Teresa M. Santos, Isabel S. Gonçalves,

Lanthanide and Transition Metal Complexes

A Zn−Al layered double hydroxide (LDH) pillared by 2,2'-bipyridine-5,5'-dicarboxylate (BDC) anions was used as a porous matrix to intercalate LnCl3 (Ln = Eu, Gd). Metal loadings of 9.0 wt % for Eu and 11 wt % for Gd were achieved, which correspond to about two lanthanide ions for every three BDC ions. The fitting of the room-temperature Eu L3-edge EXAFS for the europium-containing material revealed one shell of 7 ± 1 oxygen/nitrogen atoms at 2.41 Å. No evidence for a Eu−Cl bond was found. The emission spectra for this material display the typical Eu3+ red emission and a large broad band peaking around 460 nm, which was attributed to the emission arising from the triplet levels of free ligands not coordinated to Eu3+ ions. Measurement of the emission spectra under different excitation wavelengths and also at low temperature showed the existence of only one type of Eu3+ binding site. The 5D0 quantum efficiency was estimated to be low (7.7%), due to a relatively high nonradiative transition probability caused by the presence of water molecules in the first coordination shell. The number of water molecules was calculated as 3.6 ± 1, suggesting that the incorporated europium ions were 6-coordinate with four oxygen atoms from water molecules and two nitrogen atoms from a bidentate bipyridyl ligand.