Eu(III) and Tb(III) luminescent lanthanide systems derived from DTPA-bisamide and DTTA-based ligands incorporating bipyridine antenna

Abstract

Four new polycarboxylate ligands H 3 L n have been synthesized by the attachment of two or one 2,2′-bipyridine subunits onto a diethylenetriamine pentacarboxylic acid (DTPA-bisamide derivatives: H 3 L 1 , H 3 L 2 ) or a diethylenetriamine tricarboxylic acid (DTTA derivatives: H 3 L 3 , H 3 L 4 ) core. The neutral Eu III and Tb III complexes of these chelates have been prepared and studied from their UV–vis and luminescence data. The main photophysical characteristics of these complexes, i.e. the absorption and luminescence spectra, the metal-centred lifetimes and the overall luminescence yields ( Φ) were measured in buffered aqueous solutions. In addition the role played by non-radiative paths (vibrational energy transfer involving coordinated water molecules, involvement of ligand-to-metal charge-transfer excited states, or metal→ligand back-transfer) was investigated. In all complexes, we found that the bidentate bipyridine chromophore is not coordinated to the lanthanide ion, allowing one (Ln L 1 , Ln L 2 ) or two (Ln L 3 , Ln L 4 ) water molecules to penetrate the first coordination sphere of the metal. Although the bipyridine chromophore behaves as remote (from the binding site) light-harvesting unit for the lanthanide ion in these systems, a sizeable sensitization of the Eu- and Tb-centred luminescence can be effective (Ln L 2 , Ln L 3 , Φ=16–19% in aerated D 2O solutions). Our photophysical investigations show that overall non-radiative deactivation is not dependant of thermally activated non-radiative channels but the efficiency of the ligand→Ln intramolecular energy transfer has to be taken into account to explain the obtained results.