Synthesis and Photophysical Properties of Lanthanide Pyridinylphosphonic Tacn and Pyclen Derivatives: From Mononuclear Complexes to Supramolecular Heteronuclear Assemblies
Nadège Hamon, Léna Godec, Elsa Jourdain, Fátima Lucio‐Martínez, Carlos Platas‐Iglesias, Maryline Beyler, Loı̈c J. Charbonnière, Raphaël Tripier
Abstract
Synthetic methodologies were developed to achieve the preparation of ligands L1 and L2 consisting of tacn- and pyclen-based chelators decorated with pyridinylphosphonic pendant arms combined with ethylpicolinamide or acetate coordinating functions, respectively. Phosphonate functions have been selected for their high affinity toward Ln 3+ ions compared to their carboxylated counterparts and for their steric hindrance that favors the formation of less-hydrated complexes. Thanks to regiospecific N -functionalization of the macrocyclic backbones, the two ligands were isolated with good yields and implicated in a comprehensive photophysical study for the complexation of Eu 3+, Tb 3+, and Yb 3+ . The coordination behavior of L1 and L2 with these cations has been first investigated by means of a combination of UV–vis absorption spectroscopy, steady-state and time-resolved luminescence spectroscopy, and 1 H and 31 P NMR titration experiments. Structural characterization in solution was assessed by NMR spectroscopy, corroborated by theoretical calculations. Spectroscopic characterization of the Ln 3+ complexes of L1 and L2 was done in water and D 2 O and showed the effective sensitization of the lanthanide metal-centered emission spectra, each exhibiting typical lanthanide emission bands. The results obtained for the phosphonated ligands were compared with those reported previously for the corresponding carboxylated analogues.