Synthesis, structure and properties of 2D lanthanide coordination polymers based on N-heterocyclic arylpolycarboxylate ligands.

The reaction of 3-(2,4-dicarboxyphenyl)-2,6-pyridinedicarboxylic acid (H4dppd) with rare earth nitrates under hydrothermal conditions generated a series of new two-dimensional (2D) coordination polymers, namely {[La(Hdppd)(H2O)2·(H2O)2]n (1), [Ln2(Hdppd)2(H2O)4·(H2O)3]n [Ln = Sm (2), Eu (3)] and [Ln(Hdppd)(H2O)3·H2O]n [Ln = Gd (4), Tb (5), Dy (6), Ho (7), Er (8)] [Hdppd = 3-(2,4-dicarboxyphenyl)-2,6-pyridinedicarboxylic trivalent anion]}. The complexes were characterized by X-ray single-crystal diffraction, infrared spectroscopy, elemental analysis and thermogravimetric analysis. Luminescence spectroscopy of 3 and 5 showed bright red and green luminescences due to the 4f(n)-4f(n) transitions in Eu(3+) and Tb(3+) respectively, although the luminescence lifetime is shortened by non-radiative decay due to the presence of coordinating water molecules.

Energy transfer in Eu³⁺ doped scheelites: use as thermographic phosphor.

In this paper the luminescence of the scheelite-based CaGd₂(₁-x)Eu₂x(WO₄)₄ solid solutions is investigated as a function of the Eu content and temperature. All phosphors show intense red luminescence due to the ⁵D₀ - ⁷F₂ transition in Eu³⁺, along with other transitions from the ⁵D₁ and ⁵D₀ excited states. For high Eu³⁺ concentrations the intensity ratio of the emission originating from the ⁵D₁ and ⁵D₀ levels has a non-conventional temperature dependence, which could be explained by a phonon-assisted cross-relaxation process.

Solvent-regulated assemblies of 1D lanthanide coordination polymers with the tricarboxylate ligand.

Solvothermal reactions of the tricarboxylic acid ligand, biphenyl-3,3',5-tricarboxylic acid (H3bpta), and rare earth nitrate (Ln(NO3)3·6H2O) in the presence of KOH or DMF produced eight 1D linear coordination polymers, namely, [La(bpta)(H2O)5·(H2O)3]n (), [Pr(bpta)(H2O)5·(H2O)2.5]n (), [Nd(bpta)(H2O)5·(H2O)1.75]n (), [Sm(bpta)(H2O)5·(H2O)0.