Abstract

The lanthanide biphenyl-4,4′-dicarboxylates (bpdc) series of the general formulae Ln2(bpdc)3·nH2O, where Ln = lanthanides from La(III) to Lu(III); bpdc = C12H5(COO) 2 2− ; n = 4, 5 or 6 have been obtained by the conventional precipitation method. All prepared complexes were characterized by elemental analysis, simultaneous thermal analyses thermogravimetric-differential scanning calorimetry (TG–DSC) and TG–FT-IR, FT-IR, and FT-Raman spectroscopy as well as X-ray diffraction patterns measurements. In the whole series of analyzed complexes the bpdc2− ligand is completely deprotonated. In view of that, four carboxylate oxygen atoms are engaged in the coordination of Ln(III) ions. The synthesized compounds are polycrystalline and insoluble in water. They crystallize in the low symmetry crystal systems, like monoclinic and triclinic. Heating in the air atmosphere resulted in the multi-steps decomposition process, namely endothermic dehydration and strong exothermic decomposition processes. The dehydration process leads to the formation of stable anhydrous Ln2bpdc3 compounds which subsequently decompose to the corresponding lanthanide oxides.

Highlights

  • IntroductionCoordination polymers (PCPs) represent a unique class of crystalline open framework solids with unprecedented structures and diverse chemical composition [1, 2]

  • Synthesis of metal-based coordination polymers with novel structures constitutes an important area of research.Coordination polymers (PCPs) represent a unique class of crystalline open framework solids with unprecedented structures and diverse chemical composition [1, 2]

  • All prepared complexes were characterized by elemental analysis, simultaneous thermal analyses thermogravimetric-differential scanning calorimetry (TG–DSC) and TG–FT-IR, FT-IR, and FTRaman spectroscopy as well as X-ray diffraction patterns measurements

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Summary

Introduction

Coordination polymers (PCPs) represent a unique class of crystalline open framework solids with unprecedented structures and diverse chemical composition [1, 2]. These kinds of compounds result from molecular reactions between metal ions and bridging multidentate organic ligands, usually performed under hydro(solvo)thermal conditions [3]. The aromatic polycarboxylates are often employed in a design strategy to construct metal–organic frameworks with special topologies due to their rich coordination chemistry and the predictability of the resulting networks [4–6]. The biphenyl-4,40-dicarboxylic rigid, linear organic O-donor ligand is employed as organic linkers to construct metal– organic coordination compounds with a variety of coordination modes (Fig. 1) and different dimensionalities [8–19]

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