Two novel isostructural and heteroleptic Nd(III) and Dy(III)-organic frameworks constructed by 2,5-pyridinedicarboxylic acid and in situ generated 2-pyridinecarboxylic acid: Hydrothermal synthesis, characterization, photoluminescence properties and heterogeneous catalytic activities

AY B. , YILDIZ E. , Kani I.

POLYHEDRON, vol.130, pp.165-175, 2017 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 130
  • Publication Date: 2017
  • Doi Number: 10.1016/j.poly.2017.04.011
  • Title of Journal : POLYHEDRON
  • Page Numbers: pp.165-175


The crystal structures, heterogeneous catalytic activities and photoluminescent properties of two novel three dimensional (3D) metal organic frameworks (MOFs), [Nd(pyc)(pydc)(H2O)](n) (1) and [Dy(pyc) (pydc)(H2O)](n) (2) (H(2)pydc = pyridine-2,5-dicarboxylic acid, Hpyc = 2-pyridinecarboxylic acid) are presented. The synthesized complexes under hydrothermal conditions were characterized by the elemental analysis, inductively coupled plasma (ICP), fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), single crystal X-ray diffraction and powder X-ray diffraction (PXRD) analysis. For morphological analysis, field emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM) were used. The compounds are isostructural and each Ln(3+) (Nd(III) and Dy(III)) centers are eight-coordinated. MOFs have the distinct 3D open-framework architectures due to the presence of Hpyc ligands, which are converted from H(2)pydc ligands in-situ decarboxylation under the hydrothermal conditions. Photoluminescence properties and thermal stabilities of the compounds have been investigated. Their heterogeneous catalytic activities have also been examined on the oxidation of the thymol (T) to thymoquinone (TQ). The structures of the MOFs were stable after three catalytic cycles. The maximum T conversion values, 40.37% and 36.45% were recorded with nearly 100% selectivities by using 1 and 2, respectively. (C) 2017 Elsevier Ltd. All rights reserved.