4.7 Article

2-D and 3-D organic-inorganic hybrid lanthanide molybdates linking by pyridine-2,5-dicarboxylate

Journal

CRYSTENGCOMM
Volume 14, Issue 24, Pages 8677-8683

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ce26208h

Keywords

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Funding

  1. Natural Science Foundation of China
  2. Special Research Fund for the Doctoral Program of Higher Education
  3. Innovation Scientists and Technicians Troop Construction Projects of Henan Province
  4. Natural Science Foundation of Henan Province

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Seven organic-inorganic hybrid lanthanide dimolybdates [Ln(H2O)(6)Mo2O6(Hpydc)(pydc)]center dot nH(2)O (n = 0: Ln = La-III (1), Ce-III (2), Pr-III (3), Nd-III (4), Sm-III (5); n = 0.5: Ln = Eu-III (6)), and Na0.5H0.5[Er(H2O)(5)Mo2O6(pydc)(2)]center dot 3H(2)O (7) (H(2)pydc = pyridine-2,5-dicarboxylic acid) have been hydrothermally prepared and further characterized by elemental analyses, X-ray powder diffraction (XRPD), IR spectra, thermogravimetric (TG) analyses, and single-crystal X-ray diffraction. The common feature of 1-7 is that they all consist of Ln(III) cations and Mo-IV centers connected by oxygen atoms and H(2)pydc ligands. 1-6 show unprecedented 3D 8-connected networks with the Schlafli symbol of (3(4).4(17).5(4).6(3)), while 7 exhibits the 2D 4-connected (4(5).6) structure. Furthermore, the luminescence properties of 5 and 6 are derived from the combination of Ln cations and H(2)pydc ligands, whereas 1-4 and 7 are attributable to H(2)pydc ligands.

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