4.5 Article

Syntheses and characterizations of three coordination polymers based on dipyridylbenzoates and 1,4-bezenedicarboxylate

Journal

POLYHEDRON
Volume 28, Issue 5, Pages 975-979

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.poly.2008.12.056

Keywords

Coordination polymer; Bridging ligand; Hydrothermal method; Crystal structure; X-ray diffraction; Fluorescence

Funding

  1. National Natural Science Foundation of China [20373009, 20703008]
  2. Chang Jiang Scholars Program
  3. Program for Changjiang Scholars and the Innovative Research Team [IRT0714]
  4. Ministry of Education of China [20030183063]
  5. Science Foundation for Young Teachers of Northeast Normal University [20080502]

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Three coordination polymers, namely [Ni(3,4-pmb)(bdc)(0.5)] (1). [Co(3,5-pmb)(bdc)(0.5)] (2) and [Cd(3,5pmb)(bdc)(0.)5] (3) (3,4-pmb = 3,4-bis[4-pyridylmethyleneoxyl]benzoate, 3,5-pmb = 3.5-bis[4-pyridylmethyleneoxyl]benzoate and bdc = 1,4-benzenedicarboxylate), have been synthesized by the hydrothermal method and structurally characterized. The X-ray structural analysis reveals that the three complexes possess different structural motifs. Complex 1 has a three-dimensional (3D) threefold interpenetrated diamondiod architecture and crystallizes in the monoclinic C2/c space group, in which each Ni(II) atom is connected to four other Ni(II) centers, resulting in the formation of a (4,4) diamondoid network. Complex 2 is a (3D) fourfold interpenetrated polyrotaxane and crystallizes in the monoclinic P2(1)/c space group. It is constructed by four equivalent independent 3D units and entangled by each other give a 3D fourfold structure. Complex 3 is a 2D network in which two Cd(II) centers are bridged equivalently by four carboxylate groups of different pmb and bdc ligands, forming a paddle wheel secondary building unit (SBU) (CdO4N), and the five coordinating atoms in the CdO4N unit occupy the vertices of squarepyramidal structure. Moreover, complex 3 exhibits strong photoluminescence at room temperature. (C) 2009 Elsevier Ltd. All rights reserved.

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