Synthesis and Crystal Structure of [Pb(gly)2]n; New lead(II) Coordination Polymer with Glycine Ligand

Authors

  • Ali Morsali Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, Tehran, Iran
  • Amir Reza Abbasi Faculty of Chemistry, Razi University, Kermanshah, Iran
  • Azar Hakimifar Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, Tehran, Iran
  • Fateme Babaei Mazandaran Gas Company, Mazandaran, Iran
  • Lida Hashemi Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, Tehran, Iran
  • Michal Dusek Institute of physics ASCR Cukrovarnicka 10 162 00 Prague Czech Republic
  • Mohammad Esmaeil Ebrahimzadeh Mazandaran Gas Company, Mazandaran, Iran
  • Mojtaba Khanpour Matikolaei Mazandaran Gas Company, Mazandaran, Iran
  • Zarnoosh Shokhchashm Department of Chemistry, Payame Noor University, Abhar, Zanjan, Iran
Abstract:

[Pb(gly)2]n (1) (gly is the abbreviation of Glycine) have been synthesized and characterized by elemental analyses, IR, 1H NMR and 13C NMR spectroscopy. The single crystal structure of 1 show the complex is 2D coordination polymer with octahedral environment that is formed into 3D supramolecule through hydrogen bond. Structural determination of compound 1 reveals the Pb(II) ion is four coordinated, bonded to a nitrogen, oxygen and two carbon atoms from the Glycine ligand.The crystal structure of compound 1 consists of a 3D supramolecular compound and shows the coordination number in the Pb(II) ions is six. PbO nanoparticles were synthesized by calcination of compound 1 at 500, 550 and 600 °C under air atmosphere. Calcination of the compound 1 at these temperatures yields mixture of orthorhombic and tetragonal PbO nanoparticles and nanorods. The PbO nanostructure was characterized by scanning electron microscopy (SEM) and X-ray powder diffraction (XRD). The thermal stability of compound 1 was studied by thermal gravimetric (TG) and differential thermal analyses (DTA).

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Journal title

volume 9  issue 1

pages  8- 13

publication date 2019-01-01

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