<p>Two new zinc(II) coordination polymers [Zn(bpba)<sub>2</sub>(NO<sub>3</sub>)<sub>2</sub>]<sub>n</sub> (<b>1</b>) and [Zn(bpba)(SO<sub>4</sub>)]<sub>n</sub>•2nH<sub>2</sub>O•nDMF (<b>2</b>) were successfully synthesized by reacting zinc(II) ions with bis(4-pyridyl)benzylamine (bpba) containing different counter anions (NO₃<sup>−</sup> and SO<sub>4</sub><sup>2−</sup>). The resulting polymers were fully characterized using various experimental techniques: single-crystal X-ray diffraction analysis, elemental analysis, infrared spectra, ultraviolet/visible spectra, and thermogravimetric analysis. Single-crystal X-ray analyses revealed that the zinc(II) ions in <b>1</b> and <b>2</b> are tetra-coordinated and adopt a distorted tetrahedral geometry. Polymer <b>1</b> exhibits a one-dimensional helical chain structure, which extends into two-dimensional supramolecular networks through hydrogen bonding and C-H•••π interactions. Polymer <b>2</b> adopts a three-dimensional network structure resulting from the coordination of zinc(II) and sulfate ions as well as bpba ligands. An investigation of the solid-state photoluminescence properties of the polymers at room temperature revealed that their emissions were redshifted compared with those of the free ligand, which is attributed to metal-perturbed intra-ligand charge transfer.</p>

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Synthesis, structural characterization, and luminescence properties of zinc(II) coordination polymers containing bis(4-pyridyl)benzylamine

  • Ihsan Ullah,
  • Ngoc Tram Anh Le,
  • Kil Sik Min

摘要

Two new zinc(II) coordination polymers [Zn(bpba)2(NO3)2]n (1) and [Zn(bpba)(SO4)]n•2nH2O•nDMF (2) were successfully synthesized by reacting zinc(II) ions with bis(4-pyridyl)benzylamine (bpba) containing different counter anions (NO₃ and SO42−). The resulting polymers were fully characterized using various experimental techniques: single-crystal X-ray diffraction analysis, elemental analysis, infrared spectra, ultraviolet/visible spectra, and thermogravimetric analysis. Single-crystal X-ray analyses revealed that the zinc(II) ions in 1 and 2 are tetra-coordinated and adopt a distorted tetrahedral geometry. Polymer 1 exhibits a one-dimensional helical chain structure, which extends into two-dimensional supramolecular networks through hydrogen bonding and C-H•••π interactions. Polymer 2 adopts a three-dimensional network structure resulting from the coordination of zinc(II) and sulfate ions as well as bpba ligands. An investigation of the solid-state photoluminescence properties of the polymers at room temperature revealed that their emissions were redshifted compared with those of the free ligand, which is attributed to metal-perturbed intra-ligand charge transfer.