Two 3D Zinc(II) coordination frameworks constructed from pyrazine-2,3-dicarboxylate and 1,2-bis(4-pyridyl)ethylene


SEZER G. G., YEŞİLEL O. Z., Buyukgungor O.

JOURNAL OF MOLECULAR STRUCTURE, vol.1137, pp.562-568, 2017 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 1137
  • Publication Date: 2017
  • Doi Number: 10.1016/j.molstruc.2017.02.077
  • Journal Name: JOURNAL OF MOLECULAR STRUCTURE
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.562-568
  • Keywords: Coordination polymers, Pyrazine-2,3-dicarboxylate complexes, 1,2-bis(4-pyridyl)ethylene complexes, METAL-ORGANIC FRAMEWORKS, POLYMERS, DESIGN, INTERPENETRATION, CRYSTAL, LIGANDS, STORAGE, SERIES, MODE, ACID
  • Ondokuz Mayıs University Affiliated: Yes

Abstract

Two 3D coordination polymers, {[Zn(mu(3)-pzdc)(mu-dpeten)(0.5)]center dot 3H(2)O}(n) (1) and [Zn(mu(3)-pzdc)(mu-dpeten)(0.5)](n) (2) (H(2)pzdc = pyrazine-2,3-dicarboxylic acid and dpeten = 1,2-bis(4-pyridyl)ethylene) have been synthesized by hydrothermal methods and structurally characterized by elemental analysis, IR spectroscopy, single-crystal and powder X-ray diffraction. In complex 1, each pzdc ligand bridges three Zn(II) ions through forming two-dimensional layers. The adjacent 2D layers are further connected by dpeten ligand to generate a novel 3D framework containing one-dimensional large porous channel. It displays a 5 connected bnn hexagonal topology with point symbol {4(6).6(4)}. Although the complex 2 was obtained under the same reaction conditions together with complex 1, it exhibits 3D -> 3D a 2-fold interpenetration network with 6-connected pcu alpha-Po primitive cubic topology with point symbol {4(12).6(3)}. The adjacent three Zn(II) ions are linked by tridentate bridging pzdc ligands to form a 2D layer structure. The 2D layers are further bridged by dpeten ligand to form a 3D pillar-layered network. Moreover, thermal and photoluminescent properties of complexes 1 and 2 have also been studied. (C) 2017 Elsevier B.V. All rights reserved.