Acta Crystallographica Section E: Crystallographic Communications (Aug 2018)

Two N,N′-bis(pyridin-4-yl)pyridine-2,6-dicarboxamide coordination compounds

  • Yue-Xin Guo,
  • Hong-Cui Ma,
  • Ren Bo,
  • Ning Zhao,
  • Li-Gang Zhao,
  • Jin-Peng Li,
  • Hong-Wei Hou

DOI
https://doi.org/10.1107/S2056989018007351
Journal volume & issue
Vol. 74, no. 8
pp. 1049 – 1053

Abstract

Read online

The molecular structures of tetraaqua[N,N′-bis(pyridin-4-yl)pyridine-2,6-dicarboxamide]sulfatomanganese(II) dihydrate, [Mn(SO4)(C17H13N5O2)(H2O)4]·2H2O or [Mn(H2L1)(SO4)(H2O)4]·2H2O, (I), and tetraaquabis[N,N′-bis(pyridin-4-yl)pyridine-2,6-dicarboxamide]cadmium(II) sulfate tetrahydrate, [Cd(C17H13N5O2)2(H2O)4]SO4·4H2O or [Cd(H2O)4(H2L1)2]·SO4·4H2O, (II), both contain a central metal atom in a distorted octahedral geometry coordinated equatorially by four oxygen atoms from water molecules. In (I), the axial positions are occupied by a nitrogen atom from H2L1 and an oxygen atom from the sulfate anion, whereas in (II), the axial positions contain two nitrogen atoms from two different H2L1 ligands and the sulfate anion acts as the charge-balancing ion. π–π stacking between pyridine rings and a network of hydrogen bonds involving the water molecules and the sulfate anions play a crucial role in the molecular self-assembly of the two structures.

Keywords