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

• Main Authors: Yue-Xin Guo, Hong-Cui Ma, Ren Bo, Ning Zhao, Li-Gang Zhao, Jin-Peng Li, Hong-Wei Hou
• Format: Article
• Language: English
• Published: International Union of Crystallography 2018-08-01
• Series: Acta Crystallographica Section E: Crystallographic Communications
• Subjects: crystal structure; coordination compound; heterocyclic nitrogen ligand; MnII complex; CdII complex
• Online Access: http://scripts.iucr.org/cgi-bin/paper?S2056989018007351
• ISSN: 2056-9890

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.