Low-temperature (100 K) crystal structures of pentaaqua(5-nitrosalicylato) complexes of magnesium(II), zinc(II), cobalt(II) and nickel(II): A π–π stacked and hydrogen bonded 3D supramolecular architecture

Reactions of metal chloride or sulfate and the sodium salt of 5-nitrosalicylic acid (5-nsa) in aqueous solution result in isomorphous complexes of type [M(H2O)5(5-nsa)]+ (5-nsa)− · H2O [M = Mg (1), Zn (2), Co (3), Ni (4)] in the solid state. Structural analyses of these compounds reveal that the cationic moiety is a monomeric complex in which the metal is coordinated by five aqua ligands and one carboxylato O-atom from the 5-nitrosalicylato ligand, forming a slightly distorted octahedron. The crystal packing exhibits ionic parts assembled through extensive hydrogen bonding. The metal-bonded cationic moiety and the non-ligating anionic one are also engaged in π-stacking interactions which contribute to the crystal cohesion. The anchoring of the individual ionic subunits through π–π stacking and hydrogen bonding results in a 3D supramolecular architecture.

Reactions of metal chloride or sulfate and the sodium salt of 5-nitrosalicylic acid (5-nsa) in aqueous solution result in isomorphous complexes of type [M(H2O)5(5-nsa)]+ (5-nsa)− · H2O [M = Mg (1), Zn (2), Co (3), Ni (4)] in the solid state. The metal-bonded cationic moiety and the non-ligating anionic one are engaged in π-stacking interactions. The anchoring of the individual ionic subunits through π–π stacking and extensive hydrogen bonding results in a 3D supramolecular architecture.Figure optionsDownload as PowerPoint slide