Crystal structure of a nickel compound comprising two nickel(II) complexes with different ligand environments: [Ni(tren)(H2O)2][Ni(H2O)6](SO4)2

Acta Crystallogr E Crystallogr Commun. 2020 Feb 6;76(Pt 3):314-317. doi: 10.1107/S2056989020001358. eCollection 2020 Mar 1.

Abstract

The title compound, di-aqua-[tris-(2-amino-eth-yl)amine]-nickel(II) hexa-aqua-nickel(II) bis-(sulfate), [Ni(C6H18N4)(H2O)2][Ni(H2O)6](SO4)2 or [Ni(tren)(H2O)2][Ni(H2O)6](SO4)2, consists of two octa-hedral nickel complexes within the same unit cell. These metal complexes are formed from the reaction of [Ni(H2O)6](SO4) and the ligand tris-(2-amino-eth-yl)amine (tren). The crystals of the title compound are purple, different from those of the starting complex [Ni(H2O)6](SO4), which are turquoise. The reaction was performed both in a 1:1 and 1:2 metal-ligand molar ratio, always yielding the co-precipitation of the two types of crystals. The asymmetric unit of the title compound, which crystallizes in the space group Pnma, consists of two half NiII complexes and a sulfate counter-anion. The mononuclear cationic complex [Ni(tren)(H2O)2]2+ comprises an Ni ion, the tren ligand and two water mol-ecules, while the mononuclear complex [Ni(H2O)6]2+ consists of another Ni ion surrounded by six coordinated water mol-ecules. The [Ni(tren)(H2O)2] and [Ni(H2O)6] subunits are connected to the SO4 2- counter-anions through hydrogen bonding, thus consolidating the crystal structure.

Keywords: crystal structure; hydrogen bonding; nickel complexes; tren; tripodal ligand.

Grants and funding

This work was funded by U.S. Department of Education grant PO31S130068. National Science Foundation grant 1626103. National Institute of General Medical Sciences grant P20GM103475.