Abstract

In the title complex, [Ni(C20H22N2O4)]·0.5H2O, the NiII ion is in a slightly distorted square-planar geometry involving an N2O2 atom set of the tetra­dentate Schiff base ligand. The asymmetric unit contains one mol­ecule of the complex and half a water solvent mol­ecule. The solvent water mol­ecule lies on a crystallographic twofold rotation axis. An inter­molecular O—H⋯O hydrogen bond forms an R 2 1(4) ring motif involving a bifurcated hydrogen bond to the phenolate O atoms of the complex. In the crystal structure, mol­ecules are linked by π–π stacking inter­actions, with centroid–centroid distances in the range 3.5310 (11)–3.7905 (12) Å, forming extended chains along the b axis. In addition, there are Ni⋯Ni and Ni⋯N inter­actions [3.4404 (4)–4.1588 (4) and 3.383 (2)–3.756 (2) Å, respectively] which are shorter than the sum of the van der Waals radii of the relevant atoms. Further stabilization of the crystal structure is attained by weak inter­molecular C—H⋯O and C—H⋯π inter­actions.

Highlights

  • In the title complex, [Ni(C20H22N2O4)]0.5H2O, the NiII ion is in a slightly distorted square-planar geometry involving an

  • The solvent water molecule lies on a crystallographic twofold rotation axis

  • Interactions [3.4404 (4)–4.1588 (4) and 3.383 (2)–3.756 (2) Å, respectively] which are shorter than the sum of the van der

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Summary

Crystal data

In the title complex, [Ni(C20H22N2O4)]0.5H2O, the NiII ion is in a slightly distorted square-planar geometry involving an. N2O2 atom set of the tetradentate Schiff base ligand. The asymmetric unit contains one molecule of the complex and half a water solvent molecule. The solvent water molecule lies on a crystallographic twofold rotation axis. O—H O hydrogen bond forms an R12(4) ring motif involving a bifurcated hydrogen bond to the phenolate O atoms of the complex. Molecules are linked by – stacking interactions, with centroid–centroid distances in the range 3.5310 (11)–3.7905 (12) Å, forming extended chains along the b axis. Further stabilization of the crystal structure is attained by weak intermolecular C—H O and C—H interactions

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