Crystal structure of an indium-salicyl-hydroximate complex cation: [In(Hshi)(HO)](NO)·8.57HO.

The synthesis and crystal structure for the title compound, hexa-aqua-hexa-kis(μ-2-hy-droxy-benzene-carbo-hydrox-a-mato)bis-(2-hy-droxy-benzene-carbo-hydrox-a-m-ato)tetra-indium(III) tetra-nitrate 8.57-hydrate + unknown solvent, [In(Hshi)(HO)](NO)·8.57HO·solvent, where Hshi is salicylhydrox-imate (CHNO), are reported. The complex cation of the structure, [In(Hshi)(HO)], is a dimer with a step-like topology and possesses an inversion center that relates each [In(Hshi)(HO)] side of the complex cation. Each In ion is seven-coordinate with a penta-gonal-bipyramidal geometry, and the salicyl-hydroximate ligands have a 1- charge as only the oxime oxygen of the ligand is deprotonated. Four inter-stitial nitrate anions maintain the charge balance of the compound. One of the nitrate anions (and its symmetry equivalent) is disordered over two different orientations with an occupancy ratio of 0.557 (7) to 0.443 (7). The inter-stitial solvent water mol-ecules show substantial disorder. Approximately 8.57 water mol-ecules per formula unit were refined as disordered and partially occupied, while a suitable model could not be devised for the other extensively disordered solvent mol-ecules (water and possibly methanol as this was the synthesis solvent). Thus, these latter solvent mol-ecules were instead treated with the SQUEEZE routine [Spek (2015). . C, 9-18.] as implemented in the program , and the procedure corrected for 151 electrons within solvent-accessible voids of 367 Å.