A novel one‐dimensional thiocyanate‐bridged cobalt(III) complex: synthesis, crystal structure characterization and Hirshfeld surface analysis.

A new one‐dimensional thiocyanate‐bridged cobalt(III) Schiff base complex, namely, catena‐poly[[[4‐bromo‐2‐((Z)‐{[2‐(thiophen‐2‐yl)ethyl]imino}methyl)phenolato‐κ2N,O]cobalt(III)]‐μ‐thiocyanato‐κ2N:S], [Co(SCN)(C13H11BrNOS)2]n or [Co(μ1,3‐SCN)L2]n (1), where HL is 4‐bromo‐2‐((Z)‐{[2‐(thiophene‐2‐yl)ethyl]imino}methyl)phenol, a bidentate Schiff base prepared from the condensation reaction of 5‐bromosalicylaldehyde and 2‐(thiophen‐2‐yl)ethylamine, has been synthesized by stirring Co(ClO4)2·6H2O, the Schiff base HL and ammonium thiocyanate (in a 1:2:1 molar ratio) in ethanol medium. The complex was characterized by FT–IR, electronic spectra and single‐crystal X‐ray diffraction (SC‐XRD) studies. The SC‐XRD data suggest that the compound crystallizes in the orthorhombic space group Pca21. The CoIII ion in 1 adopts a distorted octahedral geometry, the metal sites being six‐coordinated by one thiocyanate N atom and one thiocyanate S atom in apical positions, and by two imine N atoms and two phenolate O atoms from two anionic L− ligands which form the basal plane. The thiocyanate ligand acts as a μ‐1,3 bridge, joining neighbouring CoIII atoms and forming a uniform zigzag one‐dimensional polymeric chain. The crystallographic data were also used in the Hirshfeld surface (HS) analysis, which aimed to investigate the nature and quantitative significance of any noncovalent intermolecular interactions inside the crystal lattice. The crystal void parameters have also been computed and show the molecules to be tightly packed. [ABSTRACT FROM AUTHOR]