Influence of meridional N3-ligands on supramolecular assembling and redox behavior of carboxylatocopper(II) complexes

Mononuclear phenylglyoxylato- and 4-R-benzoatocopper(II) complexes with two different 1,3-bis(2-arylimino)isoindoline ligands (aryl = pyridyl, or benzimidazolyl) have been synthesized and characterized. Coordination mode of the carboxylate ligands is very similar (monodentate) in each case, while redox behavior of the copper center is dependent on the aryl- and 4-R-substituents. The supramolecular assembly in the solid state via hydrogen bonds and π-stacking between the ligands can be influenced by the aryl-group and carboxylate ligand.

H-bonded/p-stacked supramolecular assembling and redox properties are influenced in mononuclear carboxylatocopper(II) complexes with 1,3-bis(2-arylimino)isoindoline ligands.Figure optionsDownload as PowerPoint slideHighlights
► Carboxylatocopper(II) complexes with isoindoline-based ligands synthesized.
► Redox properties of the Cu center can be controlled.
► Rich secondary interactions induce supramolecular assembling of the complexes.