Molecular Structures and Redox Properties of Homoleptic Aluminum(III) Complexes with Azobisphenolate (azp) Ligands

Abstract

To elucidate the oxidation behavior of the 2,2′-azobisphenolate (azp) ligand, a series of homoleptic 1:2 AlIII complexes of four azp derivatives (L1) with 5,5′-dichloro-, 5,5′-dimethyl-, 5,5′-di-t-butyl-, 3,3′,5,5′-tetramethyl-substituents and of one imino derivative (L2) were synthesized and obtained as TPP[Al(L)2]·solvent (TPP = tetraphenylphosphonium ion). The X-ray crystal structure analyses showed that the two ONO-tridentate ligands were meridionally coordinated to a central AlIII ion in an almost perpendicular manner to give a homoleptic octahedral coordination structure in all the AlIII complexes. The proton nuclear magnetic resonance spectra suggested that all the AlIII complexes retained the homoleptic coordination structure in solution. From the cyclic voltammetry measurements in dichloromethane solutions, all the AlIII complexes with the azp ligands showed two partially reversible oxidation waves, and an additional reversible or partially reversible reduction wave. The substitution effects on the first oxidation and reduction peak potentials were revealed in the AlIII complexes with the azp ligands. On the other hand, the imino complex showed a partially reversible oxidation wave accompanying a film deposition. The density functional theory (DFT) calculations indicated that the molecular orbital (MO) coefficients of the frontier MOs in the AlIII complexes were present on the ligands and were absent on the AlIII ion. These results confirmed that the azp ligands are susceptible to oxidation and can give a relatively stable oxidation species depending upon substituent effects.

Keywords

• azobisphenolate ligand
• aluminum complex
• redox-active ligand
• crystal structure
• redox property
• DFT calculation