Aluminum Complexes of N2O2 3– Formazanate Ligands Supported by Phosphine Oxide Donors

• Published in: Inorganic chemistry 2017-10, Vol.56 (20), p.12436-12447
• Main Authors: Maar, Ryan R, Rabiee Kenaree, Amir, Zhang, Ruizhong, Tao, Yichen, Katzman, Benjamin D, Staroverov, Viktor N, Ding, Zhifeng, Gilroy, Joe B
• Format: Article
• Language: English
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.7b01907

The synthesis and characterization of a new family of phosphine oxide supported aluminum formazanate complexes (7a,b, 8a, 9a) are reported. X-ray diffraction studies showed that the aluminum atoms in the complexes adopt an octahedral geometry in the solid state. The equatorial positions are occupied by an N2O2 3– formazanate ligand, and the axial positions are occupied by L-type phosphine oxide donors. UV–vis absorption spectroscopy revealed that the complexes were strongly absorbing (ε ≈ 30000 M–1 cm–1) between 500 and 700 nm. The absorption maxima in this region were simulated using time-dependent density functional theory. With the exception of 3-cyano-substituted complex 7b, which showed maximum luminescence intensity in the presence of excess phosphine oxide, the title complexes are nonemissive in solution and the solid state. The electrochemical properties of the complexes were probed using cyclic voltammetry. Each complex underwent sequential one-electron oxidations in potential ranges of −0.12 to 0.29 V and 0.62 to 0.97 V, relative to the ferrocene/ferrocenium redox couple. Electrochemical reduction events were observed at potentials between −1.34 and −1.75 V. In combination with tri-n-propylamine as a coreactant, complex 7b acted as an electrochemiluminescence emitter with a maximum electrochemiluminescence intensity at a wavelength of 735 nm, red-shifted relative to the photoluminescence maximum of the same compound.