Synthesis and electronic structure determination of uranium(vi) ligand radical complexes. Issue 31 (21st July 2016)

• Record Type: Journal Article
• Authors: Herasymchuk, Khrystyna; Chiang, Linus; Hayes, Cassandra E.; Brown, Matthew L.; Ovens, Jeffrey S.; Patrick, Brian O.; Leznoff, Daniel B.; Storr, Tim
• Is Part Of: Dalton transactions. Volume 45:Issue 31(2016)
• Page Start: 12576
• Page End: 12586
• Publication Date: 2016-07-21
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c6dt02089e
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Pentagonal bipyramidal uranyl (UO2 2+ ) complexes of salen ligands were prepared and the electronic structure of the one-electron oxidized species[1a–c] + were investigated in solution. Abstract : Pentagonal bipyramidal uranyl (UO2 2+ ) complexes of salen ligands, N, N ′-bis(3- tert -butyl-(5 R )-salicylidene)-1, 2-phenylenediamine, in which R = t Bu (1a ), OMe (1b ), and NMe2 (1c ), were prepared and the electronic structure of the one-electron oxidized species[1a–c] + were investigated in solution. The solid-state structures of1a and1b were solved by X-ray crystallography, and in the case of1b an asymmetric UO2 2+ unit was found due to an intermolecular hydrogen bonding interaction. Electrochemical investigation of1a–c by cyclic voltammetry showed that each complex exhibited at least one quasi-reversible redox process assigned to the oxidation of the phenolate moieties to phenoxyl radicals. The trend in redox potentials matches the electron-donating ability of the para -phenolate substituents. The electron paramagnetic resonance spectra of cations[1a–c] + exhibited g av values of 1.997, 1.999, and 1.995, respectively, reflecting the ligand radical character of the oxidized forms, and in addition, spin–orbit coupling to the uranium centre. Chemical oxidation as monitored by ultraviolet-visible-near-infrared (UV-vis-NIR) spectroscopy afforded the one-electron oxidized species. Weak low energy intra-ligand charge transfer (CT) transitions were observed for[1a–c] + indicating localization of the ligand radical to form a phenolate/phenoxyl radical species. Further analysis using density functional theory (DFT) calculations predicted a localized phenoxyl radical for[1a–c] + with a small but significant contribution of the phenylenediamine unit to the spin density. Time-dependent DFT (TD-DFT) calculations provided further insight into the nature of the low energy transitions, predicting both phenolate to phenoxyl intervalence charge transfer (IVCT) and phenylenediamine to phenoxyl CT character. Overall, [1a–c] + are determined to be relatively localized ligand radical complexes, in which localization is enhanced as the electron donating ability of the para -phenolate substituents is increased (NMe2 > OMe > t Bu).