Cooperativity‐Driven Reactivity of a Dinuclear Copper Dimethylglyoxime Complex

Abstract

In this report, we present the dinuclear copper(II) dimethylglyoxime (H$_2$dmg) complex [Cu$_2$(H$_2$dmg)(Hdmg)(dmg)]$^+$ (1), which, in contrast to its mononuclear analogue [Cu(Hdmg)$_2$] (2), is subject to a cooperativity-driven hydrolysis. The combined Lewis acidity of both copper centers increases the electrophilicity of the carbon atom in the bridging μ$_2$-O−N=C-group of H$_2$dmg and thus, facilitates the nucleophilic attack of H2O. This hydrolysis yields butane-2,3-dione monoxime (3) and NH$_2$OH that, depending on the solvent, is then either oxidized or reduced. In ethanol, NH$_2$OH is reduced to NH$_4$$^+$, yielding acetaldehyde as the oxidation product. In contrast, in CH$_3$CN, NH$_2$OH is oxidized by Cu$^{II}$ to form N$_2$O and [Cu(CH$_3$CN)4]$^+$. Herein are presented the combined synthetic, theoretical, spectroscopic and spectrometric methods that indicate and establish the reaction pathway of this solvent-dependent reaction