How Thermodynamic, Electronic, and Steric Factors Influence Mesitylcopper Oligomers

Mesitylcopper (CuMes) is a highly versatile organocopper reagent used in both organic and inorganic syntheses. It has previously been shown that CuMes exists as a tetrameric or pentameric cyclic oligomer [CuMes]<i>_n</i> (<i>n</i> = 4, 5), both in solution and in the solid state. The bonding arrangement between the [CuMes] units has qualitatively been described as localized three-center two-electron (3c-2e) bonds. However, the electronic, structural, and thermodynamic forces driving this aggregation are still not well understood. For this reason, we employed density functional theory (DFT) calculations to study mesitylcopper as a monomeric [CuMes] unit and [CuMes]<i>_n</i> oligomers with <i>n</i> = 2 to <i>n</i> = 7. We found that there is a strong electronic driving force for aggregation caused by strong mixing between the Cu's <i>d</i> orbitals and Mes's π orbitals in oligomers larger than the dimer. This mixing is only optimized in oligomers with <i>n</i> ≥ 3, where the mesityl group is no longer bonded to a single copper center but instead becomes a bridging ligand. Beyond the trimer, steric and entropic factors become relevant for determining the relative stabilities of the different aggregates, with midsized oligomers (<i>n</i> = 4-5) having the optimal balance between the electronic Cu-C bonding character, Cu···Cu attractive forces, entropy, reduced internal ring strain, and reduced steric interactions between the mesityl groups.