Ab Initio Calculations on 2,6-Dimethylphenol and 4-(2,6-Dimethylphenoxy)-2,6-dimethylphenol. Evidence of an Important Role for the Phenoxonium Cation in the Copper-Catalyzed Oxidative Phenol Coupling Reaction

TLDR: In this article, Hartree−Fock calculations with a 6-31G* basis set were performed on 2,6-dimethylphenol (DMP or monomer) and 4-(2, 6-dimmethylphenoxy)-2,6dimethyl phenol (dimer) to gain more insight into the mechanism of the copper-catalyzed oxidative phenol coupling reaction.

Abstract: Ab initio unrestricted Hartree−Fock calculations with a 6-31G* basis set were performed on 2,6-dimethylphenol (DMP or monomer) and 4-(2,6-dimethylphenoxy)-2,6-dimethylphenol (dimer) to gain more insight into the mechanism of the copper-catalyzed oxidative phenol coupling reaction. Atomic charges were determined for the phenol, phenoxyl radical, phenolate anion and phenoxonium cation (both the singlet and triplet state) of both species. Calculations for the monomer show that the only aromatic carbon atom bearing a partial positive atomic charge is the para carbon of the cation in the singlet state. In the case of the dimer, the presence of a p-phenoxy substituent results in a partial positive charge for the para carbon of the first aromatic ring in all states, but this charge is significantly higher for the singlet cation. In the singlet cationic state, the para carbon of the first aromatic ring is therefore the site most susceptible to nucleophilic aromatic substitution. This result strongly supports a pr...