om2c00202_si_002.xyz (186.38 kB)
Direct Benzene Hydroxylation with Dioxygen Induced by Copper Complexes: Uncovering the Active Species by DFT Calculations
datasetposted on 2022-07-14, 16:36 authored by Elena Borrego, Laura Tiessler-Sala, Jesus J. Lázaro, Ana Caballero, Pedro J. Pérez, Agustí Lledós
The direct oxidation of benzene into phenol using molecular oxygen at very mild temperatures can be promoted in the presence of the copper complex TpBr3Cu(NCMe) in the homogeneous phase in the presence of ascorbic acid as the source of protons and electrons. The stoichiometric nature, relative to copper, of this transformation prompted a thorough DFT study in order to understand the reaction pathway. As a result, the dinuclear species TpBr3CuII(μ-O•)(μ-OH)CuIITpBr3 is proposed as the relevant structure which is responsible for activating the arene C–H bond leading to phenol formation.
thorough dft studyoh ) cuii supcu ( ncmebr3 supdinuclear species tpdirect benzene hydroxylationcopper complex tpdirect oxidationdft calculationsactive speciestransformation promptedstoichiometric naturerelevant structurereaction pathwayphenol formationmild temperatureshomogeneous phasedioxygen inducedcopper complexesascorbic acid