On the Role of N‐Heterocyclic Carbene Salts in Alkyl Radical Generation from Alkyl Alcohols: A Computational Study

Formation of carbon‐carbon bonds through cross‐coupling reactions using readily available substrates, like alcohols, is crucial for modern organic chemistry. Recently, direct alkyl alcohol functionalization has been achieved by the use of N‐Heterocyclic Carbene (NHC) salts via in situ formation of an alcohol‐NHC adduct and its activation by a photoredox catalyst to generate carbon‐centered alkyl radicals. Experimentally, only electron deficient NHC activators work but the reasons of this behavior remain underexplored. Herein, a DFT computational study of the mechanism of alcohol activation using up to seven NHC salts is performed to shed light into the influence of their electronic properties in the alkyl radical formation. This study demonstrates that four reaction steps are involved in the transformation and characterizes how the electronic properties of the NHC salt affect each step. A fine balance of the NHC electron‐richness is proved to be determinant for this transformation. The mechanism of carbon centered radical generation from alkyl alcohols mediated by N‐heterocyclic carbene salts has been explored computationally for 7 different NHCs. The influence of the electronic properties for each mechanistic step is rationalized and has been proven to be key for reactivity.