Ruthenium-mediated nucleophilic aromatic substitution of hydrogen in benzene.

ABSTRACT: The direct functionalization of unactivated hydrocarbons remains a significant challenge in modern chemistry. In this study, we demonstrate that a simple ruthenium complex featuring a chelating ^tBuPN ligand can mediate the nucleophilic aromatic substitution of hydrogen (S_NArH) in benzene. Key intermediates were kinetically trapped in low-temperature NMR experiments, providing crucial insights into the reaction mechanism. These findings are further supported by isotopic labeling and comprehensive DFT studies. The data shows that the substitution proceeds via an unprecedented mechanism, involving reversible rear-side nucleophilic addition of the exogenous nucleophile to the ruthenium-bound benzene, followed by an intramolecular hydride migration facilitate

SUBMITTER: Melnikov S 

PROVIDER: S-EPMC12198976 | biostudies-literature | 2025 Jul

REPOSITORIES: biostudies-literature