C–H activation and nucleophilic substitution in a photochemically generated high valent iron complex

Abstract

The photochemical oxidation of a (TAML)Fe^III complex 1 using visible light generated Ru(bpy)₃³⁺ produces valence tautomers (TAML)Fe^IV (1⁺) and (TAML˙⁺)Fe^III (1-TAML˙⁺), depending on the exogenous anions. The presence of labile Cl⁻ or Br⁻ results in a ligand-based oxidation and stabilisation of a radical-cationic (TAML˙⁺)Fe^III complex, which subsequently leads to unprecedented C–H activation followed by nucleophilic substitution on the TAML aryl ring. In contrast, exogenous cyanide culminates in metal-based oxidation, yielding the first example of a crystallographically characterised S = 1 [(TAML)Fe^IV(CN)₂]²⁻ species. This is a rare report of an anion-dependent valence tautomerisation in photochemically accessed high valent (TAML)Fe systems with potential applications in the oxidation of pollutants, hydrocarbons, and water. Furthermore, the nucleophilic aromatic halogenation reaction mediated by (TAML˙⁺)Fe^III represents a novel domain for high-valent metal reactivity and highlights the possible intramolecular ligand or substrate modification pathways under highly oxidising conditions. Our findings therefore shine light on high-valent metal oxidants based on TAMLs and other potential non-innocent ligands and open new avenues for oxidation catalyst design.