In this work, we found that alkali metal cations in the electrolyte can impact the *Cl binding energy, which controls selectivity between radical-mediated electrochemical C─H chlorination and competing Cl₂ formation.

Abstract

Electrochemistry offers a promising route toward facilitating organic transformation reactions in a sustainable manner. However, there are often a multitude of factors at play; hence, it can be unclear how operating conditions can be rationally tuned to optimize selectivity. Here, we demonstrate how the identity of alkali metal cations in the electrolyte can control the selectivity of electrochemical C─H chlorination. Specifically, we obtained a 90.3% Faradaic efficiency with KCl as compared to 78.4% with LiCl for the conversion of cyclohexane to chlorocyclohexane at 1000 mA using an IrO _x electrode. Electron paramagnetic resonance spectroscopy experiments indicate a greater propensity for Cl⁻ oxidation to generate Cl radicals in the order: K⁺ > Na⁺ > Li⁺. This leads to an increase in the selectivity toward the chlorination of cyclohexane and a concomitant decrease in competitive Cl₂ formation. Density functional theory calculations and in situ Raman spectroscopy experiments indicate that this is likely due to a decrease in *Cl binding energy on IrO _x in the presence of K⁺. These findings highlight the important role of alkali metal cations, which can be a key consideration for designing electrochemical organic synthesis systems.