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Mediator-Enabled Co-Catalyzed Z -Selective Semihydrogenation via Hydride-Free Multisite Proton-Coupled Electron Transfer

Year: 2025

Type: article

Abstract: High Resolution Image Download MS PowerPoint Slide Redox mediators continue to emerge as powerful tools for driving electrochemical reactions, preventing electrode surface fouling and/or facilitating redox processes at milder operating potentials than direct electrolysis requires. In this study, we demonstrate a tandem electrocatalytic approach using a Cp 2 Co redox mediator and (dppe)CoCl 2 precatalyst to selectively hydrogenate a variety of alkynes to cis- alkenes. Controlled potential electrolysis (CPE) at the potential of the mediator ( E app = −1.45 V vs Fc +/0 ) successfully generates a variety of terminal and internal alkenes in moderate to good yields. Notably, substrates with tethered Lewis bases further drive selectivity almost exclusively for the Z isomer. Mechanistic investigation of the tandem catalytic reaction via CV and DFT point toward a multisite proton-coupled electron transfer (MS-PCET) step involving a hydride-free pathway where Cp 2 Co facilitates the reduction of alkyne- and acid-bound (dppe)Co(I)/(0). This developed methodology can be applied toward the synthesis of cis -stilbenoid natural products, as demonstrated with combretastatin A-4. It is also amenable to more practical gram-scale setup and proceeds with up to 99% Faradaic efficiency.

Source: ACS Catalysis

DOI: 10.1021/acscatal.5c08388