Ligand-Centered Electrochemical Processes Enable CO2 Reduction with a Nickel Bis(triazapentadienyl) Complex

Abstract

We report the synthesis of Ni(TAPPy)<sub>2</sub> (TAPPy = 1,3,5-triazapentadienyl-2,4-bis(2-pyridyl)) and its reactivity with CO<sub>2</sub> under reducing conditions. Electrochemical reduction of Ni(TAPPy)<sub>2 </sub>under inert gas reveals that the complex accommodates up to two additional electrons, with DFT calculations indicating that electron density is delocalized almost exclusively onto the TAPPy ligand framework. The singly reduced product [K(crypt)][Ni(TAPPy)<sub>2</sub>] (crypt = 2.2.2-cryptand) has been synthesized, and its EPR data is consistent with having ligand-based radical anion character. Controlled potential electrolysis experiments reveal that reduced Ni(TAPPy)<sub>2</sub> converts CO<sub>2</sub> to form CO; however, spectroscopic and computational data indicate that deactivation readily occurs to form Ni(L)(CO)<i><sub>n</sub></i> compounds, CO<sub>3</sub><sup>2-</sup>, and carboxylated (RCOO<sup>-</sup>) ligand decomposition products. This study highlights that redox activity at the ligand can play an important role during the reduction of CO<sub>2</sub> using transition metal complexes.

Electrocatalyst Decomposition Pathways: Torsional Strain in a Second Sphere Proton Relay Shuts Off CO2RR in a Re(2,2’-bipyridyl)(CO)3X Type Electrocatalyst

“…24 Addition of barium trifluoromethanesulfonate or magnesium salts to these solutions yield no quantifiable precipitates showing the catalyst is not operating on the CO/CO3 2disproportionation pathway. 25 CPE trials with other proton sources (PhOH, H2O etc. ), in different solvents (ACN) or at higher potentials (-2.2 V vs Fc + /Fc) did not show any improvement of TONs and FEs (Table S2).…”