Electronic Effects Drive Selectivity in CO ₂ Reduction Catalysis by Heptacoordinated Cobalt Complexes

High Resolution Image Download MS PowerPoint Slide Controlling selectivity in CO 2 reduction catalysis is essential for minimizing the formation of H 2 byproduct. We recently reported that the cobalt and iron complexes of the 1-([2,2′-bipyridin]-6-yl)- N -([2,2′-bipyridin]-6-ylmethyl)- N -(pyridin-2-ylmethyl) methanamine ligand ( L, DBPy-PyA) are efficient catalysts to selectively generate H 2 and CO, respectively. Herein we demonstrate that selectivity can be controlled not only by exchanging the metal center but also adjusting the electronic properties of the ligand. Under electrochemical conditions in acetonitrile, with 2,2,2-trifluoroethanol as a proton source, the unsubstituted CoL and the electron-rich CoL OMe predominantly produce H 2 (selectivity of 82% and 55%, respectively). In contrast, the electron-deficient CoL CF3 favors CO formation with a selectivity up to 87%. DFT calculations show that formation of the metal-hydride is favored in the case of CoL and CoL OMe, whereas it is substantially endergonic in the case of CoL CF3 . Concurrently, the binding of CO 2 and the evolution of the resulting intermediates in CoL CF3 can benefit from ligand-assisted proton transfer, as confirmed by microkinetic modeling. Catalytic tests were then conducted under photochemical conditions, affording syngas with tunable CO/H 2 ratios that follow the electronic effects of the chosen catalyst. Overall, the results underscore how ligand tuning can be a powerful handle for controlling selectivity in molecular CO 2 RR.