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Atropisomeric Hydrogen Bonding Control for CO 2 Binding and Enhancement of Electrocatalytic Reduction at Iron Porphyrins

2020; Wiley; Volume: 59; Issue: 50 Linguagem: Inglês

10.1002/anie.202010859

1521-3773

Philipp Gotico, Loïc Roupnel, Régis Guillot, Marie Sircoglou, Winfried Leibl, Zakaria Halime, Ally Aukauloo,

Metal-Catalyzed Oxygenation Mechanisms

Abstract The manipulation of the second coordination sphere for improving the electrocatalytic CO 2 reduction has led to breakthroughs with hydrogen bonding, local proton source, or electrostatic effects. We have developed two atropisomers of an iron porphyrin complex with two urea functions acting as multiple hydrogen‐bonding tweezers to lock the metal‐bound CO 2 in a similar fashion found in the carbon monoxide dehydrogenase (CODH) enzyme. The αα topological isomer with the two urea groups on the same side of the porphyrin provides a stronger binding affinity to tether the incoming CO 2 in comparison to the αβ disposition. However, the electrocatalytic activity of the αβ atropisomer outperforms its congener with one of the highest reported turnover frequencies at low overpotential. The strong H/D kinetic isotope effect (KIE) observed for the αα system indicates the existence of a tight water hydrogen‐bonding network for proton delivery which is disrupted by addition of an acid source. The small H/D KIE for the αβ isomer and the enhanced electrocatalytic performance on addition of stronger acid indicate the free access of protons to the bound CO 2 on the opposite side of the urea arm.