Proton-coupled electron transfer across benzimidazole bridges in bioinspired proton wires

• Published in: Chemical science (Cambridge) Vol. 11; no. 15; pp. 382 - 3828
• Main Authors: Odella, Emmanuel, Mora, S. Jimena, Wadsworth, Brian L, Goings, Joshua J, Gervaldo, Miguel A, Sereno, Leonides E, Groy, Thomas L, Gust, Devens, Moore, Thomas A, Moore, Gary F, Hammes-Schiffer, Sharon, Moore, Ana L
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 15-04-2020; The Royal Society of Chemistry
• Subjects: Bridges; Chemistry; Coupling (molecular); Crystallography; Density functional theory; Electrode potentials; Electron transfer; Electrons; Hydrogen bonding; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Oxidation; Phenols; Photosynthesis; Protons; Redox reactions; Solar energy conversion; Water chemistry
• ISSN: 2041-6520; 2041-6539
• DOI: 10.1039/c9sc06010c

Designing molecular platforms for controlling proton and electron movement in artificial photosynthetic systems is crucial to efficient catalysis and solar energy conversion. The transfer of both protons and electrons during a reaction is known as proton-coupled electron transfer (PCET) and is used by nature in myriad ways to provide low overpotential pathways for redox reactions and redox leveling, as well as to generate bioenergetic proton currents. Herein, we describe theoretical and electrochemical studies of a series of bioinspired benzimidazole-phenol (BIP) derivatives and a series of dibenzimidazole-phenol (BI
2
P) analogs with each series bearing the same set of terminal proton-accepting (TPA) groups. The set of TPAs spans more than 6 p
K
a
units. These compounds have been designed to explore the role of the bridging benzimidazole(s) in a one-electron oxidation process coupled to intramolecular proton translocation across either two (the BIP series) or three (the BI
2
P series) acid/base sites. These molecular constructs feature an electrochemically active phenol connected to the TPA group through a benzimidazole-based bridge, which together with the phenol and TPA group form a covalent framework supporting a Grotthuss-type hydrogen-bonded network. Infrared spectroelectrochemistry demonstrates that upon oxidation of the phenol, protons translocate across this well-defined hydrogen-bonded network to a TPA group. The experimental data show the benzimidazole bridges are non-innocent participants in the PCET process in that the addition of each benzimidazole unit lowers the redox potential of the phenoxyl radical/phenol couple by 60 mV, regardless of the nature of the TPA group. Using a series of hypothetical thermodynamic steps, density functional theory calculations correctly predicted the dependence of the redox potential of the phenoxyl radical/phenol couple on the nature of the final protonated species and provided insight into the thermodynamic role of dibenzimidazole units in the PCET process. This information is crucial for developing molecular "dry proton wires" with these moieties, which can transfer protons
via
a Grotthuss-type mechanism over long distances without the intervention of water molecules.
Experimental and theoretical methods characterize the thermodynamics of electrochemically driven proton-coupled electron transfer processes in bioinspired constructs involving multiple proton translocations over Grotthus-type proton wires.