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Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II

[Image: see text] Nature employs a Tyr(Z)-His pair as a redox relay that couples proton transfer to the redox process between P680 and the water oxidizing catalyst in photosystem II. Artificial redox relays composed of different benzimidazole–phenol dyads (benzimidazole models His and phenol models...

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Detalles Bibliográficos
Autores principales: Huynh, Mioy T., Mora, S. Jimena, Villalba, Matias, Tejeda-Ferrari, Marely E., Liddell, Paul A., Cherry, Brian R., Teillout, Anne-Lucie, Machan, Charles W., Kubiak, Clifford P., Gust, Devens, Moore, Thomas A., Hammes-Schiffer, Sharon, Moore, Ana L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445534/
https://www.ncbi.nlm.nih.gov/pubmed/28573198
http://dx.doi.org/10.1021/acscentsci.7b00125
Descripción
Sumario:[Image: see text] Nature employs a Tyr(Z)-His pair as a redox relay that couples proton transfer to the redox process between P680 and the water oxidizing catalyst in photosystem II. Artificial redox relays composed of different benzimidazole–phenol dyads (benzimidazole models His and phenol models Tyr) with substituents designed to simulate the hydrogen bond network surrounding the Tyr(Z)-His pair have been prepared. When the benzimidazole substituents are strong proton acceptors such as primary or tertiary amines, theory predicts that a concerted two proton transfer process associated with the electrochemical oxidation of the phenol will take place. Also, theory predicts a decrease in the redox potential of the phenol by ∼300 mV and a small kinetic isotope effect (KIE). Indeed, electrochemical, spectroelectrochemical, and KIE experimental data are consistent with these predictions. Notably, these results were obtained by using theory to guide the rational design of artificial systems and have implications for managing proton activity to optimize efficiency at energy conversion sites involving water oxidation and reduction.