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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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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
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author 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.
author_facet 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.
author_sort Huynh, Mioy T.
collection PubMed
description [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.
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spelling pubmed-54455342017-06-01 Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II 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. ACS Cent Sci [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. American Chemical Society 2017-05-09 2017-05-24 /pmc/articles/PMC5445534/ /pubmed/28573198 http://dx.doi.org/10.1021/acscentsci.7b00125 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle 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.
Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II
title Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II
title_full Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II
title_fullStr Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II
title_full_unstemmed Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II
title_short Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II
title_sort concerted one-electron two-proton transfer processes in models inspired by the tyr-his couple of photosystem ii
url 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
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