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受光系统II中酪氨酸-组氨酸对启发的模型中的协同单电子双质子转移过程。

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

作者信息

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

机构信息

Department of Chemistry, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, Illinois 61801, United States.

School of Molecular Sciences, Arizona State University, Tempe, Arizona 85287, United States.

出版信息

ACS Cent Sci. 2017 May 24;3(5):372-380. doi: 10.1021/acscentsci.7b00125. Epub 2017 May 9.

Abstract

Nature employs a Tyr-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-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.

摘要

自然界利用酪氨酸 - 组氨酸对作为氧化还原中继体,将质子转移与光系统II中P680和水氧化催化剂之间的氧化还原过程相耦合。已制备出由不同苯并咪唑 - 苯酚二元体(苯并咪唑模拟组氨酸,苯酚模拟酪氨酸)组成的人工氧化还原中继体,其取代基旨在模拟围绕酪氨酸 - 组氨酸对的氢键网络。当苯并咪唑取代基是强质子受体如伯胺或叔胺时,理论预测与苯酚的电化学氧化相关的协同双质子转移过程将会发生。此外,理论预测苯酚的氧化还原电位会降低约300 mV,且动力学同位素效应(KIE)较小。实际上,电化学、光谱电化学和KIE实验数据与这些预测一致。值得注意的是,这些结果是通过利用理论指导人工系统的合理设计而获得的,并且对于在涉及水氧化和还原的能量转换位点管理质子活性以优化效率具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6798/5445534/4f3fc08024e7/oc-2017-001258_0006.jpg

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