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Thermodynamics and kinetics of proton-coupled electron transfer: stepwise vs. concerted pathways

机译:质子耦合电子转移的热力学和动力学:逐步与协调的路径

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摘要

Reactions that involve transfer of an electron and a proton can proceed by stepwise pathways involving initial electron transfer (ET) or initial proton transfer (PT), or by a concerted pathway without an intermediate. The concerted mechanism is termed proton-coupled electron transfer (PCET). Understanding such reactions requires knowledge of the thermodynamics of the possible ET, PT, and PCET steps. Many reactions have a large thermochemical bias favoring the PCET pathway. This bias is often sufficient to rule out stepwise mechanisms. The ΔG °for ET, PT, or PCET has a strong influence on the rate of that step. Using the terminology of Marcus theory, PT and PCET reactions at C-H bonds have higher intrinsic barriers than such reactions at O-H or N-H bonds. The intrinsic barriers to ET and PCET are often similar when there is a small intrinsic barrier to PT. Reactions with a thermochemical bias toward PCET and with similar intrinsic barriers for all the pathways are most likely to occur by concerted PCET.
机译:涉及电子和质子转移的反应可以通过涉及初始电子转移(ET)或初始质子转移(PT)的逐步途径进行,也可以通过没有中间体的一致途径进行。协调的机制称为质子耦合电子转移(PCET)。了解此类反应需要了解可能的ET,PT和PCET步骤的热力学。许多反应具有较大的热化学偏向,有利于PCET途径。这种偏见通常足以排除逐步机制。 ET,PT或PCET的ΔG°对该步骤的速率有很大影响。使用Marcus理论的术语,C-H键上的PT和PCET反应比O-H或N-H键上的此类反应具有更高的固有壁垒。当对PT的内在障碍很小时,对ET和PCET的内在障碍通常是相似的。协调一致的PCET最有可能发生对PCET具有热化学偏向且对所有途径具有相似的内在障碍的反应。

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