Savéant Jean-Michel
Laboratoire d'Electrochimie Moléculaire, Unité Mixte de Recherche, Université Paris Diderot, Sorbonne Paris Cité, CNRS 7591, 75205 Paris Cedex 13, France; email:
Annu Rev Anal Chem (Palo Alto Calif). 2014;7:537-60. doi: 10.1146/annurev-anchem-071213-020315.
Proton-coupled electron transfers (PCET) are ubiquitous in natural and synthetic processes. This review focuses on reactions where the two events are concerted. Semiclassical models of such reactions allow their kinetic characterization through activation versus driving force relationships, estimates of reorganization energies, effects of the nature of the proton acceptor, and H/D kinetic isotope effect as well as their discrimination from stepwise pathways. Several homogeneous reactions (through stopped-flow and laser flash-quench techniques) and electrochemical processes are discussed in this framework. Once the way has been rid of the improper notion of pH-dependent driving force, water appears as a remarkable proton acceptor in terms of reorganization energy and pre-exponential factor, thanks to its H-bonded and H-bonding properties, similarly to purposely synthesized "H-bond train" molecules. The most recent developments are in modeling and description of emblematic concerted proton-electron transfer (CPET) reactions associated with the breaking of a heavy-atom bond in an all-concerted process.
质子耦合电子转移(PCET)在自然和合成过程中普遍存在。本综述聚焦于两个事件协同发生的反应。此类反应的半经典模型可通过活化与驱动力关系、重组能估计、质子受体性质的影响、H/D动力学同位素效应以及与分步途径的区分来对其进行动力学表征。在此框架下讨论了若干均相反应(通过停流和激光闪光淬灭技术)以及电化学过程。一旦摒弃了pH依赖驱动力这一不当概念,水因其氢键和形成氢键的性质,在重组能和指前因子方面表现为一种显著的质子受体,这与特意合成的“氢键链”分子类似。最新进展在于对标志性协同质子 - 电子转移(CPET)反应的建模和描述,这些反应涉及在全协同过程中重原子键的断裂。