McCarthy Brian D, Dempsey Jillian L
Department of Chemistry, University of North Carolina , Chapel Hill, North Carolina 27599-3290, United States.
Inorg Chem. 2017 Feb 6;56(3):1225-1231. doi: 10.1021/acs.inorgchem.6b02325. Epub 2017 Jan 11.
Aqueous potential-pH diagrams, commonly called Pourbaix diagrams, were originally developed to study metal corrosion in the 1930s and 1940s. Pourbaix diagrams have since been widely adopted for use across chemistry disciplines, particularly for the study of aqueous proton-coupled electron transfer reactions. Despite this enormous versatility, a clear extension of analogous diagrams to nonaqueous solvents is lacking. The problem hinges on the difficulty of defining the nonaqueous solution pH. Here, we address this issue by reporting the development of diagrams based on nonaqueous pK scales. We experimentally construct diagrams for two transition-metal complexes that undergo proton-coupled electron transfer reactivity by recording their reduction potentials in the presence of acids with varying pK values. These experimental diagrams validate the potential-pK theory and provide valuable thermochemical information for proton-coupled electron transfer reactions, including for fleetingly stable species.
水相电位-pH图,通常称为Pourbaix图,最初是在20世纪30年代和40年代为研究金属腐蚀而开发的。此后,Pourbaix图已被广泛应用于化学各学科,特别是用于研究水相质子耦合电子转移反应。尽管具有如此广泛的通用性,但缺乏将类似图明确扩展到非水溶剂的情况。问题的关键在于定义非水溶液pH值的困难。在这里,我们通过报告基于非水pK标度的图的开发来解决这个问题。我们通过记录两种过渡金属配合物在不同pK值的酸存在下的还原电位,实验构建了它们的质子耦合电子转移反应图。这些实验图验证了电位-pK理论,并为质子耦合电子转移反应提供了有价值的热化学信息,包括对短暂稳定的物种。