Gould Ian R, Wosinska Zofia M, Farid Samir
Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85287-1604, USA.
Photochem Photobiol. 2006 Jan-Feb;82(1):104-9. doi: 10.1562/2005-06-14-RA-571.
Accurate oxidation potentials for organic compounds are critical for the evaluation of thermodynamic and kinetic properties of their radical cations. Except when using a specialized apparatus, electrochemical oxidation of molecules with reactive radical cations is usually an irreversible process, providing peak potentials, E(p), rather than thermodynamically meaningful oxidation potentials, E(ox). In a previous study on amines with radical cations that underwent rapid decarboxylation, we estimated E(ox) by correcting the E(p) from cyclic voltammetry with rate constants for decarboxylation obtained using laser flash photolysis. Here we use redox equilibration experiments to determine accurate relative oxidation potentials for the same amines. We also describe an extension of these experiments to show how relative oxidation potentials can be obtained in the absence of equilibrium, from a complete kinetic analysis of the reversible redox kinetics. The results provide support for the previous cyclic voltammetry/laser flash photolysis method for determining oxidation potentials.
有机化合物准确的氧化电位对于评估其自由基阳离子的热力学和动力学性质至关重要。除了使用专门的仪器外,具有反应性自由基阳离子的分子的电化学氧化通常是一个不可逆过程,提供的是峰值电位E(p),而不是具有热力学意义的氧化电位E(ox)。在之前一项关于具有快速脱羧的自由基阳离子的胺的研究中,我们通过用激光闪光光解获得的脱羧速率常数校正循环伏安法中的E(p)来估算E(ox)。在此,我们使用氧化还原平衡实验来确定相同胺的准确相对氧化电位。我们还描述了这些实验的扩展,以展示如何在不存在平衡的情况下,通过对可逆氧化还原动力学进行完整的动力学分析来获得相对氧化电位。结果为先前用于确定氧化电位的循环伏安法/激光闪光光解方法提供了支持。