Contemporary Issues in Electron Transfer Research

化学 电子转移 分子内力 离域电子 马库斯理论 原子物理学 电子 放松(心理学) 化学物理 振动能量弛豫 反应速率常数 光谱学 分子物理学 物理化学 分子 量子力学 物理 心理学 社会心理学 有机化学 立体化学 动力学
作者
Paul F. Barbara,Thomas J. Meyer,Mark A. Ratner
出处
期刊:The Journal of Physical Chemistry [American Chemical Society]
卷期号:100 (31): 13148-13168 被引量:1559
标识
DOI:10.1021/jp9605663
摘要

This is an overview of some of the important, challenging, and problematic issues in contemporary electron transfer research. After a qualitative discussion of electron transfer, its time and distance scales, energy curves, and basic parabolic energy models are introduced to define the electron transfer process. Application of transition state theory leads to the standard Marcus formulation of electron transfer rate constants. Electron transfer in solution is coupled to solvent polarization effects, and relaxation processes can contribute to and even control electron transfer. The inverted region, in which electron transfer rate constants decrease with increasing exoergicity, is one of the most striking phenomena in electron transfer chemistry. It is predicted by both semiclassical and quantum mechanical models, with the latter appropriate if there are coupled high- or medium-frequency vibrations. The intramolecular reorganizational energy has different contributions from different vibrational modes, which, in favorable cases, can be measured on a mode-by-mode basis by resonance Raman spectroscopy. Alternatively, mode-averaging procedures are available for including multimode contributions based on absorption or emission spectra. Rate constants for intramolecular electron transfer depend on electronic coupling and orbital overlap and, therefore, on distance. Mixed-valence systems have provided an important experimental platform for investigating solvent and structural effects and the transition between localized and delocalized behavior. One of the important developments in electron transfer is the use of absorption and emission measurements to calculate electron transfer rate constants. Ultrafast electron transfer measurements have been used to uncover nonequilibrium relaxation effects, an area that presents special challenges to the understanding of the dynamics and relaxation of the coupled processes. Electron transfer in the gas phase offers substantial insights into the nature of the electron transfer process. Similarly, electron transport in conductive polymers and synthetic metals depends on the basic principles of electron transfer, with some special nuances of their own.
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