DYNAMIC SOLVENT EFFECTS ON ELECTRON-TRANSFER REACTIONS

被引:271
作者
HEITELE, H
机构
[1] Institut Für Physikalische Und Theoretische Chemie, Technischen Universität München, Garching, D-W-8046
关键词
D O I
10.1002/anie.199303591
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electron-transfer processes in solution are among the most important reactions in chemistry and biology. The huge number of redox reactions of transition metal ions and complexes, many preparatively important oxidations and reductions of organic compounds, photosynthesis, and metabolism are only a few examples where electron-transfer reactions play a pivotal role. This ubiquity, as well as their relative simplicity, makes them excellent models for the study on a molecular level of chemical reactions in solution. A particularly important question in chemical reaction dynamics in solution is the influence of the solvent on the reaction rate. In this context one distinguishes between static and dynamic solvent effects. Static effects refer to the stabilization of reactants, transition state, and products, that is, how the solvent affects the free energies of these species and the energy of activation. This interpretation of solvent effects on all kinds of chemical reactions is well established. A more recent development is the investigation of the influence of solvent dynamics on the rate of a reaction. The transfer of an electron is usually thought to be triggered by a fluctuation of the dielectric polarization in the surrounding solvent. The dynamics of such fluctuations is determined by the finite response time of the orientational polarization of the solvent. Under certain conditions this dielectric response time can become the rate-determining factor of the reaction. In this article I intend to give a review of these modern developments in the theory and experimental study of electron-transfer processes. We shall see that solvent dynamics may lead to a whole plethora of phenomena in reaction dynamics. The concepts needed for their description are not limited to electron transfer but bear relevance to many other chemical reactions in solution.
引用
收藏
页码:359 / 377
页数:19
相关论文
共 224 条
[1]   CHEMICAL-REACTION DYNAMICS IN LIQUID SOLUTION [J].
ADELMAN, SA .
ADVANCES IN CHEMICAL PHYSICS, 1983, 53 :61-223
[2]  
ADELMAN SA, 1980, ADV CHEM PHYS, V44, P143
[3]   TRANSIENT KINETICS OF CHEMICAL-REACTIONS WITH BOUNDED DIFFUSION PERPENDICULAR TO THE REACTION COORDINATE - INTRAMOLECULAR PROCESSES WITH SLOW CONFORMATIONAL-CHANGES [J].
AGMON, N ;
HOPFIELD, JJ .
JOURNAL OF CHEMICAL PHYSICS, 1983, 78 (11) :6947-6959
[4]   TEMPERATURE-DEPENDENCE OF THE INVERTED REGIME ELECTRON-TRANSFER KINETICS OF BETAINE-30 AND THE ROLE OF MOLECULAR-MODES [J].
AKESSON, E ;
JOHNSON, AE ;
LEVINGER, NE ;
WALKER, GC ;
DUBRUIL, TP ;
BARBARA, PF .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (10) :7859-7862
[5]   DYNAMIC SOLVENT EFFECTS ON ELECTRON-TRANSFER RATES IN THE INVERTED REGIME - ULTRAFAST STUDIES ON THE BETAINES [J].
AKESSON, E ;
WALKER, GC ;
BARBARA, PF .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (06) :4188-4194
[6]   ENERGY-GAP DEPENDENCE OF THE CHARGE RECOMBINATION PROCESS OF ION-PAIRS PRODUCED BY EXCITATION OF 2,6,9,10-TETRACYANOANTHRACENE METHYL-SUBSTITUTED BENZENE CHARGE-TRANSFER COMPLEXES IN ACETONITRILE [J].
ASAHI, T ;
MATAGA, N ;
TAKAHASHI, Y ;
MIYASHI, T .
CHEMICAL PHYSICS LETTERS, 1990, 171 (04) :309-313
[7]   FEMTOSECOND PICOSECOND LASER PHOTOLYSIS STUDIES ON THE DYNAMICS OF EXCITED CHARGE-TRANSFER COMPLEXES - AROMATIC HYDROCARBON-ACID ANHYDRIDE, HYDROCARBON-TETRACYANOETHYLENE, AND HYDROCARBON-TETRACYANOQUINODIMETHANE SYSTEMS IN ACETONITRILE SOLUTIONS [J].
ASAHI, T ;
MATAGA, N .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (05) :1956-1963
[8]   ROLE OF NUCLEAR TUNNELING IN AQUEOUS FERROUS FERRIC ELECTRON-TRANSFER [J].
BADER, JS ;
KUHARSKI, RA ;
CHANDLER, D .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (01) :230-236
[9]   DYNAMICS OF ACTIVATIONLESS REACTIONS IN SOLUTION [J].
BAGCHI, B ;
FLEMING, GR .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (01) :9-20