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
[71]   KINETICS OF DIABATIC AND ADIABATIC ELECTRON EXCHANGE IN ORGANIC-SYSTEMS COMPARISON OF THEORY AND EXPERIMENT [J].
GRAMPP, G ;
JAENICKE, W .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1991, 95 (08) :904-927
[72]   ESR-SPECTROSCOPIC INVESTIGATION OF THE HOMOGENEOUS ELECTRON-TRANSFER REACTIONS BETWEEN SUBSTITUTED PARA-PHENYLENEDIAMINES AND QUINONEDIIMINES, AND THE VALIDITY OF MARCUS THEORY .1. MEASUREMENTS AT 293 K [J].
GRAMPP, G ;
JAENICKE, W .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1984, 88 (04) :325-334
[73]   SOLVENT DYNAMIC IN ELECTRON-TRANSFER REACTIONS - AN APPLICATION OF KRAMERS THEORY TO HOMOGENEOUS ORGANIC ELECTRON SELF EXCHANGE [J].
GRAMPP, G ;
HARRER, W ;
HETZ, G .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1990, 94 (11) :1343-1348
[74]   THE STABLE STATES PICTURE OF CHEMICAL-REACTIONS .2. RATE CONSTANTS FOR CONDENSED AND GAS-PHASE REACTION MODELS [J].
GROTE, RF ;
HYNES, JT .
JOURNAL OF CHEMICAL PHYSICS, 1980, 73 (06) :2715-2732
[75]   MECHANISMS OF ELECTRON-TRANSFER REACTIONS - THE BRIDGED ACTIVATED COMPLEX [J].
HAIM, A .
PROGRESS IN INORGANIC CHEMISTRY, 1983, 30 :273-357
[76]  
HAIM A, 1983, PROG INORG CHEM, V30, P389
[77]  
HANGGI P, 1990, REV MOD PHYS, V62, P251, DOI 10.1103/RevModPhys.62.251
[78]   ELECTRON EXCHANGE IN THE TETRACYANOQUINODIMETHANE SYSTEM - UNEXPECTED DEPENDENCE ON SOLVENT POLARITY AND VISCOSITY [J].
HARRER, W ;
GRAMPP, G ;
JAENICKE, W .
CHEMICAL PHYSICS LETTERS, 1984, 112 (03) :263-266
[79]   INFLUENCE OF SOLVENT POLARITY ON INTRAMOLECULAR ELECTRON-TRANSFER - A CONSISTENCY TEST OF FREE-ENERGIES OF REACTION AND SOLVENT REORGANIZATION WITH EXPERIMENTAL RATES [J].
HEITELE, H ;
POLLINGER, F ;
WEEREN, S ;
MICHELBEYERLE, ME .
CHEMICAL PHYSICS, 1990, 143 (02) :325-332
[80]   THE INFLUENCE OF DIELECTRIC-RELAXATION ON INTRAMOLECULAR ELECTRON-TRANSFER [J].
HEITELE, H ;
MICHELBEYERLE, ME ;
FINCKH, P .
CHEMICAL PHYSICS LETTERS, 1987, 138 (2-3) :237-243