On the Coherent Description of Diffusion-Influenced Fluorescence Quenching Experiments II: Early Events

被引:30
作者
Angulo, Gonzalo [1 ]
Kattnig, Daniel R. [2 ]
Rosspeintner, Arnulf [2 ]
Grampp, Guenter [2 ]
Vauthey, Eric [3 ]
机构
[1] Polish Acad Sci, Inst Phys Chem, PL-01224 Warsaw, Poland
[2] Graz Univ Technol, Inst Phys & Theoret Chem, A-8010 Graz, Austria
[3] Univ Geneva, Dept Phys Chem, CH-1211 Geneva 4, Switzerland
关键词
diffusion; differential encounter theory; electron transfer; fluorescence; quenching; PHOTOINDUCED ELECTRON-TRANSFER; LONG-RANGE ELECTRON; CHARGE SEPARATION; FREE-ENERGY; DEPENDENCE; KINETICS; MODEL;
D O I
10.1002/chem.200901693
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In a previous article we showed how to perform and analyze steady-state and nanosecond time-resolved experiments on fluorescence quenching by electron transfer in a coherent manner. Now, by making use of a superior time resolution, we explore the first stages of this kind of reaction. The novel information gained enables us to merge the results on the viscosity and the driving-force dependencies of the reaction rate. A unique set of parameters for a single reaction channel suffices to describe all the results in the frame of differential encounter theory for diffusion-influenced, bimolecular, remote electron-transfer reactions. The inclusion of the solvent structure is crucial for the understanding of the reaction kinetics. To the authors' best knowledge, this is the first time that such a comprehensive set of data has been successfully and jointly explained in the field, with physically sound parameters for electron-transfer reactions.
引用
收藏
页码:2291 / 2299
页数:9
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