Electron transfer in a radical ion pair: Quantum calculations of the solvent reorganization energy

被引:13
作者
Caricato, Marco
Ingrosso, Francesca
Mennucci, Benedetta
Sato, Hirofumi
机构
[1] Univ Pisa, Dipartimento Chim & Chim Ind, I-56126 Pisa, Italy
[2] CNRS, UMR 8640 Pasteur, Dept Chim, Ecole Normale Super, F-75231 Paris 05, France
[3] Kyoto Univ, Dept Mol Engn, Kyoto 6158510, Japan
关键词
D O I
10.1021/jp0632586
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Results are presented for an investigation of intermolecular electron transfer ( ET) in solution by means of quantum calculations. The two molecules that are involved in the ET reaction form a solvent-separated radical ion pair. The solvent plays an important role in the ET between the two molecules. In particular, it can give rise to specific solute-solvent interactions with the solutes. An example of specific interactions is the formation of a hydrogen bond between a protic solvent and one of the molecules involved in the ET. We address the study of this system by means of quantum calculations on the solutes immersed in a continuum solvent. However, when the solvent can give rise to hydrogen bond formation with the negatively charged ion after ET, we explicitly consider solvent molecules in the solute cavity, determining the hydrogen bond energetic contribution to the overall interaction energy. Solute-solvent pair distribution functions, showing the different arrangement of solvent molecules before and after ET in the first solvation shell, are reported. We provide results of the solvent reorganization energy from quantum calculations for both the two isolated fragments and the ion pair in solution. Results are in agreement with available experimental data.
引用
收藏
页码:25115 / 25121
页数:7
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