Solvent nuclear quantum effects in electron transfer reactions. III. Metal ions in water. Solute size and ligand effects

2001 ◽  
Vol 114 (21) ◽  
pp. 9470-9477 ◽  
Author(s):  
Koji Ando
1997 ◽  
Vol 220 (1-2) ◽  
pp. 95-114 ◽  
Author(s):  
M.T.M. Koper ◽  
J.-H. Mohr ◽  
W. Schmickler

2003 ◽  
Vol 75 (5) ◽  
pp. 577-587 ◽  
Author(s):  
Shunichi Fukuzumi

Catalytic control of electron-transfer processes is described for a number of photoinduced and thermal electron-transfer reactions, including back electron transfer in the charge-separated state of artificial photosynthetic compounds. The intermolecular and intramolecular electron-transfer processes are accelerated by complexation of radical anions, produced in the electron transfer, with metal ions that act as Lewis acids. Quantitative measures to determine the Lewis acidity of a variety of metal ions are given in relation with the promoting effects of metal ions in the electron-transfer reactions. The mechanistic viability of metal ion catalysis in electron-transfer reactions is demonstrated by a variety of examples of both thermal and photochemical reactions that involve metal ion-promoted electron-transfer processes as the rate-determining steps, which are made possible to proceed by complexation of radical anions with metal ions.


Sign in / Sign up

Export Citation Format

Share Document