ChemInform Abstract: THE EFFECT OF THE DOUBLE LAYER ON THE RATE OF THE IRON(3+) IRON(2+) REACTION ON A PLATINUM ELECTRODE AND THE CONTEMPORARY ELECTRON TRANSFER THEORY

1977 ◽  
Vol 8 (24) ◽  
Author(s):  
Z. SAMEC ◽  
J. WEBER
1991 ◽  
Vol 95 (25) ◽  
pp. 10485-10492 ◽  
Author(s):  
Keisuke Tominaga ◽  
Gilbert C. Walker ◽  
Tai Jong Kang ◽  
Paul F. Barbara ◽  
Teresa Fonseca

1972 ◽  
Vol 50 (2) ◽  
pp. 263-269 ◽  
Author(s):  
W. R. Fawcett ◽  
P. A. Forte ◽  
R. O. Loutfy ◽  
J. M. Prokipcak

The electroreduction of 4- and 5-substituted benzofurazans was investigated at a platinum electrode in acetonitrile. Standard potentials for the reactions were linearly related to the energy of the lowest vacant molecular orbital as estimated by Hückel theory. Standard rate constants for electron transfer decreased as standard potentials in the series became more cathodic. This decrease is attributed to a double layer effect. No correlation was obtained between standard rate constants and observed hyperfine splitting constants for the anion radicals.


Nature ◽  
1988 ◽  
Vol 333 (6169) ◽  
pp. 114-114 ◽  
Author(s):  
Jim Barber

2006 ◽  
Vol 05 (03) ◽  
pp. 685-692 ◽  
Author(s):  
PING HAN ◽  
RUI-XUE XU ◽  
PING CUI ◽  
YAN MO ◽  
GUOZHONG HE ◽  
...  

The effect of solvation on ET rate processes has been investigated on the basis of the exact theory constructed in J. Phys. Chem. B110:11438, 2006. The nature of solvation has been studied in close relation with the mechanism of ET processes. The resulting Kramers' turnover and Marcus' inversion characteristics have been analyzed accordingly. The classical picture of solvation has been found to be invalid when the solvent longitudinal relaxation time is short compared with the inverse temperature.


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