Direct observation of the kinetic behavior of a charge-transfer reaction on the cation-scavenging reaction for cation radicals of N-vinylcarbazole and N-ethylcarbazole by using a pulse radiolysis technique

1980 ◽  
Vol 84 (22) ◽  
pp. 2876-2879 ◽  
Author(s):  
M. Washio ◽  
S. Tagawa ◽  
Y. Tabata
Keyword(s):  
Charge Transfer ◽  
Direct Observation ◽  
Pulse Radiolysis ◽  
Transfer Reaction ◽  
Charge Transfer Reaction ◽  
Kinetic Behavior ◽  
Cation Radicals ◽  
A Charge

Direct observation of breaking of the intramolecular H-bond, and slowing down of the proton motion and tuning its mechanism in an HBO derivative

2015 ◽  
Vol 17 (22) ◽  
pp. 14569-14581 ◽  
Author(s):  
Noemí Alarcos ◽  
Mario Gutiérrez ◽  
Marta Liras ◽  
Félix Sánchez ◽  
Miquel Moreno ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Steady State ◽  
Direct Observation ◽  
Emission Spectroscopy ◽  
Transfer Reaction ◽  
Dynamical Behavior ◽  
Charge Transfer Reaction ◽  
Slowing Down ◽  
A Charge

Exploring the mechanism of proton motion coupled to a charge-transfer reaction in a new HBO derivative in solution using steady-state and ultrafast emission spectroscopy shows an abnormal spectroscopic and dynamical behavior.

Application of the superposition principle to the study of a charge transfer reaction in cyclic chronopotentiometry. Part II

1996 ◽  
Vol 20 (1) ◽  
pp. 169-181 ◽  
Author(s):  
A. Molina ◽  
J. Gonz�lez ◽  
C. Serna ◽  
L. Camacho
Keyword(s):  
Charge Transfer ◽  
Transfer Reaction ◽  
Superposition Principle ◽  
Charge Transfer Reaction ◽  
A Charge

Electrochemical reactions at PbO2 electrodes. Part II. The exchange reaction at β-PbO2 electrodes

1967 ◽  
Vol 45 (18) ◽  
pp. 2045-2049 ◽  
Author(s):  
N. A. Hampson ◽  
P. C. Jones ◽  
R. F. Phillips
Keyword(s):  
Charge Transfer ◽  
Transfer Reaction ◽  
Adsorbed Layer ◽  
Hydrogen Ion ◽  
Charge Transfer Reaction ◽  
Galvanostatic Polarization ◽  
A Charge ◽  
Charge Transfer Coefficient ◽  
Short Time ◽  
Pbo2 Electrodes

The results of short time galvanostatic polarization experiments are described in which the maximum potential excursion is limited to ± 10 mV about the equilibrium potential.Exchange currents have been evaluated both geometrically and iteratively. The charge transfer reaction [Formula: see text]is slow. The dependence of the exchange current on the concentration of Pb(II) is consistent with a charge transfer coefficient of 0.2 in agreement with the arithmetical analysis of current–potential data.There is evidence for an adsorbed layer of hydrogen ion at the electrode.

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