A Kinetic Study of the Electron-Transfer Reaction of the Phthalimide-N-oxyl Radical (PINO) with Ferrocenes

2007 ◽  
Vol 72 (23) ◽  
pp. 8748-8754 ◽  
Author(s):  
Enrico Baciocchi ◽  
Massimo Bietti ◽  
Massimo Di Fusco ◽  
Osvaldo Lanzalunga
Keyword(s):  
Electron Transfer ◽  
Kinetic Study ◽  
Transfer Reaction ◽  
Electron Transfer Reaction

Electron Transfer Reaction of Ion Pairs: 1.  Surfactant Cobalt(III) Complexes by Fe(CN)64− in Microheterogeneous Media

2015 ◽  
Vol 229 (3) ◽  
Author(s):  
Karuppiah Nagaraj ◽  
Krishnan Senthil Murugan ◽  
Pilavadi Thangamuniyandi
Keyword(s):  
Electron Transfer ◽  
Kinetic Study ◽  
Transfer Reaction ◽  
Ion Pairs ◽  
Electron Transfer Reaction ◽  
Single Chain ◽  
Microheterogeneous Media

AbstractThe kinetic study of reduction of single chain surfactant octahedral cobalt(III) complexes,

Relative reactivities of dihydrophenazine and dihydrophenazonium radicals in electron-transfer to an azobenzene

1970 ◽  
Vol 48 (17) ◽  
pp. 2718-2721 ◽  
Author(s):  
Richard L. Reeves
Keyword(s):  
Electron Transfer ◽  
Sulfuric Acid ◽  
Kinetic Study ◽  
Rate Constant ◽  
Transfer Reaction ◽  
Order Rate Constant ◽  
Electron Transfer Reaction ◽  
Second Order ◽  
Aqueous Acetonitrile ◽  
Predominant Species

A kinetic study of the electron-transfer reaction between a model azobenzene and dihydrophenazonium ion-radical and dihydrophenazine was carried out in 0.2 N sulfuric acid in 50 v/v aqueous acetonitrile. The second-order rate constant for the dihydrophenazine is greater than that of the ion-radical by a factor of 104. It is shown that in solutions in which the ion-radical is the predominant species, the principal electron-transfer agent is the dihydrophenazine formed by dismutation of the radical.

scholarly journals Kinetic Study on Induced Electron Transfer Reaction in Pentaamminecobalt(III) Complexes of α-Hydroxy Acids by Pyridinium Fluorochromate in Micellar Medium

2011 ◽  
Vol 8 (3) ◽  
pp. 1102-1107
Author(s):  
B. Mohammed Nawaz ◽  
K. Subramani ◽  
Mansur Ahmed
Keyword(s):  
Electron Transfer ◽  
Kinetic Study ◽  
Carbonyl Compounds ◽  
Transfer Reaction ◽  
Electron Transfer Reaction ◽  
Micellar Medium ◽  
Hydroxy Acids ◽  
Uv Visible ◽  
Pyridinium Fluorochromate

Pyridinium fluorochromate (PFC) oxidation of pentaamminecobalt(III) complexes of α-hydroxy acids in micellar medium yielding nearly 100% of carbonyl compounds are ultimate products. The decrease in UV-visible absorbance at λ=502 nm for Co(III) complex corresponds to nearly 100% of the initial absorbance. The stoichiometry of unbound ligand and cobalt(III) complex is accounting for about 100% reduction at the cobalt(III) centre. The kinetic and stoichiometric results have been accounted by a suitable mechanism.

scholarly journals Electron transfer studies of a conventional redox probe in human sweat and saliva bio-mimicking conditions

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
P. Krishnaveni ◽  
V. Ganesh
Keyword(s):  
Electron Transfer ◽  
Crystalline Phase ◽  
Liquid Crystalline ◽  
Transfer Reaction ◽  
Electron Transfer Reaction ◽  
Redox Couple ◽  
Liquid Crystalline Phase ◽  
Transfer Reactions ◽  
Redox Probe ◽  
Human Sweat

AbstractModern day hospital treatments aim at developing electrochemical biosensors for early diagnosis of diseases using unconventional human bio-fluids like sweat and saliva by monitoring the electron transfer reactions of target analytes. Such kinds of health care diagnostics primarily avoid the usage of human blood and urine samples. In this context, here we have investigated the electron transfer reaction of a well-known and commonly used redox probe namely, potassium ferro/ferri cyanide by employing artificially simulated bio-mimics of human sweat and saliva as unconventional electrolytes. Typically, electron transfer characteristics of the redox couple, [Fe(CN)6]3−/4− are investigated using electrochemical techniques like cyclic voltammetry and electrochemical impedance spectroscopy. Many different kinetic parameters are determined and compared with the conventional system. In addition, such electron transfer reactions have also been studied using a lyotropic liquid crystalline phase comprising of Triton X-100 and water in which the aqueous phase is replaced with either human sweat or saliva bio-mimics. From these studies, we find out the electron transfer reaction of [Fe(CN)6]3−/4− redox couple is completely diffusion controlled on both Au and Pt disc shaped electrodes in presence of sweat and saliva bio-mimic solutions. Moreover, the reaction is partially blocked by the presence of lyotropic liquid crystalline phase consisting of sweat and saliva bio-mimics indicating the predominant charge transfer controlled process for the redox probe. However, the rate constant values associated with the electron transfer reaction are drastically reduced in presence of liquid crystalline phase. These studies are essentially carried out to assess the effect of sweat and saliva on the electrochemistry of Fe2+/3+ redox couple.

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