Influence of Proton Acceptors on the Proton-Coupled Electron Transfer Reaction Kinetics of a Ruthenium–Tyrosine Complex

2017 ◽  
Vol 121 (46) ◽  
pp. 10530-10542 ◽  
Author(s):  
J. Christian Lennox ◽  
Jillian L. Dempsey
Keyword(s):  
Electron Transfer ◽  
Reaction Kinetics ◽  
Transfer Reaction ◽  
Electron Transfer Reaction ◽  
Proton Coupled Electron Transfer ◽  
Kinetics Of

Kinetics of chain reaction driven by proton-coupled electron transfer: α-hydroxyethyl radical and bromoacetate in buffered aqueous solutions

2021 ◽  
Author(s):  
Igor Sviben ◽  
Iva Džeba ◽  
Marija Bonifačić ◽  
Ivan Ljubić
Keyword(s):  
Electron Transfer ◽  
Aqueous Solutions ◽  
Transfer Reaction ◽  
Electron Transfer Reaction ◽  
Chain Reaction ◽  
Proton Coupled Electron Transfer ◽  
Kinetics Of

The calculations unravel the role of buffers in the kinetics of the proton-coupled electron transfer reaction between α-hydroxyethyl radical and bromoacetate.

Kinetics of Electron Transfer Reaction between Co(II) and Chlorate Ions: Experimental and Modeling Study

2021 ◽  
Vol 43 (5) ◽  
pp. 559-559
Author(s):  
Mahwish Mobeen Khan and Syed Mumtaz Danish Naqvi Mahwish Mobeen Khan and Syed Mumtaz Danish Naqvi
Keyword(s):  
Electron Transfer ◽  
Transfer Reaction ◽  
High Energy ◽  
Electron Transfer Reaction ◽  
Maximum Likelihood Estimates ◽  
Oxidation Catalyst ◽  
Standard Entropy ◽  
Rate Of Reaction ◽  
Kinetics Of ◽  
Activated Complex

This research article reports original experimental and modeling detail of kinetics of the electron transfer reaction between Co(II) and chlorate ions in acetic acid solution. Design of experiment methodology has been employed to elucidate the effects of temperature and initial concentrations of reactants on the rate of reaction. Levenberg-Marquardt method has been used to fit processed kinetic data (temperatures, initial concentrations of reactants, and concentrations and rates of production of Co(III)) on to various possible rate equations. This algorithm provides a proficient mean for compensating the capricious effects of the experimental process variables and results in the maximum likelihood estimates of the kinetic parameters. The most significant rate law has been selected, on the basis of statistical analyses of the residuals between the predicted and experimental rates. The analyses suggest that the intrinsic rate of reaction is proportional to first power of chlorate concentration but for Co(II) the order is fractional (0.7455 ≈ and#190;). The effect of temperature on the observed rate constant (precision = 0.02 %) is excellently described by the Arrhenius and Eyring equations and the sluggish nature of the reaction is clearly manifested by the high energy (andgt; 93 kJ/mol), negative entropy (-28.5286 J/mol-K) and very small equilibrium constant of activation. Further fairly negative standard entropy of activation shows there is usually considerable rearrangement of energy among various degrees of freedom during the formation of activated complex and proposes an associative mechanism for formation of the activated complex. This research is performed to develop a kinetic model for the electron transfer reaction between Co(II) and chlorate ion. As a result, a redox couple of Co(II)/Co(III) has been formed which is used as a potent oxidation catalyst in chemical industries.

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