2005
DOI: 10.1016/j.electacta.2005.04.019
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Electrochemical reductive cleavage of carbon–chlorine bond in 1-chloro-2,4-dinitrobenzene

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Cited by 11 publications
(5 citation statements)
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“…3A) [33]. Moreover, in literature it is suggested that it is a reductive cleavage of the carbon-chlorine bond [34,35]; a further mechanistic discussion can be found in literature [35]. Optimized parameters ended up being the following: potential of deposition (for 60 s) of −0.20 V, electrochemical window from −0.20 to −0.50 V, potential step of 4 mV, potential pulse of 0.12 V with a scan rate of 4 mV s −1 (i.e.…”
Section: Resultsmentioning
confidence: 99%
“…3A) [33]. Moreover, in literature it is suggested that it is a reductive cleavage of the carbon-chlorine bond [34,35]; a further mechanistic discussion can be found in literature [35]. Optimized parameters ended up being the following: potential of deposition (for 60 s) of −0.20 V, electrochemical window from −0.20 to −0.50 V, potential step of 4 mV, potential pulse of 0.12 V with a scan rate of 4 mV s −1 (i.e.…”
Section: Resultsmentioning
confidence: 99%
“…. [33] By solving the above equation using the homotopy perturbation method, the substrate concentration and the current density is derived as given below:…”
Section: Homogeneous System In the Presence Of Excess Amount Of Subst...mentioning
confidence: 99%
“…32 On the other hand, in cyclic voltammetric experiments, the equations for the surface concentration are more involved in view of its dependence on the scan rate. 33 In the case of ultramicroelectrodes, 34 the surface concentrations depend upon the geometry of the electrodes as well as the mechanism under consideration. Hence it follows that explicit equations for surface concentrations pertaining to electrochemical experiments are essential to comprehend reaction mechanism.…”
Section: Mass Balance Equationmentioning
confidence: 99%
“…Reductive cleavage of carbon-halogen bonds is probably the most exhaustively studied DET process and electrochemical methods in particular have emerged as highly sensitive probes of the reaction mechanism. Numerous reports examining and/or applying the reductive cleavage of carbon-halogen bonds appeared in 2005, [62][63][64][65][66][67][68] two of which are selected for illustration.…”
Section: Cyclization Reactionsmentioning
confidence: 99%