Abstract
That anions can affect the rate of metal redox reactions has been known for a long time. More often than not, this was caused by formation of complex ions in the solution, thereby completely changing the nature of the reaction, although other causes (electrostatic effects and surface ligand bridging) have also been considered. This general field has been summarized in a review by Weaver.1 Much of the early work was carried out on mercury electrodes, usually with polarographic techniques, reviewed by de Levie.2 The anion concentration and the ratio of anion to reactant concentration were so high in practically all these reports that bulk solution complex formation could not be ignored.
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Nagy, Z. (2004). Trace-Anion Catalysis of Outer-Sphere Heterogeneous Charge-Transfer Reactions. In: White, R.E., Conway, B.E., Vayenas, C.G., Gamboa-Adelco, M.E. (eds) Modern Aspects of Electrochemistry. Modern Aspects of Electrochemistry, vol 37. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-9027-3_5
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