The kinetics of the reduction of tetraoxoiodate(VII) by n-(2-hydroxylethyl)ethylenediaminetriacetatocobaltate(II) ion in aqueous perchloric acid

The stoichiometries, kinetics and mechanism of the reduction of tetraoxoiodate(VII) ion, IO 4 − to the corresponding trioxoiodate(V) ion, IO 3 − by n -(2-hydroxylethyl)ethylenediaminetriacetatocobaltate(II) ion, [CoHEDTAOH 2 ] − have been studied in aqueous media at 28 °C, I  = 0.50 mol dm −3 (NaClO...

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Veröffentlicht in:Transition metal chemistry (Weinheim) 2009-11, Vol.34 (8), p.849-853
Hauptverfasser: Onu, A. D., Iyun, J. F., Idris, S. O.
Format: Artikel
Sprache:eng
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Zusammenfassung:The stoichiometries, kinetics and mechanism of the reduction of tetraoxoiodate(VII) ion, IO 4 − to the corresponding trioxoiodate(V) ion, IO 3 − by n -(2-hydroxylethyl)ethylenediaminetriacetatocobaltate(II) ion, [CoHEDTAOH 2 ] − have been studied in aqueous media at 28 °C, I  = 0.50 mol dm −3 (NaClO 4 ) and [H + ] = 7.0 × 10 −3  mol dm −3 . The reaction is first order in [Oxidant] and [Reductant], and the rate is inversely dependent on H + concentration in the range 5.00 × 10 −3  ≤ H + ≤ 20.00 × 10 −3  mol dm −3 studied. A plot of acid rate constant versus [H + ] −1 was linear with intercept. The rate law for the reaction is: where a  = 8.0 × 10 −4  s −1 and b  = 8.40 × 10 −3 dm 3  mol −1  s −1 . Positive salt effect was observed from the rate dependence on ionic strength studies, and added ion showed catalysis of reaction rate. An outer-sphere mechanism is proposed for the reaction.
ISSN:0340-4285
1572-901X
DOI:10.1007/s11243-009-9273-1