The kinetics of electron transfer from phenylhydrazine(S) to tris-(dimethylglyoximato) nickelate(IV), Ni(dmg)i-(dmg2-= dimethylglyoximate dianion), have been studied in aqueous medium in the range of 6.21 I pH I 12.2. The kinetics exhibit a pseudo-first-order disappearance of Ni(dmg)g-when excess S
Studies in nickel(IV) chemistry. Electron transfer kinetics of the reaction between tris(dimethylglyoximato)nickelate(IV) and hexacyanoferrate(II) in aqueous medium
โ Scribed by R. Sahu; G. Neogi; S. Acharya; R. K. Panda
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 534 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
โฆ Synopsis
The kinetics of electron transfer from hexacyanoferrate(I1) to tris(dimethylg1yoximato)nickelate(IV), Ni(dmg)g-, to produce Fe(CN)t-and Ni(dmgH)2, follows a pseudo-first-order disappearance in the Ni(1V). The pseudo-first-order rate constants hob8 are linearly dependent on [Fe(CN);-]o in a fiftyfold range of 2 X 10-4-1 X 10-2M, and the average values of k,bl[Fe(CN){-]o range from 194M-'-s-' at pH = 5.20 to 0.2M-'-s-' at pH = 9.07 in aqueous medium at 35ยฐC and fi = 0.57M. Results are interpreted in terms of a probable mechanism involving rate-determining outer sphere one-electron transfer steps from the reductant and one-protonated reductant species to the unprotonated and one-protonated Ni(1V) species present in solution. The more electrophilic one-protonated reductant species apparently reacts several orders of magnitude faster than the unprotonated one.
๐ SIMILAR VOLUMES
The kinetics of electron transfer in the redox system containing phenylhydrazine (S) and tris(dimethylglyoximato)nickelate(IV), in the presence of catalytic amounts of added CU(&, have been studied in aqueous medium at an ionic strength of 0.25M in the pH range of 6.01-9.06. The kinetics exhibit pse
Kinetics of the Cu(I1) ion-mediated acid decomposition of tris(dimethylg1yoximato)nickelate(IV), Ni(dmg);-(dmg2-= dimethylglyoximate dianion), are reported in aqueous medium in the range of 3.6 < pH < 6.6 a t 35OC and p = 0.57M. The pseudo-first-order rate constants of the disappearance of Ni(1V) (h
The kinetics of decomposition of "oxohydroxonickel(1V)" [Ni(IV)] with concomitant intramolecular electron transfer to produce hexaaquanickel(I1) and dioxygen in aqueous acid solutions show pseudo-first-order disappearance of the Ni(IV). The pseudo-first-order rate constants for the acid decompositio