Pregled bibliografske jedinice broj: 255589
Influence of Medium on the Kinetics of Oxidation of Iron(II) Ion with t-Butyl Hydroperoxide
Influence of Medium on the Kinetics of Oxidation of Iron(II) Ion with t-Butyl Hydroperoxide // Chemical Papers, 60 (2006), 4; 253-267 (međunarodna recenzija, članak, znanstveni)
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Naslov
Influence of Medium on the Kinetics of Oxidation of Iron(II) Ion with t-Butyl Hydroperoxide
Autori
Mihaljević, Branka ; Ražem, Dušan
Izvornik
Chemical Papers (0366-6352) 60
(2006), 4;
253-267
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
iron; t-butyl hydroperoxide; non-aqueous solutions; rate constant; oxidation; inner-sphere mechanism
Sažetak
The oxidation of iron(II) with tert-Butyl hydroperoxide was investigated in the absence of oxygen in water, methanol, and the dichloromethane— methanol solvent mixture (φ r = 2 : 1). The oxidation rate depends on solvent polarity ; measured in the presence of SCN– at constant 0.8 mmol dm– 3 of HCl, the rate constant increases with the polarity decrease passing from water and methanol to the dichloromethane— methanol solvent mixture. Further, in non-aqueous solutions at this acid concentration the rate constant was higher than the rate constant in the presence of Cl– only. The oxidation rate measured in the [FeCl]2+ complex in dichloromethane— methanol was slow in acidic medium and increased by decreasing the acid concentration. Approaching the physiological pH conditions the rate constant attained the value of an order of magnitude of 103 dm3 mol– 1 s– 1, while very little alteration of stoichiometry of the oxidation reaction was observed. The rate constant measured in the presence of Cl– strongly depends on electrolyte concentration at concentrations less than 0.5 mmol dm– 3of HCl, both in MeOH and the solvent mixture. Based on these results, a possible mechanism of the influence of solvent, acidity, and ligand type on the rate constant is discussed. We assume that the oxidation proceeds by an inner-sphere mechanism considering that the breakdown of the successor inner-sphere complex forming reactive alkoxyl radicals probably is the rate-limiting step.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
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