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Oxidation of 1,4-dioxane (Dio) by a copper(III) periodate complex (DPC) has been investigated spectrophotometrically both in the absence and presence of a ruthenium(III) catalyst in aqueous alkaline medium at 298 K. Stoichiometry of (1 : 8) was observed in both the reactions and the order of the reaction with respect to [DPC] was unity while the order with respect to [Dio] was <1 over the concentration range studied. Order with respect to [OH−] and [IO4−] had negative order in both cases. Order with respect to [Ru(III)] was unity. The activation parameters (ΔH# = 38 ± 2 kJ mol−1, ΔS# = −164 ± 15 J K−1 mol−1 and ΔG# = 87 ± 4 for uncatalyzed and ΔH# = 34 ± 3 kJ mol−1, ΔS# = −43 ± 2 J K−1 mol−1 and ΔG# = 47 ± 3 for catalyzed reaction) with respect to the slow step of the proposed mechanism were computed and thermodynamic quantities were also calculated. Kinetic studies suggest that [Cu(OH)2(H3IO6)]− is the reactive copper(III) species and [Ru(H2O)5(OH)]2+ is the reactive Ru(III) species.
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Naik et al. (2011) studied this question.
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