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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 881-890 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the oxidation of dimethylsulfoxide by oxohydroxoosmate(VIII) complex ions in alkaline media follow pseudo-first-order disappearance in Os(VIII). The values of the observed pseudo-first-order rate constant are linearly dependent on initial dimethylsulfoxide concentrations in a fortyfold range, and increase with increasing [OH-], leveling off at higher relative [OH-]. The results are interpreted in terms of outer sphere interactions involving dimethylsulfoxide and various species of the Os(VIII) complex. The more nucleophilic dihydroxotetraoxoosmate(VIII) ion reacts about 50 times faster than the trihydroxotrioxoosmate(VIII) species.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 945-958 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of decomposition of “oxohydroxonickel(IV)” [Ni(IV)] with concomitant intramolecular electron transfer to produce hexaaquanickel(II) and dioxygen in aqueous acid solutions show pseudo-first-order dissappearance of the Ni(IV). The pseudo-first-order rate constants for the acid decomposition (kad) satisfy \documentclass{article}\pagestyle{empty}\begin{document}$$k_{{\rm ad}} = k_{\rm d} {\rm K}_{{\rm MH}} [{\rm H}^ +]/(1 + {\rm K}_{{\rm MH}} [{\rm H}^ +])$$\end{document} where KMH and kd refer to the equilibrium protonation constant and the decomposition constant of the protonated species of the Ni(IV) respectively. The values of KMH and kd in aqueous medium at 45°C and μ = 2.0M are 25.5 ± 1M-1 and (1.7 ± 0.1) × 10-5 s-1, respectively.The kinetics of the intermolecular electron transfer from dimethyl sulfoxide (DMSO) to the Ni(IV), producing Ni(H2O)62+ and dimethyl sulfone as products, have been investigated by monitoring the formation of Ni(H2O)62+. The pseudo-first-order rate constants for the electron transfer kobs are linearly dependent on [DMSO]0 or [H+], attaining limiting values at higher relative [DMSO]0 or [H+], in accordance with \documentclass{article}\pagestyle{empty}\begin{document}$$k_{{\rm obs}} = \frac{{[{\rm DMSO}]_0 }}{{1 + K_{{\rm MH}} [{\rm H}^ +]}}\left({\frac{{k_{1{\rm x}} K_{1{\rm c}} }}{{1 + K_{1{\rm c}} [{\rm DMSO}]_0 }} + \frac{{k_{2{\rm x}} K_{2{\rm c}} }}{{1 + K_{2{\rm c}} [{\rm DMSO}]_0 }}} \right)$$\end{document} where K1c and K2c represent the formation constants of the precursors involving DMSO and the unprotonated and one-protonated Ni(IV) species, respectively, and k1x and k2x are the corresponding decomposition rate constants of the precursors. The values of K2c and k2x are (2.3 ± 0.1) × 104M-1 and 19 ± 1 s-1, respectively, at 45°C and μ = 1.0M. Results are interpreted in terms of probable mechanisms involving (1) a rate-determining decomposition of the protonated Ni(IV) followed by rapid product formation steps, and (2) precursor complex formation between DMSO and the unprotonated or the protonated species of the Ni(IV) followed by rate-determining decomposition with electron transfer.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 521-536 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics of the Cu(II) ion-mediated acid decomposition of tris (dimethylglyoximato)nickelate(IV), Ni(dmg)32- (dmg2- = dimethylglyoximate dianion), are reported in aqueous medium in the range of 3.6 ≤ pH ≤ 6.6 at 35°C and μ = 0.57 M. The pseudo-first-order rate constants of the disappearance of Ni(IV) kobs(M) satisfy the equation \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{{\rm obs(M)}} = k_{ad} + k_{dec(M)} $$\end{document} where kad refers to the pseudo-first-order rate constants for the proton-assisted decomposition of the Ni(IV) complex determined independently and is a function of [H+], and kdec(M) to that for the Cu(II) ion-mediated route and is a function of [H+] and [Cu2+]. Both kobs(M) and kdec(M) are found to increase with increasing [Cu(II)]0, tending to attain limiting values at higher relative [Cu(II)]0. At low [Cu(II)]0 the kdec(M) is found to register a decrease with increasing pH in the pH range of 3.6-4.4, then an increase in the range of 4.4-5.76, and again a decrease in the range of 5.76-6.6. Results on the Cu(II) ion-mediated acid decomposition are interpreted in terms of a probable mechanism involving pH-dependent adduct formation equilibria involving the one-protonated and the two-protonated species of Ni(IV) and the various species of Cu(II) ion in the media, followed by rate-determining acid decomposition of the adduct(s) to give Ni(II) aq. and Cu(dmgH)2. While the two-protonated Ni(IV) complex apparently reacts about five orders of magnitude faster than the one-protonated species, the aquacopper(II) reacts about two orders of magnitude slower than the hydroxoaquacopper(II).
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 19 (1987), S. 277-298 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics and mechanism of the cerium(IV) oxidation of Cr(III) complexes of a series of macrocyclic (or pseudomacrocyclic) ligands with [14]-membered intraligand ring-sizes have now been investigated at I = 1.0 M (LiClO4) Temp. 30°C. The complexes of the formulation Cr(macrocycle)(X)(H2O)(3-n)+ where X = CHCl2 and H2O, n = 0 or 1 undergo oxidation to Cr(VI) with the formation of chromium(IV) intermediates. The observed kinetic parameters for the Ce(IV) oxidation of Cr(III) macrocyclic complexes have been discussed in terms of changes brought about by the macrocyclic ligands on the Cr(III) - Cr(IV) redox potentials and in specific rates for Cr(IV) - Cr(V) conversion. On the basis of this study, it has been suggested that the trapping of Cr(IV) is easier when a macrocyclic ligand having a symmetrical intra-ligand ring size and unsaturation in the cyclic structure is coordinated equatorially. Cyclic voltammetric studies indicate the formation of Cr(IV) transient in the case of electrochemical oxidation of trans-Cr(Me4[14]tetraene)(H2O)23+.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 1001-1010 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of oxidation of thiosulfate to tetrathionate by trans-dihydroxotetraoxoosmate(VIII) in aqueous alkaline media have been studied. The oxidation follows a rate expression \documentclass{article}\pagestyle{empty}\begin{document}$$ - \frac{{d[{\rm Os(VIII})]}}{{dt}} = k3{\rm K}_{OS} {\rm K}_2 [{\rm S}_2 {\rm O}_3^{2 - }][{\rm Os(VIII})](1 + {\rm K}_{os} {\rm K}_2 [{\rm S}_2 {\rm O}_3^{2 - }])^{ - 1} $$\end{document} where KOs is the formation constant of trans-dihydroxotetraoxoosmate (VIII), and K2 and k3, respectively, represent the formation constants of the intermediate complex involving Os(VIII) and S2O32- and its decomposition constant. The KOs, K2, and k3 values have been computed to be (19.5 ± 3) dm3/mol, (6.12 ± 0.5) and (3.32 ± 0.3) × 10-1 dm3/mol s at 303 K, and I = 0.32 mol/dm3, respectively. The rate law is consistent with a mechanism envisaging the equilibrium formation of an intermediate complex involving Os(VIII) and S2O32-, followed by a rate-determining decomposition of the complex with concomitant electron transfer.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics and product analyses of the amine exchange reactions of two 2-aminopyridine derived Schiff-base ligands and their monomeric bischelate and dimeric copper(II) complexes have been studied. The Schiff-base ligands investigated underwent amine exchange reactions with n-butyl, cyclohexyl, t-butyl amines. The coordination of the Schiff-base ligands to copper(II) rendered the amine exchange reactions slower. With n-butyl and cyclohexyl amines, parallel first- and second-order terms on their concentrations are observed for the amine exchange reactions of copper(II) bischelates and dimer. The kinetic data favor a mechanism involving a rate-limiting elimination of 2-aminopyridine from a diaminoacetal intermediate in preference to a scheme in which a dissociation of the complexes into free ligands and Cu(II) may precede the amine exchange. The steric factors influence the amine exchange reactions of Cu(II) bischelates with the bulkier amines reacting slower as given by the order t-butylamine (3.3 ± 0.3 × 10-3 dm3/mol·s) 〈 cyclohexylamine (0.2 ± 0.03 dm3/mol·s) 〈 n-butylamine (2.2 ± 0.2 dm3/mol·s). The bulkiness of the t-butyl group and the constraints imposed by the changes in the coordination geometry of Cu(II) on amine exchange not only render the reactions of Cu(II) bischelates slower but also make the formation of the mixed adduct ([N-(5-methyl)-2-pyridyl salicylaldimine][N-t-butyl salicylaldimine] Cu(II)) more favored.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of electron transfer from phenylhydrazine(S) to tris-(dimethylglyoximato) nickelate(IV), Ni(dmg)32- (dmg2- = dimethylglyoximate dianion), have been studied in aqueous medium in the range of 6.21 ≤ pH ≤ 12.2. The kinetics exhibit a pseudo-first-order disappearance of Ni(dmg)32- when excess S is present. The pseudo-first-order rate constants kobs are almost linearly dependent on [S]0 for varying concentrations of the reductant. At constant [S]0, the kobs-pH profile is U shaped. The kobs values register a decrease as the [H+] is increased in the pH range of ∽12.2-9.5, remain almost constant (minimum) in the range of ∽9-8, and then again linearly increase as [H+] is increased in the pH range of ∽7-6.21. Results are interpreted in terms of a probable mechanism involving outer-sphere electron transfer from the phenylhydrazine and phenylhydrazinium cation species to the unprotonated and one-protonated species of the Ni(IV) complex. The reduction rate appears to be dependent on the nature of the species (unprotonated and one-protonated) of the oxidant Ni(IV) complex. The phenylhydrazinium cation reduces the Ni(IV) complex at least one order of magnitude faster than does the neutral reductant species. The major product of the oxidation of phenylhydrazine by the Ni(IV) complex is 4-hydroxyazobenzene with a small amount of phenol.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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