2009
DOI: 10.1016/j.molcata.2009.02.012
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Kinetic studies on the reaction between nickel(II)lactate and peroxomonosulphate ion—The effect of formaldehyde

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Cited by 12 publications
(6 citation statements)
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“…It is well known that aldehydes react with alcohol to give hemiacetals or acetals [41]. Results from this laboratory on the oxidation of Ni(II)-α-hydroxy carboxylates by PMS in the presence of formaldehyde show the formation of a hemiacetal intermediate [42,43]. Therefore, in the present study also the hydroxyl group of the tartarate and the oxo group of the product may react to form a hemiacetaltype intermediate.…”
Section: Discussionmentioning
confidence: 53%
“…It is well known that aldehydes react with alcohol to give hemiacetals or acetals [41]. Results from this laboratory on the oxidation of Ni(II)-α-hydroxy carboxylates by PMS in the presence of formaldehyde show the formation of a hemiacetal intermediate [42,43]. Therefore, in the present study also the hydroxyl group of the tartarate and the oxo group of the product may react to form a hemiacetaltype intermediate.…”
Section: Discussionmentioning
confidence: 53%
“…[5][6][7] Thus it is this weak peroxide linkage (-O-O-) that undergoes cleavage during electron transfer reactions. [8][9][10][11][12][13][14][15] However, such peroxocompounds are exceptionally sensitive to the traces of metal-ions as has been observed in trace metal-ion catalysis in large number of reactions of peroxo acids.…”
Section: 4mentioning
confidence: 99%
“…The catalytic activity and oxidation state of transition metals influence the formation of reactive species such as sulfate radicals. A sulfate radicalbased mechanism was suggested when manganese, cobalt, copper, nickel, and silver transition metals were used [29][30][31][32][33][34], and the same was suggested as one of the most efficient pathways when iron transition metal was used [35].…”
Section: Introductionmentioning
confidence: 99%