ChemInform Abstract: KINETICS AND MECHANISM OF THE OXIDATION OF L-ASCORBIC ACID BY TRIS(OXOLATO)COBALTATE(III) AND TRIS(1,10-PHENANTHROLINE)IRON(III) COMPLEXES IN AQUEOUS SOLUTION

1982 ◽  
Vol 13 (20) ◽  
Author(s):  
M. KIMURA ◽  
M. YAMAMOTO ◽  
S. YAMABE
Keyword(s):  
Aqueous Solution ◽  
Ascorbic Acid ◽  
Kinetics And Mechanism

Kinetics and mechanism of the Co(II)-assisted oxidation of l-ascorbic acid by dioxygen and nitrite in aqueous solution

2009 ◽  
pp. 10541 ◽  
Author(s):  
Elena A. Vlasova ◽  
Natalya Hessenauer-Ilicheva ◽  
Denis S. Salnikov ◽  
Evgeny V. Kudrik ◽  
Sergei V. Makarov ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Ascorbic Acid ◽  
Kinetics And Mechanism

Kinetics and mechanism of the reduction of (ImH)[trans-RuCl4(dmso)(Im)] by ascorbic acid in acidic aqueous solution

2007 ◽  
Vol 12 (6) ◽  
pp. 809-818 ◽  
Author(s):  
Malgorzata Brindell ◽  
Dorota Piotrowska ◽  
Azza A. Shoukry ◽  
Grażyna Stochel ◽  
Rudi van Eldik
Keyword(s):  
Aqueous Solution ◽  
Ascorbic Acid ◽  
Kinetics And Mechanism ◽  
Acidic Aqueous Solution

Kinetics and mechanism of the reaction of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione

1990 ◽  
Vol 55 (8) ◽  
pp. 1984-1990 ◽  
Author(s):  
José M. Hernando ◽  
Olimpio Montero ◽  
Carlos Blanco
Keyword(s):  
Aqueous Solution ◽  
Metal Ion ◽  
Activation Parameters ◽  
Enol Form ◽  
Kinetics And Mechanism ◽  
Kinetic Constants ◽  
Steric Factors ◽  
Kinetics Of ◽  
Mechanism Of The Reaction

The kinetics of the reactions of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione to form the corresponding monocomplexes have been studied spectrophotometrically in the range 5 °C to 16 °C at I 25 mol l-1 in aqueous solution. In the proposed mechanism for the two complexes, the enol form reacts with the metal ion by parallel acid-independent and inverse-acid paths. The kinetic constants for both pathways have been calculated at five temperatures. Activation parameters have also been calculated. The results are consistent with an associative activation for Fe(H2O)63+ and dissociative activation for Fe(H2O)5(OH)2+. The differences in the results for the complexes of heptanediones studied are interpreted in terms of steric factors.

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