The reaction of the hexacyanoferrate(III) ion with hydrogen peroxide

1985 ◽  
Vol 63 (4) ◽  
pp. 793-797 ◽  
Author(s):  
Donald R. Eaton ◽  
Marianne Pankratz
Keyword(s):  
Hydrogen Peroxide ◽  
Catalytic Reaction ◽  
Superoxide Radical ◽  
Catalytic Reactions ◽  
Nucleophilic Attack ◽  
Basic Solution ◽  
Cyanide Ligand ◽  
Kinetics Of

In basic solution hydrogen peroxide reduces the hexacyanoferrate(III) ion to the Fe(II) complex. The stoichiometry and kinetics of this reaction have been examined. Both a stoichiometric reduction and a catalytic reaction leading to decomposition of the hydrogen peroxide occur. The latter is largely, but not completely, photochemical in origin. The data are consistent with the involvement of a common intermediate for the stoichiometric and the thermal catalytic reactions. It is suggested that this intermediate is formed by nucleophilic attack of the hydroperoxide ion or the superoxide radical on the carbon of a cyanide ligand.

Highly sensitive in situ monitoring of catalytic reactions by surface enhancement Raman spectroscopy on multifunctional Fe3O4/C/Au NPs

Nanoscale ◽  
2014 ◽  
Vol 6 (14) ◽  
pp. 7954-7958 ◽  
Author(s):  
Wenya Cai ◽  
Xianghu Tang ◽  
Bai Sun ◽  
Liangbao Yang
Keyword(s):  
Magnetic Field ◽  
Raman Spectroscopy ◽  
Catalytic Reaction ◽  
Catalytic Reactions ◽  
In Situ Monitoring ◽  
Au Nps ◽  
Highly Sensitive ◽  
Kinetics Of ◽  
The Magnetic Field

In situ monitoring and characterizing kinetics of catalytic reaction with SERS on multifunctional Fe3O4/C/Au NPs in the magnetic field.

Kinetics of oxidation of ammonia on cobalt catalyst I model of the reactor with catalytically active wall

1982 ◽  
Vol 47 (8) ◽  
pp. 2087-2096 ◽  
Author(s):  
Bohumil Bernauer ◽  
Antonín Šimeček ◽  
Jan Vosolsobě
Keyword(s):  
Parabolic Equations ◽  
Cobalt Catalyst ◽  
Nonlinear Parabolic Equations ◽  
Catalytic Reactions ◽  
Temperature Profiles ◽  
Dimensional Model ◽  
Kinetics Of Oxidation ◽  
Nonlinear Parabolic ◽  
Catalytically Active ◽  
Kinetics Of

A two dimensional model of a tabular reactor with the catalytically active wall has been proposed in which several exothermic catalytic reactions take place. The derived dimensionless equations enable evaluation of concentration and temperature profiles on the surface of the active component. The resulting nonlinear parabolic equations have been solved by the method of orthogonal collocations.

An ESR study of the peroxidase reaction catalyzed by human methaemoglobin and methaemoglobin-haptoglobin complex

1991 ◽  
Vol 56 (4) ◽  
pp. 923-932
Author(s):  
Jana Stejskalová ◽  
Pavel Stopka ◽  
Zdeněk Pavlíček
Keyword(s):  
Hydrogen Peroxide ◽  
Ascorbic Acid ◽  
Amino Acid ◽  
Peroxidase Activity ◽  
Amino Acid Analysis ◽  
Superoxide Radical ◽  
Esr Spectra ◽  
The Other ◽  
Delocalized Electron

The ESR spectra of peroxidase systems of methaemoglobin-ascorbic acid-hydrogen peroxide and methaemoglobin-haptoglobin complex-ascorbic acid-hydrogen peroxide have been measured in the acetate buffer of pH 4.5. For the system with methaemoglobin an asymmetrical signal with g ~ 2 has been observed which is interpreted as the perpendicular region of anisotropic spectrum of superoxide radical. On the other hand, for the system with methaemoglobin-haptoglobin complex the observed signal with g ~ 2 is symmetrical and is interpreted as a signal of delocalized electron. After realization of three repeatedly induced peroxidase processes the ESR signal of the perpendicular part of anisotropic spectrum of superoxide radical is distinctly diminished, whereas the signal of delocalized electron remains practically unchanged. An amino acid analysis of methaemoglobin along with results of the ESR measurements make it possible to derive a hypothesis about the role of haptoglobin in increasing of the peroxidase activity of methaemoglobin.

Kinetics of the Imidazolium Ring-Opening of mRNA 5'-cap Analogs in Aqueous Alkali

2006 ◽  
Vol 71 (4) ◽  
pp. 567-578 ◽  
Author(s):  
Alicja Stachelska ◽  
Zbigniew J. Wieczorek ◽  
Janusz Stępiński ◽  
Marzena Jankowska-Anyszka ◽  
Harri Lönnberg ◽  
...  
Keyword(s):  
Electrostatic Interaction ◽  
Ring Opening ◽  
Nucleophilic Attack ◽  
Amino Groups ◽  
Hydroxide Ion ◽  
Methyl Group ◽  
Structural Modifications ◽  
Alkyl Groups ◽  
Imidazolium Ring ◽  
Kinetics Of

Second-order rate constants for the hydroxide-ion-catalyzed imidazolium ring-opening of several mono- and dinucleosidic analogs of mRNA 5'-cap have been determined. Intramolecular stacking of the two nucleobases in the dinucleosidic analogs, m7GpppN (m7G = 7-methylguanosine, N = 5'-linked nucleoside), and electrostatic interaction between the N-alkylated imidazolium ring and phosphate moiety have been shown to shield the m7G moiety against the nucleophilic attack of hydroxide ion. In addition, the effect of methylation of the nucleobase amino groups and replacement of the 7-methyl group with other alkyl groups have been studied. The influence of all the structural modifications studied turned out to be modest, the cleavage rates of the most and least reactive analogs (with the exception of non-phosphorylated nucleosides) differing only by a factor of 5.

Kinetics of hydrogen peroxide-sulfur(IV) reaction in rainwater collected at a northeastern U.S. site

1986 ◽  
Vol 91 (D12) ◽  
pp. 13264 ◽  
Author(s):  
Y.-N. Lee ◽  
J. Shen ◽  
P. J. Klotz ◽  
S. E. Schwartz ◽  
L. Newman
Keyword(s):  
Hydrogen Peroxide ◽  
Kinetics Of
Sign in / Sign up

Export Citation Format

Share Document