A study of the reaction of 2-pyridyl isothiocyanate with azoimide

1982 ◽  
Vol 47 (3) ◽  
pp. 877-883 ◽  
Author(s):  
Miroslav Marchalín ◽  
František Považanec ◽  
Augustin Martvoň
Keyword(s):  
Elemental Sulfur ◽  
Ethylenic Bond ◽  
Mechanism Of The Reaction

From the reaction mixture of 2-pyridyl isothiocyanate with azoimide in dioxane 5-(2-pyridyl-amino)tetrzole, 2-pyridylthiourea and elemental sulfur were isolated instead of the expected 5-(2-pyridylamino)-1,2,3,4-thiatriazole. The mechanism of the reaction mentioned was studied on the basis of the synthesis of the assumed intermediates and the isolation of the intermediates by means of compounds with an activated acetylenic or ethylenic bond.

Scanning Electron Microscope Study of Bacteria on Mineral Surfaces

1976 ◽  
Vol 34 ◽  
pp. 130-131
Author(s):  
V.K. Berry
Keyword(s):  
Oxidation Reaction ◽  
Electron Microscope Study ◽  
Elemental Sulfur ◽  
Thiobacillus Ferrooxidans ◽  
Physical Contact ◽  
Metal Sulfides ◽  
Low Grade ◽  
Mineral Surfaces ◽  
Mineral Surface ◽  
Scanning Electron Microscope Study

There are two strains of bacteria viz. Thiobacillus thiooxidansand Thiobacillus ferrooxidanswidely mentioned to play an important role in the leaching process of low-grade ores. Another strain used in this study is a thermophile and is designated Caldariella .These microorganisms are acidophilic chemosynthetic aerobic autotrophs and are capable of oxidizing many metal sulfides and elemental sulfur to sulfates and Fe2+ to Fe3+. The necessity of physical contact or attachment by bacteria to mineral surfaces during oxidation reaction has not been fairly established so far. Temple and Koehler reported that during oxidation of marcasite T. thiooxidanswere found concentrated on mineral surface. Schaeffer, et al. demonstrated that physical contact or attachment is essential for oxidation of sulfur.

Elemental sulfur in Eddy County, New Mexico

Circular ◽  
1970 ◽  
Author(s):  
Jim S. Hinds ◽  
Richard R. Cunningham
Keyword(s):  
New Mexico ◽  
Elemental Sulfur

Identification of Taste and Odour Compounds from Western Lake Ontario

1984 ◽  
Vol 19 (1) ◽  
pp. 111-118 ◽  
Author(s):  
B.G. Brownlee ◽  
D.S. Painter ◽  
R.J. Boone
Keyword(s):  
Water Supply ◽  
Water Samples ◽  
Elemental Sulfur ◽  
Lake Ontario ◽  
Direct Link ◽  
Municipal Water Supply ◽  
Municipal Water ◽  
Western Lake ◽  
Odour Concentration

Abstract During August, 1983 geosmin was identified in a municipal water supply drawn from western Lake Ontario. The geosmin concentrations were 0.01-0.07 μg L-1, within the range for threshold odour concentration of 0.01-0.2 μg L-1. 2-Methylisoborneol was not detected. The odour 'event' coincided with a dieoff of Cladophora in the lake, but we were not able to establish a direct link between the dieoff and geosmin production. Decomposing Cladophora in shoreline areas produced a strong odour in the air. 3-Methylindole, elemental sulfur, dimethyl tetrasulfide, and dimethyl pentasulfide were tentatively identified in water samples collected from these areas, but geosmin and 2-methylisoborneol were not detected.

Acetolysis of 4β-methanesulphonyloxy-6β,7aβ-cyclo-B-homo-5α-cholestane

1979 ◽  
Vol 44 (11) ◽  
pp. 3308-3320 ◽  
Author(s):  
Ladislav Kohout ◽  
Jan Fajkoš
Keyword(s):  
Mechanism Of The Reaction

Synthesis of 4β-methanesulphonyloxy-6β,7aβ-cyclo-B-homo-5α-cholestane is described. During its acetolysis a kind of conjugative stabilization of the carbocation formed was observed. The mechanism of the reaction is discussed.

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.

Kinetics and mechanism of the reaction between oxidized cytochrome c and ascorbic acid

1991 ◽  
Vol 56 (2) ◽  
pp. 478-490 ◽  
Author(s):  
Joaquin F. Perez-Benito ◽  
Conchita Arias
Keyword(s):  
Ascorbic Acid ◽  
Cytochrome C ◽  
Redox Reactions ◽  
Arrhenius Equation ◽  
Horse Heart Cytochrome ◽  
First Order ◽  
Acidic Form ◽  
Ph Range ◽  
Horse Heart Cytochrome C ◽  
Mechanism Of The Reaction

The reaction between horse-heart cytochrome c and ascorbic acid has been investigated in the pH range 5.5 – 7.1 and at 10.0 – 25.0 °C. The rate shows a first-order dependence on the concentration of cytochrome c, it increases in a non-linear way as the concentration of ascorbic acid increases, it increases markedly with increasing pH and, provided that the ionic strength of the medium is high enough, it fulfills the Arrhenius equation. The apparent activation energy increases as the pH of the solution increases. The results have been explained by means of a mechanism that includes the existence of an equilibrium between two forms (acidic and basic) of oxidized cytochrome c: cyt-H+ -Fe3+ + OH- cyt -Fe3+ + H2O, whose equilibrium constant is (6.7 ± 1.4). 108 at 25.0 °C, the acidic form being more reducible than the basic one. It is suggested that there is a linkage of hydrogenascorbate ion to both forms of cytochrome c previous to the redox reactions. Two possibilities for the oxidant-reductant linkage (binding and adsorption) are discussed in detail.

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