scholarly journals Studies on a Furane Analogue of Malachite Green. Protolytic Equilibria and Reaction Rate Constants of Furane Green in Aqueous Solutions.

1963 ◽  
Vol 17 ◽  
pp. 2091-2100 ◽  
Author(s):  
Rune Cigén ◽  
Gösta Bengtsson ◽  
Olof Theander ◽  
Akikazu Hatanaka ◽  
Jon Munch-Petersen
1962 ◽  
Vol 16 ◽  
pp. 1837-1848 ◽  
Author(s):  
Rune Cigén ◽  
Gösta Bengtsson ◽  
Svend Erik Rasmussen ◽  
A. Block-Bolten ◽  
J. M. Toguri ◽  
...  

1961 ◽  
Vol 15 ◽  
pp. 1905-1912 ◽  
Author(s):  
Rune Cigén ◽  
Jannik Bjerrum ◽  
Ole Buchardt ◽  
Gert E. Olsen ◽  
Christian Pedersen ◽  
...  

1962 ◽  
Vol 16 ◽  
pp. 192-204 ◽  
Author(s):  
Rune Cigén ◽  
Pinchas Moses ◽  
C. Krohn ◽  
K. Motzfeldt ◽  
Olof Theander ◽  
...  

1990 ◽  
Vol 68 (8) ◽  
pp. 1376-1382 ◽  
Author(s):  
Manohar Lal ◽  
H. S. Mahal

Reaction rate constants of thiyl radicals with phenothiazines, promethazine (PMZ), chlorpromazine (CPZ), prochlorperazine (PPZ), trimeperazine tarterate (TPZ), and other antioxidants, e.g., ascorbic acid and 2,2-azinobis(3-ethyl benzthiazoline-6 sulphonate) (ABTS) have been estimated using pulse radiolysis technique. In general they are quite high (108–109 M−1 s−1). The k values for cysteine, cysteamine, mercaptoethanol, and mercaptopropionic acid with similar structures and molecular weights are more or less similar for PMZ, CPZ, and PPZ.Rate constants are lower in value for [Formula: see text] radicals of phenothiazines showing that they are dependent upon the structure and the molecular weight of the compound.Rate constants are the same whether the thiyl radicals are generated from thiols or their corresponding disulphides. The k values for chlorine-containing phenothiazines, chlorpromazine, and prochlorperazine are higher than those of promothazine Keywords: pulse radiolysis, thiyl radicals, phenothiazines, ABTS, ascorbic acid.


2019 ◽  
Vol 44 (4) ◽  
pp. 300-306
Author(s):  
Joanna Drzeżdżon ◽  
Agnieszka Piotrowska-Kirschling ◽  
Lech Chmurzyński ◽  
Dagmara Jacewicz

The kinetics of the aquation reaction of the [VO(ida)(bipy)]·2H2O (VO(ida)(bipy)) complex (where ida = iminodiacetate anion and bipy = 2,2’-bipyridine) promoted by [Fe(H2O)6]3+ ions were investigated in aqueous solutions. Spectrophotometric studies were carried out at different temperatures in the range of 293.15–313.15 K. The concentration of the [Fe(H2O)6]3+ (Fe3+) ions was kept within the range of 2 × 10–4 to 8 × 10–4 mol L–1, and the concentration of VO(ida)(bipy) was 1 × 10–3 mol L–1. The values of the observable reaction rate constants were calculated based on the Glint computer program. Furthermore, the mechanism for the aquation of VO(ida)(bipy), induced by Fe(III) ions, has been proposed.


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