Mixed ligand complexes of copper with amino-acids and tartrate using differential pulse polarography. Part I

1992 ◽  
Vol 17 (1) ◽  
pp. 59-62 ◽  
Author(s):  
Hamada M. Killa ◽  
E. S. M. Mabrouk ◽  
M. M. Ghoneim
Polyhedron ◽  
1985 ◽  
Vol 4 (7) ◽  
pp. 1219-1222 ◽  
Author(s):  
H.M. Killa ◽  
M.G.Abd El Wahed ◽  
H.A. Dessouki

1991 ◽  
Vol 56 (6) ◽  
pp. 1193-1199 ◽  
Author(s):  
Hamada M. Killa ◽  
El-Sayed M. Mabrouk ◽  
Mohamed M. Ghoneim

The ternary complexes of Cd(II) with citrate anions as a primary ligand and amino acids (α-alanine and β-alanine) as a secondary ligand have been investigated using differential pulse polarography. Formation of three mixed complexes, [Cd(amino acid)(citrate)2] and [Cd(amino acid)2(citrate)] is observed in each case. The stability constants and the mixing constants of the ternary system have been calculated, as well as the stabilization constants. The electrochemical reduction was reversible and diffusion controlled. The various equilibria involved in the ternary systems are also given.


1983 ◽  
Vol 48 (10) ◽  
pp. 2903-2908 ◽  
Author(s):  
Viktor Vrabec ◽  
Oldřich Vrána ◽  
Vladimír Kleinwächter

A method is described for determining total platinum content in urine, blood plasma and tissues of patients or experimental animals receiving cis-dichlorodiamineplatinum(II). The method is based on drying and combustion of the biological material in a muffle furnace. The product of the combustion is dissolved successively in aqua regia, hydrochloric acid and ethylenediamine. The resulting platinum-ethylenediamine complex yields a catalytic current at a dropping mercury electrode allowing to determine platinum by differential pulse polarography. Platinum levels of c. 50-1 000 ng per ml of the biological fluid or per 0.5 g of a tissue can readily be analyzed with a linear calibration.


1985 ◽  
Vol 50 (3) ◽  
pp. 712-725 ◽  
Author(s):  
Jiří Barek ◽  
Lubomír Kelnar

The polarographic reduction of N,N-dimethyl-4-amino-4'-hydroxyazobenzene in water-methanol medium was investigated. Evidence is presented for adsorption of the depolarizer on the electrode, and a reduction mechanism is proposed. Conditions are indicated for the determination of this compound in the concentration range 10-4-10-6 mol/l by d.c. polarography, 10-5 to 3 . 10-7 mol/l by Tast polarography, and 10-5-3 . 10-8 mol/l by differential pulse polarography.


1986 ◽  
Vol 51 (11) ◽  
pp. 2466-2472 ◽  
Author(s):  
Jiří Barek ◽  
Antonín Berka ◽  
Ludmila Dempírová ◽  
Jiří Zima

Conditions were found for the determination of 6-mercaptopurine (I) and 6-thioguanine (II) by TAST polarography, differential pulse polarography and fast-scan differential pulse voltammetry at a hanging mercury drop electrode. The detection limits were 10-6, 8 . 10-8, and 6 . 10-8 mol l-1, respectively. A further lowering of the detection limit to 2 . 10-8 mol l-1 was attained by preliminary accumulation of the determined substances at the surface of a hanging mercury drop.


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