The "Presodium" Hydrogen Evolution at the Dropping Mercury Electrode Catalysed by Simple Cysteine Peptides

2001 ◽  
Vol 66 (3) ◽  
pp. 397-410 ◽  
Author(s):  
Pavel Mader ◽  
Věra Veselá ◽  
Vlastimil Dorčák ◽  
Michael Heyrovský

"Presodium" catalytic currents at dropping mercury electrode of cysteine, cysteinylglycine, γ-glutamylcysteine and reduced glutathione were systematically studied in weakly alkaline solutions. They consist in shifts to positive potentials of current due to reduction of the blank solution, and, under some conditions, also in formation of "catalytic prewaves". The two cases have been qualitatively interpreted as based on a suggested common mechanism, differing by the occurrence of weak catalyst adsorption in the prewave case. The catalytic activity depends on the catalyst itself (concentration, structure, conformation at the electrode, partial protonation/ionisation, partial hydrophobic/hydrophilic character) as well as on the solution (pH, ionic strength, nature and concentration of components).

1979 ◽  
Vol 57 (10) ◽  
pp. 1136-1140 ◽  
Author(s):  
Yassein M. Temerk

The adsorption and association of cytidine sulphate have been studied by using phase-sensitive ac-polarography in acidic buffer solution (pH 3.24) at the dropping mercury electrode. At low bulk concentrations, adsorbed molecules of cytidine sulphate at maximal adsorption potential (−0.7 V) are orientated in 'dilute' adsorption layer planar to the electrode surface where the interaction of π-electrons with interface favours adsorption. At bulk concentrations above a threshold value (6.6 × 10−3 M), the stacking interactions between vertically oriented molecules lead to association and formation of a compact layer; and a pit is observed. The concentration dependence of the ac-capacity current at a maximal adsorption potential (−0.7 V) shows a two-step Frumkin isotherm due to association of the adsorbed molecules. The adsorption parameters are computed and discussed.


1987 ◽  
Vol 52 (11) ◽  
pp. 2810-2818 ◽  
Author(s):  
Emil Paleček ◽  
František Jelen ◽  
Vladimír Vetterl

The behaviour of electrochemically reducible single-strand polynucleotides (poly(adenylic acid)) and poly(cytidylic acid)) was studied by the differential (derivative) pulse polarography (DPP) and by other methods. Measurements were performed with the help of the dropping mercury electrode under various conditions specified by the pulse width, pulse amplitude, drop time etc. For the faradaic and tensammetric DPP peaks the diagnostic criteria were proposed which make it possible to classify even very small DPP peaks of double helical polynucleotides.


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.


1983 ◽  
Vol 48 (2) ◽  
pp. 544-549 ◽  
Author(s):  
Jorge Alfredo Bolzan ◽  
Robert Tokoro

The electroreduction of cobalt(II) in aqueous thiocyanate solutions at the dropping mercury electrode depends on the thiocyanate concentration. At [SCN-] = 0.3 mol/l the intermediate cobalt(I)-thiocyanate complex does exist electrokinetically and may be responsible for the appearance of a peaked catalytic wave. The predecessor species of this intermediate may be CoSCN+ and Co(SCN)2 in similarity to the behaviour of cobalt(II) with cyanide and azide ions.


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