Journal ArticleDOI
Adsorption of xanthosine, inosine and 6-azauridine on the dropping mercury electrode☆
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TLDR
In this paper, the capacitance curves of inosine, xanthosine and 6-azauridine at pH 7 were determined by means of B reyer's alternating current polarography.About:
This article is published in Bioelectrochemistry and Bioenergetics.The article was published on 1977-01-01. It has received 24 citations till now. The article focuses on the topics: Xanthosine & Inosine.read more
Citations
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Journal ArticleDOI
Adsorption phenomena in the NAD+/NADH system at glassy carbon electrodes
Jacques Moiroux,Philip J. Elving +1 more
TL;DR: In this paper, a variety of electrochemical approaches have been used to investigate the adsorption of NAD*, NADH and the NAD-NXD dimer from aqueous solution at glassy carbon electrodes (GCE).
Journal ArticleDOI
Mercury Electrodes in Nucleic Acid Electrochemistry: Sensitive Analytical Tools and Probes of DNA Structure. A Review
TL;DR: This review is devoted to applications of mercury electrodes in the electrochemical analysis of nucleic acids and in studies of DNA structure and interactions.
OtherDOI
Electrochemical Analysis of Nucleic Acids
TL;DR: The sections in this article are Adsorption/Desorption Behavior of NA Components, Microanalysis of Nucleic Acid Components by Stripping Techniques, and Relations Between Structures and Electrochemical Responses of DNA.
Journal ArticleDOI
Condensed thymine films at the mercury/water interface
R. Srinivasan,R. de Levie +1 more
TL;DR: In this paper, a condensed thymine film is used to distinguish electron transfer with or without adsorption, i.e., between inner and outer-sphere electrode reactions.
Journal ArticleDOI
Adsorption of 2-thiouracil at the mercury/electrolyte interface
TL;DR: In this paper, the adsorption behavior of 2-thiouracil at the mercury/electrolyte interface was investigated by electrocapillary and capacitance measurements.
References
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Journal ArticleDOI
Studies of inter- and intramolecular interaction in mononucleotides by proton magnetic resonance.
TL;DR: The results conclusively show that these compounds, especially the purines and the purine nucleosides, associate extensively in water primarily by way of vertical stacking of base rings.
Journal ArticleDOI
Interaction and association of bases and nucleosides in aqueous solutions. V. Studies of the association of purine nucleosides by vapor pressure osmometry and by proton magnetic resonance
Journal ArticleDOI
Differentielle kapazität der elektrolytischen doppelschicht in anwesenheit einiger purin- und pyrimidinderivate
Journal ArticleDOI
The interaction of nucleosides in aqueous solution
T.N. Solie,John A. Schellman +1 more
TL;DR: In aqueous solution, in the absence of co-operative macromolecular effects, the dominant forces of interaction between nucleosides result in the parallel stacking of their constituent bases, in accord with current theory which attributes hypochomicity to base stacking.
Journal ArticleDOI
Alternating current polarography of nucleosides
TL;DR: With uridine, thymidine, and cytidine, no association of the adsorbed molecules takes place under the given experimental conditions, even at concentrations approaching saturation value, and most of the nucleosides tested are polarographically non-reducible and the maxima observed on the a.c. c.
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Electrochemical behaviour of mono- and oligonucleotides I. Effects of charge and configuration of adenine mononucleotides on their adsorption at the mercury—solution interface
P. Valenta,H.W. Nürnberg +1 more