Effect of Copper on the Oxidation Mechanisms of Tertiary and Secondary Amines of Methyl-naphthyl- cyclen-Modified Gold Electrodes

Tetraazamacrocycle such as 1,4,7,10-tetraazacyclododecane cyclen are known for efficient complexation of metallic ions and were used as an ionic recognition agents in chemical sensors in aqueous medium.The aim of this paper is to examine in more detail the oxidation mechanism of amines in cyclen before copper complexation and after copper complexation. Gold electrodes modified with mono-N-MNCyclen(mono methyl-naphtyl-cyclen) and tetra-N-MNCyclen thin films were obtained by deposition of mono-N-MNCyclen and the tetra-N-MNCyclensynthesized respectively by bisaminal route in three steps (protection, N-mono-alkylation and deprotection) and direct route. The comparative study of the electrochemical oxidation of amines in both cyclens allowed the identification of the tertiary and of the secondary amines. From the potential-pH relation and the variation of the intensities of the oxidation peaks, the redox mechanisms of both types of amines was proposed. The electrochemical redox behaviour of the amines in the copper-mono-N-MNCyclen complex was studied. From the potential-pH relation and the variation of the intensities of the oxidation peaks, the redox mechanisms of amines and the structure of the copper-mono-N-MNCyclen complex were proposed. The intensities of the oxidation peaks of the amines vary linearly with the copper concentration, in the range 10(-12) M to 10(-6) M, leading to a detection limit of of 1 pM of Cu2+.

Automated summary

The oxidation mechanism of amines in cyclen before and after copper complexation was examined in this study. Thin films of mono-N-MNCyclen and tetra-N-MNCyclen were deposited on gold electrodes, allowing for the identification of tertiary and secondary amines. The redox behavior of amines in the copper-mono-N-MNCyclen complex was studied, with a detection limit of 1 pM of Cu2+.