An Electrochemical Study on the Copolymer Formed from Piperazine and Aniline Monomers.

A study on the electrochemical oxidation of piperazine and its electrochemical copolymerization with aniline in acidic medium is presented. It was found that the homopolymerization of piperazine cannot be achieved under electrochemical conditions. A combination of electrochemistry, in situ Fourier transform infrared (FTIR), and ex situ X-ray photoelectron spectroscopy (XPS) spectroscopies was used to characterize both the chemical structure and the redox behavior of an electrochemically synthesized piperazine⁻aniline copolymer. The electrochemical sensing properties of the deposited material were also tested against ascorbic acid and dopamine as redox probes.

Improvement of chitosan solubility and bactericidity by synthesis of N-benzimidazole-O-acetyl-chitosan and its electrodeposition.

Chitosan solubility and its antibacterial activity have been improved first of all with a chemical synthesis of N-benzimidazole-O-acetyl-chitosan in acetic medium and foremost through a potentiodynamic electrodeposition of this derivative. An association of one benzimidazole and three acetyl moieties per two units of the biopolymer chain was evidenced by FTIR and 1H NMR, pH-metric titration and TG analysis. Cyclic voltammetry study of the modified polymer in acetonitrile solution reveals its anodic oxidation at a platinum disk and a progressive growing of a thin film, through the cycling of potential. An enhancement of the solubility of the biopolymer as well as its antibacterial activity against Salmonella typhimurium, Escherichia coli, Staphylococcus aureus and Pseudomoenas aeruginosa bacteria have been observed with these chemical and after electrochemical modifications.

Electrochemical and spectral studies of auto-assembled arrays of calix[4]arenequinhydrone charge-transfer complex on indium-tin oxide (ITO) glass.

A sensing materiel based on calix[4]arene molecules is electrochemically deposited on ITO electrode coated. A brown film was electrodeposited at a potential Eimp = -1.00 V versus SCE in acetonitrile solvent, however in dichloromethane solvent, a bluish film auto-assembled on the ITO electrode coated at a potential Eimp = -0.65 V versus SCE. Both films are subsequently analyzed by cyclic voltammetry and UV-Vis spectroscopy. This investigation shows that in acetonitrile solvent, the charge-transfer complex, calix[4]arenequinhydrone was formed in electrolytic solution and it was not self-assembled on the ITO electrode. The related UV-Vis spectrum shows a single absorption band towards a wavelength about 350 nm. The optical behaviour of the blue film shows two absorption bands: the first one appears on the first absorption band of the acceptor at 305 nm and the second one in the visible range at 502 nm. The band situated in the visible range correspond to a well-defined charge-transfer band indicating the presence of the charge-transfer complex, the calix[4]arenequinhydrone.