The electrochemical behavior of hexahydropyrimidine (HHP) on a boron-doped diamond electrode was studied. The obtained data were compared with the results of previous studies on the electrooxidation of HHP on platinum and gold electrodes. It was shown that different products can be obtained from one organic substance using different electrode materials.

Studies of the electrochemical behavior of hexahydropyrimidine, 1,5-diazabicyclo[3.1.0]hexane, and 1,3-diaminopropane on a gold electrode via cyclic voltammetry allow us to conclude that gold anodes are subject to corrosion in presence these compounds, yielding complexes that migrate into the solutions and discharge on the counter electrode, producing gold metal deposit. 1,5-Diazabicyclo[3.1.0]hexane is found to form complexes with gold that are much more stable that those formed by hexahydropyrimidine and 1,3-diaminopropane.

Терморасширенный графит, полученный из природного графита в результате термической обработки кислотами, был использован для удаления из водных растворов типичного антибиотика – тетрациклина. Изотерма адсорбции тетрациклина удовлетворительно описывается уравнениями Ленгмюра, Темкина и Фрейндлиха. Изучена кинетика адсорбции тетрациклина на терморасширенном графите.

The electrochemical synthesis of 3,12-dimethyl-7,8,15,16-tetraoxadispiro[5.2.5.2]hexadecane (1,2,4,5-tetraoxane) from 1,1-bis-hydroperoxy-4-methylcyclohexane on platinum electrode in a cell with separated and unseparated cathode and anode space in an aprotic solvent is conducted. The kinetics of electrochemical oxidation of 1,1-bis(hydroperoxy)-4-methylcyclohexane is studied. The current yield of the reaction is determined.

The regularities of AlkNHBr consumption in the reaction of formation of 1,2-dialkyldiaziridines in aqueous media were studied for the first time by UV spectrometry. The rate constants of particular steps of the reaction were estimated starting from the possibility of formation of the precursor of 1,2-dialkyldiaziridine, N -halogenaminal, due to the amination of the intermediate iminium cation along with the parallel halogenation of the intermediate gem -diamine. The quantum chemical calculations (DFT, B3LYP, 6–31++G(d,p) and 3–21G basis sets) were performed for the spatial and electronic structures of the compounds and indices of the local reactivity and global electrophilicity of the key intermediates of the reactions. The results of the calculations allowed us to explain the retardation of the reaction when using EtNHBr instead of MeNHBr.