Conditions of acylation of aminotetraphenylporphyrins in the presence of carbodiimides were studied. Optimal reaction conditions were determined and a number of tetraphenylporphyrin amides of various structure were synthesized.
KOH aqueous solution was carried out by cyclic voltammetry (CV). The potential ranges of oxidation-reduction processes related to the transformations of the porphyrin macrocycle, pyridyl moiety and central metal ion 15-бис(пирид-4-ил)-3,7,13,17-тетраметил-2,8,12,18-тетраэтилпорфин
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