Özet:

The study of the properties and use of natural metalloporphyrins in the development of new highly selective methods for the oxygenation of hydrocarbons at moderate temperatures is an urgent problem. The present work is devoted to the extraction of metalloporphyrins from oil residues and the creation on their basis of effective catalytic systems for the oxidation of alkenes. The separation of metalloporphyrins from oil residues was carried out using new bifunctional organic extractants having the nature of keto-alcohols and providing a greater degree of extraction of porphyrins in comparison with the known traditionally used extractants. The results of a study of a number of new bifunctional organic reagents as extractants for the selective extraction of oil porphyrins from asphaltenes are presented, their spectral characteristics are studied, the dependence of the degree of extraction on the mass ratio of the extractant and the crude oil is revealed. The best results were obtained with a mass ratio of 1:30. The isolated mixture of metalloporphyrins is first subjected to demetallization with hydrochloric acid (pH=1–2), turning into a mixture of porphyrins, then, to obtain individual metal porphyrin complexes, the required transition metal ions are introduced into the porphyrin ring by treating the mixture with these metal salts. It was shown that the yield of synthesized oil porphyrins is 42–85 %, depending on the nature of the metal. The composition and structure of the synthesized oil metalloporphyrins containing iron, cobalt, nickel, manganese are established by modern methods of physico-chemical analysis. The catalytic properties of synthesized metalloporphyrins in the epoxidation of unsaturated alkenes have been investigated. Their dioxide adducts were obtained, and a mechanism was proposed for the oxidation of alkenes with the formation of oxinoid structures as a result of the decomposition of the oxygen complexes of metal porphyrins

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