Ilya Kuzmin

A new water-soluble sulfonated cobalt(II) phthalocyanines: Synthesis, spectral, coordination and catalytic properties

Novel complexes of cobalt(II) with sulfonated derivatives of phthalocyanines are synthesized. The influence of the sulfonated groups number in peripheral substituent on solubility of macrocycle and ability to form ordered structures in solution is showed. Transition from H-aggregates to monomeric phthalocyanine structures and sandwich-type dimers was found during formation of metallophthalocyanine complexes with 1,4-diazabicyclo(2.2.2)octane. The catalytic activity of metallophthalocyanines was studied on the model of Merox process.

Novel aqueous soluble cobalt(II) phthalocyanines of tetracarboxyl-substituted: Synthesis and catalytic activity on oxidation of sodium diethyldithiocarbamate

Enhancement of the catalytic activity of phthalocyanine catalysts by immobilizing them on polymer matrix has been studied. It has been found that the immobilization of cobalt(II) phthalocyanines on polymers enhances their catalytic activity in the oxidation of sodium diethyldithiocarbamate by air oxygen under mild conditions.

Self-Association of Sulfo Derivatives of Cobalt Phthalocyanine in Aqueous Solution

Sulfo derivatives of cobalt phthalocyanine containing naphthalene fragments have been synthesized, and their self-association and molecular complexation with pyridine in aqueous solution have been studied by spectrophotometry. The dissociation constants of the dimeric associates have been determined. The effects of the number of functional groups in the peripheral substituents and of the axial ligand on the phthalocyanine dimerization process have been revealed.

Kinetics and mechanism of the oxidation of dithiocarbamic acids in the presence of Co(II) phthalocyaninetetacarboxylic acid

The present work contains kinetic data of the oxidation of sodium diethyldithiocarbamate in the presence of phthalocyanine catalysts. It is shown that the nature of the peripheral substituent has a great influence on the self- - association of phthalocyanines and on their catalytic activity. A mechanism of the oxidation of sodium diethyldithiocarbamate involving the formation of a triple complex of the substrate, the reduced form of the catalyst and oxygen is offered. It is also shown that the oxidation mechanism of dithiocarbamic acids is different from that for cysteine.

Symmetrical and difunctional substituted cobalt phthalocyanines with benzoic acids fragments: Synthesis and catalytic activity

Difunctional and symmetric phthalonitriles were synthesized by nucleophilic substitution of brome and nitro-group in 4-bromo-5-nitro-phthalonitrile for residues 4-amino-, 4-hydroxyl- and 4-sulfanyl benzoic acid. Symmetrical and difunctional substituted cobalt phthalocyanines were obtained by template synthesis based on mentioned phthalonitriles. Their spectral properties and catalytic activity in aerobic oxidation of sodium N,N-carbomoditiolate were investigated.

Catalytic properties of cobalt complexes with tetrapyrazino porphyrazine and phthalocyanine derivatives

The catalytic activity of cobalt complexes with octaphenyltetrapyrazinoporphyrazine and phthalocyanine derivatives containing branched peripheral substituents is studied in heterogeneous catalysis of the oxidation of sodium diethyldithiocarbamate (SDC) with atmospheric oxygen. Cobalt phthalocyanines are shown to display higher catalytic activity than cobalt complexes with octaphenyltetrapyrazinoporphyrazine. The highest efficiency of heterogeneous catalysts is attained at temperatures of 298–303 K.

Sulfonated Co(II) phthalocyanines covalently anchored at organic polymers as catalyst for mild oxidation of mercaptans

Current work is devoted to covalent immobilization of sulfonated derivatives of cobalt phthalocyanines “Merox catalysts” on the surfaces of polypropylene and polyethylene terephthalate. Their catalytic activity in reaction of mild oxidation of sulfur compounds to disulfides with oxygen of the air was studied. Anchoring of the catalyst on this polymer prevents its leaching and promotes its efficient recovering and recycling without significant loss of catalytic activity.