Sulfanilamide copper(II) chelates with 2-[(2-hydroxyphenyl-imino)methyl]phenolom and 1-[(2-hydroxyphenylimino)-methyl]naphthalen-2-ol

2-[(2-Hydroxyphenylimino)methyl]phenol (H 2 L 1 ) and 1-[(2-hydroxyphenylimino)methyl]naphthalen-2-ol (H 2 L 2 ) reacted with copper(II) acetate hydrate and sulfanilamide (Sf 1 ), sulfathiazole (Sf 2 ), sulfaethidole (Sf 3 ), sulfadiazine (Sf 4 ), and sulfadimidine (Sf 5 ) in ethanol to give mixed-l...

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Bibliographic Details
Published in:Russian journal of general chemistry Vol. 80; no. 7; pp. 1351 - 1354
Main Authors: Gulya, A. P., Tsapkov, V. I., Poirier, D., Aruksandei, K., Pakhontsu, E.
Format: Journal Article
Language:English
Published: Dordrecht SP MAIK Nauka/Interperiodica 01-07-2010
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Summary:2-[(2-Hydroxyphenylimino)methyl]phenol (H 2 L 1 ) and 1-[(2-hydroxyphenylimino)methyl]naphthalen-2-ol (H 2 L 2 ) reacted with copper(II) acetate hydrate and sulfanilamide (Sf 1 ), sulfathiazole (Sf 2 ), sulfaethidole (Sf 3 ), sulfadiazine (Sf 4 ), and sulfadimidine (Sf 5 ) in ethanol to give mixed-ligand copper chelates with the composition Cu(Sf 1–5 )(L 1–2 ) · n H 2 O ( n = 1, 2). All these complexes are monomeric. Salicylaldehyde imines (H 2 L 1 and H 2 L 2 ) behave as doubly deprotonated tridentate O,N,O ligands, whereas sulfanilamides (Sf 1–5 ) are unidentate ligands. Thermolysis of the synthesized complexes includes dehydration at 70–90°C, followed by complete thermal decomposition (290–380°C). The complexes [Cu(Sf 1 )(L 1 )] · 2H 2 O and [Cu(Sf 3 )(L 1 )] · H 2 O at a concentration of 10 −4 M inhibited growth and reproduction of 100% of human myeloid leukemia cells (HL-60). The inhibitory effect was 90 and 75%, respectively, at a concentration of 10 −5 M, whereas no antitumor activity was observed at a concentration of 10 −6 M.
ISSN:1070-3632
1608-3350
DOI:10.1134/S1070363210070224