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Coordination interactions of alkyl-substituted 2,2′-dipyrrolylmethene derivatives with copper(II) aminoacid complexes

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Abstract

Using the method of electron spectroscopy we showed that reaction of alkyl-substituted 2,2′-dipyrrolylmethene derivatives with copper(II) aminoacid complexes led to the formation of heteroligand complexes with two chelated metallocycles forming their coordination sphere. Formation constants of the heteroligand complexes were established and their interrelations with the structure of the aminoacid residue side group were elucidated. It was found that alongside the ability to the primary solvolytic dissociation of aminoacid complex, the main effect on the formation of combined coordination sphere of the chelate is defined by the steric factor depending on the structure of substituent in the aminoacid.

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Correspondence to E. V. Rumyantsev.

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Original Russian Text © E.V. Rumyantsev, I.E. Kolpakov, Yu.S. Marfin, E.V. Antina, 2009, published in Zhurnal Obshchei Khimii, 2009, Vol. 79, No. 3, pp. 493–497.

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Rumyantsev, E.V., Kolpakov, I.E., Marfin, Y.S. et al. Coordination interactions of alkyl-substituted 2,2′-dipyrrolylmethene derivatives with copper(II) aminoacid complexes. Russ J Gen Chem 79, 482–487 (2009). https://doi.org/10.1134/S1070363209030232

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  • DOI: https://doi.org/10.1134/S1070363209030232

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