Abstract

Crystallization under identical conditions from aqueous ethanol solutions of diethanolamine (DEA), o-nitrobenzoic acid (ONBA) and definite metal salt yields 4 different type metal complexes and one organic salt – the monoligand complex of Zn(II) with DEA (1), monoligand complex of Cu(II) with ONBA (2), mixed-ligand complex of Ni(II) with DEA and ONBA (3), supramolecular complex between monoligand complex molecule of Zn(II) with DEA and ONBA (4) and DEA+·ONBA− salt (5). In 1 two meridionally distributed DEA molecules are coordinated by a tridentate mode, 2 is a binuclear copper complex with 4 ONBA molecules which are bidentately coordinated through carboxylate groups. In 3 two DEA and two ONBA molecules are coordinated by bidentate and monodentate fashions, respectively. The compound 4 consists of a complex molecule with two facial distributed tridentate DEA molecules and ONBA ones in an outer sphere. Hence, in coordination compounds 1 and 4 Zn-complex ions with two tridentately coordinated DEA molecules are found in different isomeric forms of which a mer-distribution is recorded for the first time. The maximal enhancement of the ligands antimicrobial activity is observed for the mixed-ligand metal complex. The Zn-complex with mer-distributed ligand molecules demonstrated more antimicrobial activity in contrast to fac-isomer.

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