Synthesis, structural characterization, antimicrobial and cytotoxic effects of aziridine, 2-aminoethylaziridine and azirine complexes of copper(II) and palladium(II).

摘要

The synthesis, spectroscopic and X-ray structural characterization of copper(II) and palladium(II)complexes with aziridine ligands as 2-dimethylaziridine HNCH2CMe2 (a), the bidentate N-(2-aminoethyl)aziridines C2H4NC2H4NH2 (b) or CH2CMe2NCH2CMe2NH2 (c) as well as the unsaturatedazirine NCH2CPh (d) are reported. Cleavage of the cyclometallated Pd(II) dimer [μ-Cl(C6H4CHMeNMe2-C,N)Pd]2 with ligand a yielded compound [Cl(NHCH2CMe2)(C6H4CHMe2NMe2-C,N)Pd] (1a). Thereaction of the aziridine complex trans-[Cl2Pd(HNC2H4)2] with an excess of aziridine in the presence ofAgOTf gave the ionic chelate complex trans-[(C2H4NC2H4NH2-N,N′)2Pd](OTf)2 (2b) which contains thenew ligand b formed by an unexpected insertion and ring opening reaction of two aziridines (“aziridinedimerization”). CuCl2 reacted in pure HNC2H4 or HNCH2CMe2 (b) again by “dimerization” to give thetris-chelated ionic complex [Cu(C2H4NC2H4NH2-N,N′)3]Cl2 (3b) or the bis-chelated complex [CuCl(C2H2Me2NC2H2Me2NH2-N,N′)2]Cl (4c). By addition of 2H-3-phenylazirine (d) to PdCl2, trans-[Cl2Pd(NCH2CPh)2] (5d) was formed. All new compounds were characterized by NMR, IR and mass spectraand also by X-ray structure analyses (except 3b). Additionally the cytotoxic effects of these complexeswere examined on HL-60 and NALM-6 human leukemia cells and melanoma WM-115 cells. Theantimicrobial activity was also determined. The growth of Gram-positive bacterial strains (S. aureus,S. epidermidis, E. faecalis) was inhibited by almost all tested complexes at the concentrations of37.5–300.0 μg mL−1. However, MIC values of complexes obtained for Gram-negative E. coli and P.aeruginosa, as well as for C. albicans yeast, mostly exceeded 300 μg mL−1. The highest antibacterialactivity was achieved by complexes 1a and 2b. Complex 2b also inhibited the growth of Gram-negativebacteria.