Abstract

The synthesis, characterization and the biological study of a series of Ni(ll)2(carboxylato)2 [12- MCNi(II)N(shi)2(pko)2-4][12-MCNi(ii)N(sh03(pko)-4] (CH3OH)3(H3O) fused 12-membered metallacrowns with 10 metal ions and commercial available herbicides or anti-inflammatory drugs as carboxylato ligands are reported. All the compounds have a mixed ligand composition with salicylhydroxamic acid and di-2-pyridylketonoxime as chelate agents. The compounds construct metallacrown cores {[12-MCNi(n)N(sj02(pko)2-4][12-MCNi(ll)N(shO3(pko)-4]}2+ following the pattern [-Ni-O-N-]4. The neutral decanuclear [Ni(II)(A)]2[12-MCNi(II)N(shi)2(pko)2-4][12-MCNi(II)N(pko)3(pko)-4] fused metallacrown, consists of two [12-MCM(ox)N(ligand)-4] units the {Ni(ll)(A)[12-MCNi(II)N(shi)2(pko)2-4]} and {Ni(II)(A)[12-MCNi(II)N(shi)3(pko)-4]} with 1+ and 1- charge, respectively. Each metallacrown unit has four ring Ni(II) ions and one additional encapsulated Ni(II) ion in planar arrangement. The anionic unit is bonded with cationic one creating binuclear moieties. The herbicide or antiiflammatory carboxylato ligands are bridging the central octahedral nickel atom with a ring metal ion in a bindetate fashion. The effect on DNA and their antibacterial activity was examined. The changes in the mobility can be attributed to the altered structures of the pDNA treated with Ni(II) complexes. Evaluating the data of the antibacterial activity of the compounds tested, we can conclude that nickel complexes present strong antibacterial activity.

Highlights

  • Metallomacrocycles have gained increasing attention over the past decade due to their potentially unique properties

  • Metallacrowns* resemble crown ethers in their repeating pattern of u, x, O-X-X-O with the oxygen atoms oriented toward the center of a cavity/2-27/. [9-MCoN0g,nd)-3] /2-4/, 12-MCuox)N0igat,d-4] /5-12/and [15-MCM(ox)N(iigand)-5]/13-18/metallacrowns with cavity size 0.35 A, 0.60 A and 0.77 A respectively and metal ions Mn Fe Ni Cu and vVo, [12-MC-6]/26/, [16-MC-8]/27/, [18

  • All metallacrowns are soluble in methanol, CHCI3, DMF, DMSO and there are no electrolytes in these solvents

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Summary

Introduction

Metallomacrocycles have gained increasing attention over the past decade due to their potentially unique properties. [12-MCNi(II)N(shO2(pko)2"4][12-MCi(U)N(shO3ko)’4] (CH3OH)3(H20) fused 12-membered metallacrowns with 10 metal ions and commercial available herbicides or anti-inflammatory drugs as carboxylato ligands (Scheme 1). The products resulting from DNA-compound interactions were separated by electrophoresis on agarose gels (1%), which contained lag/ml ethidium bromide in 40 mM

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