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Antibacterial Activities and Nuclease Properties of Two New Ternary Copper(ll) Complexes with 2-(4'-Thiazolyl)- benzimidazole and 2,2'-Bipyridine/1,10-phenanthroline

Antibacterial Activities and Nuclease Properties of Two New Ternary Copper(ll) Complexes with 2-(4'-Thiazolyl)- benzimidazole and 2,2'-Bipyridine/1,10-phenanthroline
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摘要 Two new complexes: [Cu(TBZ)(bipy)Cl]Cl[H2O (1) and [Cu(TBZ)(phen)CI]CloH20 (2) [TBZ=2-(4'-thiazolyl)- benzimidazole, phen = 1,10-phenanthroline and bipy =2,2'-bipyridine] have been synthesized and characterized by elemental analysis, molar conductivity, IR, and UV-vis methods. Complex 2, structurally characterized by single-crystal X-ray crystallography, crystallizes in the monoclinic space group P21/c in a unit cell of a = 0.85257(12) nm, b=2.5358(4) nm, c=1.15151(13) nm, β=118.721(8)°, V=2.183.2(5) nm^3, Z=4, Dc=1.624 gocm 3, μ= 1.367 mm^-1. The complexes, free ligands and chloride copper(II) salt were each tested for their ability to inhibit the growth of two gram-positive (B. subtilis and S. aureus) and two gram-negative (Salmonella and E. coli) bacteria. The complexes showed good antibacterial activities against the microorganisms. The interaction between the com- plexes and calf thymus DNA in aqueous solution was investigated adopting electronic absorption spectroscopy, fluorescence spectroscopy, viscosity measurements and cyclic voltammetry. Results suggest that the two complexes can bind to DNA by intercalative mode. In addition, the result of agarose gel electrophoresis suggested that the complexes can cleave the plasmid DNA at physiological pH and room temperature. Mechanistic studies with different inhibiting reagents reveal that hydroxyl radicals, and a singlet oxygen-like copper-oxo species are all involved in the DNA scission process mediated by the complexes. Two new complexes: [Cu(TBZ)(bipy)Cl]Cl[H2O (1) and [Cu(TBZ)(phen)CI]CloH20 (2) [TBZ=2-(4'-thiazolyl)- benzimidazole, phen = 1,10-phenanthroline and bipy =2,2'-bipyridine] have been synthesized and characterized by elemental analysis, molar conductivity, IR, and UV-vis methods. Complex 2, structurally characterized by single-crystal X-ray crystallography, crystallizes in the monoclinic space group P21/c in a unit cell of a = 0.85257(12) nm, b=2.5358(4) nm, c=1.15151(13) nm, β=118.721(8)°, V=2.183.2(5) nm^3, Z=4, Dc=1.624 gocm 3, μ= 1.367 mm^-1. The complexes, free ligands and chloride copper(II) salt were each tested for their ability to inhibit the growth of two gram-positive (B. subtilis and S. aureus) and two gram-negative (Salmonella and E. coli) bacteria. The complexes showed good antibacterial activities against the microorganisms. The interaction between the com- plexes and calf thymus DNA in aqueous solution was investigated adopting electronic absorption spectroscopy, fluorescence spectroscopy, viscosity measurements and cyclic voltammetry. Results suggest that the two complexes can bind to DNA by intercalative mode. In addition, the result of agarose gel electrophoresis suggested that the complexes can cleave the plasmid DNA at physiological pH and room temperature. Mechanistic studies with different inhibiting reagents reveal that hydroxyl radicals, and a singlet oxygen-like copper-oxo species are all involved in the DNA scission process mediated by the complexes.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2011年第7期1380-1388,共9页 中国化学(英文版)
关键词 ternary copper(ll) complexes COPPER 2-(4'-thiazolyl)benzimidazole DNA DNA cleavage antibacterial activity ternary copper(ll) complexes, copper, 2-(4'-thiazolyl)benzimidazole, DNA, DNA cleavage, antibacterial activity
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  • 1Keene, F. R.; Smith, J. A.; Collins, J. G. Coord. Chem. Rev.2009, 253, 2021.
  • 2Yu, H. J.; Huang, S. M.; Li, L. Y.; Jia, H. N.; Chao, H.; Mao, Z. W.; Liu, J. Z.; Ji, L. N. J. lnorg. Biochem. 2009,103, 881.
  • 3Gao, E. J.; Liu, L.; Zhu, M. C.; Wu, Q. Chin. J Chem. 2009, 27, 1285,.
  • 4Patel, M. N.; Parmar, P. A.; Gandhi, D. S. Bioorg. Med. Chem. 2010, 18, 1227.
  • 5Wang, B. D.; Yang, Z. Y.; Crewdson, P.; Wang, D. Q. J. Inorg. Biochem. 2007, 101, 1492.
  • 6Turel, I. Coord. Chem. Rev. 2002, 232, 27.
  • 7Weder, J. E.; Dillon, C. T.; Hambley, T. W.; Kennedy, B. J.; Lay, P. A.; Biffin, J. R.; Regtop, H. L.; Davies, N. M. Co- ord. Chem. Rev. 2002, 232, 95.
  • 8Efthimiadou, E. K.; Sanakis, Y.; Katsarou, M.; Raptopoulou C. P.; Karaliota, A.; Katsaros, N.; Psomas, G. J. Inorg. Biochem. 2006, 100, 1378.
  • 9Sorenson, J. R. J. Prog. Med. Chem. 1989, 26, 437.
  • 10Sorenson, J. R. J. Handbook of Metal-Ligand Interactions in Biologicalfluids, Vol. 2, 1st ed., Marcel Decker, New York, 1995, p. 1318.

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