Citation:
LIU Wen-Qian, ZHOU Shi-Lei, FAN Ming-Zhu, PAN Zhi-Quan, CHEN Yun-Feng. Synthesis and Crystal Structure of a Dinuclear Cu(II) Complex Based on a Carboxyl-substituted 1H-1,2,3-Triazole and Its DNA Cleavage Activity[J]. Chinese Journal of Structural Chemistry,
;2015, 34(6): 917-924.
doi:
10.14102/j.cnki.0254-5861.2011-0634
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The novel dinuclear copper complex [Cu2(H2O)2(DMF)2(L)2] (1, H2L=5-phenyl-2H-1,2,3-triazole-4-carboxylic acid, DMF=N,N-dimethyl-formamide) has been synthesized and characterized by X-ray single-crystal diffraction. The compound crystallizes in triclinic system, space group P1 with a=9.591, b=10.508, c=15.515 Å, β=75.11°, V=1446.2 Å3, Z=2, Mr=683.62, Dc=1.570 g/cm3, μ=1.531 mm-1, F(000)=700, the final R=0.0404 and wR=0.1130 for 5327 observed reflections with I>2σ(I). In each unit of the complex, two Cu2+ ions coordinated with two triazole ligands to form a dimeric [5,6,5] tricyclic structure. The central Cu atom is five-coordinated, and each copper atom shows a square pyramidal geometry. The crystal structure is stabilized by the inversion-related O-H···O hydrogen bond and C-H···O hydrogen bonding interactions to form a layer structure. Fluorescent spectra show an obvious quenching of fluorescence compared with free 1,2,3-triazole ligand. The results of agarose gel electrophoresis indicate that this complex can cleave the plasmid supercoiled DNA within shorter time in the 50-folds excess of ascorbate under physiological conditions, providing a new example in the research for artificial metal nucleic acid enzyme.
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