Synthesis,Crystal Structure and Antitumor Activity in Vitro of a New Benzoate Binuclear CupperⅡ)Comp

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The title compound,[Cu2(C7H5O2)4(C2H6O)2],was synthesized by the reaction of benzoic acid,copper acetate and ethanol in an aqueous solution.Trypan blue dye exclusion method was used in experiment.X-ray single-crystal analysis has revealed that compound 1 (C32H32Cu2O10)crystallizes in the monoclinic system,space group C2/c,Mr=703.66,a=47.340(5),b=6.6613(4),C=22.028(2)(A),β=113.284(4)°,V=6380.6(10)(A)3,Z=8,Dc=1.465 g/cm3,F(000)=2896,μ=1.388 mm-1,the final R=0.0515 and wR=O.1172 for 5712 observed reflections with I>2σ(I).X-ray crystal structure analysis suggests that compound [Cu2[C7H5Oz]4(C2H6O)2]has a binuclear structure with two Cu(п)atoms coordinated by four benzoate groups and two ethanol molecules.The crystal packing is stabilized by intermolecular O-H-O hydrogen bonds.The compound inhibits the proliferation of K562 cells(chronic myeloid leukemic cells)significantly and dose-dependently in 48 h,and IC50 of K562 is 17.μg/mL by trypan blue dye exclusion method.
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