摘要
A new Schiff base compound, 4,4′-hydrazine-1,2-diylidenebis（methanylylidene）- bis（2- ethoxyphenol） （C18H20N2O4）, has been synthesized by the condensation of 3-ethoxy-4- hydroxybenzaldehyde and 80% hydrazine hydrate in an ethanol solution. The compound was characterized by 1H NMR, MS and single-crystal X-ray diffraction. The crystal belongs to the monoclinic system, space group P21/n with a = 5.2421（5）, b = 10.3700（8）, c = 14.9906（11）A, β = 97.6030（10）°, Z = 2, V= 807.73（12） A, Dc = 1.350 g/cm3, Mr = 328.36, λ（MoKa） = 0.71073 A,μ = 0.096 mm-1, F（000） = 348, R = 0.041 and wR = 0.0136. The two benzene rings are coplanar. The molecule adopts an E,E configuration about the central C=N functional bonds. A total of 3938 unique reflections were collected, of which 1440 with I 〉 2σ（I） were observed. A different type of intermolecular hydrogen bond, O-H…N, exists in the crystal. The title complex molecules are connected through hydrogen bonds to generate a two-dimensional network. The preliminary antibacterial activity results showed that the title compound exhibits antibacterial activity against Staphylococcus aureus.
A new Schiff base compound, 4,4′-hydrazine-1,2-diylidenebis（methanylylidene）- bis（2- ethoxyphenol） （C18H20N2O4）, has been synthesized by the condensation of 3-ethoxy-4- hydroxybenzaldehyde and 80% hydrazine hydrate in an ethanol solution. The compound was characterized by 1H NMR, MS and single-crystal X-ray diffraction. The crystal belongs to the monoclinic system, space group P21/n with a = 5.2421（5）, b = 10.3700（8）, c = 14.9906（11）A, β = 97.6030（10）°, Z = 2, V= 807.73（12） A, Dc = 1.350 g/cm3, Mr = 328.36, λ（MoKa） = 0.71073 A,μ = 0.096 mm-1, F（000） = 348, R = 0.041 and wR = 0.0136. The two benzene rings are coplanar. The molecule adopts an E,E configuration about the central C=N functional bonds. A total of 3938 unique reflections were collected, of which 1440 with I 〉 2σ（I） were observed. A different type of intermolecular hydrogen bond, O-H…N, exists in the crystal. The title complex molecules are connected through hydrogen bonds to generate a two-dimensional network. The preliminary antibacterial activity results showed that the title compound exhibits antibacterial activity against Staphylococcus aureus.
基金
Supported by the Fundamental Research Funds for the Central Universities (2012ZM0035)
