A new sulfanilamide Schiff-base compound N,N -(p-phenyl sulfanilamide)-5,6-dimethoxy-pyrimidine-(2-hydroxyl benzene) methylidene has been synthesized by the condensation of equimolar salicylaldehyde and 4-(p-amin...A new sulfanilamide Schiff-base compound N,N -(p-phenyl sulfanilamide)-5,6-dimethoxy-pyrimidine-(2-hydroxyl benzene) methylidene has been synthesized by the condensation of equimolar salicylaldehyde and 4-(p-amino phenyl sulfanilamide)-5,6-dimethoxy-pyrimidine in an anhydrous ethanol solution.The compound was characterized by elemental analysis,IR spectra,and single-crystal X-ray diffraction.The crystal belongs to the monoclinic system,space group P21/c with a=19.0425(11),b=11.1914(6),c=9.0075(5),β=93.9650(10)°,Z= 4, V= 1915.01(18) A3,Dc = 1.437 g/cm^3, Mr = 414.43, λ(MoKa) = 0.71073 A,μ= 2.09 mm^-1, F(000) = 864, R = 0.0385 and wR = 0.1224.展开更多
基金supported by the Natural Science Foundation of Jiangxi Province (2008GZH0064)the Sustentation Fund of Education Department from Jiangxi Province (GJJ08275)
文摘A new sulfanilamide Schiff-base compound N,N -(p-phenyl sulfanilamide)-5,6-dimethoxy-pyrimidine-(2-hydroxyl benzene) methylidene has been synthesized by the condensation of equimolar salicylaldehyde and 4-(p-amino phenyl sulfanilamide)-5,6-dimethoxy-pyrimidine in an anhydrous ethanol solution.The compound was characterized by elemental analysis,IR spectra,and single-crystal X-ray diffraction.The crystal belongs to the monoclinic system,space group P21/c with a=19.0425(11),b=11.1914(6),c=9.0075(5),β=93.9650(10)°,Z= 4, V= 1915.01(18) A3,Dc = 1.437 g/cm^3, Mr = 414.43, λ(MoKa) = 0.71073 A,μ= 2.09 mm^-1, F(000) = 864, R = 0.0385 and wR = 0.1224.