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机构地区:[1]School of Material Science & Chemistry Engineering,Jiangxi University of Science and Technology [2]Department of Pharmacy,Gannan Medical University
出 处:《Chinese Journal of Structural Chemistry》2010年第1期69-73,共5页结构化学(英文)
基 金:supported by the Natural Science Foundation of Jiangxi Province (2008GZH0064);the Sustentation Fund of Education Department from Jiangxi Province (GJJ08275)
摘 要: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.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.
关 键 词:Schiff base SULFANILAMIDE crystal structure fluorescent property
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