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出 处:《Chinese Journal of Structural Chemistry》2017年第11期1797-1802,共6页结构化学(英文)
基 金:financially supported by the Natural Science Foundation of Hunan Province(2017JJ3093);the Scientific Research Fund of Hunan Provincial Education Department(No.16B104)
摘 要:Three new o-hydroxy Schiff bases, L1, L2 and L3, were derived from the 1:1 M condensation of substituted salicylaldehyde with tris base and were characterized by FT-IR, ^1H NMR and ^13C NMR spectroscopies. The crystal structure of L1 was also determined by single-crystal X-ray analysis, and it exists as a zwitterionic form in the solid state, with the H atom of the phenol group being transferred to the imine N atom. It adopts an E-configuration about the central C=N double bond. In addition, the biological activity assay was carried out and the results show that the Schiff-base compounds have a diverse range of biological activities against the fungi tested, which suggests great potential applications in antifungal fields in the future.Three new o-hydroxy Schiff bases, L1, L2 and L3, were derived from the 1:1 M condensation of substituted salicylaldehyde with tris base and were characterized by FT-IR, ^1H NMR and ^13C NMR spectroscopies. The crystal structure of L1 was also determined by single-crystal X-ray analysis, and it exists as a zwitterionic form in the solid state, with the H atom of the phenol group being transferred to the imine N atom. It adopts an E-configuration about the central C=N double bond. In addition, the biological activity assay was carried out and the results show that the Schiff-base compounds have a diverse range of biological activities against the fungi tested, which suggests great potential applications in antifungal fields in the future.
关 键 词:Schiff base crystal biological activity
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