期刊文献+

Synthesis and Crystal Structure of 2-Hydroxybenzoic Acid [1-(3,5-Dibromo-2-hydroxyphenyl)methylidene]hydrazide Methanol 被引量:1

Synthesis and Crystal Structure of 2-Hydroxybenzoic Acid [1-(3,5-Dibromo-2-hydroxyphenyl)methylidene]hydrazide Methanol
在线阅读 下载PDF
导出
摘要 A new Schiff base compound, 2-hydroxybenzoic acid [1-(3,5-dibromo-2-hydroxyphenyl) methylidene]hydrazide methanol (C14H10Br2N2O3·CH3OH), has been synthesized by the condensation of equimolar 3,5-dibromosalicylaldehyde and 2-hydroxybenzoic acid hydrazide in a methanol solution. The compound was characterized by elemental analysis, IR spectra, and singlecrystal X-ray diffraction. The compound consists of a Schiff base moiety 2-hydroxybenzoic acid [1-(3,5-dibromo-2-hydroxyphenyl)methylidene]hydrazide and a lattice methanol molecule. The crystal belongs to the monoclinic system, space group P21/n with a = 7.183(1), b = 15.673(2), c = 15.001(2) A, β = 98.345(2)°, Z = 4, V = 1670.9(4) A^3, Dc = 1.773 g/cm^3, Mr = 446.10, λ(MoKα) = 0.71073 , μ = 4.872 mm^-1, F(000) = 880, R = 0.0458 and wR = 0.0963. A total of 3445 unique reflections were collected, of which 2236 with I 〉 2σ(Ⅰ) were observed. As expected, the molecule adopts a trans configuration about the C=N double bond. The two benzene rings are nearly coplanar (mean deviation from the combined plane is 0.061(4) ), with the dihedral angle of 7.9(3)°. The preliminary biological tests show that the compound has moderate antibacterial activities. A new Schiff base compound, 2-hydroxybenzoic acid [1-(3,5-dibromo-2-hydroxyphenyl) methylidene]hydrazide methanol (C14H10Br2N2O3·CH3OH), has been synthesized by the condensation of equimolar 3,5-dibromosalicylaldehyde and 2-hydroxybenzoic acid hydrazide in a methanol solution. The compound was characterized by elemental analysis, IR spectra, and singlecrystal X-ray diffraction. The compound consists of a Schiff base moiety 2-hydroxybenzoic acid [1-(3,5-dibromo-2-hydroxyphenyl)methylidene]hydrazide and a lattice methanol molecule. The crystal belongs to the monoclinic system, space group P21/n with a = 7.183(1), b = 15.673(2), c = 15.001(2) A, β = 98.345(2)°, Z = 4, V = 1670.9(4) A^3, Dc = 1.773 g/cm^3, Mr = 446.10, λ(MoKα) = 0.71073 , μ = 4.872 mm^-1, F(000) = 880, R = 0.0458 and wR = 0.0963. A total of 3445 unique reflections were collected, of which 2236 with I 〉 2σ(Ⅰ) were observed. As expected, the molecule adopts a trans configuration about the C=N double bond. The two benzene rings are nearly coplanar (mean deviation from the combined plane is 0.061(4) ), with the dihedral angle of 7.9(3)°. The preliminary biological tests show that the compound has moderate antibacterial activities.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2007年第5期547-550,共4页 结构化学(英文)
基金 This work was supported by the Natural Science Foundation of Gansu Province (No. 3ZS061-A25-026) ‘Qing Lan’ Talent Engineering Funds by Lanzhou Jiaotong University
关键词 Schiff base ACYLHYDRAZONE crystal structure antibacterial activity Schiff base, acylhydrazone, crystal structure, antibacterial activity
  • 相关文献

参考文献1

二级参考文献10

  • 1Sheldrick, G. M. SHELXS 97, Program for the Solution of Crystal Structure, University of Goettingen, Germany 1997.
  • 2Sheldrick, G. M. SHELXL 97, Program for the Refinement of Crystal Structure, University of Goettingen, Germany 1997.
  • 3Karayannis, N. M.; Pytlewski, L. L.; Mikulski, C. M. Coord. Chem. Rev. 1973,11, 93-159.
  • 4Drew, M. G. B.: Glaves, L. R.: Hudsom, M. J. J. Chem. Soc., Dalton Trans. 1985, 771-775.
  • 5Gong, Y. Q.; Jiang, M. C. Synth. React. Inorg. Met-Org. Chem. 1990, 20, 1115-1123.
  • 6Hussain, M. S.Schlemper, E. O. J. Chem. Soc., Dalton Trans. 1982, 751-755.
  • 7Gerald. D.: Bettina, H.: Gerald. H. Tetrahedron. Asymmetry 1999, 10, 3297-3307.
  • 8Gong, Y. Q.; Chen. C. G.Huan, X. F. J. Hangzhou Univ. (Nat. Sci.) 1993, 20, 438-442.
  • 9Gong, Y. Q.: Chen, C. G.; Huan, X. F. Synth. React. Inorg. Mel-Org. Chem. 1994, 24, 877-889.
  • 10Liang, H.: Chen, X. B.Hu, R. X.; Chen. Z. F. Acta Chim. Sinica 2002, 60, 939-946.

共引文献4

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部