Thermal and spectral studies of Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) complexes with 3-(anilinomethylene)-2-methoxychroman-4-one

被引:0
作者
Agnieszka Dziewulska-Kułaczkowska
机构
[1] Maria Curie-Skłodowska University,Department of General and Coordination Chemistry, Faculty of Chemistry
来源
Journal of Thermal Analysis and Calorimetry | 2012年 / 109卷
关键词
Complexes; Chromanone; TG-DSC; IR; X-ray powder diffraction;
D O I
暂无
中图分类号
学科分类号
摘要
The complexes Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) with 3-(anilinomethylene)-2-methoxychroman-4-one were synthesized and characterized by elemental analysis, conductivity, infrared and UV–Vis spectroscopy, 1H NMR, X-ray diffraction patterns, magnetic susceptibility and thermal analysis (TG/DTG/DSC). The X-ray analysis shows that the studied compounds crystallize in the triclinic crystal system and they are no isostructural complexes. The unit cell parameters for these chelates were presented. The molecules of solvent are in the outside coordination sphere of the complexes. The chelates have different thermal stability and they decompose in air atmosphere in three steps. The coordination of metal ions is through nitrogen atom from ligand and oxygen atom present in 4-position of γ-pyrone. The studied chelates have electrolyte (1:1) and non-electrolyte nature. They are high-spin complexes with octahedral coordination and the weak ligand fields.
引用
收藏
页码:7 / 15
页数:8
相关论文
共 126 条
  • [1] Wang BD(2009)Synthesis, characterization, cytotoxic activity and DNA binding Ni(II) complex with the 6-hydroxy chromone-3-carbaldehyde thiosemicarbazone J Org Chem 694 4069-4075
  • [2] Yang ZY(2002)A benzopyran derivative substituted at position 3 Acta Cryst C58 405-406
  • [3] Lu MH(2006)Synthesis, characterization, and DNA- binding properties of the Ln(III) complexes with 6-hydroxy chromone-3-carbaldehyde-(2’-hydroxy) benzoyl hydrazone Bioorg Med Chem 14 6012-6021
  • [4] Hai J(2006)In vivo antitumor, in vitro antibacterial activity and alkylating properties of phosphorohydrazine derivaties of coumarin and chromone Eur J Med Chem 41 1301-1309
  • [5] Wang Q(2002)A versatile route to 2-alkyl-/aryl-amino-3-formyl-and heteroannelated-chromones, through a facile nucleophilic substitution at C2 in 2-( Tetrahedron 58 2471-2480
  • [6] Chen ZN(2009)-methylanilino)-3-formylchromones Cancer Chemother Pharmacol 63 1007-1016
  • [7] Rybarczyk-Pirek AJ(2010)Studies of structure-activity relationship on plant polyphenol-induced suppression of human liver cancer cells J Therm Anal Calorim 100 519-526
  • [8] Małecka M(2003)Thermochemistry of chromone and coumarin-3-carboxylic acid Bioorg Med Chem Lett 13 2561-2563
  • [9] Grabowski SJ(2004)Formylchromone derivatives as a novel class of protein tyrosine phosphatase 1B inhibitors Spectrochim Acta A60 995-1000
  • [10] Nawrot-Modranka J(2001)FTIR and FTR spectral studies of 2-amino-6-bromo -3-fromylchromone Tetrahedron 57 3455-3464