[Cu(S-benzyl-β-N-(2-acetylpyrid-2-yl)methylenedithiocarbazate(1-))(saccharinate)] | 937032-48-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 三唑并嘧啶类
• 英文名称: [Cu(S-benzyl-β-N-(2-acetylpyrid-2-yl)methylenedithiocarbazate(1-))(saccharinate)]
• 英文别名: Cu(NNS')sac)]
• CAS: 937032-48-9
• 化学式: C₂₂H₁₈CuN₄O₃S₃
• 分子量: 546.154
• InChiKey: QFAWHIHDJLKADI-UHFFFAOYSA-L

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
  None
• 环数：
  None
• sp3杂化的碳原子比例：
  None
• 拓扑面积：
  None
• 氢给体数：
  None
• 氢受体数：
  None

反应信息

• 作为产物：
  描述：

  [1-(2-pyridine)ethylidene]hydrazinecarbodithioic acid phenylmethyl ester 、 [Cu(sac)₂(H₂O)₄]*2H₂O 以 乙醇 、 水 为溶剂， 以75%的产率得到[Cu(S-benzyl-β-N-(2-acetylpyrid-2-yl)methylenedithiocarbazate(1-))(saccharinate)]
  参考文献：
  名称：

  Synthesis, characterization and bioactivity of mixed-ligand Cu(II) complexes containing Schiff bases derived from S-benzyldithiocarbazate and saccharinate ligand and the X-ray crystal structure of the copper-saccharinate complex containing S-benzyl-β-N-(acetylpyrid-2-yl)methylenedithiocarbazate

  摘要：

  Mixed-ligand complexes of general formula, [Cu(NNS)(sac)] (NNS' = S-benzyl-beta-N-(2-acetylpyrid-2-yl)methylenedithiocarbazate, NNS '' = S-benzyl-beta-N-(2-benzoylpyrid-2-yl)methylenedithiocarbazate and NNS''' = S-benzyl-beta-N-(6-methylpyrid-2-yl)methylenedithiocarbazate, sac= the saccharinate anion) have been synthesized by reacting [Cu(sac)(2)(H2O)(4)] center dot 2H(2)O with the appropriate ligands in ethanol and characterized by various physico-chemical techniques. Magnetic and spectral evidence indicate that the complexes are four-coordinate in which the Schiff bases coordinate as NNS ligands and the sac- anion coordinates as a unidentate N-donor ligand. An X-ray crystallographic structural analysis of [Cu(NNS')(sac)] shows that the complex has a distorted square-planar geometry with the Schiff base coordinated to the copper (II) ion as a uninegatively charged tridentate chelating agent via the pyridine nitrogen atom, the azomethine nitrogen atom and the thiolate sulphur atom while the fourth coordination position is occupied by the N-bonded saccharinate anion. The complexes have been evaluated for their biological activities against selected pathogens and cancer cell lines. They display weak activity against the pathogenic bacteria and fungi. The complexes were highly active against the leukemic cell line (HL-60) but only [Cu(NNS')(sac)] was found to exhibit strong cytotoxicity against the ovarian cancer cell line (Caov-3). All complexes were inactive against the breast cancer cell line (MCF-7). (C) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.poly.2006.03.007