[Ni(1,10-phenanthroline)(thiodiglycolate(2-))(H2O)] | 724425-41-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 菲咯啉
• 英文名称: [Ni(1,10-phenanthroline)(thiodiglycolate(2-))(H2O)]
• CAS: 724425-41-6
• 化学式: C₁₆H₁₄N₂NiO₅S
• 分子量: 405.054
• InChiKey: ZJULEYJHLXDYSG-UHFFFAOYSA-L

计算性质

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

• 作为产物：
  描述：

  1,10-菲罗啉 、 Ni(thiodiacetate)(H2O)3 以 乙醇 、 水 为溶剂， 以78%的产率得到[Ni(1,10-phenanthroline)(thiodiglycolate(2-))(H2O)]
  参考文献：
  名称：

  Syntheses and study on nickel(II) complexes with thiodiglycolic acid and nitrogen-donor ligands. X-ray structures of [Ni(bpy)(tdga)(H2O)] · 4H2O and [(en)Ni(μ-tdga)2Ni(en)] · 4H2O (tdgaH2=thiodiglycolic acid)

  摘要：

  Mixed-ligand Ni(II) complexes involving thiodiglycolate(2-) anion (tdga) and nitrogen-donor ligands in the coordination sphere have been prepared. The complexes of composition [Ni(bpy)(tdga)(H2O)].4H(2)O (1), [(en)Ni(mu-tdga)(2)Ni(en)].4H(2)O (2), [Ni(phen)(tdga)(H2O)] (3), [Ni(1,8-dan)(tdga)(H2O)] (4), [Ni(nphen)(tdga)(H2O)].H2O (5), [Ni(ampy)(tdga)(H2O)] (6), where bpy = 2,2'-bipyridine,en = ethylenediamine,phen = 1,10-phenanthroline, 1,8-dan = 1,8-diaminonaphthalene, nphen = 5-nitro-1,10-phenanthroline and ampy = 2-(aminomethyl)-pyridine, have been characterized by elemental analysis, IR and UV-Vis spectroscopies, and magnetic susceptibility measurements. Room temperature effective magnetic moments for 1-6 are ranging from 3.06 to 3.28 mu(eff)/mu(B). and thus indicating that nickel atoms are six-coordinated in a deformed octahedral arrangement in all the prepared complexes. This conclusion has been confirmed by single-crystal X-ray analysis of [Ni(bpy)(tdga)(H2O)].4H(2)O (1). A binuclear structure of complex [(en)Ni(mu-tdga)(2)Ni(en)].4H(2)O (2) has been anticipated in connection with study of its magnetic properties over the 1.8-300 K temperature range (J = 4.35 cm(-1), D = 5.53 cm(-1), zJ = -0.94 cm(-1) for g = 2.00) and unambiguously proved by a single-crystal X-ray analysis. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.poly.2004.03.005