N-(3,5-dibromopyridin-2-yl)picolinamide | 1210410-10-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: N-(3,5-dibromopyridin-2-yl)picolinamide
• CAS: 1210410-10-8
• 化学式: C₁₁H₇Br₂N₃O
• 分子量: 357.004
• InChiKey: LISJDQZQYRBIQN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.25
• 重原子数：
  17.0
• 可旋转键数：
  2.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  54.88
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  甲醇 、 N-(3,5-dibromopyridin-2-yl)picolinamide 、 nickel dibromide 以 甲醇 为溶剂， 以78%的产率得到
  参考文献：
  名称：

  N-(Pyridin-2-yl)picolinamide tetranickel clusters: Synthesis, structure and ethylene oligomerization

  摘要：

  A series of N-(pyridin-2-yl)picolinamide derivatives was synthesized and characterized. Tetranickel complexes were obtained by stoichiometric reaction of NiBr2 and corresponding ligands, and characterized by elemental and spectroscopic analysis. Moreover, the coordination pattern of complex 3a was confirmed by single-crystal X-ray diffraction. In the structure, two ligands linked two nickel atoms to form a unit, and two units were bridged via mu(3)-OMe and mu(2)-Br to form a tetranickel cluster. These Ni(II) complexes were investigated in ethylene oligomerization and found to exhibit remarkable catalytic activities upon activation with MAO. Reaction conditions as well as ligand environment significantly affected the catalytic performance of the nickel complexes: the highest activity could be achieved to be 2.7 x 10(6) g mol(-1) Ni h(-1). (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.poly.2009.06.079
• 作为产物：
  描述：

  2-吡啶甲酸 、 2-氨基-3,5-二溴吡啶 在 三氯化磷 作用下， 以 5,5-dimethyl-1,3-cyclohexadiene 为溶剂， 反应 24.0h， 以77%的产率得到N-(3,5-dibromopyridin-2-yl)picolinamide
  参考文献：
  名称：

  N-(Pyridin-2-yl)picolinamide tetranickel clusters: Synthesis, structure and ethylene oligomerization

  摘要：

  A series of N-(pyridin-2-yl)picolinamide derivatives was synthesized and characterized. Tetranickel complexes were obtained by stoichiometric reaction of NiBr2 and corresponding ligands, and characterized by elemental and spectroscopic analysis. Moreover, the coordination pattern of complex 3a was confirmed by single-crystal X-ray diffraction. In the structure, two ligands linked two nickel atoms to form a unit, and two units were bridged via mu(3)-OMe and mu(2)-Br to form a tetranickel cluster. These Ni(II) complexes were investigated in ethylene oligomerization and found to exhibit remarkable catalytic activities upon activation with MAO. Reaction conditions as well as ligand environment significantly affected the catalytic performance of the nickel complexes: the highest activity could be achieved to be 2.7 x 10(6) g mol(-1) Ni h(-1). (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.poly.2009.06.079