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[(2-tolylpyridine)BrNi((2-tolyl-κC2)pyridine-κN)] | 956298-32-1

中文名称
——
中文别名
——
英文名称
[(2-tolylpyridine)BrNi((2-tolyl-κC2)pyridine-κN)]
英文别名
——
[(2-tolylpyridine)BrNi((2-tolyl-κC2)pyridine-κN)]化学式
CAS
956298-32-1
化学式
C24H21BrN2Ni
mdl
——
分子量
476.038
InChiKey
YUAZXKOTAQMCIB-UHFFFAOYSA-M
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

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

  • 作为反应物:
    描述:
    [(2-tolylpyridine)BrNi((2-tolyl-κC2)pyridine-κN)] 在 t-BuOK 作用下, 以 乙醚 为溶剂, 以34%的产率得到[Ni((2-tolyl-κC2)pyridine-κN)2]
    参考文献:
    名称:
    Heterolytic CH-bond activation in the synthesis of Ni{(2-aryl-κC2)pyridine-κN}2 and derivatives
    摘要:
    Thermolysis of Ni(OTf)(2) in 2-phenyl-pyridine or 2-tolyl-pyridine afforded the cationic chelate derivatives, [bis(2-aryl-pyridine)Ni{(2aryl-kappa C-2)pyridine-kappa N]OTf (aryl = phenyl, 1a; tolyl, 1b). Addition of KBr to 1a and LiBr to 1b provided the bromides, (2-aryl-pyridine)BrNi{ (2-aryl-KC2)pyridine-KN} (aryl = phenyl, 2a; tolyl, 2b). When subjected to KO'Bu in Et2O, the bromides generated the entitled bis-cyclometalated compounds, Ni((2-aryl-KC2)pyridine-kappa N-2 (aryl = phenyl, 3a; tolyl, 3b). These compounds insert diphenylacetylene into one cyclometalate arm to produce [(2-aryl-kappa C-2)pyridine-KN]Ni[2-(2-(1,2-diphenylethenyl-kappa C-2)aryl)pyridine-KN] (aryl = phenyl, 4a; p-tolyl, 4b). X-ray crystallographic studies were conducted on la, 2a, 3a and 4a, and a brief DFT study of 3a confirmed its low spin configuration and rippled geometry. (C) 2007 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2007.06.047
  • 作为产物:
    参考文献:
    名称:
    Heterolytic CH-bond activation in the synthesis of Ni{(2-aryl-κC2)pyridine-κN}2 and derivatives
    摘要:
    Thermolysis of Ni(OTf)(2) in 2-phenyl-pyridine or 2-tolyl-pyridine afforded the cationic chelate derivatives, [bis(2-aryl-pyridine)Ni{(2aryl-kappa C-2)pyridine-kappa N]OTf (aryl = phenyl, 1a; tolyl, 1b). Addition of KBr to 1a and LiBr to 1b provided the bromides, (2-aryl-pyridine)BrNi{ (2-aryl-KC2)pyridine-KN} (aryl = phenyl, 2a; tolyl, 2b). When subjected to KO'Bu in Et2O, the bromides generated the entitled bis-cyclometalated compounds, Ni((2-aryl-KC2)pyridine-kappa N-2 (aryl = phenyl, 3a; tolyl, 3b). These compounds insert diphenylacetylene into one cyclometalate arm to produce [(2-aryl-kappa C-2)pyridine-KN]Ni[2-(2-(1,2-diphenylethenyl-kappa C-2)aryl)pyridine-KN] (aryl = phenyl, 4a; p-tolyl, 4b). X-ray crystallographic studies were conducted on la, 2a, 3a and 4a, and a brief DFT study of 3a confirmed its low spin configuration and rippled geometry. (C) 2007 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2007.06.047
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