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(2,6-diisopropylphenyl)-{1-[6-(3,5-dimethyl-pyrazol-1-yl)pyridin-2-yl]ethylidene} amine | 1190071-25-0

中文名称
——
中文别名
——
英文名称
(2,6-diisopropylphenyl)-{1-[6-(3,5-dimethyl-pyrazol-1-yl)pyridin-2-yl]ethylidene} amine
英文别名
(2,6-diisopropylphenyl)-(1-(6-(3,5-dimethylpyrazol-1-yl)pyridin-2-yl)ethylidene) amine;2-[1-(2,6-diisopropylphenylimino)ethyl]-6-(3,5-dimethylpyrazol-1-yl)pyridine;1-[6-(3,5-dimethylpyrazol-1-yl)pyridin-2-yl]-N-[2,6-di(propan-2-yl)phenyl]ethanimine
(2,6-diisopropylphenyl)-{1-[6-(3,5-dimethyl-pyrazol-1-yl)pyridin-2-yl]ethylidene} amine化学式
CAS
1190071-25-0
化学式
C24H30N4
mdl
——
分子量
374.529
InChiKey
NURPQPCPGSJSDF-UHFFFAOYSA-N
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):
    6.1
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    43.1
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (2,6-diisopropylphenyl)-{1-[6-(3,5-dimethyl-pyrazol-1-yl)pyridin-2-yl]ethylidene} amine 、 cobalt(II) chloride 以 四氢呋喃 为溶剂, 反应 24.0h, 以93%的产率得到2-[1-(2,6-diisopropylphenylimino)ethyl]-6-(3,5-dimethylpyrazol-1-yl)pyridine cobaltdichloride
    参考文献:
    名称:
    Polymerization of 1,3-butadiene catalyzed by pincer cobalt(II) complexes derived from 2-(1-arylimino)-6-(pyrazol-1-yl)pyridine ligands
    摘要:
    A new class of air stable and structurally well-defined cobalt complexes with unsymmetrical pincer type ligands ([2-(ArN=CMe)-6-(PY)C5H3N]CoCl2) (Ar = -C6H5, PY = pyrazol-1-yl, 5a; Ar = 2,4,6-Me3C6H2 Py=pyrazol-1-yl, 5b; Ar = 2,6-(Pr2C6H3)-Pr-1. Py = pyrazol-1-yl, 5c; Ar = -C6H5, Py = 3,5-Me(2)pyrazol-1-yl, 5d; Ar=2,4,6-Me3C6H2, Py 3,5-Me(2)pyrazol-1-yl, 5e; Ar = 2,6-(Pr2C6H3)-Pr-i, Py = 3,5-Me(2)pyrazol-1-yl, 5f; Ar = 2,6-(Pr2C6H3)-Pr-i, Py 3,5-(i)Pr(2)pyrazol-1-yl, 5g and [2-(O=CMe)-6-(3,5-diphenylpyrazol-1-y1)C3H3N]CoCl2 5h) were prepared and the molecular structures of 5a, 5c and 5f were determined by single crystal X-ray crystallography. Upon activation by methylaluminoxane (MAO) in toluene at room temperature, all complexes initiate polymerization of 1,3-butadiene (polymer yields: 65-99%), affording polybutadiene with excellent cis-1,4 regularity (97.5-98.7%). The polymer yields and properties in terms of molecular weight and distribution are well controlled by the substituents on iminoaryl rings and pyrazole rings. Selectivity switch from cis-1,4 to syndio-1,2 was also achievable by adding phosphine as microstructure regulator. (C) 2013 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.apcata.2013.04.026
  • 作为产物:
    参考文献:
    名称:
    Polymerization of 1,3-butadiene catalyzed by pincer cobalt(II) complexes derived from 2-(1-arylimino)-6-(pyrazol-1-yl)pyridine ligands
    摘要:
    A new class of air stable and structurally well-defined cobalt complexes with unsymmetrical pincer type ligands ([2-(ArN=CMe)-6-(PY)C5H3N]CoCl2) (Ar = -C6H5, PY = pyrazol-1-yl, 5a; Ar = 2,4,6-Me3C6H2 Py=pyrazol-1-yl, 5b; Ar = 2,6-(Pr2C6H3)-Pr-1. Py = pyrazol-1-yl, 5c; Ar = -C6H5, Py = 3,5-Me(2)pyrazol-1-yl, 5d; Ar=2,4,6-Me3C6H2, Py 3,5-Me(2)pyrazol-1-yl, 5e; Ar = 2,6-(Pr2C6H3)-Pr-i, Py = 3,5-Me(2)pyrazol-1-yl, 5f; Ar = 2,6-(Pr2C6H3)-Pr-i, Py 3,5-(i)Pr(2)pyrazol-1-yl, 5g and [2-(O=CMe)-6-(3,5-diphenylpyrazol-1-y1)C3H3N]CoCl2 5h) were prepared and the molecular structures of 5a, 5c and 5f were determined by single crystal X-ray crystallography. Upon activation by methylaluminoxane (MAO) in toluene at room temperature, all complexes initiate polymerization of 1,3-butadiene (polymer yields: 65-99%), affording polybutadiene with excellent cis-1,4 regularity (97.5-98.7%). The polymer yields and properties in terms of molecular weight and distribution are well controlled by the substituents on iminoaryl rings and pyrazole rings. Selectivity switch from cis-1,4 to syndio-1,2 was also achievable by adding phosphine as microstructure regulator. (C) 2013 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.apcata.2013.04.026
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文献信息

  • Ruthenium(II) complex catalysts bearing a pyridyl-supported pyrazolyl-imine ligand for transfer hydrogenation of ketones
    作者:Miao Zhao、Zhengkun Yu、Shenggang Yan、Yang Li
    DOI:10.1016/j.jorganchem.2009.05.028
    日期:2009.9
    ine ligands and their ruthenium(II) and nickel(II) NNN complexes were synthesized. The Ru(II) complex catalysts have been fully characterized and exhibited good to excellent catalytic activity in the transfer hydrogenation (TH) of ketones in refluxing 2-propanol. These results have demonstrated rare examples of active ruthenium(II) NNN complex catalysts that do not feature a N–H functionality for TH
    合成了新型的半不对称的不对称的2-(1-芳基)-6-(吡唑-1-基)吡啶配体及其(II)和(II)NNN配合物。Ru(II)络合物催化剂已得到充分表征,并在回流的2-丙醇中的转移加(TH)中表现出良好的催化活性。这些结果证明了稀有的活性(II)NNN络合物催化剂的实例,这些催化剂不具有TH的N–H官能度。
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