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(Z)-1-dicyclohexylphosphanyl-N-[(E)-(1-dicyclohexylphosphanyl-3,3-dimethylbutan-2-ylidene)amino]-3,3-dimethylbutan-2-imine;diiodonickel | 496770-14-0

中文名称
——
中文别名
——
英文名称
(Z)-1-dicyclohexylphosphanyl-N-[(E)-(1-dicyclohexylphosphanyl-3,3-dimethylbutan-2-ylidene)amino]-3,3-dimethylbutan-2-imine;diiodonickel
英文别名
——
(Z)-1-dicyclohexylphosphanyl-N-[(E)-(1-dicyclohexylphosphanyl-3,3-dimethylbutan-2-ylidene)amino]-3,3-dimethylbutan-2-imine;diiodonickel化学式
CAS
496770-14-0
化学式
C36H66IN2NiP2*I
mdl
——
分子量
901.38
InChiKey
ZYHSQNKCYPJEDC-GBJMTVQWSA-L
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):
    13.94
  • 重原子数:
    43
  • 可旋转键数:
    11
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    24.7
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    nickel(II) iodide 、 以 丙酮 为溶剂, 以41%的产率得到(Z)-1-dicyclohexylphosphanyl-N-[(E)-(1-dicyclohexylphosphanyl-3,3-dimethylbutan-2-ylidene)amino]-3,3-dimethylbutan-2-imine;diiodonickel
    参考文献:
    名称:
    Cationic nickel(II) complexes with azine diphosphines—structural and electrochemical study
    摘要:
    Nickel(II) complexes of azine diphosphine ligands, PR2CH2C(Bu-t)NNC(Bu-t)CH2PR2 (R = Ph, Bu-t, Pr-i, C6H11), were prepared for the first time by reactions of anhydrous NiX2 (X = Cl, Br, I) with ligands. Complexes are cationic, the counterion being either simple halide anion or, in two cases, 1/2[NiCl4](2-). The azine diphosphines are coordinated terdentately in (E,Z) configuration forming thereby a bicyclic ligand frame (five and six-membered ring) with diphosphine bite angles 160-165degrees. A balance of stereoelectronic factors governing square planar versus tetrahedral coordination of the ligands is suggested. Structures of four of the complexes with bulky ligands (R = Bu-t, X- = Cl-, Br-, I-; R = C6H11, X- = 1/2[NiCl](2-)) were determined by X-ray diffraction and qualitative Huckel MO calculations on model undistorted square planar [trans-NiX(NH2)(PH3)(2)](+) were carried out to elucidate the contributions of steric and electronic factors. Two reduction and two oxidation processes depending on the substituent R and the halide were identified from cyclic voltammetry data on the complexes. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(02)00982-9
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