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[(2,6-iPr2C6H3)NC(Me)C(Me)NH(2,6-iPr2C6H3)AlMe2] | 1424662-19-0

中文名称
——
中文别名
——
英文名称
[(2,6-iPr2C6H3)NC(Me)C(Me)NH(2,6-iPr2C6H3)AlMe2]
英文别名
——
[(2,6-iPr<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)NC(Me)C(Me)NH(2,6-iPr2C<sub>6</sub>H<sub>3</sub>)AlMe<sub>2</sub>]化学式
CAS
1424662-19-0
化学式
C30H47AlN2
mdl
——
分子量
462.698
InChiKey
NUQRCEHVKLIWRI-FAIYXUOWSA-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):
    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

  • 作为产物:
    描述:
    2-N,3-N-bis[2,6-di(propan-2-yl)phenyl]but-2-ene-2,3-diamine三甲基铝正己烷甲苯 为溶剂, 反应 6.0h, 以67%的产率得到[(2,6-iPr2C6H3)NC(Me)C(Me)NH(2,6-iPr2C6H3)AlMe2]
    参考文献:
    名称:
    Synthesis and Reactions of a Redox-Active α-Diimine Aluminum Complex
    摘要:
    The reaction of the ene-diamine LH2 (L = [ArNC(Me)C(Me)NAr](2-), Ar = 2,6-iPr(2)C(6)H(3)) with AlMe3 and AlEt3 yielded the aluminum dimethyl complex (LH)AlMe2 (1) and the radical (L-center dot)AlEt2 (2; L-center dot = [ArNC(Me)C(Me)-NAr](center dot-)), respectively. Treatment of 2 with O-2 and TEMPO (2,2,6,6-tetramethylpiperidin-l-oxyl) led to hydrogen abstraction from the methyl group at the ligand backbone to give the diamagnetic species (L*)AlEt2 (3; L* = [ArN= C(Me)C(CH2)NAr](-)) and (L*)Al(TEMPO)(Et) (4). In contrast, the reaction of 2 with iodine resulted in the iodination of the Al-C bonds and yielded the radical (L-center dot)AlI2 (5). Reaction of 2 with BCl3 led to electron transfer between the alpha-diimine radicals with the formation of the aluminum cation [(L-0)AlCl2](+)[AlCl4](-) (6; L-0 = ArN=C(Me)(Me)C=NAr) and the diazaborole LBCl (7). The structures of compounds 2, 3, and 7 have been determined by X-ray single-crystal diffraction, and the paramagnetic species 2 has been characterized by EPR measurements.
    DOI:
    10.1021/om300920y
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