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| 1350542-32-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1350542-32-3
化学式
C34H62ClHfNP2Si2
mdl
——
分子量
816.935
InChiKey
NNJJQUOIVLWTIN-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:
    氘代苯 为溶剂, 生成
    参考文献:
    名称:
    Hafnium alkyl complexes of the anionic PNP pincer ligand and possible alkylidene formation
    摘要:
    The diarylamido-based PNP pincer ligand can be used successfully for support of organometallic Hf complexes (PNP - [(4-Me-2-(Pr2P)-Pr-i-C6H3)(2)N]). (PNP)HfCl3 (3) was prepared via reaction of (PNP)Li (2) with HfCl4(OEt2). Reactions of (PNP) HfCl3 with alkyl Grignards led to triple alkylation to produce (PNP) HfMe3 (4) with a small methyl or only double alkylation to give (PNP)Hf(CH2SiMe3)(2)Cl (5) with a larger alkyl. Structures of 3, 4, and 5 in the solid state were established by X-ray diffraction studies. Structures of the alkyl complexes 4 and 5 display remarkably irregular coordination environments about Hf, while in 3 it is approximately octahedral. Compound 4 was found to be thermally stable at 75 degrees C. On the other hand, thermolysis of 5 at similar conditions led to a mixture of products, the major one of which is believed to be a Hf alkylidene on the basis of in situ NMR spectroscopic observations (e.g., delta 248.2 ppm in the C-13{H-1} NMR spectrum). (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2011.07.017
  • 作为产物:
    描述:
    (三甲基硅基)甲基氯化镁1,4-二氧六环乙醚 为溶剂, 以77%的产率得到
    参考文献:
    名称:
    Hafnium alkyl complexes of the anionic PNP pincer ligand and possible alkylidene formation
    摘要:
    The diarylamido-based PNP pincer ligand can be used successfully for support of organometallic Hf complexes (PNP - [(4-Me-2-(Pr2P)-Pr-i-C6H3)(2)N]). (PNP)HfCl3 (3) was prepared via reaction of (PNP)Li (2) with HfCl4(OEt2). Reactions of (PNP) HfCl3 with alkyl Grignards led to triple alkylation to produce (PNP) HfMe3 (4) with a small methyl or only double alkylation to give (PNP)Hf(CH2SiMe3)(2)Cl (5) with a larger alkyl. Structures of 3, 4, and 5 in the solid state were established by X-ray diffraction studies. Structures of the alkyl complexes 4 and 5 display remarkably irregular coordination environments about Hf, while in 3 it is approximately octahedral. Compound 4 was found to be thermally stable at 75 degrees C. On the other hand, thermolysis of 5 at similar conditions led to a mixture of products, the major one of which is believed to be a Hf alkylidene on the basis of in situ NMR spectroscopic observations (e.g., delta 248.2 ppm in the C-13{H-1} NMR spectrum). (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2011.07.017
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