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| 171569-11-2

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
171569-11-2
化学式
C62H74F6N4O6S2Zn
mdl
——
分子量
1214.81
InChiKey
NMLQFQPYBKNQLZ-QCRJGZHHSA-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:
    Trifluoro-methanesulfonic acid 4-[(1Z,4Z,9Z,15Z)-2,8,12,18-tetrahexyl-3,7,13,17-tetramethyl-15-(4-trifluoromethanesulfonyloxy-phenyl)-porphyrin-5-yl]-phenyl ester 、 zinc(II) acetate dihydrate甲醇氯仿 为溶剂, 以99%的产率得到
    参考文献:
    名称:
    Exploration of the Stille Coupling Reaction for the Synthesis of Functional Polymers
    摘要:
    The palladium-catalyzed Stille coupling reaction was used for preparing functionalized, conjugated polymers. This reaction has several advantages, two of which are that it requires mild reaction conditions and produces high yields. Several factors which affect the polymerization processes were investigated, such as the catalyst composition and concentration, different solvents and ligands, and structures of monomers. It was found that solvents that could keep the macromolecules in solution and stabilize the palladium(0) catalyst would yield polymers with high molecular weights. If a Pd(II) compound was used as the catalyst, a stoichiometric adjustment of the distannyl monomer was necessary to enhance the molecular weight of the resulting polymer. In general, it was found that a combination of an electron-rich distannyl monomer and an electron-deficient dihalide (ditriflate) monomer forms polymers with relatively high molecular weights. To further demonstrate the versatility of the Stille reaction for polycondensations, different types of conjugated polymers with different properties and applications, such as liquid crystalline conjugated polymers and conjugated photorefractive polymers, were synthesized.
    DOI:
    10.1021/ja00155a007
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