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| 178114-70-0

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
178114-70-0
化学式
C37H31ClOP2Pd
mdl
——
分子量
695.473
InChiKey
VXGMJNCZVNMFPX-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:
    乙腈 、 silver tetrafluoroborate 以 二氯甲烷 为溶剂, 生成
    参考文献:
    名称:
    Copolymerization of ethylene and carbon monoxide by phosphinite-modified palladium catalysts
    摘要:
    Novel palladium complexes with bidentate phosphinite and mixed phosphine-phosphinite ligands of the general formula [((PP)-P-Lambda)Pd(Me)Cl] were prepared. After halide abstraction, these complexes are highly active catalysts for the copolymerization of ethylene and CO, yielding high molecular weight polyketones with activities of up to 30000 mol per mol Pd. The preference of cis- or cans-coordination, depending on the chelate ring size, was investigated. In complexes with up to 11-membered chelates, a cis-fixation of the ligands is observed, whereas bigger chelates afforded catalytically inactive trans-complexes.
    DOI:
    10.1016/0022-328x(95)06046-y
  • 作为产物:
    描述:
    chloromethyl(1,5-cyclooctadiene)palladium(II) 、 以 为溶剂, 以99%的产率得到
    参考文献:
    名称:
    Copolymerization of ethylene and carbon monoxide by phosphinite-modified palladium catalysts
    摘要:
    Novel palladium complexes with bidentate phosphinite and mixed phosphine-phosphinite ligands of the general formula [((PP)-P-Lambda)Pd(Me)Cl] were prepared. After halide abstraction, these complexes are highly active catalysts for the copolymerization of ethylene and CO, yielding high molecular weight polyketones with activities of up to 30000 mol per mol Pd. The preference of cis- or cans-coordination, depending on the chelate ring size, was investigated. In complexes with up to 11-membered chelates, a cis-fixation of the ligands is observed, whereas bigger chelates afforded catalytically inactive trans-complexes.
    DOI:
    10.1016/0022-328x(95)06046-y
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