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diferrocenyl(trityloxy)cyclopropenylium tetrafluoroborate | 862772-15-4

中文名称
——
中文别名
——
英文名称
diferrocenyl(trityloxy)cyclopropenylium tetrafluoroborate
英文别名
——
diferrocenyl(trityloxy)cyclopropenylium tetrafluoroborate化学式
CAS
862772-15-4
化学式
BF4*C42H33Fe2O
mdl
——
分子量
752.222
InChiKey
XOHOGSNJSAFTAS-UHFFFAOYSA-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

  • 作为反应物:
    参考文献:
    名称:
    Diferrocenylcyclopropenyl cations. Synthesis, structures, and some chemical properties
    摘要:
    Synthesis of diferrocenyleyclopropenyl tetrafluoroborates with hetero-substituents in the three-membered ring, viz., ethoxy, trityloxy, ferrocenyl(phenyl)methoxy, N,N-diethylamino, piperidino, and morpholino, is described. The spatial structure of diferrocenyl(morpholino)cyclopropenyl tetralluoroborate was established based on the data from X-ray diffraction analysis. Under the action of potassium tert-butoxide, all the diferrocenylcyclopropenyl tetrafluoroborates undergo three-membered ring-opening with formation of the corresponding 2,3-diferrocenylacrylic acid derivatives. A mechanism of the ring-opening is suggested. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2005.04.014
  • 作为产物:
    描述:
    2,3-diferrocenylcyclopropenone 、 trityl tetrafluoroborate 以 二氯甲烷 为溶剂, 以85%的产率得到diferrocenyl(trityloxy)cyclopropenylium tetrafluoroborate
    参考文献:
    名称:
    Diferrocenylcyclopropenyl cations. Synthesis, structures, and some chemical properties
    摘要:
    Synthesis of diferrocenyleyclopropenyl tetrafluoroborates with hetero-substituents in the three-membered ring, viz., ethoxy, trityloxy, ferrocenyl(phenyl)methoxy, N,N-diethylamino, piperidino, and morpholino, is described. The spatial structure of diferrocenyl(morpholino)cyclopropenyl tetralluoroborate was established based on the data from X-ray diffraction analysis. Under the action of potassium tert-butoxide, all the diferrocenylcyclopropenyl tetrafluoroborates undergo three-membered ring-opening with formation of the corresponding 2,3-diferrocenylacrylic acid derivatives. A mechanism of the ring-opening is suggested. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2005.04.014
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