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2-methylnaphth-1-yl ferrocenoyl selenide | 779339-33-2

中文名称
——
中文别名
——
英文名称
2-methylnaphth-1-yl ferrocenoyl selenide
英文别名
——
2-methylnaphth-1-yl ferrocenoyl selenide化学式
CAS
779339-33-2
化学式
C22H18FeOSe
mdl
——
分子量
433.191
InChiKey
LYIAPYORUIKIFR-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:
    描述:
    2-methylnaphth-1-yl ferrocenoyl selenide苯硫酚 以 further solvent(s) 为溶剂, 以0%的产率得到二茂铁甲醛
    参考文献:
    名称:
    Synthesis, reactivity, electrochemical and crystallographic studies of diferrocenoyl diselenide and ferrocenoyl selenides
    摘要:
    Diacyl diselenide (8), diacyl selenide (9) and acyl selenol esters (10-12) incorporating the ferrocenoyl substituent have been synthesized from ferrocene carboxylic acid (13). The new compounds (8-10) have been characterized by multinuclear NMR (H-1, C-13, Se-77), IR spectroscopy and electrospray mass spectrometry. All compounds (8-13) undergo a one electron reversible oxidation at significantly more positive potential than ferrocene. The structures of the diselenide and selenide (8 and 10) have been confirmed by single crystal X-ray diffraction. The absolute structure parameter of 8 indicates that it crystallizes in an enan-tiomerically pure form. The peroxidase-like activities of the diselenide (8) and selenides (9-12) have been determined by the thiol assay. (C) 2004 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2004.06.054
  • 作为产物:
    描述:
    ferrocenoyl chloridebis(2-methyl-1-naphthyl) diselenide 在 LiBHEt3 作用下, 以 四氢呋喃 为溶剂, 以94%的产率得到2-methylnaphth-1-yl ferrocenoyl selenide
    参考文献:
    名称:
    Synthesis, reactivity, electrochemical and crystallographic studies of diferrocenoyl diselenide and ferrocenoyl selenides
    摘要:
    Diacyl diselenide (8), diacyl selenide (9) and acyl selenol esters (10-12) incorporating the ferrocenoyl substituent have been synthesized from ferrocene carboxylic acid (13). The new compounds (8-10) have been characterized by multinuclear NMR (H-1, C-13, Se-77), IR spectroscopy and electrospray mass spectrometry. All compounds (8-13) undergo a one electron reversible oxidation at significantly more positive potential than ferrocene. The structures of the diselenide and selenide (8 and 10) have been confirmed by single crystal X-ray diffraction. The absolute structure parameter of 8 indicates that it crystallizes in an enan-tiomerically pure form. The peroxidase-like activities of the diselenide (8) and selenides (9-12) have been determined by the thiol assay. (C) 2004 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2004.06.054
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