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dicarbonyl(methylcyclopentadienyl)-3-(2-methoxy-6-phenylpyrylium)iron(II) hexafluorophosphate | 714960-55-1

中文名称
——
中文别名
——
英文名称
dicarbonyl(methylcyclopentadienyl)-3-(2-methoxy-6-phenylpyrylium)iron(II) hexafluorophosphate
英文别名
——
dicarbonyl(methylcyclopentadienyl)-3-(2-methoxy-6-phenylpyrylium)iron(II) hexafluorophosphate化学式
CAS
714960-55-1
化学式
C20H17FeO4*F6P
mdl
——
分子量
522.164
InChiKey
RXVDYKYTXNWINU-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

反应信息

  • 作为产物:
    描述:
    六氟磷酸银 、 [FeI(CO)2(η5-C5H4CH3)] 、 苯乙炔丙炔酸甲酯二氯甲烷 为溶剂, 以20%的产率得到dicarbonyl(methylcyclopentadienyl)-3-(2-methoxy-6-phenylpyrylium)iron(II) hexafluorophosphate
    参考文献:
    名称:
    Synthesis and Electrochemistry of Iron-Pyrylium Complexes
    摘要:
    The syntheses and characterization of three cationic iron-pyrylium complexes (2(+), [2-OMe-3-Fp-5,6-Ph2(C5HO)] (+); 3(+), [2-OMe-3-Fp-6-Ph(C5H2O)](+); 4(+), [2-OMe-3-Fp'-6-Ph (C5H2O)] (+))that result from the sequential addition of methyl propiolate and PhC=CR (R = Ph, H) to FpBF(4) (Fp = eta(5)-C5H5(CO)(2)Fe) or Fp'PF6 (Fp' = eta(5)-(C5H4Me)(CO)(2)Fe) are presented. The initially formed cationic Fp-methyl propiolate complex is shown to convert into a complicated mixture that includes the corresponding vinylidene and alkynyl complexes. The iron-pyrylium complexes have been characterized by H-1 NMR and IR spectroscopy, elemental analysis, FAB-MS, electrochemical, and fiber-optic-IR and ESR spectroelectrochemical techniques. These metal-pyrylium complexes undergo electron transfer at the pyrylium ring rather than at the metal center. The subsequent chemistry of the neutral species 2(.), 3(.), and 4(.) is strongly influenced by the nature of the substituents on the ring. The sterically protected complex 2+ undergoes chemically and electrochemically reversible reductions. The complexes 3+ and 4+ undergo dimerization reactions after reduction presumably through the 4-position of the pyrylium ring.
    DOI:
    10.1021/om0343420
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