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[3,3-(biphenyl-2,2'-diyl)-1,1-bis(diphenylphosphino)allene]tetracarbonyliron | 1313574-11-6

中文名称
——
中文别名
——
英文名称
[3,3-(biphenyl-2,2'-diyl)-1,1-bis(diphenylphosphino)allene]tetracarbonyliron
英文别名
——
[3,3-(biphenyl-2,2'-diyl)-1,1-bis(diphenylphosphino)allene]tetracarbonyliron化学式
CAS
1313574-11-6
化学式
C43H28FeO4P2
mdl
——
分子量
726.487
InChiKey
JVGJMHWOPGHKHJ-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

  • 作为产物:
    描述:
    diiron nonacarbonyl3,3-(biphenyl-2,2'-diyl)-1,1-bis(diphenylphosphino)lallene四氢呋喃 为溶剂, 以19%的产率得到[3,3-(biphenyl-2,2'-diyl)-1,1-bis(diphenylphosphino)allene]tetracarbonyliron
    参考文献:
    名称:
    κ1- and κ2-Complexes of Fluorenylidene–Allenyl Phosphines and Phosphine Oxides with Palladium Chloride and Iron Carbonyl: Displacement of Trimethylsilyl by Diphenylphosphino via a Stabilized Carbanion
    摘要:
    An attempt to prepare 3,3-(biphenyl-2,2'-diyl)-1-diphenylphosphino-1-(trimethylsilyl)allene, 15, by treatment of 3,3- (bipheny1-2,2'-diyl)-1-lithio-1-(trimethylsilyl)allene with chlorodiphenylphosphine led instead to 3,3-(biphenyl-2,2'-diyl)-1,1-bis(diphenylphosphino)allene, 14. The proposed mechanism invokes attack on the trimethylsilyl group in 15 by liberated chloride to form a stabilized anion that reacts with a second molecule of the chlorophosphine. The diphosphine, 14, reacts with di-iron nonacarbonyl to form monodentate 14-Fe(CO)(4) and the chelate 14-Fe(CO)(3). 9-Ethynyl-9H-fluoren-9-ol and chlorodiphenylphosphine form 3,3-(biphenyl-2,2'-diyl)-1-diphenylphosphinylallene, which is readily deprotonated by triethylamine to generate a stabilized fluorenyl anion, which reacts with a second molecule of the chlorophosphine to furnish 3,3-(biphenyl-2,2'-diyl)-1-diphenylphosphino-1-diphenylphosphinylallene, 26. This bis-phosphine-monoxide (BPMO) reacts with di-iron nonacarbonyl to form initially monodentate P-bonded 26-Fe(CO)(4), which loses a carbonyl, allowing the adjacent allene double bond in 26-Fe(CO)(3) to coordinate to iron and leave the phosphine oxide uncoordinated. In contrast, the BPMO, 26, and (PhCN)(2)PdCl2 yield the phosphine-coordinated, chlorine-bridged dimer 34 and also the chelate 35, in which the palladium is linked to both the diphenylphosphino and diphenylphosphinyl groups via phosphorus and oxygen, respectively. Surprisingly, chlorodiphenylphosphine and 1,4-bis(9-hydroxy-9H-fluorenyl)buta-1,3-diyne, 37, do not yield the expected 3,4-bis(phosphinyl)hexa-1,2,4,5-tetraene, 33, but rather the 1-chloro-2-diphenylphosphinocyclobutene, 38, bearing a spiro-bonded fluorenylidene and a fluorenylidene-allene. All new compounds were characterized by P-31 NMR spectroscopy and X-ray crystallography.
    DOI:
    10.1021/om200357v
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