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(N3P3(OPh)(OCH2CF3)3(η-C5H4)2Fe)n | 136657-22-2

中文名称
——
中文别名
——
英文名称
(N3P3(OPh)(OCH2CF3)3(η-C5H4)2Fe)n
英文别名
——
(N3P3(OPh)(OCH2CF3)3(η-C5H4)2Fe)n化学式
CAS
136657-22-2
化学式
C22H19F9FeN3O4P3
mdl
——
分子量
709.164
InChiKey
DVCLZPSGEXUFFC-MRAYHFNWSA-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:
    N3P3(OPh)(OCH2CF3)3(η-C5H4)2Fe 在 六氯环三磷腈 作用下, 以 melt 为溶剂, 以25%的产率得到(N3P3(OPh)(OCH2CF3)3(η-C5H4)2Fe)n
    参考文献:
    名称:
    Strain-induced ring-opening polymerization of ferrocenylorganocyclotriphosphazenes: a new synthetic route to poly(organophosphazenes)
    摘要:
    The strained transannular ferrocenylcyclotriphosphazenes N3P3(OCH2CF3)4(eta-C5H4)2Fe, N3P3R(OCH2CF3)3(eta-C5H4)2Fe [R = OPh, R = Me, R = Ph (R geminal to Cp), and R = Ph (nongeminal to Cp)], and N3P3R2(OCH2CF3)2(eta-C5H4)2Fe [R = Ph (geminal to Cp) and R = Ph (nongeminal to Cp)] undergo ring-opening polymerization when heated at 250-degrees-C in the presence of a small amount (1%) of (NPCl2)3, which functions as a polymerization initiator. The cyclic trimers N3P3(OPh)(OCH2CF3)3(eta-C5H4)2Fe, N3P3Me(OCH2CF3)3(eta-C5H4)2Fe, and N3P3Ph2(OCH2CF3)2(eta-C5H4)2Fe (Ph groups nongeminal to Cp) also polymerize at 250-degrees-C but in the absence of (NPCl2)3. These transformations are the first examples of uncatalyzed ring-opening polymerization of cyclic phosphazenes that lack phosphorus-halogen bonds. By contrast,the sterically crowded cyclotriphosphazene N3P3(OPh)4(eta-C5H4)2Fe undergoes ring expansion to the corresponding cyclic hexamer when heated at 250-degrees-C in the presence or absence of (NPCl2)3, but it does not polymerize. When heated in the absence of (NPCl2)3, N3P3(OCH2CF3)4(eta-C5H4)2Fe, N3P3(OPh)(OCH2CF3)3(eta-C5H4)2Fe, and N3P3Ph(OCH2CF3)3(eta-C5H4)2Fe (Ph nongeminal to Cp) also undergo ring expansion to form the corresponding cyclic hexamers. The Lewis acid BCl3 initiates the ring-opening polymerization of N3P3(OCH2CF3)4(eta-C5H4)2Fe and catalyzes the ring expansion of N3P3(OPh)4(eta-C5H4)2Fe. Possible explanations for the differences in thermal behavior are given. The implications of these results for the mechanisms of phosphazene ring-opening polymerization and ring-ring equilibration are also discussed.
    DOI:
    10.1021/ja00025a026
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