| 172973-81-8

• CAS: 172973-81-8
• 化学式: C₂₂H₂₉FePSi₂
• 分子量: 436.464
• InChiKey: LENBBJVMMHXNEY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.97
• 重原子数：
  26.0
• 可旋转键数：
  5.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  0.0
• 氢给体数：
  0.0
• 氢受体数：
  0.0

反应信息

• 作为反应物：
  描述：

  以 neat (no solvent) 为溶剂， 以66%的产率得到iron(II) 1,1'-(phenylphosphanediyl)bis(3-(trimethylsilyl)cyclopenta-2,4-dien-1-ide)
  参考文献：
  名称：

  应变的，倾斜的磷桥连的[1]二茂铁磷烯的热开环聚合（ROP）：聚二茂铁膦和聚二茂铁膦的合成

  摘要：

  A series of phosphorus(III)-bridged [1]ferrocenophanes Fe[(eta-C(5)H(3)R)(eta-C(5)H(3)R')]PX (X = Ph, R = R' = H (3); X = Cl, R = R' = H (4); X = Ph, R = H, R' = (II)Bu (5); X = Ph, R = R' = SiMe(3) (6)) have been synthesized via the reaction of Fe[(eta-C(5)H(3)R'Li)(eta-C(5)H(3)R'Li)]. nTMEDA with PXCl(2) (X = Cl, Ph). The reaction of 6 with an excess of elemental sulfur resulted in the quantitative formation of the phosphorus(V)-bridged species Fe[eta-C(5)H(3)SiMe(3)]P-2(S)Ph (7). The new compounds 4-7 were characterized by multinuclear NMR, by mass spectrometry and, in the cases of 4, 6, and a, by single-crystal X-ray diffraction and elemental analysis. Ring-tilt angles (alpha) for 4 and 6 were found to be typical of phosphorus(III)-bridged [1]ferrocenophanes (4, 27.0(6)degrees; 6, 27.5(6)degrees) whereas in the case of the phosphorus(V)-bridged species 7 the tilt angle was slightly less (alpha = 25.3(3)degrees). The thermal ring-opening polymerization of 3, 5, and 6 at 120-250 degrees C yielded the poly(ferrocenylphosphines) 8-10, respectively. These materials were characterized by multinuclear NMR and by elemental analysis. The molecular weight of the trimethylsilyl-substituted polymer 10 was determined by GPC in THF versus polystyrene standards to be M(w) = 66 000, PDI = 1.98, whereas 8 and 9 failed to elute from the GPC column. The phosphorus(V)-bridged species 7 also underwent thermal ring-opening polymerization to yield the poly(ferrocenylphosphine sulfide) 13 which was analyzed by GPC (M(w) = 22 000, PDI = 1.24); thermally-induced elimination of S(SiMe(3))(2) from the ring-opened polymer was identified as a side reaction. The macromolecular reactions of 8-10 with elemental sulfur yielded the poly(ferrocenylphosphine sulfides) 11-13. These were structurally characterized by multinuclear NMR and elemental analysis and their molecular distributions were analyzed by GPC (M(w) = 18 000-65 000, PDI = 1.5-2.3).

  DOI：

  10.1021/om00012a017
• 作为产物：
  描述：

  、 苯基二氯化磷 以 正己烷 为溶剂， 以16%的产率得到
  参考文献：
  名称：

  应变的，倾斜的磷桥连的[1]二茂铁磷烯的热开环聚合（ROP）：聚二茂铁膦和聚二茂铁膦的合成

  摘要：

  A series of phosphorus(III)-bridged [1]ferrocenophanes Fe[(eta-C(5)H(3)R)(eta-C(5)H(3)R')]PX (X = Ph, R = R' = H (3); X = Cl, R = R' = H (4); X = Ph, R = H, R' = (II)Bu (5); X = Ph, R = R' = SiMe(3) (6)) have been synthesized via the reaction of Fe[(eta-C(5)H(3)R'Li)(eta-C(5)H(3)R'Li)]. nTMEDA with PXCl(2) (X = Cl, Ph). The reaction of 6 with an excess of elemental sulfur resulted in the quantitative formation of the phosphorus(V)-bridged species Fe[eta-C(5)H(3)SiMe(3)]P-2(S)Ph (7). The new compounds 4-7 were characterized by multinuclear NMR, by mass spectrometry and, in the cases of 4, 6, and a, by single-crystal X-ray diffraction and elemental analysis. Ring-tilt angles (alpha) for 4 and 6 were found to be typical of phosphorus(III)-bridged [1]ferrocenophanes (4, 27.0(6)degrees; 6, 27.5(6)degrees) whereas in the case of the phosphorus(V)-bridged species 7 the tilt angle was slightly less (alpha = 25.3(3)degrees). The thermal ring-opening polymerization of 3, 5, and 6 at 120-250 degrees C yielded the poly(ferrocenylphosphines) 8-10, respectively. These materials were characterized by multinuclear NMR and by elemental analysis. The molecular weight of the trimethylsilyl-substituted polymer 10 was determined by GPC in THF versus polystyrene standards to be M(w) = 66 000, PDI = 1.98, whereas 8 and 9 failed to elute from the GPC column. The phosphorus(V)-bridged species 7 also underwent thermal ring-opening polymerization to yield the poly(ferrocenylphosphine sulfide) 13 which was analyzed by GPC (M(w) = 22 000, PDI = 1.24); thermally-induced elimination of S(SiMe(3))(2) from the ring-opened polymer was identified as a side reaction. The macromolecular reactions of 8-10 with elemental sulfur yielded the poly(ferrocenylphosphine sulfides) 11-13. These were structurally characterized by multinuclear NMR and elemental analysis and their molecular distributions were analyzed by GPC (M(w) = 18 000-65 000, PDI = 1.5-2.3).

  DOI：

  10.1021/om00012a017