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(η5:η1:η5:η1-Et8-calix[4]pyrrolyl)(Gd(SiMe3)2)2 | 1360146-18-4

中文名称
——
中文别名
——
英文名称
(η5:η1:η5:η1-Et8-calix[4]pyrrolyl)(Gd(SiMe3)2)2
英文别名
——
(η5:η1:η5:η1-Et8-calix[4]pyrrolyl)(Gd(SiMe3)2)2化学式
CAS
1360146-18-4
化学式
C48H84Gd2N6Si4
mdl
——
分子量
1172.08
InChiKey
WTXQTQVZVDWKLJ-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:
    [(Me3Si)2N]3Gd(µ-Cl)Li(THF)3meso-octaethylporphyrinogen甲苯 为溶剂, 以53%的产率得到(η5:η1:η5:η1-Et8-calix[4]pyrrolyl)(Gd(SiMe3)2)2
    参考文献:
    名称:
    Synthesis and Characterization of Organolanthanide Complexes with a Calix[4]-pyrrolyl Ligand and Their Catalytic Activities toward Hydrophosphonylation of Aldehydes and Unactivated Ketones
    摘要:
    The alkali metal salt free dinuclear trivalent lanthanide amido complexes (eta(5):eta(1):eta(5):eta(1)-Et-8-calix[4]-pyrrolyl){LnN-(SiMe3)(2)}(2) (Ln = Nd (2), Sm (3), Gd (4)) were prepared through the silylamine elimination reactions of calix[4]-pyrrole [Et2C(C4H2NH)](4) (1) with 2 equiv of [(Me3Si)(2)N](3)Ln(mu-Cl)Li(THF)(3) (Ln = Nd, Sm, Gd) in toluene at 110 degrees C. The complexes were fully characterized by elemental, spectroscopic, and single-crystal X-ray analyses. Studies on the catalytic activity of the new lanthanide amido complexes revealed that these complexes can be used as efficient catalysts for hydrophosphonylation of aldehydes and unactivated ketones, affording the products in high yields by employing a low catalyst loading (0.1 mol %) at room temperature in a short time (20 min). Noteworthy is that it is the first application of calix[4]-pyrrolyl-supported lanthanide amides as catalysts to catalyze the hydrophosphonylation of aldehydes and unactivated ketones under mild conditions.
    DOI:
    10.1021/om2008925
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