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chlorodioxo(2-(ferrocenylmethyleneamino)ethylato)(tetrahydrofuran)molybdenum(VI) | 1178577-90-6

中文名称
——
中文别名
——
英文名称
chlorodioxo(2-(ferrocenylmethyleneamino)ethylato)(tetrahydrofuran)molybdenum(VI)
英文别名
——
chlorodioxo(2-(ferrocenylmethyleneamino)ethylato)(tetrahydrofuran)molybdenum(VI)化学式
CAS
1178577-90-6
化学式
C17H22ClFeMoNO4
mdl
——
分子量
491.606
InChiKey
UDDPSCUDEQGMCY-UHFFFAOYSA-M
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:
    2-(二茂铁基亚甲基氨基)乙醇Molybdenum, dichlorodioxobis(tetrahydrofuran)-四氢呋喃 为溶剂, 以88%的产率得到chlorodioxo(2-(ferrocenylmethyleneamino)ethylato)(tetrahydrofuran)molybdenum(VI)
    参考文献:
    名称:
    Synthesis and catalytic performance for olefin epoxidation of a novel dioxomolybdenum (VI) (ferrocenylmethyleneamino)alcoholate complex
    摘要:
    A novel dioxomolybdenum (VI) complex of (ferrocenylmethyleneamino) alcoholate was easily synthesized via the reaction of MoO2Cl2(THF)(2) with N-hydroxyethyl ferrocenylimine ligand [(eta(5)-C5H5)Fe{(eta(5)-C5H4)-CH=N-CH2-CH2-OH}], and characterized by FR-IR, H-1 NMR, UV-Vis spectroscopy and elemental analysis. In the presence of the catalytic amount of the dioxomolybdenum (VI) complex, good to excellent selectivities of epoxides (77-95%) were obtained for epoxidation of styrene and cyclohexene with tertbutyl hydroperoxide (TBHP) as oxidant in 1,2-dichloroethane at 12 h. Higher initial activity of the complex was observed for the catalyzed styrene epoxidation (451 mol mol(Mo) (1) h (1)) than that of cyclohexene epoxidation (164 mol molMo (1) h (1)) at 1 h. Meanwhile, influences of reaction temperature, solvents, reaction time as well as catalyst amount for olefin epoxidation were also investigated. (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2009.05.033
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