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2,7,13,18-tetramethyl-3,6,14,17-tetraazatricyclo-[17.3.1.1]-tetracosa-1(23),8(24),9,11,19,21-hexane-9,11,20,22-tetraol | 1178976-24-3

中文名称
——
中文别名
——
英文名称
2,7,13,18-tetramethyl-3,6,14,17-tetraazatricyclo-[17.3.1.1]-tetracosa-1(23),8(24),9,11,19,21-hexane-9,11,20,22-tetraol
英文别名
2,7,13,18-Tetramethyl-3,6,14,17-tetrazatricyclo[17.3.1.18,12]tetracosa-1(23),8(24),9,11,19,21-hexaene-9,11,20,22-tetrol;2,7,13,18-tetramethyl-3,6,14,17-tetrazatricyclo[17.3.1.18,12]tetracosa-1(23),8(24),9,11,19,21-hexaene-9,11,20,22-tetrol
2,7,13,18-tetramethyl-3,6,14,17-tetraazatricyclo-[17.3.1.1]-tetracosa-1(23),8(24),9,11,19,21-hexane-9,11,20,22-tetraol化学式
CAS
1178976-24-3
化学式
C24H36N4O4
mdl
——
分子量
444.574
InChiKey
SAHWGXMGAFZFRE-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):
    1.1
  • 重原子数:
    32
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    129
  • 氢给体数:
    8
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    2,7,13,18-tetramethyl-3,6,14,17-tetraazatricyclo-[17.3.1.1]-tetracosa-1(23),8(24),9,11,19,21-hexane-9,11,20,22-tetraol 、 copper(II) acetate monohydrate 以 乙醇 为溶剂, 生成 [Cu2(2,7,13,18-tetramethyl-3,6,14,17-tetraazatricyclo-[17.3.1.1]-tetracosa-1(23),8(24),9,11,19,21-hexane-9,11,20,22-tetraol(4-))]
    参考文献:
    名称:
    Synthesis, characterization and catalytic oxidation of cyclohexane using a novel host (zeolite-Y)/guest (binuclear transition metal complexes) nanocomposite materials
    摘要:
    Transition metal (M = Mn(II), Co(II), Ni(II) and Cu(II)) complexes with octahydro-Schiff base (H-4-N4O4) = 2,7,13,18-tetramethyl-3,6,14,17-tetraazatricyclo-[17.3.1.1]-tetracosa-1(23), 2,6,8(24), 9,11,13,17,19,21-decaene-9,11,20,22-tetraol; H-4([H](8)-N4O4) = 2,7,13,, 18-tetramethyl-3,6,14,17-tetraazatricyclo-[17.13.1. 1.]-tetracosa-1(23), 8(24), 9,11,19,21-hexane-9,11,20,22-tetraol) have been encapsulated in nanopores of zeolite-Y; [M([H](8)-N4O4)]@NaY; with Flexible Ligand Method (FLM) for the first time. The new Host-Guest Nanocomposite Materials (HGNM) was characterized by several techniques: chemical analysis, spectroscopic methods (DRS, FT-IR and UV/Vis), BET technique, conductometric and magnetic measurements. The catalytic activities for oxidation of cyclohexane with HGNM complexes are reported. Zeolite encapsulated octahydro-Schiff base copper(II) complex; [Cu([H](8)-N4O4)]@NaY; was found to be more active than the corresponding cobalt(II), manganese(II) and nickel(II) complexes for cyclohexane oxidation. The catalytic properties of the complexes are influenced by their geometry and by the steric environment of the active sites. HGNM are stable enough to be reused and are suitable to be utilized as partial oxidation catalysts. The encapsulated catalysts systems; [M([H](8)-N4O4)]@NaY; were more active than the corresponding neat complexes; [M([H](8)-N4O4)))]. (C) 2009 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2009.04.028
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文献信息

  • Synthesis, characterization and catalytic oxidation of cyclohexane using a novel host (zeolite-Y)/guest (binuclear transition metal complexes) nanocomposite materials
    作者:Masoud Salavati-Niasari、Zohreh Salimi、Mahdi Bazarganipour、Fatemeh Davar
    DOI:10.1016/j.ica.2009.04.028
    日期:2009.8
    Transition metal (M = Mn(II), Co(II), Ni(II) and Cu(II)) complexes with octahydro-Schiff base (H-4-N4O4) = 2,7,13,18-tetramethyl-3,6,14,17-tetraazatricyclo-[17.3.1.1]-tetracosa-1(23), 2,6,8(24), 9,11,13,17,19,21-decaene-9,11,20,22-tetraol; H-4([H](8)-N4O4) = 2,7,13,, 18-tetramethyl-3,6,14,17-tetraazatricyclo-[17.13.1. 1.]-tetracosa-1(23), 8(24), 9,11,19,21-hexane-9,11,20,22-tetraol) have been encapsulated in nanopores of zeolite-Y; [M([H](8)-N4O4)]@NaY; with Flexible Ligand Method (FLM) for the first time. The new Host-Guest Nanocomposite Materials (HGNM) was characterized by several techniques: chemical analysis, spectroscopic methods (DRS, FT-IR and UV/Vis), BET technique, conductometric and magnetic measurements. The catalytic activities for oxidation of cyclohexane with HGNM complexes are reported. Zeolite encapsulated octahydro-Schiff base copper(II) complex; [Cu([H](8)-N4O4)]@NaY; was found to be more active than the corresponding cobalt(II), manganese(II) and nickel(II) complexes for cyclohexane oxidation. The catalytic properties of the complexes are influenced by their geometry and by the steric environment of the active sites. HGNM are stable enough to be reused and are suitable to be utilized as partial oxidation catalysts. The encapsulated catalysts systems; [M([H](8)-N4O4)]@NaY; were more active than the corresponding neat complexes; [M([H](8)-N4O4)))]. (C) 2009 Elsevier B. V. All rights reserved.
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