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dibanzo-1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane | 1075689-94-9

中文名称
——
中文别名
——
英文名称
dibanzo-1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane
英文别名
dibenzo-1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane;Bzo2[16]aneN4;5,15-Diphenyl-2,6,12,16-tetrazatricyclo[15.3.1.17,11]docosa-1(20),7(22),8,10,17(21),18-hexaene-3,13-dione;5,15-diphenyl-2,6,12,16-tetrazatricyclo[15.3.1.17,11]docosa-1(20),7(22),8,10,17(21),18-hexaene-3,13-dione
dibanzo-1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane化学式
CAS
1075689-94-9
化学式
C30H28N4O2
mdl
——
分子量
476.578
InChiKey
PMGIRCAFLXTHLR-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):
    4.6
  • 重原子数:
    36
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    82.3
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    硫酸氧钒水合物dibanzo-1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane 在 (C2H5)3N 作用下, 以 乙醇 为溶剂, 生成 [VO(dibenzo-1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane)]SO4
    参考文献:
    名称:
    Synthesis, characterization and liquid-phase hydroxylation of phenol with hydrogen peroxide over host (nanopores of zeolite-Y)/guest (oxovanadium(IV) complexes of tetraaza macrocyclic ligands) nanocatalyst
    摘要:
    Oxovanadium(IV) tetraaza complexes of [14]aneN(4)n: 1,5,8,12-tetraaza-2,9-dioxo-4,11-diphenylcyclotetradecane; [16]aneN(4): 1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane; Bzo(2)[14]aneN(4): dibenzo-1,5,8,12-tetraaza-2,9-dioxo-4,11-diphenylcyclotetradecane and Bzo(2)[16] aneN(4): dibenzo-1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane have been encapsulated in the nanopores of zeolite-Y by a two-step process in the liquid phase: (i) adsorption of [bis(diamine)VO(IV)] (diamine = 1,2-diaminoethane, 1,3-diaminopropane, 1,2-diaminobenzene, 1,3-diaminobenzene); [VO(N-N)(2)](2+)-NaY; in the nanopores of the zeolite-Y and (ii) in situ condensation of the oxovanadium(IV) precursor complex with ethylcinnamate. The new host-guest nanocatalysts were characterized by several techniques: chemical analysis and spectroscopic methods (FT-infrared (FT-IR), ultraviolet-visible (UV-Vis), X-ray diffraction (XRD), nitrogen adsorption and diffuse reflectance spectra (DRS)) technique. The analytical data indicated a composition corresponding to the mononuclear complex of tetraaza ligand. The characterization data showed the absence of extraneous complexes, retention of zeolite crystalline structure and encapsulation in the nanopores. Liquid-phase selective hydroxylation of phenol with H2O2 to a mixture of catechol and hydroquinone in CH3CN have been reported using oxovanadium(IV) tetraaza complexes encapsulated in zeolite-Y as catalysts. All these catalysts are more selective toward catechol formation. (c) 2008 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2008.09.043
  • 作为产物:
    参考文献:
    名称:
    乙苯在主体(沸石-Y)/客体(四氮杂大环配体的铜(II)配合物)纳米复合材料上的合成、表征和催化氧化
    摘要:
    14 元和 16 元四氮杂大环配体的 Cu(II) 配合物已通过液相中的两步法封装在沸石-Y 的纳米孔中:(1)吸附 [双(二胺)铜(II)] (二胺 = 1,2-二氨基乙烷、1,3-二氨基丙烷、1,2-二氨基苯和 1,3-二氨基苯);[Cu(N–N)2]2+–NaY;在沸石-Y 的纳米孔中和 (2) 铜 (II) 前体络合物与肉桂酸乙酯的原位缩合。新的主客体纳米复合材料通过化学分析和光谱方法进行了表征。使用叔丁基过氧化氢作为氧化剂,“纯”和包封的复合物在 333 K 下对乙苯的氧化表现出良好的催化活性。
    DOI:
    10.1080/00958972.2010.510557
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文献信息

  • Synthesis, characterization of cobalt(II) complex nanoparticles encapsulated within nanoreactors of zeolite-Y and their catalytic activities
    作者:Masoud Salavati-Niasari
    DOI:10.1016/j.molcata.2009.05.018
    日期:2009.9
    Cobalt(II) complex nanoparticles of [14]aneN(4): 1,5,8,12-tetraaza-2,9-dioxo-4,11-diphenylcyclotetradecane [16]aneN(4): 1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane; Bzo(2)[14]aneN(4): dibenzo-1,5,8,12-tetraaza-2,9-dioxo-4,11-diphenylcyclotetradecane and Bzo(2)[16]aneN(4): dibenzo-1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane have been encapsulated in the nanopores of zeolite-Y by a two-step process in the liquid phase: (i) adsorption of [bis(diamine)cobalt(II)] (diamine = 1,2-diaminoethane, 1,3-diaminopropane, 1,2-diaminobenzene, 1,3-diaminobenzene): [Co(N-N)(2)](2+)-NaY; in the nanopores of the zeolite-Y. and (ii) in situ condensation of the cobalt(II) precursor complex with ethylcinnamate. The new complex nanoparticles entrapped in the nanoreactor of zeolite-Y were characterized by several techniques: BET, chemical analysis and spectroscopic methods (FT-IR, UV-vis, XRD, and DRS). These complexes (neat and encapsulated) were used for epoxidation of styrene with O-2 as oxidant in different solvents. Electronic spectra of the reaction mixture indicated that the oxidation proceeds through a free radical mechanism. (C) 2009 Elsevier B.V. All rights reserved.
  • Synthesis, characterization and catalytic oxidation of cyclohexene with molecular oxygen with host (nanopores of zeolite-Y)/guest (Ni(II) complexes of 14- and 16-membered tetraaza dioxo diphenyl macrocyclic ligands) nanocomposite materials
    作者:Masoud Salavati-Niasari
    DOI:10.1016/j.poly.2008.06.033
    日期:2008.9
    Ni(II) complexes of [14]aneN(4): 1,5,8,12-tetraaza-2,9-dioxo-4,11-diphenylcyclotetradecane; [16]aneN(4): 1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane; Bzo(2)[14]aneN(4): dibenzo-1,5,8,12-tetraaza-2,9-dioxo-4,11-diphenylcyclotetradecane and Bzo(2)[16]aneN(4): dibenzo-1,5,9,13-tetraaza-2,10-dioxo-4,12-diphenylcyclohexadecane have been encapsulated in the nanopores of zeolite-Y by a two-step process in the liquid phase: (i) adsorption of [bis(diamine)nickel(II)] (diamine = 1,2-diaminoethane, 1,3-diaminopropane, 1,2-diaminobenzene, 1,3-diaminobenzene); [Ni(N-N)(2)](2+)-NaY; in the nanopores of the zeolite-Y, and (ii) in situ condensation of the nickel(II) precursor complex with ethylcinnamate. The new host-guest nanocomposite materials (HGNM) were characterized by several techniques: chemical analysis and spectroscopic methods (FT-IR, UV/Vis, XRD and DRS) and the BET technique. These complexes were used for oxidation of cyclohexene with molecular oxygen. (C) 2008 Elsevier Ltd. All rights reserved.
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