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benzo[i]benzo[6',7']quinoxalino[2',3':9,10]phenanthro[4,5-abc]phenazine | 1228192-02-6

中文名称
——
中文别名
——
英文名称
benzo[i]benzo[6',7']quinoxalino[2',3':9,10]phenanthro[4,5-abc]phenazine
英文别名
3,14,22,33-Tetrazadecacyclo[18.18.2.02,15.04,13.06,11.016,40.021,34.023,32.025,30.035,39]tetraconta-1(39),2,4,6,8,10,12,14,16(40),17,19,21,23,25,27,29,31,33,35,37-icosaene
benzo[i]benzo[6',7']quinoxalino[2',3':9,10]phenanthro[4,5-abc]phenazine化学式
CAS
1228192-02-6
化学式
C36H18N4
mdl
——
分子量
506.566
InChiKey
KKOKMEKPJIJLJR-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

物化性质

  • 熔点:
    >300 °C
  • 密度:
    1.491±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.6
  • 重原子数:
    40
  • 可旋转键数:
    0
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    2,3-二氨基萘芘- 4,5,9,10 -四酮吡啶 作用下, 反应 72.0h, 以40%的产率得到benzo[i]benzo[6',7']quinoxalino[2',3':9,10]phenanthro[4,5-abc]phenazine
    参考文献:
    名称:
    高度稳定的四氮杂十四碳烯和四氮杂八碳烯染料的简便合成
    摘要:
    稳定,可调且色彩鲜艳:据报道,可以直接合成高度稳定的π扩展的四氮杂庚并四氮杂十八碳烯染料。首次还观察到based基氮杂并苯的氧化行为,以及for原子氮杂并具有<11个线性稠合环的第三次还原波。
    DOI:
    10.1002/asia.200900373
点击查看最新优质反应信息

文献信息

  • Mechanochemical Synthesis, Photophysical Properties, and X-ray Structures of N-Heteroacenes
    作者:Prasit Kumar Sahoo、Chandan Giri、Tuhin Subhra Haldar、Rakesh Puttreddy、Kari Rissanen、Prasenjit Mal
    DOI:10.1002/ejoc.201600005
    日期:2016.3
    chromatographic purifications could be avoided after the solvent-free syntheses. The UV/Vis absorption spectra of the pyrazaacenes show intense absorption bands in the near-IR region. The single-crystal X-ray analyses of selected pyrazaacene derivatives showed pairwise π–π interactions and some C–H···π interactions, which could account for some of the photophysical features of the compounds in the solid
    所描述的机械化学方法是概念验证的一个例子,在该方法中,在无溶剂球磨条件下实现了基于溶液的乏味、收率低且困难的氮杂并苯合成;该方法简单、高产、省时、环保。合成的化合物还包括氮杂并苯(N-杂并苯),它们是含有结构单元的辛苯类似物。该化合物微溶于普通溶剂,无溶剂合成后可避免柱层析纯化。氮杂并苯的紫外/可见吸收光谱在近红外区域显示出强烈的吸收带。选定的氮杂并苯衍生物的单晶 X 射线分析显示成对的 π-π 相互作用和一些 C-H…π 相互作用,
  • ORGANIC THIN FILM TRANSISTOR
    申请人:LG Chem, Ltd.
    公开号:EP1836731B1
    公开(公告)日:2017-10-11
  • PYRENE DERIVATIVES AND ORGANIC ELECTRONIC DEVICE USING PYRENE DERIVATIVES
    申请人:LG CHEM, LTD.
    公开号:EP1828343B1
    公开(公告)日:2016-12-07
  • Organic thin film transistor
    申请人:Hwang Ho In
    公开号:US20070023749A1
    公开(公告)日:2007-02-01
    The present invention relates to an organic thin film transistor which includes an organic layer comprising an organic compound facilitating the ohmic contact between a semi-conducting layer and electrodes and serving as the semi-conducting layer. The organic thin film transistor according to the present invention has excellent electric contact between the semiconductor layer and the source electrode/drain electrode, and thus can be widely used as components for electric/electronic devices. As a result, as the materials for the source electrode or the drain electrode in the organic thin film transistor, materials which are less expensive and excellent in processibility though they have a low work function as the materials can be used.
  • Pyrene derivatives and organic electronic device using pyrene derivatives
    申请人:Lee Hoon Dong
    公开号:US20070069203A1
    公开(公告)日:2007-03-29
    The present invention provides an organic electronic device using the compound of the formula (1) and a pyrene derivative having a new structure.
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