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2-(phthalimidomethyl)triphenylene | 166898-50-6

中文名称
——
中文别名
——
英文名称
2-(phthalimidomethyl)triphenylene
英文别名
2-(Triphenylen-2-ylmethyl)isoindole-1,3-dione;2-(triphenylen-2-ylmethyl)isoindole-1,3-dione
2-(phthalimidomethyl)triphenylene化学式
CAS
166898-50-6
化学式
C27H17NO2
mdl
——
分子量
387.437
InChiKey
DWPIRXHLEVVPMA-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):
    6.1
  • 重原子数:
    30
  • 可旋转键数:
    2
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    37.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-(phthalimidomethyl)triphenylene一水合肼 作用下, 以 乙醇 为溶剂, 反应 2.0h, 以94%的产率得到2-(aminomethyl)triphenylene
    参考文献:
    名称:
    New Sensitizer-Modified Calix[4]arenes Enabling Near-UV Excitation of Complexed Luminescent Lanthanide Ions
    摘要:
    The synthesis is described of a series of calix[4]arenes with three different sensitizer chromophores (''antenna'') attached to the lower rim via a short spacer. In the Eu3+ and Tb3+ complexes of these calixarenes, photoexcitation of the antenna can induce lanthanide emission via intramolecular energy transfer. Although the higher energy of the Tb3+ luminescent state makes it more difficult to sensitize than in the case of Eu3+, especially a triphenylene antenna is found to have strong sensitizing ability toward not only Eu3+ but also Tb3+, allowing excitation of the lanthanide with wavelengths extending to 350 nm.
    DOI:
    10.1021/ja00142a004
  • 作为产物:
    参考文献:
    名称:
    New Sensitizer-Modified Calix[4]arenes Enabling Near-UV Excitation of Complexed Luminescent Lanthanide Ions
    摘要:
    The synthesis is described of a series of calix[4]arenes with three different sensitizer chromophores (''antenna'') attached to the lower rim via a short spacer. In the Eu3+ and Tb3+ complexes of these calixarenes, photoexcitation of the antenna can induce lanthanide emission via intramolecular energy transfer. Although the higher energy of the Tb3+ luminescent state makes it more difficult to sensitize than in the case of Eu3+, especially a triphenylene antenna is found to have strong sensitizing ability toward not only Eu3+ but also Tb3+, allowing excitation of the lanthanide with wavelengths extending to 350 nm.
    DOI:
    10.1021/ja00142a004
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文献信息

  • [EN] HOLE INJECTOR POLYMERS<br/>[FR] POLYMERES INJECTEURS DE TROUS
    申请人:THOMSON-CSF
    公开号:WO1999065961A1
    公开(公告)日:1999-12-23
    (EN) The invention relates to a new type of material that can be used for visual presentation in electroluminescent displays. The invention consists of straight-chain polymers containing active groups in terms of hole injection in an electroluminescent material. The above-mentioned active groups can be of a monopyrazoline or monoamine type.(FR) L'invention concerne un nouveau type de matériaux susceptibles d'être utilisés en visualisation dans des écrans électroluminescents. Il s'agit de polymères à chaînes latérales comportant des groupements actifs en terme d'injection de trous dans un matériau électroluminescent. Ces groupements actifs peuvent être de type monopyrazoline ou de type monoamine.
  • New Sensitizer-Modified Calix[4]arenes Enabling Near-UV Excitation of Complexed Luminescent Lanthanide Ions
    作者:Frank J. Steemers、Willem Verboom、David N. Reinhoudt、Erik B. van der Tol、Jan W. Verhoeven
    DOI:10.1021/ja00142a004
    日期:1995.9
    The synthesis is described of a series of calix[4]arenes with three different sensitizer chromophores (''antenna'') attached to the lower rim via a short spacer. In the Eu3+ and Tb3+ complexes of these calixarenes, photoexcitation of the antenna can induce lanthanide emission via intramolecular energy transfer. Although the higher energy of the Tb3+ luminescent state makes it more difficult to sensitize than in the case of Eu3+, especially a triphenylene antenna is found to have strong sensitizing ability toward not only Eu3+ but also Tb3+, allowing excitation of the lanthanide with wavelengths extending to 350 nm.
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