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3,7-Diphenylimidazo[4,5-f]benzimidazole | 1013425-27-8

中文名称
——
中文别名
——
英文名称
3,7-Diphenylimidazo[4,5-f]benzimidazole
英文别名
——
3,7-Diphenylimidazo[4,5-f]benzimidazole化学式
CAS
1013425-27-8
化学式
C20H14N4
mdl
——
分子量
310.358
InChiKey
XCRUVCSCVOBEHZ-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):
    4.36
  • 重原子数:
    24.0
  • 可旋转键数:
    2.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    35.64
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    3,7-Diphenylimidazo[4,5-f]benzimidazolelithium diisopropyl amide 、 zinc(II) chloride 、 作用下, 以 四氢呋喃 为溶剂, 反应 3.25h, 以84%的产率得到2,6-Diiodo-3,7-diphenylimidazo[4,5-f]benzimidazole
    参考文献:
    名称:
    有机电致发光材料和器件
    摘要:
    公开了一种有机电致发光材料和器件。所述有机电致发光材料是一系列具有脱氢苯并二咪唑或脱氢苯并二吡咯及其类似结构的新型化合物,可用作电致发光器件中的电荷传输材料、电荷注入材料及类似材料。这些新型化合物具有深LUMO能级,在电荷传输材料、电荷注入材料等领域中具有更好的潜力和优良的应用前景。还公开了一种电致发光器件和化合物组合。
    公开号:
    CN113087711B
  • 作为产物:
    描述:
    碘苯benzobis(imidazole)copper(l) iodide1,10-菲罗啉potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 48.0h, 以19%的产率得到3,7-Diphenylimidazo[4,5-f]benzimidazole
    参考文献:
    名称:
    有机电致发光材料和器件
    摘要:
    公开了一种有机电致发光材料和器件。所述有机电致发光材料是一系列具有脱氢苯并二咪唑或脱氢苯并二吡咯及其类似结构的新型化合物,可用作电致发光器件中的电荷传输材料、电荷注入材料及类似材料。这些新型化合物具有深LUMO能级,在电荷传输材料、电荷注入材料等领域中具有更好的潜力和优良的应用前景。还公开了一种电致发光器件和化合物组合。
    公开号:
    CN113087711B
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文献信息

  • Modular Fluorescent Benzobis(imidazolium) Salts:  Syntheses, Photophysical Analyses, and Applications
    作者:Andrew J. Boydston、Peter D. Vu、Olga L. Dykhno、Vicki Chang、Alvin R. Wyatt、Adam S. Stockett、Eric T. Ritschdorff、Jason B. Shear、Christopher W. Bielawski
    DOI:10.1021/ja7102247
    日期:2008.3.1
    A series of benzobis(imidazolium) (BBI) salts has been prepared and studied as a new class of versatile fluorescent materials. Using a high yielding, modular synthetic strategy, 13131 salts with a range of functionality poised for investigating fundamental and applications-oriented characteristics, including emission wavelength tunability, solvatochromism, red-edge excitation, chemical stability, multiphoton excitation, and protein conjugation, were prepared in overall yields of 40-97%. Through structural variation, the BBIs exhibited lambda(em) ranging between 329 and 561 nm while displaying Phi(f)s up to 0.91. In addition, the emission characteristics of these salts were found to exhibit strong solvent dependencies with Stokes shifts ranging from 4570 to 13 793 cm(-1), depending on the nature of the BBI core. Although red-edge effects for BBI salts with Br and BF4 counterions were found to be similar, unique characteristics were displayed by an analogue with MeSO4 anions. The stability of an amphiphilic BBI was quantified in aqueous solutions of varying pH, and > 85% of the emission intensity was retained after 2 h at pH 3-9. Through multiphoton excitation experiments in aqueous solutions, a BBI salt was found to exhibit three-photon fluorescence action cross sections similar to serotonin. The application of BBI salts as fluorescent protein tags was demonstrated by conjugating bovine serum albumin to a maleimide-functionalized derivative.
  • ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES
    申请人:BEIJING SUMMER SPROUT TECHNOLOGY CO., LTD.
    公开号:US20210296594A1
    公开(公告)日:2021-09-23
    Organic electroluminescent materials and devices are disclosed. The organic electroluminescent materials are novel dehydrobenzodiimidazole or dehydrobenzodipyrrole or its analogous structure compounds, which can be used as charge transporting materials or charge injection materials or the like in an electroluminescent device. These novel compounds have deep LUMO energy level, and have better potential and excellent application prospecty in the field of charge-transporting materials, charge injection materials or the like. An organic electroluminescent device and a compound formulation are also disclosed.
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