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1,7-diphenyl-1,7-dihydrobenzo[1,2-d:4,5-d']diimidazole | 1000054-24-9

中文名称
——
中文别名
——
英文名称
1,7-diphenyl-1,7-dihydrobenzo[1,2-d:4,5-d']diimidazole
英文别名
——
1,7-diphenyl-1,7-dihydrobenzo[1,2-d:4,5-d']diimidazole化学式
CAS
1000054-24-9
化学式
C20H14N4
mdl
——
分子量
310.358
InChiKey
DEIGATOKUQRUEM-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

  • 沸点:
    567.6±60.0 °C(Predicted)
  • 密度:
    1.27±0.1 g/cm3(Predicted)

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:
    1,7-diphenyl-1,7-dihydrobenzo[1,2-d:4,5-d']diimidazole硫酸二甲酯乙腈 为溶剂, 以99%的产率得到3,5-dimethyl-1,7-diphenylbenzobis(imidazolylium) methylsulfate
    参考文献:
    名称:
    Modular Fluorescent Benzobis(imidazolium) Salts:  Syntheses, Photophysical Analyses, and Applications
    摘要:
    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.
    DOI:
    10.1021/ja7102247
  • 作为产物:
    描述:
    甲酸4,6-dinitro-N1,N3-diphenylbenzene-1,3-diamine 在 palladium on activated charcoal 碳酸氢钠 作用下, 反应 48.0h, 以95%的产率得到1,7-diphenyl-1,7-dihydrobenzo[1,2-d:4,5-d']diimidazole
    参考文献:
    名称:
    Phase-Tunable Fluorophores Based upon Benzobis(imidazolium) Salts
    摘要:
    A new series of highly photoluminescent benzobis(imidazolium) salts with tunable electronic and physical properties is described. Systematic structural manipulations provided a set of materials that were not only fluorescent in the condensed state but also displayed tunable glass transition temperatures ranging from -0.3 to 113 degrees C. Upon heating, these robust materials flowed while maintaining their emissive properties. Further phase tuning was demonstrated through the synthesis of two thermotropic liquid-crystalline fluorescent benzobis(imidazolium) salts.
    DOI:
    10.1021/ja075963d
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