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2-(10-bromoanthr-9-yl)-1-n-dodecyl-4,5-diphenylimidazole | 1192255-63-2

中文名称
——
中文别名
——
英文名称
2-(10-bromoanthr-9-yl)-1-n-dodecyl-4,5-diphenylimidazole
英文别名
2-(10-Bromoanthracen-9-yl)-1-dodecyl-4,5-diphenylimidazole
2-(10-bromoanthr-9-yl)-1-n-dodecyl-4,5-diphenylimidazole化学式
CAS
1192255-63-2
化学式
C41H43BrN2
mdl
——
分子量
643.71
InChiKey
XCLYUYKFHURTQR-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):
    13.7
  • 重原子数:
    44
  • 可旋转键数:
    14
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2-(anthracen-9-yl)-4,5-diphenyl-1H-imidazole四丁基溴化铵 、 sodium hydroxide 作用下, 以 二硫化碳丁酮 为溶剂, 反应 3.0h, 生成 2-(10-bromoanthr-9-yl)-1-n-dodecyl-4,5-diphenylimidazole
    参考文献:
    名称:
    Synthesis and optical behaviors of 2-(9-phenanthrenyl)-, 2-(9-anthryl)-, and 2-(1-pyrenyl)-1-alkylimidazole homologues
    摘要:
    Eight 2-(9-phenanthrenyl)-, 2-(9-anthryl)- and 2-(I-pyrenyl)-1-alkyl-benzimidazole compounds, three 2-(9-anthryl)-1-alkylphenanthroimidazole compounds and five 4,5-diphenyl-1-alkyl-2-(9-anthryl)imidazole compounds were synthesized by alkylation reactions of the corresponding benzimidazole, phenanthroimidazole or imidazole compounds. 2-(10-Bromo-9-anthryl)-1-alkyl-benzimidazole compounds were prepared by bromination reaction of 2-(9-anthryl)-1-alkylbenzimidazole compounds. All the synthesized compounds were characterized by elemental analysis, H-1 NMR, C-13 NMR, MS or HRMS; their absorption coefficients (epsilon), maximum absorption lambda(amax). fluorescence emission maximum lambda(em), Stokes shifts and fluorescence quantum yields (Phi(F)) in ethyl acetate were determined; their fluorescent lifetimes (T-1 and T-2) were measured in ethyl acetate and in solid state, respectively. The crystal structure of 2-(9-anthryl)-1-n-butyl-4,5-diphenylimidazole (12a) was determined to be triclinic, space group P-1 types, using single crystal X-ray crystallography technique. The results showed that these compounds exhibited moderate fluorescence-emission abilities and higher solubility in most organic solvents than their corresponding starting materials. The relationships between the optical behaviors and structures for these compounds were discussed. (C) 2009 Published by Elsevier B.V.
    DOI:
    10.1016/j.saa.2009.06.020
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