1,1'-(9,9-diethyl-9H-fluorene-2,7-diyl)bis(methylene)bis(2,4,5-triphenyl-1H-imidazole) | 1426959-06-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 芴
• 英文名称: 1,1'-(9,9-diethyl-9H-fluorene-2,7-diyl)bis(methylene)bis(2,4,5-triphenyl-1H-imidazole)
• 英文别名: 1-[[9,9-Diethyl-7-[(2,4,5-triphenylimidazol-1-yl)methyl]fluoren-2-yl]methyl]-2,4,5-triphenylimidazole；1-[[9,9-diethyl-7-[(2,4,5-triphenylimidazol-1-yl)methyl]fluoren-2-yl]methyl]-2,4,5-triphenylimidazole
• CAS: 1426959-06-9
• 化学式: C₆₁H₅₀N₄
• 分子量: 839.095
• InChiKey: BPVRLUZFWIQGOF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  14.8
• 重原子数：
  65
• 可旋转键数：
  12
• 环数：
  11.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  35.6
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2,7-bis(bromomethyl)-9,9-diethylfluorene 、 2,4,5-三苯基咪唑 在 苄基三乙基氯化铵 、 sodium hydroxide 作用下， 以 水 、 苯 为溶剂， 以54%的产率得到1,1'-(9,9-diethyl-9H-fluorene-2,7-diyl)bis(methylene)bis(2,4,5-triphenyl-1H-imidazole)
  参考文献：
  名称：

  Synthesis, optical properties, and blue electroluminescence of fluorene derivatives containing multiple imidazoles bearing polyaromatic hydrocarbons

  摘要：

  Fluorene decorated with multiple imidazole units in a non-conjugated fashion and featuring polyaromatic hydrocarbons such as anthracene or pyrene were synthesized and characterized as blue emitters suitable for application in organic light-emitting diodes. The optical absorption and emission peak profiles remained unaltered on increasing the imidazole loading on fluorene. But the molar extinction coefficient progressively increased on introduction of additional imidazole unit attributable to the increment in the chromophore density. Replacement of phenyl group at the C-2 of imidazole nucleus with polyaromatic hydrocarbons such as anthracene and pyrene led to a red-shift in the absorption and emission spectra due to their characteristic absorption features. All the compounds exhibited high thermal decomposition temperature in the range 395-509 degrees C showing significant thermal robustness. The anthracene and pyrene derivatives were demonstrated as efficient blue emitters in 4,4'-di(9H-carbazol-9-y1)-1,1'-biphenyl host for multilayered organic light-emitting diodes. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2013.01.046

文献信息

• Synthesis, optical properties, and blue electroluminescence of fluorene derivatives containing multiple imidazoles bearing polyaromatic hydrocarbons
  作者：Dhirendra Kumar、K.R. Justin Thomas、Yu-Lin Chen、Yung-Cheng Jou、Jwo-Huei Jou

  DOI：10.1016/j.tet.2013.01.046

  日期：2013.3

  Fluorene decorated with multiple imidazole units in a non-conjugated fashion and featuring polyaromatic hydrocarbons such as anthracene or pyrene were synthesized and characterized as blue emitters suitable for application in organic light-emitting diodes. The optical absorption and emission peak profiles remained unaltered on increasing the imidazole loading on fluorene. But the molar extinction coefficient progressively increased on introduction of additional imidazole unit attributable to the increment in the chromophore density. Replacement of phenyl group at the C-2 of imidazole nucleus with polyaromatic hydrocarbons such as anthracene and pyrene led to a red-shift in the absorption and emission spectra due to their characteristic absorption features. All the compounds exhibited high thermal decomposition temperature in the range 395-509 degrees C showing significant thermal robustness. The anthracene and pyrene derivatives were demonstrated as efficient blue emitters in 4,4'-di(9H-carbazol-9-y1)-1,1'-biphenyl host for multilayered organic light-emitting diodes. (C) 2013 Elsevier Ltd. All rights reserved.