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2-(4-(trifluoromethyl)phenyl)-4,5-bis(4-hydroxyphenyl)imidazole | 1414863-66-3

中文名称
——
中文别名
——
英文名称
2-(4-(trifluoromethyl)phenyl)-4,5-bis(4-hydroxyphenyl)imidazole
英文别名
4-[4-(4-hydroxyphenyl)-2-[4-(trifluoromethyl)phenyl]-1H-imidazol-5-yl]phenol
2-(4-(trifluoromethyl)phenyl)-4,5-bis(4-hydroxyphenyl)imidazole化学式
CAS
1414863-66-3
化学式
C22H15F3N2O2
mdl
——
分子量
396.369
InChiKey
FOTKJKWKVOAYLZ-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):
    5.2
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    69.1
  • 氢给体数:
    3
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    2-氯-5-硝基三氟甲苯2-(4-(trifluoromethyl)phenyl)-4,5-bis(4-hydroxyphenyl)imidazolepotassium carbonate 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 8.0h, 以93%的产率得到2-(4-trifluoromethylphenyl)-4,5-bis(4-(4-nitro-2-trifluoromethylphenoxy)phenyl)imidazole
    参考文献:
    名称:
    Novel para-linked and CF3-substituted poly(amide-ether-imidazole)s: Solubility, optical and thermal properties
    摘要:
    A new photoactive fluorinated diamine, 2-(4-trifluoromethylphenyl)-4,5-bis(4-(4-amino-2-trifluoromethylphenoxy)phenyl)imidazole (TFIA), was synthesized and used for preparation of novel fluorinated poly(amide-ether-imidazole)s (PAEIs) by using direct polycondensation of the diamine with various dicarboxylic acids. The resulting PAEIs were amorphous and had intrinsic viscosity [eta] in the range of 0.68-0.80 dL/g. The weight average (M,) and number average (M-n) molecular weights of one of the polymer, measured by GPC, were 18,600 g/mol and 11,500 g/mol, respectively. These polymers were readily soluble in a variety of organic solvents and formed low-colored and flexible thin films via solution casting. Their values of cut-off wavelength (lambda(o)) were in the range of 380-390 nm, and all PAEIs films exhibited high optical transparency. According to thermal analysis, these polymers exhibited glass transition temperatures (T-g)s in the range of 160-250 degrees C, initial decomposition temperature (T-i) from 295 to 400 degrees C and temperature of 10% weight loss (T-10%) from 400 to 490 degrees C in N-2. These polymers exhibited strong UV-vis absorption at 310 nm in solution and in films and their fluorescence emission peaks appeared around 430-520 nm with the quantum yields in solution varied from 10% to 29%. (C) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2012.07.014
  • 作为产物:
    描述:
    参考文献:
    名称:
    Novel para-linked and CF3-substituted poly(amide-ether-imidazole)s: Solubility, optical and thermal properties
    摘要:
    A new photoactive fluorinated diamine, 2-(4-trifluoromethylphenyl)-4,5-bis(4-(4-amino-2-trifluoromethylphenoxy)phenyl)imidazole (TFIA), was synthesized and used for preparation of novel fluorinated poly(amide-ether-imidazole)s (PAEIs) by using direct polycondensation of the diamine with various dicarboxylic acids. The resulting PAEIs were amorphous and had intrinsic viscosity [eta] in the range of 0.68-0.80 dL/g. The weight average (M,) and number average (M-n) molecular weights of one of the polymer, measured by GPC, were 18,600 g/mol and 11,500 g/mol, respectively. These polymers were readily soluble in a variety of organic solvents and formed low-colored and flexible thin films via solution casting. Their values of cut-off wavelength (lambda(o)) were in the range of 380-390 nm, and all PAEIs films exhibited high optical transparency. According to thermal analysis, these polymers exhibited glass transition temperatures (T-g)s in the range of 160-250 degrees C, initial decomposition temperature (T-i) from 295 to 400 degrees C and temperature of 10% weight loss (T-10%) from 400 to 490 degrees C in N-2. These polymers exhibited strong UV-vis absorption at 310 nm in solution and in films and their fluorescence emission peaks appeared around 430-520 nm with the quantum yields in solution varied from 10% to 29%. (C) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2012.07.014
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