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1,3-bis(2,2-diphenylethenyl)-9-methyl-2-methoxycarbazol | 1219943-25-5

中文名称
——
中文别名
——
英文名称
1,3-bis(2,2-diphenylethenyl)-9-methyl-2-methoxycarbazol
英文别名
1,3-Bis(2,2-diphenylethenyl)-2-methoxy-9-methylcarbazole;1,3-bis(2,2-diphenylethenyl)-2-methoxy-9-methylcarbazole
1,3-bis(2,2-diphenylethenyl)-9-methyl-2-methoxycarbazol化学式
CAS
1219943-25-5
化学式
C42H33NO
mdl
——
分子量
567.73
InChiKey
OZZFBWSQORHXAM-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):
    11.6
  • 重原子数:
    44
  • 可旋转键数:
    7
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    14.2
  • 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:
    1,3-bis(2,2-diphenylethenyl)-9H-carbazol-2-ol碘甲烷 在 sodium sulfate 、 potassium hydroxide 作用下, 反应 3.0h, 以62%的产率得到1,3-bis(2,2-diphenylethenyl)-9-methyl-2-methoxycarbazol
    参考文献:
    名称:
    Easily functionalizable carbazole based building blocks with extended conjugated systems for optoelectronic applications
    摘要:
    Carbazole based building blocks, possessing diphenylethenyl fragments, have been synthesized. Condensation of the carbazol-2-ol with diphenylacetaldehyde yields 1,3-substituted derivatives. Change of the synthesis sequence, however, (i.e., substitution at the hydroxyl and NH groups, followed by the condensation reaction) results in the 3,6-substituted products. Thermal, optical, electro-chemical and photophysical properties of the synthesized derivatives have been investigated. Room temperature hole-drift mobilities, evaluated using xerographic time-of-flight technique, were found to exceed 10(-4) cm(2) V-1 s(-1) at strong electric fields. The obtained results indicate high charge mobility for molecularly doped polymers, especially considering the fact that these measurements were carried out under ambient conditions and not in high vacuum. Commercial availability and relative cheapness of the starting materials, simple synthetic method, number of sites available for easy functionalization and covalent linking to other molecules makes these precursors attractive building blocks for the construction of more complex low-molecular-weight or polymeric materials for optoelectronic applications. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.02.086
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文献信息

  • Easily functionalizable carbazole based building blocks with extended conjugated systems for optoelectronic applications
    作者:Giedre Bubniene、Tadas Malinauskas、Maryte Daskeviciene、Vygintas Jankauskas、Vytautas Getautis
    DOI:10.1016/j.tet.2010.02.086
    日期:2010.4
    Carbazole based building blocks, possessing diphenylethenyl fragments, have been synthesized. Condensation of the carbazol-2-ol with diphenylacetaldehyde yields 1,3-substituted derivatives. Change of the synthesis sequence, however, (i.e., substitution at the hydroxyl and NH groups, followed by the condensation reaction) results in the 3,6-substituted products. Thermal, optical, electro-chemical and photophysical properties of the synthesized derivatives have been investigated. Room temperature hole-drift mobilities, evaluated using xerographic time-of-flight technique, were found to exceed 10(-4) cm(2) V-1 s(-1) at strong electric fields. The obtained results indicate high charge mobility for molecularly doped polymers, especially considering the fact that these measurements were carried out under ambient conditions and not in high vacuum. Commercial availability and relative cheapness of the starting materials, simple synthetic method, number of sites available for easy functionalization and covalent linking to other molecules makes these precursors attractive building blocks for the construction of more complex low-molecular-weight or polymeric materials for optoelectronic applications. (C) 2010 Elsevier Ltd. All rights reserved.
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