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5,5'-bis(9,9-dimethylfluoren-2-yl)-1-methyl-1-phenyldithienosilole | 1402411-31-7

中文名称
——
中文别名
——
英文名称
5,5'-bis(9,9-dimethylfluoren-2-yl)-1-methyl-1-phenyldithienosilole
英文别名
4,10-Bis(9,9-dimethylfluoren-2-yl)-7-methyl-7-phenyl-3,11-dithia-7-silatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene
5,5'-bis(9,9-dimethylfluoren-2-yl)-1-methyl-1-phenyldithienosilole化学式
CAS
1402411-31-7
化学式
C45H36S2Si
mdl
——
分子量
668.998
InChiKey
DQXDEPDTJOYBBX-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):
    10.84
  • 重原子数:
    48
  • 可旋转键数:
    3
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    56.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    4,10-Diiodo-7-methyl-7-phenyl-3,11-dithia-7-silatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene 、 tris(9,9-dimethylfluoren-2-yl)indium 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 作用下, 以 四氢呋喃乙醚正己烷 为溶剂, 反应 10.0h, 以0.18 g的产率得到5,5'-bis(9,9-dimethylfluoren-2-yl)-1-methyl-1-phenyldithienosilole
    参考文献:
    名称:
    Synthesis and characterization of fluorene and carbazole dithienosilole derivatives for potential applications in organic light-emitting diodes
    摘要:
    Several fluorene or carbazole-based dithienosiloles (DTSs) have been synthesized and their thermal, photophysical, and electrochemical properties have been systematically investigated. These compounds show high thermal stability with glass transition temperature above 110 degrees C as well as decomposition temperatures at similar to 400 degrees C. Intense green emission is observed in the spectral region of 500-510 nm for all compounds (Phi(PL)=0.31-0.80), that is, attributed to both the 5,5 '-substituents of the DTS ring and DTS-based pi-pi* transition. Based on the emission spectra at 77 K, the triplet energy for these compounds was calculated to be within 2.1-2.2 eV, indicating that they may be used as host materials for red emitters in organic light-emitting diodes (OLEDs). All compounds exhibit reversible oxidation and possess low-lying LUMO energies, owing to the conjugated fluorene/carbazole substituents on the DTS. This along with the high thermal/electrochemical stabilities and high fluorescent quantum efficiencies makes the new DTSs compounds promising candidates for use in OLEDs as emitters, host and electron-transporting materials. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.08.056
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