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1-(meso-phenyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene)-2,5-di-2-thienyl-1H-pyrrole | 1092925-01-3

中文名称
——
中文别名
——
英文名称
1-(meso-phenyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene)-2,5-di-2-thienyl-1H-pyrrole
英文别名
——
1-(meso-phenyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene)-2,5-di-2-thienyl-1H-pyrrole化学式
CAS
1092925-01-3
化学式
C31H26BF2N3S2
mdl
——
分子量
553.507
InChiKey
JRUSYPFNJONQDC-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

物化性质

  • 熔点:
    226-227 °C

计算性质

  • 辛醇/水分配系数(LogP):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    1,4-双(2-噻吩基)-1,4-丁二酮8-(4-苯胺基)氟硼吡咯 在 p-toluenesulfonic acid 作用下, 以 甲苯 为溶剂, 以85%的产率得到1-(meso-phenyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene)-2,5-di-2-thienyl-1H-pyrrole
    参考文献:
    名称:
    A new conducting polymer bearing 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) subunit: Synthesis and characterization
    摘要:
    A new monomer system based on thiophene, pyrrole and 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene dye (SNS-BODIPY) was synthesized and its corresponding polymer (PSNS-BODIPY) was obtained via repetitive cycling or constant potential electrolysis in 0.1 M tetrabutylammonium hexafluorophosphate dissolved in dichloromethane. The PSNS-BODIPY film has very stable and well-defined reversible redox couples during p-doping process. Multi-electrochromic polymer film has a band gap of 2.9 eV with two absorption bands in its neutral state at 351 and 525 nm, attributed to the polymer backbone and BODIPY subunits, respectively. The percentage transmittance changes between both states (neutral and oxidized) were found as 12.1% for 351 nm and 17.7% for 525 nm in the visible region as well as 46.2% for 1050 nm in the near-infrared region. Beyond the robustness, the PSNS-BODIPY film has high redox stability (retaining 53.3% of its electroactivity at 351 nm after 2000 switching) with a low response time of 1.0 s. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.electacta.2008.06.062
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