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4,4-difluoro-8-[3',5'-bis(decyloxy)phenyl]-2,6-diiodo-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene | 1094812-00-6

中文名称
——
中文别名
——
英文名称
4,4-difluoro-8-[3',5'-bis(decyloxy)phenyl]-2,6-diiodo-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene
英文别名
4,4-difluoro-8-(3,5-bis(decyloxy)phenyl)-2,6-diiodo-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene
4,4-difluoro-8-[3',5'-bis(decyloxy)phenyl]-2,6-diiodo-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene化学式
CAS
1094812-00-6
化学式
C39H57BF2I2N2O2
mdl
——
分子量
888.511
InChiKey
LEQQANIWBOSMHL-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):
    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

  • 作为反应物:
    描述:
    4,4-difluoro-8-[3',5'-bis(decyloxy)phenyl]-2,6-diiodo-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene5-乙炔基-2-吡啶-2-基吡啶 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide二异丙胺 作用下, 以 四氢呋喃 为溶剂, 反应 24.0h, 以80%的产率得到4,4-difluoro-8-[3',5'-bis(decyloxy)phenyl]-2,6-bis(2'',2'''-bipyridine-5''-ethynyl)-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene
    参考文献:
    名称:
    基于硼氮杂吲哚发色团的新型分子构件:在荧光金属超分子配位聚合物中的应用
    摘要:
    明亮的聚合物:描述了由通用的官能化双联吡啶(硼双联吡啶)生色团组成的荧光配位聚合物,如图所示。聚合是通过荧光发射强度的变化和峰值发射波长的变化来表示的。
    DOI:
    10.1002/chem.200802538
  • 作为产物:
    描述:
    4,4-difluoro-8-[3',5'-bis(decyloxy)phenyl]-2-iodo-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene碘酸 作用下, 以 为溶剂, 以95%的产率得到4,4-difluoro-8-[3',5'-bis(decyloxy)phenyl]-2,6-diiodo-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene
    参考文献:
    名称:
    Phenylethynyl-BODIPY Oligomers: Bright Dyes and Fluorescent Building Blocks
    摘要:
    Boradiazaindacene dyes were converted Into phenylethynyl-BODIPY oligomers via a cycle of reactions, notably including Sonogashira couplings. As expected, as the number, n, of repeating units Increases, peak absorption and emission wavelengths are shifted to the red end of the visible spectrum, albeit with smaller increments as n Increases, Decyl groups help to keep the solubility remarkably high, and in addition to being very bright red-emitting fluorophores, their rigid rod-like structures could allow their use as functional building blocks.
    DOI:
    10.1021/ol802446e
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文献信息

  • Tetrastyryl-Bodipy Dyes: Convenient Synthesis and Characterization of Elusive Near IR Fluorophores
    作者:Onur Buyukcakir、O. Altan Bozdemir、Safacan Kolemen、Sundus Erbas、Engin U. Akkaya
    DOI:10.1021/ol9019056
    日期:2009.10.15
    1,3,5,7-Tetramethyl-Bodipy derivatives undergo Knoevenagel-type condensations with aromatic aldehydes to ultimately yield tetrastyryl-Bodipy derivatives. The resulting dyes absorb and emit strongly in the near IR. As the versatility of the Bodipy dyes are fully appreciated, these new tetrastyryl dyes are likely to be featured in a variety of functional supramolecular systems.
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