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8-Chloro-2,2-difluoro-4-phenyl-3-oxa-9-aza-1-azonia-2-boranuidabicyclo[4.4.0]deca-1(10),4,6,8-tetraene | 1446022-19-0

中文名称
——
中文别名
——
英文名称
8-Chloro-2,2-difluoro-4-phenyl-3-oxa-9-aza-1-azonia-2-boranuidabicyclo[4.4.0]deca-1(10),4,6,8-tetraene
英文别名
8-chloro-2,2-difluoro-4-phenyl-3-oxa-9-aza-1-azonia-2-boranuidabicyclo[4.4.0]deca-1(10),4,6,8-tetraene
8-Chloro-2,2-difluoro-4-phenyl-3-oxa-9-aza-1-azonia-2-boranuidabicyclo[4.4.0]deca-1(10),4,6,8-tetraene化学式
CAS
1446022-19-0
化学式
C12H8BClF2N2O
mdl
——
分子量
280.469
InChiKey
JKTGLCUTNJOCNG-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):
    2.77
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    26
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    8-Chloro-2,2-difluoro-4-phenyl-3-oxa-9-aza-1-azonia-2-boranuidabicyclo[4.4.0]deca-1(10),4,6,8-tetraene苯乙酮 在 sodium hydride 、 三氟化硼乙醚三乙胺 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 54.0h, 以16%的产率得到4,4,14,14-Tetrafluoro-6,12-diphenyl-5,13-dioxa-1,3-diazonia-4,14-diboranuidatricyclo[8.4.0.03,8]tetradeca-1(10),2,6,8,11-pentaene
    参考文献:
    名称:
    Synthesis and Fluorescence Properties of Pyrimidine Mono- and Bisboron Complexes
    摘要:
    Novel fluorescent mono- and bisboron complexes based on pyrimidine bearing beta-iminoenolate ligands were synthesized, and their fluorescence properties were investigated. The nonsubstituted and trifluoromethyl-substituted monoboron complexes showed higher fluorescence quantum yield in solid state than in solution. The dimethylamino derivative of the monoboron complex exhibited positive solvatochromism in the fluorescence spectra. The bisboron complex showed significantly higher molar absorption coefficient and red-shifted maximum absorption and maximum fluorescence wavelengths than the corresponding monoboron complex.
    DOI:
    10.1021/jo400879g
  • 作为产物:
    参考文献:
    名称:
    Strategy to enhance solid-state fluorescence and aggregation-induced emission enhancement effect in pyrimidine boron complexes
    摘要:
    尽管非-, 三氟甲基- 和氰基取代衍生物显示了AIEE效应,但甲氧基- 和二甲基胺基取代的类似物在溶液中表现出相对强烈的荧光。
    DOI:
    10.1039/c4dt03318c
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文献信息

  • Strategy to enhance solid-state fluorescence and aggregation-induced emission enhancement effect in pyrimidine boron complexes
    作者:Yasuhiro Kubota、Kouhei Kasatani、Hiroki Takai、Kazumasa Funabiki、Masaki Matsui
    DOI:10.1039/c4dt03318c
    日期:——

    Although non-, trifluoromethyl-, and cyano-substituted derivatives showed AIEE effects, methoxy- and dimethylamino-substituted analogues resulted in relatively strong fluorescence in solution.

    尽管非-, 三氟甲基- 和氰基取代衍生物显示了AIEE效应,但甲氧基- 和二甲基胺基取代的类似物在溶液中表现出相对强烈的荧光。
  • Synthesis and Fluorescence Properties of Pyrimidine Mono- and Bisboron Complexes
    作者:Yasuhiro Kubota、Yousuke Ozaki、Kazumasa Funabiki、Masaki Matsui
    DOI:10.1021/jo400879g
    日期:2013.7.19
    Novel fluorescent mono- and bisboron complexes based on pyrimidine bearing beta-iminoenolate ligands were synthesized, and their fluorescence properties were investigated. The nonsubstituted and trifluoromethyl-substituted monoboron complexes showed higher fluorescence quantum yield in solid state than in solution. The dimethylamino derivative of the monoboron complex exhibited positive solvatochromism in the fluorescence spectra. The bisboron complex showed significantly higher molar absorption coefficient and red-shifted maximum absorption and maximum fluorescence wavelengths than the corresponding monoboron complex.
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