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2,7-bis-(4-(N,N-diphenylamino)phen-1-yl)-9,9’-dimethylfluorene | 239475-90-2

中文名称
——
中文别名
——
英文名称
2,7-bis-(4-(N,N-diphenylamino)phen-1-yl)-9,9’-dimethylfluorene
英文别名
4-[9,9-dimethyl-7-[4-(N-phenylanilino)phenyl]fluoren-2-yl]-N,N-diphenylaniline
2,7-bis-(4-(N,N-diphenylamino)phen-1-yl)-9,9’-dimethylfluorene化学式
CAS
239475-90-2
化学式
C51H40N2
mdl
——
分子量
680.892
InChiKey
LTIHUWGSTKWDDJ-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

  • 密度:
    1.174±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    14.2
  • 重原子数:
    53
  • 可旋转键数:
    8
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    6.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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:
    2,7-二溴-9,9-二甲基芴4-硼酸三苯胺四(三苯基膦)钯 、 sodium carbonate 作用下, 以 四氢呋喃 为溶剂, 以60%的产率得到2,7-bis-(4-(N,N-diphenylamino)phen-1-yl)-9,9’-dimethylfluorene
    参考文献:
    名称:
    Efficient Greenish Blue Electrochemiluminescence from Fluorene and Spirobifluorene Derivatives
    摘要:
    The spectroscopic and electrochemical behavior as well as electrogenerated chemiluminescence (ECL) of a series of donor g-pi-donor derivatives bearing triphenylamine groups as donor connected to a fluorene, 2,7-bis-(4-(N,N-diphenylamino)phen-1-yl)-9,9'-dimethylfluorene (1), or spirobifluorene core, 2,7-bis-(4-(N,N-diphenylamino)phen-1-yl)-9,9'-spirobifluorene (2) and 2,2',7,7'-tetrakis(4-(N,N-diphenylamino)phen-l-yl)-9,9'-spirobifluorene (3), were investigated. Besides a high photoluminescence (PL) quantum yield in solution (between 81 and 87%), an efficient radical ions annihilation process induces intense greenish blue ECL emission that could be seen with the naked eye. Only the tetrasubstituted spirobifluorene derivative (compound 3) shows weak ECL obtained by a direct annihilation mechanism. Because the energy of the annihilation reaction is higher than the energy required to form the singlet excited state, the S-route could be considered the pathway followed by the ECL process in these molecules. The ECL emissions recorded by direct ion-ion annihilation show two bands compared to the single structureless PL band. The ECL spectra obtained by a coreactant approach using benzoylperoxide as a coreagent show no differences relative to that produced by annihilation, except for an increasing of ECL intensity for all compounds.
    DOI:
    10.1021/ja3054018
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文献信息

  • FLUORENYLENE COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE USING SAME
    申请人:SAITOH AKIHITO
    公开号:US20070155998A1
    公开(公告)日:2007-07-05
    A novel pyrenylfluorenylene compound is provided which is represented by the general formula (1):
    提供一种新型的芘基芴烯化合物,其通式表示为(1):
  • ORGANIC LIGHT EMITTING DEVICE
    申请人:LG Chem, Ltd.
    公开号:EP3579292B1
    公开(公告)日:2020-08-05
  • ORGANIC ELECTROLUMESCENCE DEVICE
    申请人:Hosokawa Chishio
    公开号:US20070142671A1
    公开(公告)日:2007-06-21
    Materials for organic electroluminescence devices are represented by following general formula [1]: wherein A represents a chrysene group, X 1 to X 4 each independently represent a substituted or unsubstituted arylene group having 6 to 30 carbon atoms, X 1 and X 2 may be bonded to each other, X 3 and X 4 may be bonded to each other, Y 1 to Y 4 each independently represent an organic group represented by general formula [2], a to d each represent an integer of 0 to 2 and, a+b+c+d≧0; general formula [2] being: wherein R 1 to R 4 each independently represent hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 20 carbon atoms, cyano group or form a triple bond by a linkage of R 1 and R 2 or R 3 and R 4 , Z represents a substituted or unsubstituted aryl group having 6 to 20 carbon atoms and n represents 0 or 1.
  • PYRENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE DEVICE MAKING USE OF THE SAME
    申请人:Ito Mitsunori
    公开号:US20090058270A1
    公开(公告)日:2009-03-05
    Provided is an organic electroluminescence device including one or two or more organic thin-film layers having at least a light emitting layer interposed between a negative electrode and a positive electrode, in which the light emitting layer contains a pyrene derivative of a specified structure and an amine compound of a specified structure. The organic electroluminescence device excels in heat resistance, ensures long life and high luminous efficiency, and is capable of emitting blue, green and red lights.
  • ASYMMETRIC FLUORENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT CONTAINING THE SAME
    申请人:Ito Mitsunori
    公开号:US20090261711A1
    公开(公告)日:2009-10-22
    Provided is an organic electroluminescence device which includes an organic thin film layer composed of one or more layers including at least one light emitting layer, the organic thin film layer being interposed between a cathode and an anode, in which at least one layer of the organic thin layer contains an asymmetric fluorene-based derivative compound of a specific structural formula and an amine compound of a specific structural formula. This organic electroluminescence device has excellent heat resistance and a long lifetime and can emit any of blue, green, and red lights at a high luminous efficiency.
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