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[bis(2-(2',4'-difluorophenyl)-4-tert-butyl-pyridine)iridium(μ-chloride)2iridium-bis(2-(2',4'-difluorophenyl)-4-tert-butyl-pyridine)] | 889101-47-7

中文名称
——
中文别名
——
英文名称
[bis(2-(2',4'-difluorophenyl)-4-tert-butyl-pyridine)iridium(μ-chloride)2iridium-bis(2-(2',4'-difluorophenyl)-4-tert-butyl-pyridine)]
英文别名
——
[bis(2-(2',4'-difluorophenyl)-4-tert-butyl-pyridine)iridium(μ-chloride)2iridium-bis(2-(2',4'-difluorophenyl)-4-tert-butyl-pyridine)]化学式
CAS
889101-47-7
化学式
C60H56Cl2F8Ir2N4
mdl
——
分子量
1440.46
InChiKey
VRDLRERGZQIFQQ-UHFFFAOYSA-L
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:
    参考文献:
    名称:
    Investigating photoluminescence and electroluminescence of iridium(III)-based blue-emitting phosphors
    摘要:
    The syntheses of two new cyclometalated ligands [2-(2',4'-difluorophenyl)-4-tert-butylpyridine (F(2)(t)Buppy) and 2-(2',4'-difluorophenyl)-4-oxyhexylpyridine (F(2)HexOppy)] were carried out. Blue-light emitting iridium(III) complex dopants [Ir(F(2)Buppy)(2)(acac/pic)] (acac = acetylacetone; pic = picolinic acid) and [Ir(F(2)HeXOppy)(2)(acac/pic)] were prepared using these cyclometalated ligands with acetylacetone and picolinic acid as their ancillary ligands. The structure of the complexes, [Ir(F(2)(t)Buppy)(2)(acac)] and [Ir(F(2)(t)Buppy)(2)(pic)] were authenticated by X-ray single-crystal structure analysis and showed an octahedral geometry. Comparative absorption and emission spectra of thin-films as well as their solution samples were studied. The variation of the lowest emitting states to their corresponding unsubstituted complexes, [Ir(F(2)ppy)(2)(acac/pic)] was also discussed. The electroluminescent (EL) device was fabricated using [Ir(F(2)(t)Buppy)(2)(pic)] as the dopant (D-I) into the emitting layer and compared with two other EL devices where [Ir(F(2)MeOppy)(2)(acac)] (D-II) and FIrpic (D-III) dopants were used in the same device structure. The lower driving voltages obtained for D-I with respect to D-II and D-III devices were rationalized. The exceptional lowering of the luminance yield of the substituted dopants containing devices, D-I and D-II, to that of D-III which contains the unsubstituted dopant was also investigated. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2005.08.033
  • 作为产物:
    描述:
    氯化铱(III) 水合物4-(tert-butyl)-2-(2,4-difluorophenyl)pyridine 在 HCl 作用下, 以 乙二醇乙醚 为溶剂, 以70%的产率得到[bis(2-(2',4'-difluorophenyl)-4-tert-butyl-pyridine)iridium(μ-chloride)2iridium-bis(2-(2',4'-difluorophenyl)-4-tert-butyl-pyridine)]
    参考文献:
    名称:
    Investigating photoluminescence and electroluminescence of iridium(III)-based blue-emitting phosphors
    摘要:
    The syntheses of two new cyclometalated ligands [2-(2',4'-difluorophenyl)-4-tert-butylpyridine (F(2)(t)Buppy) and 2-(2',4'-difluorophenyl)-4-oxyhexylpyridine (F(2)HexOppy)] were carried out. Blue-light emitting iridium(III) complex dopants [Ir(F(2)Buppy)(2)(acac/pic)] (acac = acetylacetone; pic = picolinic acid) and [Ir(F(2)HeXOppy)(2)(acac/pic)] were prepared using these cyclometalated ligands with acetylacetone and picolinic acid as their ancillary ligands. The structure of the complexes, [Ir(F(2)(t)Buppy)(2)(acac)] and [Ir(F(2)(t)Buppy)(2)(pic)] were authenticated by X-ray single-crystal structure analysis and showed an octahedral geometry. Comparative absorption and emission spectra of thin-films as well as their solution samples were studied. The variation of the lowest emitting states to their corresponding unsubstituted complexes, [Ir(F(2)ppy)(2)(acac/pic)] was also discussed. The electroluminescent (EL) device was fabricated using [Ir(F(2)(t)Buppy)(2)(pic)] as the dopant (D-I) into the emitting layer and compared with two other EL devices where [Ir(F(2)MeOppy)(2)(acac)] (D-II) and FIrpic (D-III) dopants were used in the same device structure. The lower driving voltages obtained for D-I with respect to D-II and D-III devices were rationalized. The exceptional lowering of the luminance yield of the substituted dopants containing devices, D-I and D-II, to that of D-III which contains the unsubstituted dopant was also investigated. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2005.08.033
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文献信息

  • WO2008/56799
    申请人:——
    公开号:——
    公开(公告)日:——
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