3-[9-(4-Methylphenyl)carbazol-2-yl]-9-phenylcarbazole

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 3-[9-(4-Methylphenyl)carbazol-2-yl]-9-phenylcarbazole
• 英文别名: 3-[9-(4-methylphenyl)carbazol-2-yl]-9-phenylcarbazole
• 化学式: C₃₇H₂₆N₂
• 分子量: 498.6
• InChiKey: ASWURXONAAYEOU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.1
• 重原子数：
  39
• 可旋转键数：
  3
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.03
• 拓扑面积：
  9.9
• 氢给体数：
  0
• 氢受体数：
  0

文献信息

• HOST MATERIALS FOR OLED APPLICATION
  申请人：Universal Display Corporation

  公开号：US20140291638A1

  公开（公告）日：2014-10-02

  The present disclosure provides novel compounds containing dibenzo[fg,op]tetracene and larger all-benzenoid moiety that can be used as hosts for phosphorescent emitters providing low-voltage, high-efficiency and high-stability devices.

  本公开提供了含有二苯并[fg，op]四环和更大的全苯基基团的新型化合物，可用作荧光发射体的宿主，提供低电压、高效率和高稳定性的设备。
• Organic electroluminescent materials and devices
  申请人：Universal Display Corporation

  公开号：US11127905B2

  公开（公告）日：2021-09-21

  Novel compounds that contain azadibenzofuran, azadibenzothiophene, and azadibenzoselenophene with fused rings that can be used as a host material in phosphorescent OLEDs is disclosed.

  本发明公开了含有偶氮二苯并呋喃、偶氮二苯并噻吩和偶氮二苯并硒吩的具有融合环的新型化合物，这些化合物可用作磷光 OLED 的主材料。
• Organic Luminescent Compound With Delayed Fluorescence
  申请人：UNIVERSAL DISPLAY CORPORATION

  公开号：US20140145149A1

  公开（公告）日：2014-05-29

  Novel organic compounds containing an imidazole core and electron donor and acceptor fragments are provided. By selection of the disclosed donor and acceptor groups, compounds exhibiting small singlet-triplet gaps are obtained. These compounds are useful in OLED devices as host materials or as delayed fluorescent emitters.
• ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES
  申请人：Universal Display Corporation

  公开号：US20160149139A1

  公开（公告）日：2016-05-26

  A composition formed of a mixture of two compounds having similar thermal evaporation properties that are pre-mixed into an evaporation source that can be used to co-evaporate the two compounds into an emission layer in OLEDs via vacuum thermal evaporation process is disclosed. The first and second compounds can have an evaporation temperature T 1 and T 2 , respectively, of 150 to 350° C., and the absolute value of T 1 −T 2 can be less than 20° C. The first compound can have a concentration C 1 in the mixture and a concentration C 2 in a film formed by evaporating the mixture in a vacuum deposition tool at a constant pressure between 1×10 −6 Torr to 1×10 −9 Torr, at a 2 Å/sec deposition rate on a surface positioned at a predefined distance away from the mixture being evaporated, where the absolute value of (C 1 −C 2 )/C 1 is less than 5%.
• SPECIFICALLY SUBSTITUTED BENZOFURO- AND BENZOTHIENOQUINOLINES FOR ORGANIC LIGHT EMITTING DIODES
  申请人：IDEMITSU KOSAN CO., LTD.

  公开号：US20190161497A1

  公开（公告）日：2019-05-30

  Specifically substituted benzofuro- and benzothienoquinolines and their use in electronic devices, especially electroluminescent devices. When used as charge transport material, charge blocker material and/or host material in electroluminescent devices, the specifically substituted benzofuro- and benzothienoquinolines may provide improved efficiency, stability, manufacturability, or spectral characteristics of electroluminescent devices and reduced driving voltage of electroluminescent devices.