3-chloro-[1,1':3',1"]terphenyl

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3-chloro-[1,1':3',1"]terphenyl
• 英文别名: 3-chloro-1,1′:3′,1″-terphenyl；3-Chloro-1,1':3',1''-terphenyl；1-chloro-3-(3-phenylphenyl)benzene
• 化学式: C₁₈H₁₃Cl
• 分子量: 264.754
• InChiKey: FLGLFUIDRYWVDL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.2
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  3-chloro-[1,1':3',1"]terphenyl 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 四(三苯基膦)钯 、 potassium acetate 、 potassium carbonate 作用下， 以 四氢呋喃 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 63.0h， 生成
  参考文献：
  名称：

  유기 화합물, 유기 광전자 소자 및 표시 장치

  摘要：

  这是关于有机光电子元件和显示器件中包含的有机化合物，其化学式表示为1。在化学式1中，L到L，Ar，Ar，n1，n2，m1到m4如规范中所述。

  公开号：

  KR20170124412A
• 作为产物：
  描述：

  (E)-6-(3-chlorophenyl)-1-phenylhex-1-en-5-yn-3-yl acetate 在 N-苯基马来酰亚胺 、 platinum(II) iodide 作用下， 以 甲苯 为溶剂， 反应 24.0h， 以90%的产率得到3-chloro-[1,1':3',1"]terphenyl
  参考文献：
  名称：

  PtI₂-catalyzed cyclization of 3-acyloxy-1,5-enynes with the elimination of HOAc and a benzyl shift: synthesis of unsymmetrical m-terphenyls

  摘要：

  开发了一种新的1,5-炔烃环化反应，通过消除HOAc和苯甲基转移来合成m-联苯。

  DOI：

  10.1039/c4ob02336f

文献信息

• 축합환 화합물, 및 이를 포함한 유기 발광 소자
  申请人：SAMSUNG SDI CO., LTD. 삼성에스디아이 주식회사(119980018058) Corp. No ▼ 110111-0394174BRN ▼124-81-31282

  公开号：KR20150084657A

  公开（公告）日：2015-07-22

  축합환 화합물 및 상기 축합환 화합물을 포함한 유기 발광 소자가 제시된다.

  有机发光器件包括聚合环化合物和上述聚合环化合物。
• 유기 발광 화합물 및 이를 이용한 유기 전계 발광 소자
  申请人：Solus Advanced Materials co., Ltd. 솔루스첨단소재 주식회사(120190660630) Corp. No ▼ 214911-0058927BRN ▼668-81-01406

  公开号：KR20160076884A

  公开（公告）日：2016-07-01

  본 발명은 캐리어 수송능 및 발광능 등이 우수한 신규의 화합물 및 이를 하나 이상의 유기물층에 포함함으로써 낮은 구동 전압과, 높은 발광 효율, 및 향상된 수명 특성 등을 갖는 유기 전계 발광 소자에 관한 것이다.

  This invention relates to an organic electroluminescent device having low driving voltage, high luminous efficiency, and improved lifespan characteristics by incorporating a novel compound with excellent carrier transport and luminescent properties into one or more organic layers.
• COMPOSITION FOR ORGANIC OPTOELECTRIC DEVICE AND ORGANIC OPTOELECTRIC DEVICE AND DISPLAY DEVICE
  申请人：SAMSUNG SDI CO., LTD.

  公开号：US20170309831A1

  公开（公告）日：2017-10-26

  Disclosed are a composition for an organic optoelectric device including at least one of a first host compound represented by a combination of Chemical Formula 1 and Chemical Formula 2, and at least one of a second host compound represented by Chemical Formula 3, an organic optoelectric device including the same, and a display device. Details of Chemical Formulae 1 to 3 are the same as defined in the specification.
• PLURALITY OF HOST MATERIALS, ORGANIC ELECTROLUMINESCENT COMPOUND, AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME
  申请人：ROHM AND HAAS ELECTRONIC MATERIALS KOREA LTD.

  公开号：US20240090324A1

  公开（公告）日：2024-03-14

  The present disclosure relates to a plurality of host materials, an organic electroluminescent compound, and an organic electroluminescent device comprising the same. An organic electroluminescent device having improved driving voltage, luminous efficiency, and/or lifespan properties compared to a conventional organic electroluminescent device can be provided by including the specific combination of compounds according to the present disclosure as a plurality of host materials or by including the compound according to the present disclosure.
• ORGANIC LIGHT EMITTING DEVICE
  申请人：LG CHEM, LTD.

  公开号：US20230200229A1

  公开（公告）日：2023-06-22

  Provided is an organic light-emitting device with improved driving voltage, efficiency, and lifetime, comprising: an anode; a cathode; a light emitting layer between the anode and the cathode; an electron blocking layer between the anode and the light-emitting layer; and a hole transport layer between the electron blocking layer and the anode, wherein the light-emitting layer includes a compound of Formula 1, a compound of Formula 2, and a compound of Formula 3: where A is a benzene ring condensed with two adjacent pentagonal rings, B is a benzene ring condensed with two adjacent pentagonal rings, and the other substituents are as defined in the specification.