6-bromo-1-iodo-naphthalene | 1261510-93-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 6-bromo-1-iodo-naphthalene
• 英文别名: 6-Bromo-1-iodonaphthalene
• CAS: 1261510-93-3
• 化学式: C₁₀H₆BrI
• 分子量: 332.966
• InChiKey: BCTQEGIUJORLRI-UHFFFAOYSA-N

物化性质

• 沸点：
  362.0±15.0 °C(Predicted)
• 密度：
  2.057±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  2.0
• 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：

  4-(naphthalen-2-yl(phenyl)amino)phenylboronic acid 、 乙二醇二甲醚 、 2M-sodium carbonate 、 6-bromo-1-iodo-naphthalene 生成 [4-(6-bromo-naphthalene-2-yl)-phenyl]-naphthalene-2-yl-phenyl-amine
  参考文献：
  名称：

  摘要：

  DOI：

文献信息

• Asymmetrical Aryl Amine Derivative for Organic Electroluminescence Devices, Method for Preparing Same, Organic Thin Film for Organic Electroluminescence Devices and Organic Electroluminescence Device Using Same
  申请人：Kim Sang Dong

  公开号：US20120032152A1

  公开（公告）日：2012-02-09

  Provided are asymmetric arylamine derivatives for an organic electroluminescent element, represented by the formula (1), which is prepared by sequentially inducing a secondary amine and a tertiary amine to an aryl compound Ar core so that they do not include a symmetrical axis and a symmetrical surface in a molecule, a manufacturing method of the same, an organic thin layer material including the asymmetric arylamine derivatives, and an organic electroluminescent element employing the same: wherein Ar represents a C 10 -C 20 divalent aryl group, Ar 1 is a divalent C 6 -C 30 aryl group, and Ar 2 to Ar 5 each independently represents a divalent C 6 -C 30 aryl group, at least one of Ar 2 to Ar 5 having a different structure when the secondary amine and the tertiary amine in Ar are substituted at symmetrical positions, and Ar 2 to Ar 5 having the same structure or different structures when the secondary amine and the tertiary amine in Ar are substituted at asymmetrical positions. The asymmetric arylamine derivative can be used in forming an organic thin layer for an organic electroluminescent element. When the organic electroluminescent element is formed using a dopant as an emitting material, the asymmetric arylamine derivative exhibits superb emission efficiency and an excellent lifetime characteristic in a blue wavelength region.

  本发明提供了一种不包括对称轴和对称面的分子结构的非对称芳基胺衍生物，用于有机电致发光元件，其公式表示为（1），通过将二级胺和三级胺顺序引入到芳基化合物Ar核中制备而成，该化合物包括一个制备方法，包括非对称芳基胺衍生物的有机薄层材料以及使用该材料的有机电致发光元件。其中，Ar表示C10-C20二价芳基基团，Ar1表示C6-C30二价芳基基团，Ar2到Ar5各自独立表示C6-C30二价芳基基团，当二级胺和三级胺在Ar中被置换在对称位置时，Ar2到Ar5中至少一个具有不同的结构，当二级胺和三级胺在Ar中被置换在非对称位置时，Ar2到Ar5具有相同的结构或不同的结构。该非对称芳基胺衍生物可用于形成有机电致发光元件的有机薄层。当使用掺杂剂作为发射材料制备有机电致发光元件时，该非对称芳基胺衍生物在蓝色波长区域表现出卓越的发射效率和优异的寿命特性。
• N-(4-(8-(PHENYL)NAPHTHALEN-2-YL)PHENYL)-N,N'-DI(PHENYL)-AMINE DERIVATIVES AND RELATED COMPOUNDS FOR USE IN ORGANIC ELECTROLUMINESCENCE DEVICES
  申请人：Samsung Display Co., Ltd.

  公开号：EP3518303A1

  公开（公告）日：2019-07-31

  Provided is an organic electroluminescence device including a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, and a second electrode disposed on the electron transport region, in which the hole transport region includes a monoamine compound represented by Formula 1, such as e.g. an N-(4-(8-(phenyl)naphthalen-2-yl)phenyl)-N,N'-di(phenyl)-amine derivative or a structurally related compound, thereby attaining high emission efficiency. FIG. 1

  提供了一种有机电致发光器件，包括第一电极、设置在第一电极上的空穴传输区、设置在空穴传输区上的发射层、设置在发射层上的电子传输区以及设置在电子传输区上的第二电极，其中空穴传输区包括由式1表示的单胺化合物，例如N-(4-(8-(苯基)萘-2-基)苯基)-N,N'-二(苯基)-胺衍生物或结构相关的化合物。例如 N-(4-(8-(苯基)萘-2-基)苯基)-N,N'-二(苯基)-胺衍生物或结构相关的化合物，从而获得高发射效率。 图 1
• ORGANIC ELECTROLUMINESCENCE DEVICE AND MONOAMINE COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE
  申请人：SAMSUNG DISPLAY CO., LTD.

  公开号：US20190237668A1

  公开（公告）日：2019-08-01

  An organic electroluminescence device includes a first electrode, a hole transport region on the first electrode, an emission layer on the hole transport region, an electron transport region on the emission layer, and a second electrode on the electron transport region. The hole transport region includes a monoamine compound represented by the following Formula 1:
• US8586211B2
  申请人：——

  公开号：US8586211B2

  公开（公告）日：2013-11-19