9-[3-(10-Naphthalen-1-ylanthracen-9-yl)phenyl]naphtho[1,2-b][1]benzofuran

• 分子结构分类: 有机化合物 - 木脂素、新木脂素和相关化合物 - 芳基萘木脂素
• 英文名称: 9-[3-(10-Naphthalen-1-ylanthracen-9-yl)phenyl]naphtho[1,2-b][1]benzofuran
• 英文别名: 9-[3-(10-naphthalen-1-ylanthracen-9-yl)phenyl]naphtho[1,2-b][1]benzofuran
• 化学式: C₄₆H₂₈O
• 分子量: 596.728
• InChiKey: HWIVQEYZVWOHTR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  13.5
• 重原子数：
  47
• 可旋转键数：
  3
• 环数：
  10.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  13.1
• 氢给体数：
  0
• 氢受体数：
  1

文献信息

• ORGANIC ELECTROLUMINESCENCE ELEMENT AND ELECTRONIC APPARATUS
  申请人：IDEMITSU KOSAN CO., LTD.

  公开号：US20210005826A1

  公开（公告）日：2021-01-07

  An organic electroluminescence device comprising a cathode, an anode and an organic layer disposed between the cathode and the anode, wherein the organic layer comprises a fluorescent emitting layer and the fluorescent emitting layer comprises a first compound, a second compound having a hole mobility larger than that of the first compound, and a dopant material showing a fluorescent spectrum with a half width of 30 nm or less; and an organic electroluminescence device comprising a cathode, an anode and an organic layer disposed between the cathode and the anode, wherein the organic layer comprises a fluorescent emitting layer and the fluorescent emitting layer comprises a first compound, a third compound having an affinity larger than that of the first compound, and a dopant material showing a fluorescent spectrum with a half width of 30 nm or less and the content of the third compound in the fluorescent emitting layer is less than that of the first compound in the fluorescent emitting layer are excellent in their performance.

  一种有机电致发光装置，包括阴极、阳极以及设置在阴极和阳极之间的有机层，其中所述有机层包括荧光发射层，且所述荧光发射层包括第一化合物、第二化合物和掺杂材料，所述第二化合物的空穴迁移率大于所述第一化合物，且所述掺杂材料显示的荧光光谱半宽为30纳米或更小；以及一种有机电致发光装置，包括阴极、阳极以及设置在阴极和阳极之间的有机层，其中所述有机层包括荧光发射层，且所述荧光发射层包括第一化合物、第三化合物和掺杂材料，所述第三化合物与所述第一化合物的亲和力更大，且所述掺杂材料显示的荧光光谱半宽为30纳米或更小，且所述第三化合物在荧光发射层中的含量小于所述第一化合物在荧光发射层中的含量，这些装置的性能都十分出色。
• Organic electroluminescence device and novel compound
  申请人：IDEMITSU KOSAN CO., LTD.

  公开号：US10249832B1

  公开（公告）日：2019-04-02

  To provide an organic electroluminescence device having a high luminous efficiency and a novel compound that can be used as a material for an organic electroluminescence device having a high luminous efficiency. A compound represented by the following formula (3-I), wherein at least one of R1 to R7 and R10 to R11 is —N(R36)(R37). R31 to R37 are independently a hydrogen atom, a substituted or unsubstituted alkyl group including 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group including 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms.

  提供一种具有高发光效率的有机电致发光器件和一种可用作具有高发光效率的有机电致发光器件材料的新化合物。 以下式（3-I）所代表的化合物，其中R1至R7和R10至R11中的至少一个是—N(R36)(R37)。R31至R37独立地是氢原子，包括1至50个碳原子的取代或未取代的烷基基团，包括3至50个环碳原子的取代或未取代的环烷基基团，包括6至50个环碳原子的取代或未取代的芳基基团或包括5至50个环原子的取代或未取代的单价杂环基团。
• ORGANIC ELECTROLUMINESCENT ELEMENT, ELECTRONIC DEVICE, AND COMPOUND
  申请人：IDEMITSU KOSAN CO.,LTD.

  公开号：US20200212315A1

  公开（公告）日：2020-07-02

  An organic electroluminescence device includes: an anode; a cathode and a first organic layer between the anode and the cathode, the first organic layer containing a first compound represented by a formula (2) below. In the formula (2), at least one combination of adjacent two or more of R 201 to R 216 is mutually bonded to form a saturated ring, mutually bonded to form an unsaturated ring, or not mutually bonded, and R 201 to R 216 forming neither the saturated ring nor the unsaturated ring each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group, or the like.

  一种有机电致发光器件，包括：阳极；阴极和第一有机层，在阳极和阴极之间，第一有机层包含一个由下式（2）表示的第一化合物。在式（2）中，相邻的两个或更多的R201到R216中的至少一个组合互相结合形成饱和环，互相结合形成不饱和环，或不互相结合，而R201到R216中既不形成饱和环也不形成不饱和环的各自独立地表示氢原子、取代或未取代的烷基或类似物。
• NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENCE DEVICE
  申请人：IDEMITSU KOSAN CO., LTD.

  公开号：US20190214579A1

  公开（公告）日：2019-07-11

  A compound represented by the formula (1) below. At least one set of two or more adjacent groups among R 1 to R 11 forms a substituted or unsubstituted heterocyclic ring, or forms a ring represented by the formula (2) below, or at least one of R 1 to R 4 is a group represented by the formula (3) below.

  一个由下式（1）表示的化合物。其中R1到R11中至少有一组相邻的两个或更多基团形成替代或未替代的杂环，或形成下式（2）表示的环，或者R1到R4中至少有一个是下式（3）表示的基团。
• ANTHRACENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE ELEMENT USING SAME
  申请人：Idemitsu Kosan Co., Ltd.

  公开号：US20150325800A1

  公开（公告）日：2015-11-12

  An anthracene derivative represented by the following formula (1): wherein in the formula (1), L 1 is selected from a single bond and a linking group, and the linking group is selected from a divalent arylene group, a divalent heterocyclic group, and a group formed by linking of 2 to 4 of divalent arylene groups and/or divalent heterocyclic groups. Ar 1 is selected from the following formulas (2) and (3). In the formulas (2) and (3), X is selected from an oxygen atom and a sulfur atom. In the formula (2), any one of R 11 to R 14 is used for bonding to L 1 . In the formula (3), any one of R 21 to R 24 is used for bonding to L 1 . Ar 2 is selected from a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms and a substituted or unsubstituted heterocyclic group including 5 to 50 ring atoms.

  以下为翻译结果： 一种蒽衍生物，其化学式如下（1）：在式（1）中，L1选自单键和连接基，连接基选自二价芳基基团、二价杂环基团以及由2至4个二价芳基基团和/或二价杂环基团连接而成的基团。Ar1选自以下化学式（2）和（3）。在式（2）和（3）中，X选自氧原子和硫原子。在式（2）中，R11至R14中的任意一个用于与L1结合。在式（3）中，R21至R24中的任意一个用于与L1结合。Ar2选自包含6至50个环碳原子的取代或未取代芳基团和包含5至50个环原子的取代或未取代杂环基团。