18-[3-(10-Naphthalen-2-ylanthracen-9-yl)phenyl]-21-oxapentacyclo[12.7.0.02,7.08,13.015,20]henicosa-1(14),2,4,6,8,10,12,15(20),16,18-decaene

• 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: 18-[3-(10-Naphthalen-2-ylanthracen-9-yl)phenyl]-21-oxapentacyclo[12.7.0.02,7.08,13.015,20]henicosa-1(14),2,4,6,8,10,12,15(20),16,18-decaene
• 英文别名: 18-[3-(10-naphthalen-2-ylanthracen-9-yl)phenyl]-21-oxapentacyclo[12.7.0.02,7.08,13.015,20]henicosa-1(14),2,4,6,8,10,12,15(20),16,18-decaene
• 化学式: C₅₀H₃₀O
• 分子量: 646.8
• InChiKey: CIGRSFYNROVECR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  14.8
• 重原子数：
  51
• 可旋转键数：
  3
• 环数：
  11.0
• 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

• 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。
• ORGANIC LIGHT-EMITTING DEVICE
  申请人：SAMSUNG DISPLAY CO., LTD.

  公开号：US20160218297A1

  公开（公告）日：2016-07-28

  An organic light-emitting device includes a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer and an electron transport region between the emission layer and the second electrode. The organic layer includes a first material represented by Formula 1 and a second material represented by Formula 2. The organic light-emitting device including the first and second materials may have improved efficiency and lifetime.
• ORGANIC ELECTROLUMINESCENCE ELEMENT AND ELECTRONIC DEVICE
  申请人：IDEMITSU KOSAN CO., LTD.

  公开号：US20180130968A1

  公开（公告）日：2018-05-10

  An organic electroluminescence device includes: an anode; a cathode; an emitting layer disposed between the anode and the cathode; and a hole transporting layer disposed between the anode and the emitting layer. The emitting layer contains a first compound represented by a formula (1) and a fluorescent second compound. The hole transporting layer contains a third compound represented by a formula (3). In the formula (1), Z 1 is represented by a formula (1a). A cyclic structure represented by a formula (1b) or (1c) may be fused to Z 1 . Each of X 1 and X 2 is an oxygen atom, a sulfur atom, NR A or CR B R C .
• US9947879B2
  申请人：——

  公开号：US9947879B2

  公开（公告）日：2018-04-17
• [EN] ANTHRACENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE ELEMENT USING SAME<br/>[FR] DÉRIVÉ D'ANTHRACÈNE ET ÉLÉMENT ÉLECTROLUMINESCENT ORGANIQUE L'UTILISANT
  申请人：IDEMITSU KOSAN CO

  公开号：WO2014141725A1

  公开（公告）日：2014-09-18

  下記式（１）で表されるアントラセン誘導体。式（１）中、Ｌ１は単結合及び連結基から選択され、前記連結基は、２価のアリーレン基、２価の複素環基、及び、２価のアリーレン基及び／又は２価の複素環基が２～４個連結して形成される基から選択される。Ａｒ１は下記式（２）及び（３）から選択される。式（２）、（３）中、Ｘは酸素原子及び硫黄原子から選択される。式（２）中、Ｒ１１～Ｒ１４のいずれか１つはＬ１との結合に用いられる。式（３）中、Ｒ２１～Ｒ２４のいずれか１つはＬ１との結合に用いられる。Ａｒ２は、置換もしくは無置換の環形成炭素数６～５０のアリール基及び置換もしくは無置換の環形成原子数５～５０の複素環基から選択される。