2-甲基-苯并(b)萘并(2,3-d)噻吩 | 83656-84-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 中文名称: 2-甲基-苯并(b)萘并(2,3-d)噻吩
• 英文名称: 2-methylbenzonaphtho<2,3-d>thiophene
• 英文别名: 10-methylbenzo[b]naphtho[1,2-d]thiophene；Benzo(b)naphtho(2,3-d)thiophene, 2-methyl-；2-methylnaphtho[2,3-b][1]benzothiole
• CAS: 83656-84-2
• 化学式: C₁₇H₁₂S
• 分子量: 248.348
• InChiKey: LJJIWDOMGATCMS-UHFFFAOYSA-N

物化性质

• 保留指数：
  406.07;413.67;414.69

计算性质

• 辛醇/水分配系数(LogP)：
  5.6
• 重原子数：
  18
• 可旋转键数：
  0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  28.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  naphthalen-2-yl(p-tolyl)sulfane 在 palladium(II) trifluoroacetate 、 silver(I) acetate 、 potassium carbonate 作用下， 反应 24.0h， 以57%的产率得到2-甲基-苯并(b)萘并(2,3-d)噻吩
  参考文献：
  名称：

  二苯并噻吩的合成钯催化双Ç ？二芳基硫醚的H活化

  摘要：

  据报道，钯通过氧化脱氢环化反应，使二芳基硫醚的双CH官能化形成二苯并噻吩（DBT）。该协议以中等到良好的产量提供了各种DBT，并具有对多种底物的耐受性。通过该方法成功合成了苯并[1,2- b：4,5- b '] bis [ b ]苯并噻吩，用作场效应晶体管的有机半导体。

  DOI：

  10.1002/chem.201402265

文献信息

• Organic Compound, Light-Emitting Element, Light-Emitting Device, Electronic Apparatus, and Lighting Device
  申请人：Semiconductor Energy Laboratory Co., Ltd.

  公开号：US20200216428A1

  公开（公告）日：2020-07-09

  A novel compound is provided. In addition, a light-emitting element with high emission efficiency and a long lifetime is provided. An organic compound represented by General Formula (G0), including a dibenzocarbazole skeleton and two amine skeletons. In General Formula (G0), A represents a substituted or unsubstituted dibenzocarbazole skeleton. The dibenzocarbazole skeleton and the amine skeletons may be bonded to each other through or not through an arylene group. In addition, a light-emitting element including the compound is provided.

  提供了一种新型化合物。此外，提供了一种具有高发射效率和长寿命的发光元件。一种由通用公式（G0）表示的有机化合物，包括一个二苯并咔唑骨架和两个胺骨架。在通用公式（G0）中，A代表一个取代或未取代的二苯并咔唑骨架。二苯并咔唑骨架和胺骨架可以通过芳基或非芳基团相互结合或不相互结合。此外，提供了一种包含该化合物的发光元件。
• Organic Compound, Light-Emitting Device, Light-Emitting Apparatus, Electronic Device, Display Device, and Lighting Device
  申请人：Semiconductor Energy Laboratory Co., Ltd.

  公开号：US20210139445A1

  公开（公告）日：2021-05-13

  A novel organic compound is provided. Alternatively, an organic compound that exhibits light emission with favorable chromaticity is provided. Alternatively, an organic compound that exhibits blue light emission with favorable chromaticity is provided. Alternatively, a light-emitting device with favorable emission efficiency is provided. Alternatively, an organic compound having a high carrier-transport property is provided. Alternatively, an organic compound with favorable reliability is provided. An organic compound having at least one amino group in which any one of a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, and a substituted or unsubstituted carbazolyl group is bonded to any one of a substituted or unsubstituted naphthobisbenzofuran skeleton, a substituted or unsubstituted naphthobisbenzothiophene skeleton, and a substituted or unsubstituted naphthobenzothienobenzofuran skeleton is provided.

  提供了一种新型有机化合物。或者提供一种表现出有利色度的光发射的有机化合物。或者提供一种表现出有利色度的蓝光发射的有机化合物。或者提供一种具有良好发射效率的发光装置。或者提供一种具有高载流子传输性能的有机化合物。或者提供一种具有良好可靠性的有机化合物。提供了一种有机化合物，其中任何一种取代或未取代的二苯并呋喃基团，取代或未取代的二苯并噻吩基团和取代或未取代的咔唑基团中的至少一个氨基与取代或未取代的萘并苯并呋喃骨架、取代或未取代的萘并苯并噻吩骨架和取代或未取代的萘苯并噻吩苯并呋喃骨架中的任何一个键合。
• [EN] ORGANIC ELECTROLUMINESCENT COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME<br/>[FR] COMPOSÉ ÉLECTROLUMINESCENT ORGANIQUE ET DISPOSITIF ÉLECTROLUMINESCENT ORGANIQUE LE COMPRENANT
  申请人：ROHM & HAAS ELECT MATERIALS KOREA LTD

  公开号：WO2020032574A1

  公开（公告）日：2020-02-13

  The present disclosure relates to an organic electroluminescent compound represented by formula 1 and an organic electroluminescent device comprising the same. By comprising the organic electroluminescent compound of the present disclosure, an organic electroluminescent device having improved driving voltage, luminous efficiency, and/or lifespan characteristics can be provided.

  本公开涉及一种由式1表示的有机电致发光化合物和包含其的有机电致发光器件。通过包含本公开的有机电致发光化合物，可以提供具有改善驱动电压、发光效率和/或寿命特性的有机电致发光器件。
• Pratap, Ram; Tominaga, Yoshinori; Castle, Raymond N., Journal of Heterocyclic Chemistry, 1982, vol. 19, p. 865 - 869
  作者：Pratap, Ram、Tominaga, Yoshinori、Castle, Raymond N.、Lee, Milton L.

  DOI：——

  日期：——
• PRATAP, RAM;TOMINAGA, YOSHINORI;CASTLE, R. N.;LEE, M. L., J. HETEROCYCL. CHEM., 1982, 19, N 4, 865-869
  作者：PRATAP, RAM、TOMINAGA, YOSHINORI、CASTLE, R. N.、LEE, M. L.

  DOI：——

  日期：——