2-[4,4-Bis(4-methylphenyl)indeno[1,2-b]thiophen-2-yl]-4,4-bis(4-methylphenyl)indeno[1,2-b]thiophene | 1173057-64-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 双噻吩和低聚噻吩
• 英文名称: 2-[4,4-Bis(4-methylphenyl)indeno[1,2-b]thiophen-2-yl]-4,4-bis(4-methylphenyl)indeno[1,2-b]thiophene
• 英文别名: 2-[4,4-bis(4-methylphenyl)indeno[1,2-b]thiophen-2-yl]-4,4-bis(4-methylphenyl)indeno[1,2-b]thiophene
• CAS: 1173057-64-1
• 化学式: C₅₀H₃₈S₂
• 分子量: 702.984
• InChiKey: ROKPGCCYFMLXJG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  14
• 重原子数：
  52
• 可旋转键数：
  5
• 环数：
  10.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  56.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2-bromo-4,4-di-p-tolyl-4H-indeno[1,2-b]thiophene 、 2-(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)-8,8-di-p-tolyl-8H-3-thia-cyclopenta[a]indene 在 potassium phosphate 、 四(三苯基膦)钯 、 三叔丁基膦 作用下， 以 1,4-二氧六环 、 水 、 甲苯 为溶剂， 反应 48.0h， 以65%的产率得到2-[4,4-Bis(4-methylphenyl)indeno[1,2-b]thiophen-2-yl]-4,4-bis(4-methylphenyl)indeno[1,2-b]thiophene
  参考文献：
  名称：

  Structural effects on the hole mobilities of indenothiophene-embedded homologs

  摘要：

  A systematic study of the relationship between the structures and the non-dispersive hole mobilities (Lip to 10(-3) cm(2) V-1 s(-1)) of a homologous series of amorphous indenothiophene-containing materials is described. The hole mobilities were dependent mainly on the length and rigidity of the pi-conjugated backbone and the peripheral substituents. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2009.02.148

文献信息

• Structural effects on the hole mobilities of indenothiophene-embedded homologs
  作者：Teng-Chih Chao、Ken-Tsung Wong、Wen-Yi Hung、Tei-Hung Hou、Wei-Jiun Chen

  DOI：10.1016/j.tetlet.2009.02.148

  日期：2009.7

  A systematic study of the relationship between the structures and the non-dispersive hole mobilities (Lip to 10(-3) cm(2) V-1 s(-1)) of a homologous series of amorphous indenothiophene-containing materials is described. The hole mobilities were dependent mainly on the length and rigidity of the pi-conjugated backbone and the peripheral substituents. (C) 2009 Elsevier Ltd. All rights reserved.