4,7-bis(3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepin-6-yl)benzo[c][1,2,5]thiadiazole | 1234785-24-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻二唑类
• 英文名称: 4,7-bis(3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepin-6-yl)benzo[c][1,2,5]thiadiazole
• 英文别名: 4,7-Bis(3,3-didecyl-2,4-dihydrothieno[3,4-b][1,4]dioxepin-6-yl)-2,1,3-benzothiadiazole；4,7-bis(3,3-didecyl-2,4-dihydrothieno[3,4-b][1,4]dioxepin-6-yl)-2,1,3-benzothiadiazole
• CAS: 1234785-24-0
• 化学式: C₆₀H₉₆N₂O₄S₃
• 分子量: 1005.63
• InChiKey: GKUNVSKRYCGTPO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  25
• 重原子数：
  69
• 可旋转键数：
  38
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.77
• 拓扑面积：
  147
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  4,7-二溴-2,1,3-苯并噻二唑 、 tri-n-butyl(3,3-di-n-decyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepin-8-yl)stannane 在 bis-triphenylphosphine-palladium(II) chloride 作用下， 以 甲苯 为溶剂， 以60%的产率得到4,7-bis(3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepin-6-yl)benzo[c][1,2,5]thiadiazole
  参考文献：
  名称：

  Donor−Acceptor Polymer Electrochromes with Tunable Colors and Performance

  摘要：

  To demonstrate the effect of donor (D) and acceptor (A) units on the structure property relationships of electrochromic polymers, design, synthesis, characterization and polymerization of a series of D A type systems, 1-5, based on thiophene, 3,4-ethylenedioxythiophene, and 3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine as D units and 2,1,3-benzoselenadiazole, 2,1,3-benzothiadiazole and 2-decyl-2H-benzo[d][1,2,3]triazole as A units are highlighted. It is found that these units play key roles on the redox behavior, band gap, neutral state color, and the electrochromic performance (stability, optical contrast, coloration efficiency, and switching time) of the system. It is noted that electropolymerization of these D-A systems provides processable low band gap electrochromes, P1-P5, exhibiting high redox stability, coloration efficiency, transmittance and/or contrast ratio and low response time. Furthermore, P1-P5 reflect various hues of blue and green pallets of the RGB color-space in the neutral state. In particular, it is noteworthy that P5 is an excellent blue-to-colorless polymeric electrochrome, which, to our best knowledge, exhibits the highest optical contrast and coloration efficiency among the D A type systems. The panoramic breadth of the neutral state colors and intriguing features of these polymeric materials further confirm that D A approach allows engineering tunable electrochromes, which hold promise for commercialization of polymeric ROB electrochromics.

  DOI：

  10.1021/cm100805g

文献信息

• Donor−Acceptor Polymer Electrochromes with Tunable Colors and Performance
  作者：Merve İçli、Melek Pamuk、Fatih Algi、Ahmet M. Önal、Atilla Cihaner

  DOI：10.1021/cm100805g

  日期：2010.7.13

  To demonstrate the effect of donor (D) and acceptor (A) units on the structure property relationships of electrochromic polymers, design, synthesis, characterization and polymerization of a series of D A type systems, 1-5, based on thiophene, 3,4-ethylenedioxythiophene, and 3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine as D units and 2,1,3-benzoselenadiazole, 2,1,3-benzothiadiazole and 2-decyl-2H-benzo[d][1,2,3]triazole as A units are highlighted. It is found that these units play key roles on the redox behavior, band gap, neutral state color, and the electrochromic performance (stability, optical contrast, coloration efficiency, and switching time) of the system. It is noted that electropolymerization of these D-A systems provides processable low band gap electrochromes, P1-P5, exhibiting high redox stability, coloration efficiency, transmittance and/or contrast ratio and low response time. Furthermore, P1-P5 reflect various hues of blue and green pallets of the RGB color-space in the neutral state. In particular, it is noteworthy that P5 is an excellent blue-to-colorless polymeric electrochrome, which, to our best knowledge, exhibits the highest optical contrast and coloration efficiency among the D A type systems. The panoramic breadth of the neutral state colors and intriguing features of these polymeric materials further confirm that D A approach allows engineering tunable electrochromes, which hold promise for commercialization of polymeric ROB electrochromics.