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3,5-dihexyldithieno[3,2-b:2',3'-d]thiophene-2,6-dialdehyde | 1256918-75-8

中文名称
——
中文别名
——
英文名称
3,5-dihexyldithieno[3,2-b:2',3'-d]thiophene-2,6-dialdehyde
英文别名
5,9-Dihexyl-3,7,11-trithiatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene-4,10-dicarbaldehyde;5,9-dihexyl-3,7,11-trithiatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene-4,10-dicarbaldehyde
3,5-dihexyldithieno[3,2-b:2',3'-d]thiophene-2,6-dialdehyde化学式
CAS
1256918-75-8
化学式
C22H28O2S3
mdl
——
分子量
420.661
InChiKey
SCAGSFGUTSTNKR-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    9.3
  • 重原子数:
    27
  • 可旋转键数:
    12
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    119
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    1,10-邻二氮杂菲-5,6-二酮3,5-dihexyldithieno[3,2-b:2',3'-d]thiophene-2,6-dialdehyde 在 ammonium acetate 、 溶剂黄146 作用下, 反应 2.0h, 以65%的产率得到2-(6-(1H-imidazo[4,5-f][1,10]phenanthrolin-2-yl)-3,5-dihexyldithieno[3,2-b:2',3'-d]thien-2-yl)-1H-imidazo[4,5-f][1,10]phenanthroline
    参考文献:
    名称:
    Synthesis and study of novel supramolecular nanocomposites containing aryl-imidazo-phenanthroline-based metallo-polymers (H-donors) and surface-modified ZnO nanoparticles (H-acceptors)
    摘要:
    Four novel metallo-polymers (P1-P4) containing aryl-imidazo-phenanthrolines (AIP) ligands (incorporated with phenyl and fused-thiophene cores) were synthesized and characterized. Interestingly, P1-P4 exhibited electrochromism during the oxidation processes of cyclic voltammogram studies. In addition, P1-P4 were blended with surface-modified pyridyl-ZnO nanoparticles (ZnOpy as proton acceptors) to form nanocomposites, where P3-P4 were functionalized with carboxylic acid pendants (as proton donors) on the polymer backbones to study for the H-bonded effects on surface-modified ZnOpy nanoparticles. In order to investigate the nanocomposites containing metallo-polymers P1-P4 and surface-modified ZnOpy nanoparticles, nanocomposites P1-P4/ZnOpy were characterized by UV-visible (UV) absorption spectra, Fourier transform infrared (FT-IR), photoluminescence (PL) spectra, time-resolved photoluminescence decays, X-ray diffraction (XRD) measurements, and transmission electron microscopy (TEM) analyses. In contrast to nanocomposites P1/ZnOpy and P2/ZnOpy, higher crystallinities with a distinct layered-structure of H-bonded nanocomposites P3/ZnOpy and P4/ZnOpy in XRD measurements were induced by the introduction of surface-modified ZnOpy nanoparticles to metallopolymers P3 and P4, correspondingly. Furthermore, due to the supramolecular interactions of surface-modified ZnOpy nanoparticles with metallo-polymers P3-P4, TEM images verified that ZnOpy nanoparticles were more homogeneously distributed in nanocomposites P3-P4/ZnOpy (with H-bonds) than those in P1-P2/ZnOpy (without H-bonds), respectively. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.10.031
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同类化合物

锡烷,1,1'-(3,6-二辛基噻吩[3,2-B]噻吩-2,5-二基)双[1,1,1-三甲基- 苯胺,N-[3,4,6-三[(1-甲基乙基)硫代]-1H,3H-噻吩并[3,4-c]噻吩并-1-亚基]- 并四噻吩 四苯基噻吩并[3,2-b]噻吩 噻吩酮[2,3-b]噻吩-2-羧酸 噻吩并[3,2-b]噻吩-2-羧酸乙酯 噻吩并[3,2-b]噻吩-2-甲腈 噻吩并[3,2-b]噻吩-2,5-二羧醛 噻吩并[3,2-b]噻吩 噻吩并[3,2-b!噻吩-2-羧酸甲酯 噻吩并[3,2-B]噻吩-2-甲酸 噻吩并[3,2-B]噻吩-2,5-二基二硼酸 噻吩[32-B]噻吩-2-硼酸频呢醇酯 噻吩[3,2-b]噻吩-2-硼酸 噻吩[3,2-B]噻吩-2,5-二羧酸 噻吩[3,2-B]噻吩,2,5-二溴-3,6-二辛基- 噻吩[2,3-B]噻吩 二噻吩并[3,2-b:2',3'-d]噻吩-2,6-二甲醛 二噻吩并[2,3-b:3',2'-d]噻吩 二噻吩[3,2-b:2',3'-d]噻吩-2-硼酸 二噻吩[3,2-B:2',3'-D]噻吩-2,6-二羧酸 二噻吩[3,2-B:2',3'-D]噻吩-2,5-二羧酸乙酯 二噻吩[3,2-B:2',3'-D]噻吩 6-溴噻吩并[3,2-B]噻吩-2-甲酸 5-甲酰基噻吩并[2,3-b]噻吩-2-磺酰胺 5-溴-3,4-二甲基噻吩基[2,3-b]噻吩-2-甲醛 5-氰基-3,4-二甲基噻吩并[2,3-B]噻吩-2-羧酸乙酯 5-己基噻吩并[3,2-B]噻吩-2-硼酸频哪醇酯 5-乙酰基-3,4-二甲基噻吩并[2,3-b]噻吩-2-甲腈 5,10-双((2-己基癸基)氧基)噻吩并[2,3-d:2',3'-d']苯并[1,2-b:4,5-b'二噻吩 4,6-二氢噻吩并[3,4-b]噻吩-2-羧酸甲酯 4,6-二氢噻吩并[3,4-b]噻吩-2-羧酸 3-溴噻吩[3,2-b]噻吩 3-溴-6-癸基噻吩并[3,2-b]噻吩-2-甲醛 3-溴-5-碘噻吩-2-羧酸甲酯 3-氯噻吩并[2,3-B]噻吩-2-羧酸 3-氯噻吩基并[2,3-B]噻吩-2-羰酰氯 3-壬基噻吩并[3,2-B]噻吩 3-十一烷基噻吩并[3,2-b]噻吩 3,7-双十七烷基噻吩并[3,2-B]噻吩并[2',3':4,5]噻吩并[2,3-D]噻吩 3,6-双(5-溴噻吩并[3,2-b]噻吩-2-基)-2,5-双(2-辛基癸基)吡咯并[3,4-c]吡咯-1,4(2H,5H)-二酮 3,6-二辛基噻吩并[3,2-b]噻吩 3,6-二甲氧基噻吩并[3,2-b]噻吩 3,6-二溴噻吩[3,2-b]噻吩 3,6-二己基噻吩并[3,2-b]噻吩 3,5-二溴二噻吩[3,2-b:2',3'-d]噻吩 3,4-二甲基噻吩并噻吩 3,4-二甲基噻吩并[2,3-b]噻吩-2-羧酸甲酯 3,4-二甲基噻吩并[2,3-B]噻吩-2-甲醛 3,4-二甲基噻吩(2,3-b)噻吩-2,5-二羧酸