摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-[3,4,5-tris(dodecyloxy)phenyl]-2-tributylstannyl dithieno[3,2-b:2',3'-a]thiophene | 1422273-19-5

中文名称
——
中文别名
——
英文名称
6-[3,4,5-tris(dodecyloxy)phenyl]-2-tributylstannyl dithieno[3,2-b:2',3'-a]thiophene
英文别名
——
6-[3,4,5-tris(dodecyloxy)phenyl]-2-tributylstannyl dithieno[3,2-b:2',3'-a]thiophene化学式
CAS
1422273-19-5
化学式
C62H106O3S3Sn
mdl
——
分子量
1114.43
InChiKey
IGXQRABQELOIJC-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):
    22.8
  • 重原子数:
    69.0
  • 可旋转键数:
    47.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.77
  • 拓扑面积:
    27.69
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    6-[3,4,5-tris(dodecyloxy)phenyl]-2-tributylstannyl dithieno[3,2-b:2',3'-a]thiophene四(三苯基膦)钯 、 ammonium acetate 、 溶剂黄146 作用下, 以 甲苯 为溶剂, 反应 24.0h, 生成 3-(5-(5-{6-[3,4,5-tris(dodecyloxy)phenyl]dithieno[3,2-b:2',3'-a]thienyl})-2-(4-hexylthiazol-2-yl)-4-hexylthiazole)-2-cyanoacrylic acid
    参考文献:
    名称:
    Synthesis of metal-free organic dyes containing tris(dodecyloxy)phenyl and dithienothiophenyl units and a study of their mesomorphic and photovoltaic properties
    摘要:
    In this study we synthesized three metal-free organic dyes (Cpd11, Cpd16, and Cpd22) featuring 3,4,5-tris(dodecyloxy)phenyl and cyanoacrylic acid moieties as electron-donor and electron-acceptor/anchoring units, respectively, linked through various dithienothiophenyl conjugated spacers. Cpd16 exhibits mesomorphic properties, confirmed through polarizing optical microscopy, differential scanning calorimetly, and X-ray diffraction (XRD), due to the appropriate ratio of the lengths of its flexible chain to its rigid core. Molecular modeling of Cpd16, and its d-spacing determined from XRD data, verified the existence of a tilt angle in the SmC phase. Among these metal-free organic dyes, a dye-sensitized solar cell incorporating Cpd16 exhibited the best performance, presumably because of its better packing and its mesomorphic properties; the power conversion efficiency was 3.72% (V-oc=0.58 V; J(sc)=9.98 mA cm(-2); FF=0.65) under simulated AM 1.5 irradiation (100 mW cm(-2)). (c) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2013.01.009
  • 作为产物:
    描述:
    2-tributylstannyldithieno[3,2-b;2',3'-d]thiophene 在 四(三苯基膦)钯正丁基锂 作用下, 以 四氢呋喃正己烷甲苯 为溶剂, 反应 50.0h, 生成 6-[3,4,5-tris(dodecyloxy)phenyl]-2-tributylstannyl dithieno[3,2-b:2',3'-a]thiophene
    参考文献:
    名称:
    Synthesis of metal-free organic dyes containing tris(dodecyloxy)phenyl and dithienothiophenyl units and a study of their mesomorphic and photovoltaic properties
    摘要:
    In this study we synthesized three metal-free organic dyes (Cpd11, Cpd16, and Cpd22) featuring 3,4,5-tris(dodecyloxy)phenyl and cyanoacrylic acid moieties as electron-donor and electron-acceptor/anchoring units, respectively, linked through various dithienothiophenyl conjugated spacers. Cpd16 exhibits mesomorphic properties, confirmed through polarizing optical microscopy, differential scanning calorimetly, and X-ray diffraction (XRD), due to the appropriate ratio of the lengths of its flexible chain to its rigid core. Molecular modeling of Cpd16, and its d-spacing determined from XRD data, verified the existence of a tilt angle in the SmC phase. Among these metal-free organic dyes, a dye-sensitized solar cell incorporating Cpd16 exhibited the best performance, presumably because of its better packing and its mesomorphic properties; the power conversion efficiency was 3.72% (V-oc=0.58 V; J(sc)=9.98 mA cm(-2); FF=0.65) under simulated AM 1.5 irradiation (100 mW cm(-2)). (c) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2013.01.009
点击查看最新优质反应信息

同类化合物

齐留通钠 齐留通相关物质A 齐留通亚砜 齐留通-d4 齐留通 雷洛昔芬杂质 邻联甲苯胺砜 试剂4,8-Bis(3,5-dioctyl-2-thienyl)-2,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[1,2-b:4,5-b']dithiophene 试剂1,1'-[4,8-Bis[4-(2-ethylhexyl)-3,5-difluorophenyl]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl]bis[1,1,1-trimethylstannane] 苯并噻吩-7-醇 苯并噻吩-4-硼酸频哪醇酯 苯并噻吩-3-羧酸甲酯 苯并噻吩-3-硼酸 苯并噻吩-2-羰酰氯 苯并噻吩-2-羧酸肼 苯并噻吩-2-羧酸 苯并噻吩-2-硼酸 苯并噻吩-2-氨基甲酸叔丁酯 苯并噻吩 苯并[c]噻吩 苯并[b]噻吩-7-胺 苯并[b]噻吩-7-羧酸乙酯 苯并[b]噻吩-7-甲醛 苯并[b]噻吩-7-甲腈 苯并[b]噻吩-6-醇 苯并[b]噻吩-6-胺 苯并[b]噻吩-6-羧酸乙酯 苯并[b]噻吩-6-羧酸 苯并[b]噻吩-6-甲腈 苯并[b]噻吩-5-甲腈,2-甲酰基- 苯并[b]噻吩-5-甲磺酰氯 苯并[b]噻吩-4-羧酸甲酯 苯并[b]噻吩-4-羧酸 苯并[b]噻吩-4-甲醛 苯并[b]噻吩-4-甲腈 苯并[b]噻吩-4-基甲醇 苯并[b]噻吩-3-胺盐酸盐 苯并[b]噻吩-3-胺 苯并[b]噻吩-3-羧酸-(2-二烯丙基氨基乙酯) 苯并[b]噻吩-3-硼酸频哪酯 苯并[b]噻吩-3-甲醛肟 苯并[b]噻吩-3-甲酰胺 苯并[b]噻吩-3-基乙酸酯 苯并[b]噻吩-3-乙酸 苯并[b]噻吩-3-乙酰氯 苯并[b]噻吩-3-乙腈 苯并[b]噻吩-2-胺盐酸盐 苯并[b]噻吩-2-羧酸6-氨基-3-氯-甲酯 苯并[b]噻吩-2-羧酸,5-氯-3-(1-甲基乙氧基)- 苯并[b]噻吩-2-羧酸,3-羟基-5-甲氧基-,甲基酯