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4-Methoxy-5-(4-methoxyphenyl)-2-thiophen-2-yl-1,3-thiazole | 1376711-57-7

中文名称
——
中文别名
——
英文名称
4-Methoxy-5-(4-methoxyphenyl)-2-thiophen-2-yl-1,3-thiazole
英文别名
4-methoxy-5-(4-methoxyphenyl)-2-thiophen-2-yl-1,3-thiazole
4-Methoxy-5-(4-methoxyphenyl)-2-thiophen-2-yl-1,3-thiazole化学式
CAS
1376711-57-7
化学式
C15H13NO2S2
mdl
——
分子量
303.406
InChiKey
CGAWBXSKBAWMPQ-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):
    4.3
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    87.8
  • 氢给体数:
    0
  • 氢受体数:
    5

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:
    4-Methoxy-5-(4-methoxyphenyl)-2-thiophen-2-yl-1,3-thiazole哌啶正丁基锂 作用下, 以 四氢呋喃正己烷乙腈 为溶剂, 反应 6.5h, 生成
    参考文献:
    名称:
    4-Methoxy-1,3-thiazole based donor-acceptor dyes: Characterization, X-ray structure, DFT calculations and test as sensitizers for DSSC
    摘要:
    Four donor-(pi-conjugated-bridge)-acceptor type dyes A-D were designed and synthesized. These new compounds use an unconventional 4-hydroxy-1,3-thiazole building block as an additional chromophore for light harvesting and to extend the pi-conjugated system of the molecules. The synthetic route involved a double N-arylation Hartwig-Buchwald reaction using Pd(dba)(2) as precatalyst and P(Bu-t)(3) as ligand. Two different triarylamines and a 4-methoxyphenyl group were used as electron donor moieties. The electron acceptor (anchoring) group was 2-cyanoacrylic acid for all dyes, whereas the pi-spacer was varied and the influence was investigated. The dyes were thoroughly characterized using photophysical and electrochemical methods and by density functional theory calculations. Additionally, they were evaluated in nanocrystalline TiO2-based dye-sensitized solar cells (DSSCs). The DSSCs were prepared with and without deoxycholic acid (DCA) as a co-adsorbent to inhibit dye aggregation. The efficiencies obtained were low for DSSCs fabricated without DCA, but were significantly improved for DCCS with co-adsorbed DCA. Additionally, the X-ray structure of dye D was obtained, demonstrating the stereochemistry and planar geometry of the molecule. The DSSC based on dye A showed an efficiency of eta = 1.70% (J(sc) = 4.49 mA cm(-2), V-OC = 0.61 V, FF = 0.62) under 100 mW cm(-2) simulated AM 1.5 G solar irradiation compared to eta = 4.1% of the standard N-3 obtained under same conditions. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2012.02.014
  • 作为产物:
    参考文献:
    名称:
    4-Methoxy-1,3-thiazole based donor-acceptor dyes: Characterization, X-ray structure, DFT calculations and test as sensitizers for DSSC
    摘要:
    Four donor-(pi-conjugated-bridge)-acceptor type dyes A-D were designed and synthesized. These new compounds use an unconventional 4-hydroxy-1,3-thiazole building block as an additional chromophore for light harvesting and to extend the pi-conjugated system of the molecules. The synthetic route involved a double N-arylation Hartwig-Buchwald reaction using Pd(dba)(2) as precatalyst and P(Bu-t)(3) as ligand. Two different triarylamines and a 4-methoxyphenyl group were used as electron donor moieties. The electron acceptor (anchoring) group was 2-cyanoacrylic acid for all dyes, whereas the pi-spacer was varied and the influence was investigated. The dyes were thoroughly characterized using photophysical and electrochemical methods and by density functional theory calculations. Additionally, they were evaluated in nanocrystalline TiO2-based dye-sensitized solar cells (DSSCs). The DSSCs were prepared with and without deoxycholic acid (DCA) as a co-adsorbent to inhibit dye aggregation. The efficiencies obtained were low for DSSCs fabricated without DCA, but were significantly improved for DCCS with co-adsorbed DCA. Additionally, the X-ray structure of dye D was obtained, demonstrating the stereochemistry and planar geometry of the molecule. The DSSC based on dye A showed an efficiency of eta = 1.70% (J(sc) = 4.49 mA cm(-2), V-OC = 0.61 V, FF = 0.62) under 100 mW cm(-2) simulated AM 1.5 G solar irradiation compared to eta = 4.1% of the standard N-3 obtained under same conditions. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2012.02.014
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文献信息

  • 4-Methoxy-1,3-thiazole based donor-acceptor dyes: Characterization, X-ray structure, DFT calculations and test as sensitizers for DSSC
    作者:Roberto Menzel、Daniel Ogermann、Stephan Kupfer、Dieter Weiß、Helmar Görls、Karl Kleinermanns、Leticia González、Rainer Beckert
    DOI:10.1016/j.dyepig.2012.02.014
    日期:2012.9
    Four donor-(pi-conjugated-bridge)-acceptor type dyes A-D were designed and synthesized. These new compounds use an unconventional 4-hydroxy-1,3-thiazole building block as an additional chromophore for light harvesting and to extend the pi-conjugated system of the molecules. The synthetic route involved a double N-arylation Hartwig-Buchwald reaction using Pd(dba)(2) as precatalyst and P(Bu-t)(3) as ligand. Two different triarylamines and a 4-methoxyphenyl group were used as electron donor moieties. The electron acceptor (anchoring) group was 2-cyanoacrylic acid for all dyes, whereas the pi-spacer was varied and the influence was investigated. The dyes were thoroughly characterized using photophysical and electrochemical methods and by density functional theory calculations. Additionally, they were evaluated in nanocrystalline TiO2-based dye-sensitized solar cells (DSSCs). The DSSCs were prepared with and without deoxycholic acid (DCA) as a co-adsorbent to inhibit dye aggregation. The efficiencies obtained were low for DSSCs fabricated without DCA, but were significantly improved for DCCS with co-adsorbed DCA. Additionally, the X-ray structure of dye D was obtained, demonstrating the stereochemistry and planar geometry of the molecule. The DSSC based on dye A showed an efficiency of eta = 1.70% (J(sc) = 4.49 mA cm(-2), V-OC = 0.61 V, FF = 0.62) under 100 mW cm(-2) simulated AM 1.5 G solar irradiation compared to eta = 4.1% of the standard N-3 obtained under same conditions. (C) 2012 Elsevier Ltd. All rights reserved.
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