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1-(4,6-二氢噻吩并[3,4-b]噻吩-2-基)-2-乙基-1-己酮 | 1194605-72-5

中文名称
1-(4,6-二氢噻吩并[3,4-b]噻吩-2-基)-2-乙基-1-己酮
中文别名
1-(4,6-二氢噻吩并[3,4-B]噻吩-2-基)-2-乙基-1-己酮
英文名称
1-(4,6-dibromothieno[3,4-b]thiophen-2-yl)-2-ethylhexan-1-one
英文别名
2-ethyl-1-(4,6-dihydrothieno[3,4-b]thiophen-2-yl)hexan-1-one;1-(4,6-Dihydrothieno[3,4-b]thiophen-2-yl)-2-ethylhexan-1-one
1-(4,6-二氢噻吩并[3,4-b]噻吩-2-基)-2-乙基-1-己酮化学式
CAS
1194605-72-5
化学式
C14H20OS2
mdl
——
分子量
268.444
InChiKey
QECXUUREYNIHHP-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

物化性质

  • 沸点:
    430.1±45.0 °C(Predicted)
  • 密度:
    1.125

计算性质

  • 辛醇/水分配系数(LogP):
    4.5
  • 重原子数:
    17
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    70.6
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2934999090

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:
    1-(4,6-二氢噻吩并[3,4-b]噻吩-2-基)-2-乙基-1-己酮2,3-二氯-5,6-二氰基-1,4-苯醌 作用下, 以 二氯甲烷 为溶剂, 以76.3%的产率得到2-ethyl-1-(thieno[3,4-b]thiophen-2-yl)hexan-1-one
    参考文献:
    名称:
    Design, synthesis and photophysical properties of A-D-A-D-A small molecules for photovoltaic application
    摘要:
    A series of linear-conjugated small molecule compounds featured with the acceptor-donor-acceptor-donor-acceptor (A-D-A-D-A) structure were designed, synthesized and characterized. The films of the compounds showed a broad UV-Vis absorption range of 300-800 nm with high molar absorption coefficient of more than 1.0 x 10(4) cm(-1). Their hole-mobility can be as high as 1.0 x 10(-3) cm(2) V-1 s(-1). The compounds have a compatible HOMO energy level of -5.0 eV to PC71BM and a high solubility up to 20 mg mL(-1) in chloroform. Therefore, compounds can blend with PC71BM in the chloroform and form an active layer for a photovoltaic cell device by spin-coating of the blend solution. A maximum power conversion efficiency of 3.2% was achieved with the DERH3TT solar cell device. These results indicate that the A-D-A-D-A small molecules with electron-withdrawing dyes as terminals are promising candidates for the high efficiency solution processed organic photovoltaic cells. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2015.05.009
  • 作为产物:
    描述:
    2-乙基己酰氯 在 sodium sulfide 、 aluminum (III) chloride 、 四氯化钛 作用下, 以 甲醇二氯甲烷 为溶剂, 生成 1-(4,6-二氢噻吩并[3,4-b]噻吩-2-基)-2-乙基-1-己酮
    参考文献:
    名称:
    Design, synthesis and photophysical properties of A-D-A-D-A small molecules for photovoltaic application
    摘要:
    A series of linear-conjugated small molecule compounds featured with the acceptor-donor-acceptor-donor-acceptor (A-D-A-D-A) structure were designed, synthesized and characterized. The films of the compounds showed a broad UV-Vis absorption range of 300-800 nm with high molar absorption coefficient of more than 1.0 x 10(4) cm(-1). Their hole-mobility can be as high as 1.0 x 10(-3) cm(2) V-1 s(-1). The compounds have a compatible HOMO energy level of -5.0 eV to PC71BM and a high solubility up to 20 mg mL(-1) in chloroform. Therefore, compounds can blend with PC71BM in the chloroform and form an active layer for a photovoltaic cell device by spin-coating of the blend solution. A maximum power conversion efficiency of 3.2% was achieved with the DERH3TT solar cell device. These results indicate that the A-D-A-D-A small molecules with electron-withdrawing dyes as terminals are promising candidates for the high efficiency solution processed organic photovoltaic cells. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2015.05.009
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文献信息

  • Synthesis of a Low Band Gap Polymer and Its Application in Highly Efficient Polymer Solar Cells
    作者:Jianhui Hou、Hsiang-Yu Chen、Shaoqing Zhang、Ruby I. Chen、Yang Yang、Yue Wu、Gang Li
    DOI:10.1021/ja9064975
    日期:2009.11.4
    HOMO level of the PBDTTT-based polymer was successfully reduced by introducing an keton group in place of the ester group. The average PCE of the PBDTTT-based devices reached 6.3% with a champion PCE result of 6.58%. Due to its highly efficient photovoltaic performance and more feasible synthesis approach, PBDTTT-C has the potential to be successfully applied in the large-scale manufacturing of polymer solar cells.
  • CONJUGATED POLYMERS WITH CARBONYL SUBSTITUTED THIENO [3,4-B]THIOPHENE UNITS FOR POLYMER SOLAR CELL ACTIVE LAYER MATERIALS
    申请人:Solarmer Energy, Inc.
    公开号:EP2456810B1
    公开(公告)日:2016-08-17
  • CONJUGATED POLYMERS WITH CARBONYL SUBSTITUTED THIENO[3,4-B]THIOPHENE UNITS FOR POLYMER SOLAR CELL ACTIVE LAYER MATERIALS
    申请人:Hou Jianhui
    公开号:US20110017956A1
    公开(公告)日:2011-01-27
    In one embodiment of the present disclosure, a series of conjugated polymers used, among other things, as polymer solar cell or polymer photovoltaic device active layer materials, is provided. In one embodiment, the conjugated polymers have the general structure and formula shown in (I), wherein: R1 and R2 are independently selected from proton, halogens, alkyls, aryls and substituted aryls; Ar is selected from the group consisting of monocyclic, bicyclic and polycyclic arylene, or monocyclic, bicyclic and polycyclic heteroarylene. In another embodiment, the conjugated photovoltaic polymers are comprised of repeated units having the general structure of formula (II), wherein, R1, R2, R3, R4, R5, and R6 are independently selected from proton, alkyls, halogens, aryls, substituted aryls, and other kinds of substituents. Synthesis methods of several polymers of the present disclosure are provided, and absorption spectra and electrochemical cyclic voltammetry data of some polymers, and also the photovoltaic properties of the polymers in this present disclosure are also provided.
  • CONJUGATED POLYMERS WITH CARBONYL-SUBSTITUTED THIENO [3,4-B] THIOPHENE UNITS FOR POLYMER SOLAR CELL ACTIVE LAYER MATERIALS
    申请人:Solarmer Energy, Inc.
    公开号:US20130123449A1
    公开(公告)日:2013-05-16
    In one embodiment of the present disclosure, a series of conjugated polymers used, among other things, as polymer solar cell or polymer photovoltaic device active layer materials, is provided. In one embodiment, the conjugated polymers have the general structure and formula shown in (I), wherein: R1 and R2 are independently selected from proton, halogens, alkyls, aryls and substituted aryls; Ar is selected from the group consisting of monocyclic, bicyclic and polycyclic arylene, or monocyclic, bicyclic and polycyclic heteroarylene. In another embodiment, the conjugated photovoltaic polymers are comprised of repeated units having the general structure of formula (II), wherein, R1, R2, R3, R4, R5, and R6 are independently selected from proton, alkyls, halogens, aryls, substituted aryls, and other kinds of substituents. Synthesis methods of several polymers of the present disclosure are provided, and absorption spectra and electrochemical cyclic voltammetry data of some polymers, and also the photovoltaic properties of the polymers in this present disclosure are also provided.
  • US8372945B2
    申请人:——
    公开号:US8372945B2
    公开(公告)日:2013-02-12
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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 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-2,5-二羧酸乙酯 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-乙酰基-3,4-二甲基噻吩并[2,3-b]噻吩-2-甲腈 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-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 3-十一烷基噻吩并[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 3,4-二甲基(2,3-b)-噻吩-2,5-二羧酸二乙酯 3,4-二甲基(2,3-B)并噻吩-2,5-二甲腈 3,4-二溴噻吩[2,3-b]噻吩 3,4-二氨基噻吩并[2,3-b]噻吩-2,5-二羧酸二乙酯 2-辛基-噻吩[3,2-B]并二噻吩 2-甲酰基并二噻吩