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

2,5-bis(3,4-dibutylthien-2-yl)selenophene | 1338368-15-2

中文名称
——
中文别名
——
英文名称
2,5-bis(3,4-dibutylthien-2-yl)selenophene
英文别名
——
2,5-bis(3,4-dibutylthien-2-yl)selenophene化学式
CAS
1338368-15-2
化学式
C28H40S2Se
mdl
——
分子量
519.718
InChiKey
QIMWPXZCAPJGRY-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):
    9.57
  • 重原子数:
    31.0
  • 可旋转键数:
    14.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    2,5-bis(3,4-dibutylthien-2-yl)selenophene 在 bis-triphenylphosphine-palladium(II) chloride 、 mercury(II) acetate 、 cesium fluoride 作用下, 以 四氢呋喃氯仿 为溶剂, 反应 94.5h, 生成 2,5-bis(3,4-dibutyl-2,2'-bithien-5-yl)selenophene
    参考文献:
    名称:
    Dicyanovinylene-Substituted Selenophene–Thiophene Co-oligomers for Small-Molecule Organic Solar Cells
    摘要:
    We report on the design, synthesis, and characterization of a series of terminal dicyanovinylene-substituted quinquechalcogenophenes as light-harvesting small-molecule donor materials for organic solar cells. The spectroscopic, electrochemical, and thermal properties of these pentamers were investigated. The replacement of thiophene unit(s) by selenophene(s) results in a bathochromic shift of the longest wavelength absorption band with concomitant increase of the molar extinction coefficient. Cyclic voltammetry measurements revealed fully reversible oxidation and irreversible reduction processes. The highest occupied and lowest unoccupied molecular orbital (HOMO/LUMO) energy levels were determined from electrochemical measurements and lie in the range of -5.6 and -3.8 eV. Vacuum-deposited bulk-heterojunction solar cells fabricated with the novel chalcogenophenes as donor and C-60 as acceptor displayed high open-circuit voltages of up to 1 V, short-circuit currents close to 8 mA.cm(-2), and power conversion efficiencies over 3%.
    DOI:
    10.1021/cm201392c
  • 作为产物:
    描述:
    3,4-二丁基噻吩potassium phosphatetris-(dibenzylideneacetone)dipalladium(0)正丁基锂 、 tri tert-butylphosphoniumtetrafluoroborate 作用下, 以 四氢呋喃 为溶剂, 反应 22.0h, 生成 2,5-bis(3,4-dibutylthien-2-yl)selenophene
    参考文献:
    名称:
    Dicyanovinylene-Substituted Selenophene–Thiophene Co-oligomers for Small-Molecule Organic Solar Cells
    摘要:
    We report on the design, synthesis, and characterization of a series of terminal dicyanovinylene-substituted quinquechalcogenophenes as light-harvesting small-molecule donor materials for organic solar cells. The spectroscopic, electrochemical, and thermal properties of these pentamers were investigated. The replacement of thiophene unit(s) by selenophene(s) results in a bathochromic shift of the longest wavelength absorption band with concomitant increase of the molar extinction coefficient. Cyclic voltammetry measurements revealed fully reversible oxidation and irreversible reduction processes. The highest occupied and lowest unoccupied molecular orbital (HOMO/LUMO) energy levels were determined from electrochemical measurements and lie in the range of -5.6 and -3.8 eV. Vacuum-deposited bulk-heterojunction solar cells fabricated with the novel chalcogenophenes as donor and C-60 as acceptor displayed high open-circuit voltages of up to 1 V, short-circuit currents close to 8 mA.cm(-2), and power conversion efficiencies over 3%.
    DOI:
    10.1021/cm201392c
点击查看最新优质反应信息