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

3,6-dibutoxy-4,5-di(2-thienyl)phthalonitrile | 365218-22-0

中文名称
——
中文别名
——
英文名称
3,6-dibutoxy-4,5-di(2-thienyl)phthalonitrile
英文别名
3,6-Dibutoxy-4,5-dithiophen-2-ylbenzene-1,2-dicarbonitrile
3,6-dibutoxy-4,5-di(2-thienyl)phthalonitrile化学式
CAS
365218-22-0
化学式
C24H24N2O2S2
mdl
——
分子量
436.599
InChiKey
XNKRZBIHEIOQDM-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):
    6.5
  • 重原子数:
    30
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    123
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    3,6-dibutoxy-4,5-di(2-thienyl)phthalonitrile1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 正己醇 为溶剂, 反应 18.0h, 以20%的产率得到[1,4,8,11,15,18,22,25-octabutoxy-2,3,9,10,16,17,23,24-octa(2-thienyl)phthalocyaninato]cobalt(II)
    参考文献:
    名称:
    Elongation of the π-System of Phthalocyanines by Introduction of Thienyl Substituents at the Peripheral β Positions. Synthesis and Characterization
    摘要:
    1,4,8,11,15,18,22,25-Octabutoxyphthalocyanines ((OBu)(8)Pcs) having eight 2-thienyl (1) and [2,2 ' -bithiophene] -5-yl (2) groups at beta positions and their zinc(II) and cobalt(II) derivatives were prepared from 2-thienyl- (3) or [2,2 ' -bithiophenel-5-yl (4)-substituted phthalonitriles in moderate to good yields. The electronic absorption spectra of the Pes showed red-shifted Q-bands relative to P-unsubstituted (OBu)8Pcs. The longer substituent, the [2,2 ' -bithiophene]-5-yl group, is more effective than the 2-thienyl group in enlarging the a-conjugated system of the Pcs. The ring oxidation potential obtained by cyclic voltammetry shifted cathodically with increasing chain length, indicating destabilization of the HOMOs. Due to the shift of the Q-band, 2-thienyl- and [2,2 ' -bithiophene]-5-yl-substituted Pes exhibit a remarkable color change from the original green color.
    DOI:
    10.1021/jo010384r
  • 作为产物:
    描述:
    2-三丁基甲锡烷基噻吩4,5-dibromo-3,6-dibutoxyphthalonitrile 在 bis-triphenylphosphine-palladium(II) chloride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 36.0h, 以83.4%的产率得到3,6-dibutoxy-4,5-di(2-thienyl)phthalonitrile
    参考文献:
    名称:
    Elongation of the π-System of Phthalocyanines by Introduction of Thienyl Substituents at the Peripheral β Positions. Synthesis and Characterization
    摘要:
    1,4,8,11,15,18,22,25-Octabutoxyphthalocyanines ((OBu)(8)Pcs) having eight 2-thienyl (1) and [2,2 ' -bithiophene] -5-yl (2) groups at beta positions and their zinc(II) and cobalt(II) derivatives were prepared from 2-thienyl- (3) or [2,2 ' -bithiophenel-5-yl (4)-substituted phthalonitriles in moderate to good yields. The electronic absorption spectra of the Pes showed red-shifted Q-bands relative to P-unsubstituted (OBu)8Pcs. The longer substituent, the [2,2 ' -bithiophene]-5-yl group, is more effective than the 2-thienyl group in enlarging the a-conjugated system of the Pcs. The ring oxidation potential obtained by cyclic voltammetry shifted cathodically with increasing chain length, indicating destabilization of the HOMOs. Due to the shift of the Q-band, 2-thienyl- and [2,2 ' -bithiophene]-5-yl-substituted Pes exhibit a remarkable color change from the original green color.
    DOI:
    10.1021/jo010384r
点击查看最新优质反应信息

文献信息

  • Elongation of the π-System of Phthalocyanines by Introduction of Thienyl Substituents at the Peripheral <i>β</i> Positions. Synthesis and Characterization
    作者:Tsuyoshi Muto、Tetsuji Temma、Mutsumi Kimura、Kenji Hanabusa、Hirofusa Shirai
    DOI:10.1021/jo010384r
    日期:2001.9.1
    1,4,8,11,15,18,22,25-Octabutoxyphthalocyanines ((OBu)(8)Pcs) having eight 2-thienyl (1) and [2,2 ' -bithiophene] -5-yl (2) groups at beta positions and their zinc(II) and cobalt(II) derivatives were prepared from 2-thienyl- (3) or [2,2 ' -bithiophenel-5-yl (4)-substituted phthalonitriles in moderate to good yields. The electronic absorption spectra of the Pes showed red-shifted Q-bands relative to P-unsubstituted (OBu)8Pcs. The longer substituent, the [2,2 ' -bithiophene]-5-yl group, is more effective than the 2-thienyl group in enlarging the a-conjugated system of the Pcs. The ring oxidation potential obtained by cyclic voltammetry shifted cathodically with increasing chain length, indicating destabilization of the HOMOs. Due to the shift of the Q-band, 2-thienyl- and [2,2 ' -bithiophene]-5-yl-substituted Pes exhibit a remarkable color change from the original green color.
查看更多