1,1'-[1,4-Phenylenedi(ethene-2,1-diyl)]bis(4-ethoxybenzene) | 197653-10-4

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: 1,1'-[1,4-Phenylenedi(ethene-2,1-diyl)]bis(4-ethoxybenzene)
• 英文别名: 1,4-bis[2-(4-ethoxyphenyl)ethenyl]benzene
• CAS: 197653-10-4
• 化学式: C₂₆H₂₆O₂
• 分子量: 370.491
• InChiKey: HWKABBAQOPAUCC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.1
• 重原子数：
  28
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  4-乙氧基苯甲醛 、 [p-phenylenebis(methylene)]bis[triphenylphosphonium] dichloride 在 sodium ethanolate 作用下， 以 乙醇 为溶剂， 生成 1,1'-[1,4-Phenylenedi(ethene-2,1-diyl)]bis(4-ethoxybenzene)
  参考文献：
  名称：

  Alkoxylated p-phenylenevinylene oligomers: Synthesis and spectroscopic and electrochemical properties

  摘要：

  Twenty-one n-alkoxy substituted phenylenevinylene oligomers were synthesized, varying in size, number and position of the OR groups. IR,MS and solubility data are presented. NMR measurements provided the molecular structure as well as information about conformations and molecular dynamics. UV and of cyclic voltammetric data give correlations of chemical structure (number and position of OR substituents) with separate HOMO and LUMO energies. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)00871-5

文献信息

• Alkoxylated p-phenylenevinylene oligomers: Synthesis and spectroscopic and electrochemical properties
  作者：Henri Ndayikengurukiye、Sven Jacobs、Wim Tachelet、Johan Van Der Looy、Anne Pollaris、Herman J. Geise、Magda Claeys、Jean M. Kauffmann、Silvia Janietz

  DOI：10.1016/s0040-4020(97)00871-5

  日期：1997.10

  Twenty-one n-alkoxy substituted phenylenevinylene oligomers were synthesized, varying in size, number and position of the OR groups. IR,MS and solubility data are presented. NMR measurements provided the molecular structure as well as information about conformations and molecular dynamics. UV and of cyclic voltammetric data give correlations of chemical structure (number and position of OR substituents) with separate HOMO and LUMO energies. (C) 1997 Elsevier Science Ltd.