(E)-1,2-bis(4-propoxyphenyl)ethene | 36931-02-9

• 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: (E)-1,2-bis(4-propoxyphenyl)ethene
• 英文别名: 4,4'-dipropoxy-trans-stilbene；4,4'-Dipropoxy-trans-stilben；1-propoxy-4-[(E)-2-(4-propoxyphenyl)ethenyl]benzene
• CAS: 36931-02-9
• 化学式: C₂₀H₂₄O₂
• 分子量: 296.409
• InChiKey: MZXFDZDAALOFJJ-AATRIKPKSA-N

物化性质

• 沸点：
  441.5±14.0 °C(Predicted)
• 密度：
  1.033±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  22
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 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：

  1-(溴甲基)-4-丙氧基苯 在 sodium ethanolate 作用下， 以 乙醇 、 xylene 为溶剂， 生成 (E)-1,2-bis(4-propoxyphenyl)ethene
  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

• Structural Requirements for Palladium Catalyst Transfer on a Carbon–Carbon Double Bond
  作者：Masataka Nojima、Yoshihiro Ohta、Tsutomu Yokozawa

  DOI：10.1021/jacs.5b03113

  日期：2015.5.6

  Intramolecular transfer of (Bu3PPd)-Bu-t(0) on a carbon carbon double bond (C=C) was investigated by using Suzuki-Miyaura coupling reaction of dibromostilbenes with aryl boronic acid or boronic acid esters in the presence of various additives containing C=C as a model. Substituent groups at the ortho position of C=C of stilbenes are critical for selective intramolecular catalyst transfer and may serve to suppress formation of the bimolecular C=C-Pd-C=C complex that leads to intermolecular transfer of (Bu3PPd)-Bu-t(0).
• Stilbene derivatives. New class of room temperature nematic liquids
  作者：William R. Young、Arieh Aviram、Robert J. Cox

  DOI：10.1021/ja00766a054

  日期：1972.5
• Tadros et al., Journal of the Chemical Society, 1954, p. 2351
  作者：Tadros et al.

  DOI：——

  日期：——
• [EN] WATER-DISPERSIBLE COPOLYMER CONTAINING UVA AND UVB LIGHT-ABSORBING MONOMERS<br/>[FR] COPOLYMERE SE DISPERSANT DANS L'EAU ET CONTENANT DES NOMOMERES ABSORBANT LA LUMIERE UVA ET UVB
  申请人：UNILEVER PLC

  公开号：WO1993022366A1

  公开（公告）日：1993-11-11

  (EN) The invention is concerned with novel water-dispersible or water-soluble copolymers which contain at least one UVA light-absorbing monomer, one UVB light-absorbing monomer, one hydrophilic monomer, and optionally one hydrophobic monomer component. The UVA light-absorbing monomer absorbs at $g(l)max ultraviolet light in the 320 - 400 nm range. The UVB light-absorbing monomer absorbs at $g(l)max ultraviolet light in the 290 - 320 nm range.(FR) L'invention concerne de nouveaux copolymères se dispersant ou se dissolvant dans l'eau et qui contiennent au moins un nomomère absorbant la lumière UVA, un monomère absorbant la lumière UVB, un nomomère hydrophile et, le cas échéant, un monomère hydrophobe. Le monomère absorbant la lumière UVA a un maximum d'absorption dans l'ultraviolet à $g(l)max dans la gamme de 320 - 400 nm. Le monomère absorbant la lumière UVB a un maximum d'absorption dans l'ultraviolet $g(l)max dans la gamme de 290 - 320 nm.
• 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.