(E)-4-[(4-pentyloxyphenyl)diazenyl]phenol | 123948-12-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 偶氮苯
• 英文名称: (E)-4-[(4-pentyloxyphenyl)diazenyl]phenol
• CAS: 123948-12-9
• 化学式: C₁₇H₂₀N₂O₂
• 分子量: 284.358
• InChiKey: BDKCUHWOKIOERC-VHEBQXMUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.38
• 重原子数：
  21.0
• 可旋转键数：
  7.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  54.18
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  (E)-4-[(4-pentyloxyphenyl)diazenyl]phenol 生成
  参考文献：
  名称：

  Novel calamitic side-chain metallomesogenic polymers with ferrocene in the backbone: synthesis and properties of thermotropic liquid-crystalline poly(ferrocenylsilanes)

  摘要：

  制备出了主链为聚（二茂铁硅烷）、侧链为 4-戊氧基-4′-羟基己氧基偶氮苯或 4-戊氧基-4′-羟基十一烷氧基偶氮苯丙烯酸酯的新型热致金属聚合物；每种材料都呈现出向列介相。

  DOI：

  10.1039/a607238k
• 作为产物：
  描述：

  对乙酰氨基酚 在 盐酸 、 水 、 sodium nitrite 作用下， 生成 (E)-4-[(4-pentyloxyphenyl)diazenyl]phenol
  参考文献：
  名称：

  Novel calamitic side-chain metallomesogenic polymers with ferrocene in the backbone: synthesis and properties of thermotropic liquid-crystalline poly(ferrocenylsilanes)

  摘要：

  制备出了主链为聚（二茂铁硅烷）、侧链为 4-戊氧基-4′-羟基己氧基偶氮苯或 4-戊氧基-4′-羟基十一烷氧基偶氮苯丙烯酸酯的新型热致金属聚合物；每种材料都呈现出向列介相。

  DOI：

  10.1039/a607238k

文献信息

• Functionalization of poly(metallocenes) via hydrosilylation: synthesis and properties of thermotropic liquid crystalline poly(ferrocenylsilanes)
  作者：Xiao-Hua Liu、Duncan W. Bruce、Ian Manners

  DOI：10.1016/s0022-328x(97)00254-4

  日期：1997.12

  Hydrosilylation of poly(ferrocenylmethylhydrosilane) [Fe(η-C5H4)2SiMeH]n with 1-hexene and ethyl acrylate was achieved using Karstedt's catalyst with degrees of functionalization of ca 80%. Using a similar strategy, 4-pentoxy-4′-hydroxyhexanoxyazobenzene or 4-pentoxy-4′-hydroxyundecyloxyazo-benzene acrylate side chains were successfully attached to the poly(metallocene) main chain. The resulting functionalized

  聚（ferrocenylmethylhydrosilane）的氢化硅烷化的[Fe（η-C 5 H ^ 4）2 SiMeH] Ñ与1-己烯和丙烯酸乙酯使用的Karstedt的配合度的CA 80％官能化的催化剂来实现的。使用类似的策略，将4-戊氧基-4'-羟基己氧基偶氮苯或4-戊氧基-4'-羟基十一烷基氧基偶氮苯丙烯酸酯侧链成功连接到聚（茂金属）主链上。所得的官能化的聚（二茂铁基硅烷）代表骨架中具有二茂铁基团的热敏性热侧链液晶聚合物的第一个实例。
• The Initial and Photoinduced 3D Orientational Order in Polymethacrylates with Azobenzene Side Groups
  作者：O. Yaroshchuk、T. Bidna、O. Nadtoka、L. Olkhovyk、V. Syromyatnikov、L. C. Chien

  DOI：10.1080/15421400590954353

  日期：2005.6.1

  The combination of the transmission null ellipsometry and total absorption method, earlier approved for several polymer classes, is applied to study 3D orientational configurations of azachromophores in polymethacrylates with azobenzene side groups. The transformation of the initial orientation due to the photoexcitation of azoehromophores is investigated. The dependence of the orientational configuration on the structure of azochromophore fragments and its concentration in the polymers are also studied. In the non-irradiated films, azochromofores strive to be aligned normally to the film plate. Under irradiation, if reorientation mechanism of the photoinduced ordering prevails, the azochromophores reorient perpendicularly to the polarization direction of the exciting light, E-ex, and in the saturation state they are randomly distributed in the plane perpendicular to E-ex This implies that the induced structure is mainly influenced by the photoordering, while selfordering of polymer chains is not effective or overcome, presumably because of high T-g of polymethacrylates. In case when photoselection ordering mechanism dominates, 3D distribution of azochromophores in the saturation state of irradiation is isotropic due to a strong exhaustion of the number of anisotropic trans isomers. The transient photoinduced orientations are biaxial independently on the dominating ordering mechanism. The reduction of the azochromophore's concentration in polymers reduces the anisotropy rate but not influence the trends described above. The observed regularities were earlier described for several other classes of photosensitive polymers and so they may be common rules for photoordering in the photochromic media.