(E)-N-hexadecyl-4-(2-(4-(dimethylamino)phenyl)ethylene)pyridinium tetrakis(1-phenyl-3-methyl-4-benzoyl-5-pyrazolonato)ytterbium(III) | 158595-45-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: (E)-N-hexadecyl-4-(2-(4-(dimethylamino)phenyl)ethylene)pyridinium tetrakis(1-phenyl-3-methyl-4-benzoyl-5-pyrazolonato)ytterbium(III)
• 英文别名: (E)-N-hexadecyl-N',N'-dimethylamino-stilbazolium tetrakis(1-phenyl-3-methyl-4-benzoyl-5-pyrazolonato) ytterbium(III)；A16Yb(PMBP)4
• CAS: 158595-45-0
• 化学式: C₃₁H₄₉N₂*C₆₈H₅₂N₈O₈Yb
• 分子量: 1731.99
• InChiKey: FXNVQCUQPKPESI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
  None
• 环数：
  None
• sp3杂化的碳原子比例：
  None
• 拓扑面积：
  None
• 氢给体数：
  None
• 氢受体数：
  None

反应信息

• 作为反应物：
  描述：

  (E)-N-hexadecyl-4-(2-(4-(dimethylamino)phenyl)ethylene)pyridinium tetrakis(1-phenyl-3-methyl-4-benzoyl-5-pyrazolonato)ytterbium(III) 生成 ytterbium(III) oxide
  参考文献：
  名称：

  含半花青的镧系元素配合物的液晶行为

  摘要：

  四种镧系元素配合物(E)-N-十六烷基-4-(2-(4-(二甲氨基)苯基)亚乙基)吡啶鎓四(1-苯基-3-甲基-4-苯甲酰基-5-吡唑啉酮)的液晶行为）镧系元素（La、Nd、Dy 和 Yb）(III) 已通过使用差示扫描量热法 (DSC)、热重和差热分析 (TG-DTA) 以及偏光显微镜进行了研究。除镧络合物外，其他三种络合物均表现出具有典型近晶镶嵌结构的介晶行为。这是自发现取代双（酞菁）镥的圆盘状中间相以来，关于镧系金属晶体的第二份报告。

  DOI：

  10.1016/0038-1098(95)00221-9
• 作为产物：
  描述：

  氢化镱 、 4-苯甲酰基-3-甲基-1-苯基-2-吡唑-5-酮 、 1-n-hexadecyl-4-[4-N,N-(dimethylamino)styryl]pyridinium bromide 在 NaOH 作用下， 以 乙醇 为溶剂， 以52%的产率得到(E)-N-hexadecyl-4-(2-(4-(dimethylamino)phenyl)ethylene)pyridinium tetrakis(1-phenyl-3-methyl-4-benzoyl-5-pyrazolonato)ytterbium(III)
  参考文献：
  名称：

  含半花菁生色团的镧系元素络合物的近红外光致发光

  摘要：

  三个（E）-N-十六烷基-N '，N的近红外发光特性描述了′-二甲基氨基-噻唑四（1-苯基-3-甲基-4-苯甲酰基-5-吡唑并萘基）镧系元素（III）配合物。这三种分别包含三价钕，和的配合物在紫外线照射下在乙腈溶液中显示出近红外发光。已经测量了发光衰减时间。配合物由带有长烷基链的带正电的半菁发色团和四（吡唑并萘）镧系元素（III）阴离子组成。由于在吡唑并酮配体中不存在α-氢原子，并且由于配体球被四个双齿配体饱和，因此与例如喹啉酸酯配合物相比，发光性能得到增强。

  DOI：

  10.1016/j.poly.2007.08.005

文献信息

• Langmuir Film-Forming and Second Harmonic Generation Properties of Lanthanide Complexes
  作者：Chunhui Huang、Kezhi Wang、Guangxian Xu、Xinsheng Zhao、Xiaoming Xie、Yu Xu、Yunqi Liu、Lingge Xu、Tiankai Li

  DOI：10.1021/j100039a029

  日期：1995.9

  A series of amphiphilic lanthanide complexes were designed and synthesized, in which the lanthanide complex anions act both as the counterions of hemicyanine and as the spacer within a Langmuir-Blodgett (LB) film. Studies on the surface pressure-area (pi-A) isotherms of these complexes show that the film-forming properties can be clearly improved if appropriate beta-diketone ligands were chosen. The effects of molecular structures of the complexes, including the variation of lanthanide central ions, the structures of beta-diketone ligands, and the length of alkyl chains in hemicyanines, on the film-forming properties of the materials are discussed. From second-harmonic generation experiments, the largely enhanced second-order molecular hyperpolarizability of lanthanide complexes with good film-forming properties were obtained compared with the hemicyanine iodide. This effect may be due in part to the local field effect but primarily molecular ordering and ordered segregation of hemicyanine chromophores by the bulky lanthanide complex anions. The charge separation of the hemicyanine chromophores was supported by the crystal structure of a model complex. The homogeneity of the film was verified by low angle X-ray diffraction and also by the linear relationship of the absorbance vs the number of layers of the LB films of a selected complex.