| 1571083-41-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• CAS: 1571083-41-4
• 化学式: C₁₈H₂₈N₂O₉
• 分子量: 416.428
• InChiKey: OKCLJBCKOSSULB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.67
• 重原子数：
  29.0
• 可旋转键数：
  18.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  160.49
• 氢给体数：
  4.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  在 N,N'-二环己基碳二亚胺 、 1-羟基苯并三唑 作用下， 以 四氢呋喃 为溶剂， 反应 35.0h， 以10.52 g的产率得到1,13-bismaleimido-4,7,10-trioxatridecane
  参考文献：
  名称：

  A Dual-Cure, Solid-State Photoresist Combining a Thermoreversible Diels–Alder Network and a Chain Growth Acrylate Network

  摘要：

  A Die Is Alder (DA) network containing dissolved multiacrylate monomers is demonstrated as a novel two-stage reactive polymer network, with a potential application in self-supporting stereolithography. Initially, a thermoreversible Die Is Alder "scaffold" network is formed, containing unreacted acrylate monomers and photoinitiator. During photopatterning with light at 15 mW/cm(2) from a 365 nm source for 16 s of exposure at either ambient temperature or 70 degrees C, both acrylates and unreacted maleimides polymerize to form a permanent, covalently cross-linked network structure that simultaneously maintains the thermoreversible characteristics afforded by the underlying DA network. Light exposure of a DA network containing between 25 and 50 wt % acrylate monomer resulted in a sharp increase in cross-link density and a 60 degrees C jump in glass transition temperature of the material. As a result of the temperature-dependent DA equilibrium, the temperature of the film during light exposure has dramatic effects on the resulting acrylate conversion (as measured by FT-IR) and mechanical behavior (as measured by DMA) of the complex dynamic network structure. For example, despite the irreversible acrylate network, the rubbery modulus of the material decreases above the glass transition temperature due to the presence of the dynamic thermosensitive DA network. The shape of the modulus curve was also affected by the ratio of DA monomers to acrylate monomers; higher DA monomer content resulted in greater temperature sensitivity of the rubbery modulus in light-exposed films. 3D structures with feature sizes ranging from 50 to 500 pm were produced in geometries such as stacked rectangles and "logpile" structures. In the unexposed regions, free acrylate and maleimide groups were shown to tolerate temperatures as high as 120 degrees C with no premature gel formation observed. Removal of unexposed material during the development step was achieved at 120 degrees C, where the Diels-Alder equilibrium shifts toward the furan and maleimide reactants and the network depolymerizes. Finally, a process was developed for the fabrication of 3D microstructures via layer-by-layer photopatterning. The process is highly repeatable and results in complete elimination of unexposed regions. Additionally, excess quantities of the unexposed mixture may be stored at 4 degrees C for at least several weeks and then reused by heating to 120 degrees C to fully depolymerize the DA network, subsequently using the liquid mixture to make films.

  DOI：

  10.1021/ma500244r
• 作为产物：
  描述：

  马来酸酐 、 4,7,10-三氧-1,13-十三烷二胺 以 二氯甲烷 为溶剂， 反应 2.0h， 生成
  参考文献：
  名称：

  A Dual-Cure, Solid-State Photoresist Combining a Thermoreversible Diels–Alder Network and a Chain Growth Acrylate Network

  摘要：

  A Die Is Alder (DA) network containing dissolved multiacrylate monomers is demonstrated as a novel two-stage reactive polymer network, with a potential application in self-supporting stereolithography. Initially, a thermoreversible Die Is Alder "scaffold" network is formed, containing unreacted acrylate monomers and photoinitiator. During photopatterning with light at 15 mW/cm(2) from a 365 nm source for 16 s of exposure at either ambient temperature or 70 degrees C, both acrylates and unreacted maleimides polymerize to form a permanent, covalently cross-linked network structure that simultaneously maintains the thermoreversible characteristics afforded by the underlying DA network. Light exposure of a DA network containing between 25 and 50 wt % acrylate monomer resulted in a sharp increase in cross-link density and a 60 degrees C jump in glass transition temperature of the material. As a result of the temperature-dependent DA equilibrium, the temperature of the film during light exposure has dramatic effects on the resulting acrylate conversion (as measured by FT-IR) and mechanical behavior (as measured by DMA) of the complex dynamic network structure. For example, despite the irreversible acrylate network, the rubbery modulus of the material decreases above the glass transition temperature due to the presence of the dynamic thermosensitive DA network. The shape of the modulus curve was also affected by the ratio of DA monomers to acrylate monomers; higher DA monomer content resulted in greater temperature sensitivity of the rubbery modulus in light-exposed films. 3D structures with feature sizes ranging from 50 to 500 pm were produced in geometries such as stacked rectangles and "logpile" structures. In the unexposed regions, free acrylate and maleimide groups were shown to tolerate temperatures as high as 120 degrees C with no premature gel formation observed. Removal of unexposed material during the development step was achieved at 120 degrees C, where the Diels-Alder equilibrium shifts toward the furan and maleimide reactants and the network depolymerizes. Finally, a process was developed for the fabrication of 3D microstructures via layer-by-layer photopatterning. The process is highly repeatable and results in complete elimination of unexposed regions. Additionally, excess quantities of the unexposed mixture may be stored at 4 degrees C for at least several weeks and then reused by heating to 120 degrees C to fully depolymerize the DA network, subsequently using the liquid mixture to make films.

  DOI：

  10.1021/ma500244r