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The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
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The formation of a solution is an example of a spontaneous process, a process that occurs under specified conditions without energy from some external source.
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解读影响电场的因素在溶液-固体界面中介聚合和脱聚合.

Zhinan Fu1, Nicolás Arisnabarreta1, Kunal S Mali2

  • 1Division of Molecular Imaging and Photonics, Department of Chemistry, Celestijnenlaan 200F, Leuven, 3001, Belgium.

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概括
此摘要是机器生成的。

强大的电场 (EF) 可逆控制2D聚合的酸在石墨上的二维聚合. 扫描道显微镜尖端偏差的切换极性驱动脱聚合和单体吸附,影响分子自我组装.

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科学领域:

  • 表面科学是一门科学.
  • 纳米技术纳米技术
  • 材料化学 材料化学

背景情况:

  • 强大的电场 (EF) 影响分子结构和反应性.
  • 扫描道显微镜 (STM) 可以探测和操纵纳米级的分子组件.
  • 二维聚合物 (2DPs) 为先进材料提供独特的特性.

研究的目的:

  • 在石墨上研究控制电场介导的氧基2DPs在石墨上的聚合和脱聚合的因素.
  • 了解溶剂极性和单体度在EF驱动的2D聚合中的作用.
  • 阐明单体网络和2DP域之间可逆转换背后的机制.

主要方法:

  • 使用扫描道显微镜 (STM) 将电场应用于石墨表面上的酸烯基单体.
  • 系统地改变溶剂特性 (极性前极性,极性近极性,非极性) 来评估它们的影响.
  • 研究了单体度和时间依赖性对聚合过程的影响.

主要成果:

  • 电场 (EF) 不能启动二维聚合物 (2DP) 域的核化.
  • 脱聚合和随后的单体溶解是由基质偏差的极性变化引发的.
  • 单体网络和2DP域之间的可逆过渡与偏差诱导的单体吸附/脱附有关.

结论:

  • 在石墨上基于氧的系统的可逆二维聚合是通过电场极性可控的.
  • 单体的偏差诱导吸附和脱附是驱动观察到的可逆转变的关键机制.
  • 当地单体度变化受到吸附/脱附的影响,在EF介导的 (去) 聚合中起着至关重要的作用.