离子液体
微粘度
化学
阳离子聚合
动力学
化学物理
离子键合
伦敦分散部队
氢键
色散(光学)
聚合
粘度
离子
化学工程
高分子化学
聚合物
材料科学
有机化学
分子
膜
催化作用
范德瓦尔斯力
生物化学
物理
量子力学
光学
复合材料
工程类
标识
DOI:10.1016/j.eurpolymj.2020.109778
摘要
Ionic liquids are liquids composed entirely of ions – large organic cations and inorganic or organic anions. Due to different kind of interactions between cationic and anionic moieties, such as electrostatic interactions but also dispersion forces and hydrogen bonding, they are inhomogeneous on microscale forming polar and non-polar domains. The nature of ionic liquids, making them distinctly different from conventional organic solvents, may affect the kinetics of chemical reactions proceeding in these solvents. Specific interactions between components of ionic liquid result in relatively high viscosity of those media and especially may affect microviscosity in the close vicinity of reacting species. Specific non-directional interactions such as electrostatic or dispersion forces and directional interactions, such as e.g. hydrogen bonding between components of ionic liquids and reactants may affect both translational and rotational mobility of reaction species as well as activation parameters. These factors which should be considered when analyzing the kinetics of radical polymerization in ionic liquid media are briefly but critically discussed in this mini-review.
科研通智能强力驱动
Strongly Powered by AbleSci AI