| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5201950 | Polymer Degradation and Stability | 2014 | 6 Pages |
Abstract
Aminolysis reaction between polyarylsulfones and organic amines was investigated. A bimolecular nucleophilic substitution mechanism was proposed. The nucleophilic reagent attacks the aryl ether bond carbon on the aryl ring carrying substituents with strong electron-attracting character. 1H NMR and 1H-1H COSY NMR spectroscopies were adopted to characterize the chemical structure of the products, the terminal groups especially. The effect of polyarylsulfone structure on the reactivity was studied by comparing the reaction rates. The aminolysis kinetics of polyethersulfone with ethylenediamine at different temperature and reagent concentration was studied in detail. The molar mass of the aminolyzed product was determined by GPC and theoretical deduction, and they showed great consistency.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Linghui Wang, Yue Cui, Nachuan Wang, Hong Zhang, Baoku Zhu, Liping Zhu, Youyi Xu,