Wang Tongtong, Gao Dali, Yin Hua, Zhao Jiawei, Wang Xingguo, Niu Hui
Department of Polymer Science and Engineering, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, China.
SINOPEC (Beijing) Research Institute of Chemical Industry Co., Ltd., Beijing 100013, China.
Polymers (Basel). 2024 Feb 5;16(3):441. doi: 10.3390/polym16030441.
The Diels-Alder (D-A) reaction between furan and maleimide is a thermally reversible reaction that has become a vital chemical technique for designing polymer structures and functions. The kinetics of this reaction, particularly in polymer bulk states, have significant practical implications. In this study, we investigated the feasibility of utilizing infrared spectroscopy to measure the D-A reaction kinetics in bulk-state polymer. Specifically, we synthesized furan-functionalized polystyrene and added a maleimide small-molecule compound to form a D-A adduct. The intensity of the characteristic absorption peak of the D-A adduct was quantitatively measured by infrared spectroscopy, and the dependence of conversion of the D-A reaction on time was obtained at different temperatures. Subsequently, the D-A reaction apparent kinetic coefficient and the Arrhenius activation energy were calculated. These results were compared with those determined from H-NMR in the polymer solution states.
呋喃与马来酰亚胺之间的狄尔斯-阿尔德(D-A)反应是一种热可逆反应,已成为设计聚合物结构和功能的重要化学技术。该反应的动力学,特别是在聚合物本体状态下的动力学,具有重要的实际意义。在本研究中,我们研究了利用红外光谱法测量本体状态聚合物中D-A反应动力学的可行性。具体而言,我们合成了呋喃功能化的聚苯乙烯,并添加了马来酰亚胺小分子化合物以形成D-A加合物。通过红外光谱法定量测量D-A加合物特征吸收峰的强度,并在不同温度下获得D-A反应转化率随时间的变化关系。随后,计算了D-A反应的表观动力学系数和阿伦尼乌斯活化能。将这些结果与在聚合物溶液状态下通过H-NMR测定的结果进行了比较。