Song Lidao, Wei Wei, Farooq Muhammad Amjad, Xiong Huiming
Department of Polymer Science, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
Frontiers Science Center for Transformative Molecules, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
ACS Macro Lett. 2020 Nov 17;9(11):1542-1546. doi: 10.1021/acsmacrolett.0c00696. Epub 2020 Oct 19.
Nontraditional polyurethane (PU) has been successfully synthesized by anionic copolymerization of some typical aryl isocyanates and epoxides with ammonium halide onium salt (Lewis base) as the initiator and triisobutylaluminum (Lewis acid) as the activator and the synergistic coordinator. In contrast to the traditional step-growth approach, this chain-growth copolymerization can maintain the anionic propagation site and exhibit some living features with a high activity, by which the copolymers synthesized have narrow molecular weight distributions and discrete end groups. The copolymer is primarily constituted by a urethane linkage, and the byproducts of isocyanurate trimer and oxazolidinone can be effectively suppressed as the polymerization proceeds. Density functional theory (DFT) calculations were also performed to support the proposed reaction mechanism.
通过以卤化铵鎓盐(路易斯碱)为引发剂、三异丁基铝(路易斯酸)为活化剂和协同配位剂,使一些典型的芳基异氰酸酯与环氧化物进行阴离子共聚,成功合成了非传统聚氨酯(PU)。与传统的逐步增长方法不同,这种链式增长共聚能够保持阴离子增长位点,并表现出一些具有高活性的活性特征,据此合成的共聚物具有窄的分子量分布和离散的端基。该共聚物主要由脲烷键构成,随着聚合反应的进行,异氰脲酸酯三聚体和恶唑烷酮的副产物能够得到有效抑制。还进行了密度泛函理论(DFT)计算以支持所提出的反应机理。