Severson Sarah M, Ren Bai-Hao, Cayzer May, Keresztes Ivan, Johnson Mary L, Lu Xiao-Bing, Coates Geoffrey W
Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York 14853-1301, United States.
State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials, Dalian University of Technology, Dalian 116024, China.
J Am Chem Soc. 2025 Jan 8;147(1):801-810. doi: 10.1021/jacs.4c13550. Epub 2024 Dec 18.
Direct incorporation of malonate units into polymer backbones is a synthetic challenge. Herein, we report the alternating and controlled anionic copolymerization of epoxides and Meldrum's acid (MA) derivatives to access poly(alkyl malonates) using (-bis(salicylidene)phenylenediamine)AlCl and a tris(dialkylamino)cyclopropenium chloride cocatalyst. This unique copolymerization yields a malonate-containing repeat unit while releasing a small molecule upon MA-derivative ring-opening. Mechanistic and computational studies reveal that the nature of the small molecule released influences overall polymerization kinetics, side reaction behavior, and molecular weight control. Controlled copolymerization of MA derivatives with a range of epoxides ultimately yields a library of new poly(alkyl malonates) with diverse and tunable thermal properties.
将丙二酸酯单元直接引入聚合物主链是一项合成挑战。在此,我们报道了使用(-双(水杨醛亚胺)苯二胺)氯化铝和三(二烷基氨基)环丙烯鎓氯化物助催化剂,通过环氧化物与丙二酸亚异丙酯(MA)衍生物的交替和可控阴离子共聚来制备聚(烷基丙二酸酯)。这种独特的共聚反应产生了含丙二酸酯的重复单元,同时在MA衍生物开环时释放出一个小分子。机理和计算研究表明,释放出的小分子的性质影响整体聚合动力学、副反应行为和分子量控制。MA衍生物与一系列环氧化物的可控共聚最终产生了一系列具有多样且可调热性能的新型聚(烷基丙二酸酯)。