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Highly Active Organic Lewis Pairs for the Copolymerization of Epoxides with Cyclic Anhydrides: Metal-Free Access to Well-Defined Aliphatic Polyesters
來源:張興宏教授個(gè)人網(wǎng)站 發(fā)布日期:2019-04-02
作者:Lan-Fang Hu, Cheng-Jian Zhang, Hai-Lin Wu, Jia-Liang Yang, Bin Liu, Han-Yi Duan, and Xing-Hong Zh
關(guān)鍵字:Epoxides with Cyclic Anhydrides,Metal-Free,
論文來源:期刊
具體來源:Macromolecules 2018, 51, 3126?3134
發(fā)表時(shí)間:2018年

Polyester synthesis from the alternating copolymerization of epoxides with cyclic anhydrides via a metal-free route remains a key challenge. This work reports the development of a highly active organocatalytic route for the copolymerization of a spectrum of epoxides and cyclic anhydrides. Fully alternating polyesters were synthesized by a variety of organic Lewis acid?base pairs including organoboranes and quaternary onium salts. The effect of the acidity, type, and size of Lewis pairs on the catalytic activity and selectivity of the copolymerization is

presented. The undesirable transesterification and etherification were effectively suppressed even in the case of complete conversion of the cyclic anhydride. This could be ascribed to the formation of a unique tetracoordinate bond-carboxylate (or alkoxide) anion. The Lewis pairs

are highly active, with a turnover frequency of 102 and 303 h?1 for the copolymerization of propylene oxide with maleic anhydride and phthalic anhydride, respectively, at 80 °C. Block polyester with narrow polydispersity of 1.05 was achieved via a sequential addition strategy. This work provides robust organocatalysts for the selective copolymerization of epoxides with cyclic anhydrides.


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