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Lewis Pairs for Ring-Opening Alternating Copolymerization of Cyclic Anhydrides and Epoxides

Abstract

Simple and highly active catalytic process for ring-opening alternating copolymerization (ROAC) of cyclic anhydrides and epoxides still remains a key challenge. Herein, we described an effective group of versatile and nontoxic zinc dicarbyl/amine Lewis pairs for the ROAC in this work. The facile route showed high catalytic activity (TOF ≤ 210 h-1 at 110 ºC) and perfectly alternating selectivity (> 99%). An unexpected highly regioselective ring-opening of asymmetric epoxides (PO, ECH and SO) was also achieved by the combination of zinc alkyls (or aryls) and amines. Of unique, deprotonation side reaction of α-H of anhydrides with organic bases was uncovered, and subsequently was inhibited by using nonpolar solvents and Lewis acid/base pairs. Thus, an array of polyesters was synthesized by the coupling of various anhydrides (PA, CHA, SA and NA) and epoxides (CHO, PO, ECH and SO) under the same Lewis pairs. Further variable temperature 1H NMR spectra and MALDI TOF MS analysis were performed to understand possible mechanism and microstructure. The experimental results indicated that zwitterionic alkoxides and carboxylates intermediate alternately formed to enhance ester repeat units in chain initiation and propagation. This work provides a simple and green catalytic strategy to prepare diversified polyesters from the ROAC process of cyclic anhydrides and epoxides with considerable catalytic activity and alternating selectivity.

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Publication details

The article was received on 29 Oct 2017, accepted on 05 Dec 2017 and first published on 06 Dec 2017


Article type: Paper
DOI: 10.1039/C7GC03261G
Citation: Green Chem., 2017, Accepted Manuscript
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    Lewis Pairs for Ring-Opening Alternating Copolymerization of Cyclic Anhydrides and Epoxides

    H. Ji, B. Wang, L. Pan and Y. Li, Green Chem., 2017, Accepted Manuscript , DOI: 10.1039/C7GC03261G

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