4.7 Article

Alkali metal carbonate catalyzed copolymerization of anhydrides and epoxides: a simple, efficient and versatile approach to well-defined alternating polyesters

Journal

POLYMER CHEMISTRY
Volume 14, Issue 14, Pages 1630-1638

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2py01507b

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Ring-opening alternating copolymerization (ROAC) using alkali metal carbonates (AMCs) as efficient and environmentally benign catalysts is reported. The ROAC of phthalate anhydride (PA) and propylene oxide (PO) is catalyzed efficiently by AMC at 100 degrees C, producing polyesters with perfectly alternating structures. The structural and functional diversity of the resultant polyesters can be expanded by using various epoxide monomers and alcohol initiators. The cooperative catalysis of AMC accelerates the generation of the alternating structure.
Ring-opening alternating copolymerization (ROAC) has recently become an attractive strategy for polyester synthesis. To date, ROAC catalysts have been restricted to organometallics and organic super-bases. In this work, we report ROAC using alkali metal carbonates (AMCs), one of the most common, simple, and inexpensive reagents in the laboratory, as efficient and environmentally benign catalysts. The ROAC of phthalate anhydride (PA) and propylene oxide (PO) can be catalyzed efficiently by AMC at 100 degrees C to afford polyesters with perfectly alternating structures. The structural and functional diversity of the resultant polyesters can be expanded by using various epoxide monomers and alcohol initiators. An alkali metal cation dissociated from the AMC successively activates the anhydride and the epoxide, and the carbonate anion activates the terminated hydroxyl. The cooperative catalysis accelerates the generation of the alternating structure.

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