催化作用
聚酯纤维
邻苯二甲酸酐
环氧化物
高分子化学
聚碳酸酯
聚合
化学
共聚物
有机化学
聚合物
琥珀酸酐
材料科学
双酚A
对苯二甲酸
马来酸酐
酰氯
氯化物
邻苯二甲酸
环氧丙烷
作者
Fatemeh Niknam,David Hermann Lamparelli,Assunta D’Amato,Vito Speranza,Francesca Aliberti,Roberto Pantani,Antonio Buonerba,Carmine Capacchione
标识
DOI:10.1016/j.eurpolymj.2026.114830
摘要
The ring-opening copolymerization (ROCOP) of various epoxides with cyclic anhydrides derived from β-myrcene and isoprene, named MDA and IDA respectively, was achieved using [OSSO]-type iron(III) (1) or chromium(III) (2) catalysts in combination with bis(triphenylphosphine)iminium chloride (PPNCl). In all binary ROCOP reactions, polyesters with anhydride conversion > 99% and tunable glass-transition temperatures ( T g = from − 2 to 98 °C) were obtained. The Cr(III) catalyst increased polymerization rates, while Fe(III) delivered comparable polymer properties, supporting iron as a more sustainable catalyst platform. Sequential ROCOP using two cyclic anhydrides, for example MDA followed by phthalic anhydride (PA), afforded multiblock copolymers with > 95% overall conversion. Extending this chemistry to one-pot epoxide/anhydride/CO 2 terpolymerizations enabled a switch from polyester to polycarbonate formation, with up to 82% of the consumed epoxide incorporated as carbonate linkages at low catalyst loading (0.10 mol%). Nuclear Magnetic Resonance (NMR) spectroscopy analyses indicated minimal polyether formation and controlled block architectures, highlighting the Fe(III) catalyst as a selective and versatile system for sustainable, renewable polymers.
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