Insertion of CO2 to 2-methyl furoate promoted by a cobalt hypercrosslinked polymer catalyst to obtain a monomer of CO2-based biopolyesters†

Elizabeth Rangel-Rangel, Beatriz Fuerte-Díez, Marta Iglesias and Eva M. Maya
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Abstract

2,5-Furan Dicarboxylic methyl Ester (FDME), a highly valued monomer for the synthesis of biobased polyesters, has been prepared through a new synthetic strategy that consists of the direct carboxylation of methyl furoate in two steps: the first one involves a solvent-free reaction using a moderate CO2 pressure (10 bar), a base (Cs2CO3) and a cobalt-based heterogeneous catalyst (HCP-Salphen-Co) for 6 h, which was prepared using mechanochemical polymerization. The second step consists of an acid esterification using standard conditions. The CO2-based FDME synthesized with this strategy was successfully reacted with a diol derived from vanillin, thus obtaining a CO2 and a completely bio-based polyester which exhibited high thermal stability with a starting degradation temperature of 250 °C and a glass transition temperature of 104 °C.

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在超交联聚合物钴催化剂的促进下,将二氧化碳插入糠酸 2-甲酯,从而获得二氧化碳基生物聚酯单体
2,5-呋喃二羧酸甲酯(FDME)是一种用于合成生物基聚酯的高价值单体,它是通过一种新的合成策略制备的,该策略包括分两步对糠酸甲酯进行直接羧化:第一步是使用中等二氧化碳压力(10 巴)、碱(Cs2CO3)和钴基异相催化剂(HCP-Salphen-Co)进行 6 小时的无溶剂反应,该催化剂是通过机械化学聚合法制备的。第二步是在标准条件下进行酸酯化。采用这种策略合成的二氧化碳基 FDME 成功地与香兰素衍生的二元醇发生了反应,从而获得了二氧化碳和完全生物基的低聚酯,这种低聚酯具有很高的热稳定性,起始降解温度为 250°C,玻璃化转变温度为 104°C。
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