The combination of the Williamson and Tishchenko reactions produced a series of new α,ω-diene functionalized carboxylic ester, by which serials of polyesters have been prepared successfully.
The design and preparation of polymers by using biobased chemicals is regarded as an important strategy towards a sustainable polymer chemistry. Herein, two aromatic diols, 4-(hydroxymethyl)-2-methoxyphenol and 2-(4-(hydroxymethyl)-2-methoxyphenoxy)ethanol, have been prepared in good yields through the direct reduction of vanillin and hydroxyethylated vanillin (4-(2-hydroxyethoxy)-3-methoxybenzaldehyde) using NaBH4, respectively. The diols were submitted to traditional polycondensation and polyaddition with acyl chlorides and diisocyanatos, and serials of new polyesters and polyurethanes were prepared in high yields with moderate molecular weight ranging from 17,000 to 40,000 g mol−1. Their structures were characterized by 1H NMR, 13C NMR and FTIR, and their thermal properties were studied by TGA and differential scanning calorimetry (DSC), indicating that the as-prepared polyesters and polyurethanes have Tg in the range of 16.2 to 81.2 °C and 11.6 to 80.4 °C, respectively.
Polymerization of α,ω-diene functionalized carbonate monomers prepared from bio-based eugenol and 2-methoxy-4-vinylphenol through thiol–ene click and ADMET polymerizations produced polycarbonates with moderate molecular weight satisfactory thermal properties.
The significant development of catalytic biomass conversion has provided a large library of chemicals ready for subsequent upgrading to polymerisable monomers for the design and preparation of sustainable polymers. In this study, hydroxyethylation of eugenol by using green ethylene carbonate as alkylation reagent and cheap tetrabutylammonium iodide ionic liquids as green solvents and catalysts produced 2-(4-allyl-2-methoxyphenoxy)ethan-1-ol with a 85% yield, which could be used to construct an in situ CO 2 capture and conversion system by taking the reversible chemistry of alcoholic compounds with CO 2 in the presence of superbases, on which α,ω-diene functionalized carbonate monomers were successfully prepared and were applied in thiol-ene click and acyclic diene metathesis polymerisation (ADMET), producing a series of poly(thioether carbonate)s and unsaturated aromatic aliphatic polycarbonates with moderate molecular weights and satisfactory thermal properties. The structures of the formed CO 2 reversible ILs, the polymerisable monomers and the corresponding polymers were fully characterized by various technologies.
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