Polyesters with both cyclic topology and chemical recyclability are attractive. Here, the alternating copolymerization of cyclic anhydride and o-phthalaldehyde to synthesize a series of cyclic and recyclable polyesters are reported for the first time. Besides readily available monomers, the copolymerization is carried out at 25 °C, uses common Lewis/Brønsted acids as catalysts, and achieves high yields within 1 h. The resulting polyesters possess well-defined alternating sequences, high-purity cyclic topology, and tunable structures using distinct two monomer sets. Of interest, the copolymerization manifests obvious chemical reversibility as revealed by kinetic and thermodynamic studies, making the unprecedented polyesters easy to recycle to their distinct two monomers in a closed loop at high temperatures. This work furnishes a facile and efficient method to synthesize cyclic polyesters with closed-loop recyclability.
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http://dx.doi.org/10.1002/advs.202306072 | DOI Listing |
ChemSusChem
January 2025
Peking University, Chemistry, 292 Chengfu Rd, 100871, Beijing, CHINA.
Polyesters featuring a linear topology and in-chain 1,3-cyclobutane rings, synthesized via ring-opening polymerization (ROP) of 2-oxabicyclo[2.1.1]hexan-3-one (4R-BL, R = Bu, Ph) through a coordination-insertion mechanism, display excellent thermal and hydrolytic stability, making them promising candidates for sustainable circular materials.
View Article and Find Full Text PDFACS Macro Lett
January 2025
Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, People's Republic of China.
Efficient synthesis of cyclic polymers remains a frontier challenge. We report here that macromolecular transesterification during a pseudoblock copolymerization process can be utilized for such a purpose. Organobase-catalyzed ring-opening alternating copolymerization of 3,4-dihydrocoumarin and epoxide is conducted with four-armed poly(ethylene oxide) (PEO) as a macroinitiator.
View Article and Find Full Text PDFBiomacromolecules
January 2025
Dalian Key Laboratory of Green Manufacturing Technology for Fine Chemicals Production, College of Environmental and Chemical Engineering, Dalian University, Dalian 116622, P. R. China.
The development of biobased polyesters with the combination of high UV shielding and degradability is a significant challenge. Herein, three 4-membered cyclic monomers containing two pyrrolidone and two furan rings were prepared by the aza-Michael addition of biobased bifuran diamine and dimethyl itaconate (DMI). They were available in melt polycondensation reactions with various diols to synthesize biobased polyesters.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Polymer Synthesis Laboratory, Laboratory, Chemistry Program, KAUST Catalysis Center, Physical Sciences and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal 23955, Saudi Arabia.
Khirurgiia (Mosk)
December 2024
Petrovsky National Research Center of Surgery, Moscow, Russia.
Objective: To evaluate the mechanical properties of poly(L-lactide) cage prototypes on cadaveric models of the lumbar spine ram model.
Material And Methods: Prototypes of neck devices were developed on the Ender 2v2 3D printer («Shenzhen Creality 3D Technology Co., Ltd.
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