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Fixing carbon dioxide as a polymer material is an effective and environmentally beneficial approach for reducing the harm of CO greenhouse gas. In this paper, carbon dioxide and cyclohexene oxide were used as co-monomers, and a chiral binuclear cobalt complex with a biphenyl linker was employed as the catalyst to successfully prepare a poly(cyclohexenylene carbonate) with high stereoregularity. The influence of catalyst structure, CO pressure, and operating temperature on the copolymerization rate and polymer structure were systematically investigated. Optimal catalyst structure and operating conditions were determined, resulting in an excellent poly(cyclohexenylene carbonate) with a stereoregularity as high as 93.5%. Performance testing revealed that the polyester had a molecular weight of approximately 20 kg/mol, a glass transition temperature of 129.7 °C, an onset decomposition temperature of 290 °C, and a tensile strength of 42.8 MPa. These results demonstrate high thermal stability and mechanical strength, indicating the potential for expanding the applications of aliphatic polycarbonate materials.
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http://dx.doi.org/10.3390/molecules28135235 | DOI Listing |
Molecules
July 2023
State Key Laboratory of Coking Coal Resources Development and Comprehensive Utilization, Pingdingshan 467002, China.
Fixing carbon dioxide as a polymer material is an effective and environmentally beneficial approach for reducing the harm of CO greenhouse gas. In this paper, carbon dioxide and cyclohexene oxide were used as co-monomers, and a chiral binuclear cobalt complex with a biphenyl linker was employed as the catalyst to successfully prepare a poly(cyclohexenylene carbonate) with high stereoregularity. The influence of catalyst structure, CO pressure, and operating temperature on the copolymerization rate and polymer structure were systematically investigated.
View Article and Find Full Text PDFJ Am Chem Soc
June 2002
Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77842, USA.
The air-stable, chiral (salen)Cr(III)Cl complex (3), where H(2)salen = N,N'-bis(3,5-di-tert-butyl-salicylidene)-1,2-cyclohexene diamine, has been shown to be an effective catalyst for the coupling of cyclohexene oxide and carbon dioxide to afford poly(cyclohexenylene carbonate), along with a small quantity of its trans-cyclic carbonate. The thus produced polycarbonate contained >99% carbonate linkages and had a M(n) value of 8900 g/mol with a polydispersity index of 1.2 as determined by gel permeation chromatography.
View Article and Find Full Text PDF