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Synthesis of Biobased Long-Chain Polyesters by Acyclic Diene Metathesis Polymerization and Tandem Hydrogenation and Depolymerization with Ethylene

[Image: see text] Acyclic diene metathesis (ADMET) polymerization of biobased α,ω-dienes of bis(undec-10-enoate) with diols (1,4-butanediol, isosorbide, isomannide, and 1,4-cyclohexanedimethanol) afforded high-molecular weight unsaturated polyesters, and subsequent tandem hydrogenation (H(2) 1.0 MPa...

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Detalles Bibliográficos
Autores principales: Nomura, Kotohiro, Chaijaroen, Permpoon, Abdellatif, Mohamed Mehawed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391851/
https://www.ncbi.nlm.nih.gov/pubmed/32743205
http://dx.doi.org/10.1021/acsomega.0c01965
Descripción
Sumario:[Image: see text] Acyclic diene metathesis (ADMET) polymerization of biobased α,ω-dienes of bis(undec-10-enoate) with diols (1,4-butanediol, isosorbide, isomannide, and 1,4-cyclohexanedimethanol) afforded high-molecular weight unsaturated polyesters, and subsequent tandem hydrogenation (H(2) 1.0 MPa, 50 °C, 3 h) gave the saturated polymers upon addition of a small amount of Al(2)O(3) (1.0–1.7 wt %). Subsequent reaction of the unsaturated polymers with ethylene afforded the oligomers (by depolymerization and degradation).