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Unraveling substituent effects on the glass transition temperatures of biorenewable polyesters

Converting biomass-based feedstocks into polymers not only reduces our reliance on fossil fuels, but also furnishes multiple opportunities to design biorenewable polymers with targeted properties and functionalities. Here we report a series of high glass transition temperature (T(g) up to 184 °C) po...

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Detalles Bibliográficos
Autores principales: Yu, Xiaopeng, Jia, Junteng, Xu, Shu, Lao, Ka Un, Sanford, Maria J., Ramakrishnan, Ramesh K., Nazarenko, Sergei I., Hoye, Thomas R., Coates, Geoffrey W., DiStasio, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056526/
https://www.ncbi.nlm.nih.gov/pubmed/30038298
http://dx.doi.org/10.1038/s41467-018-05269-3
Descripción
Sumario:Converting biomass-based feedstocks into polymers not only reduces our reliance on fossil fuels, but also furnishes multiple opportunities to design biorenewable polymers with targeted properties and functionalities. Here we report a series of high glass transition temperature (T(g) up to 184 °C) polyesters derived from sugar-based furan derivatives as well as a joint experimental and theoretical study of substituent effects on their thermal properties. Surprisingly, we find that polymers with moderate steric hindrance exhibit the highest T(g) values. Through a detailed Ramachandran-type analysis of the rotational flexibility of the polymer backbone, we find that additional steric hindrance does not necessarily increase chain stiffness in these polyesters. We attribute this interesting structure-property relationship to a complex interplay between methyl-induced steric strain and the concerted rotations along the polymer backbone. We believe that our findings provide key insight into the relationship between structure and thermal properties across a range of synthetic polymers.