Author
Listed:
- Xiaopeng Yu
(Cornell University)
- Junteng Jia
(Cornell University)
- Shu Xu
(University of Minnesota)
- Ka Un Lao
(Cornell University)
- Maria J. Sanford
(Cornell University)
- Ramesh K. Ramakrishnan
(University of Southern Mississippi)
- Sergei I. Nazarenko
(University of Southern Mississippi)
- Thomas R. Hoye
(University of Minnesota)
- Geoffrey W. Coates
(Cornell University)
- Robert A. DiStasio
(Cornell University)
Abstract
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 (Tg 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 Tg 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.
Suggested Citation
Xiaopeng Yu & Junteng Jia & Shu Xu & Ka Un Lao & Maria J. Sanford & Ramesh K. Ramakrishnan & Sergei I. Nazarenko & Thomas R. Hoye & Geoffrey W. Coates & Robert A. DiStasio, 2018.
"Unraveling substituent effects on the glass transition temperatures of biorenewable polyesters,"
Nature Communications, Nature, vol. 9(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05269-3
DOI: 10.1038/s41467-018-05269-3
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