Biobased poly(2,5‐furandimethylene succinate‐co‐butylene succinate) crosslinked by reversible Diels–Alder reaction
Publication type: Journal Article
Publication date: 2013-11-11
SJR: —
CiteScore: —
Impact factor: —
ISSN: 0887624X, 10990518
Materials Chemistry
Organic Chemistry
Polymers and Plastics
Abstract
ABSTRACT
We synthesized biobased poly(2,5‐furandimethylene succinate‐co‐butylene succinate) [P(FS‐co‐BS)] copolymers by polycondensation of 2,5‐bis(hydroxymethyl)furan, 1,4‐butanediol, and succinic acid. These copolymers could be crosslinked to form network polymers by means of a reversible Diels–Alder reaction with bis‐maleimide. The thermal properties, mechanical properties, and healing abilities of the P(FS‐co‐BS)s and the network polymers were investigated. The mechanical properties of the network polymers depended on the comonomer composition of the P(FS‐co‐BS)s and the maleimide/furan ratio in the network polymers. Some of the copolymers exhibited healing ability at room temperature, and their healing efficiency was enhanced by solvent or heat. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014, 52, 216–222
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44
Total citations:
44
Citations from 2025:
1
(2.27%)
The most citing journal
Citations in journal:
4
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MLA
Cite this
GOST
Copy
Ikezaki T. et al. Biobased poly(2,5‐furandimethylene succinate‐co‐butylene succinate) crosslinked by reversible Diels–Alder reaction // Journal of Polymer Science, Part A: Polymer Chemistry. 2013. Vol. 52. No. 2. pp. 216-222.
GOST all authors (up to 50)
Copy
Ikezaki T., Matsuoka R., HATANAKA K., Yoshie N. Biobased poly(2,5‐furandimethylene succinate‐co‐butylene succinate) crosslinked by reversible Diels–Alder reaction // Journal of Polymer Science, Part A: Polymer Chemistry. 2013. Vol. 52. No. 2. pp. 216-222.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/pola.26990
UR - https://onlinelibrary.wiley.com/doi/10.1002/pola.26990
TI - Biobased poly(2,5‐furandimethylene succinate‐co‐butylene succinate) crosslinked by reversible Diels–Alder reaction
T2 - Journal of Polymer Science, Part A: Polymer Chemistry
AU - Ikezaki, Tabito
AU - Matsuoka, Reishi
AU - HATANAKA, Kenichi
AU - Yoshie, Naoko
PY - 2013
DA - 2013/11/11
PB - Wiley
SP - 216-222
IS - 2
VL - 52
SN - 0887-624X
SN - 1099-0518
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2013_Ikezaki,
author = {Tabito Ikezaki and Reishi Matsuoka and Kenichi HATANAKA and Naoko Yoshie},
title = {Biobased poly(2,5‐furandimethylene succinate‐co‐butylene succinate) crosslinked by reversible Diels–Alder reaction},
journal = {Journal of Polymer Science, Part A: Polymer Chemistry},
year = {2013},
volume = {52},
publisher = {Wiley},
month = {nov},
url = {https://onlinelibrary.wiley.com/doi/10.1002/pola.26990},
number = {2},
pages = {216--222},
doi = {10.1002/pola.26990}
}
Cite this
MLA
Copy
Ikezaki, Tabito, et al. “Biobased poly(2,5‐furandimethylene succinate‐co‐butylene succinate) crosslinked by reversible Diels–Alder reaction.” Journal of Polymer Science, Part A: Polymer Chemistry, vol. 52, no. 2, Nov. 2013, pp. 216-222. https://onlinelibrary.wiley.com/doi/10.1002/pola.26990.