Biobased poly(2,5‐furandimethylene succinate‐ co ‐butylene succinate) crosslinked by reversible Diels–Alder reaction-Reference-Cited by-同舟云学术

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Biobased poly(2,5‐furandimethylene succinate‐ co ‐butylene succinate) crosslinked by reversible Diels–Alder reaction

Published:2013-11-11 Issue:2 Volume:52 Page:216-222
ISSN:0887-624X
Container-title:Journal of Polymer Science Part A: Polymer Chemistry
language:en
Short-container-title:J. Polym. Sci. Part A: Polym. Chem.

Author:

Ikezaki Tabito¹,Matsuoka Reishi¹,Hatanaka Kenichi¹,Yoshie Naoko¹

Affiliation:

1. Institute of Industrial ScienceThe University of Tokyo4‐6‐1 KomabaMeguro‐ku Tokyo153‐8505 Japan

Funder

Institute of Industrial Science, the University of Tokyo

Publisher

Wiley

Subject

Materials Chemistry,Organic Chemistry,Polymers and Plastics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pola.26990

Reference33 articles.

1. The irruption of polymers from renewable resources on the scene of macromolecular science and technology

2. How well can renewable resources mimic commodity monomers and polymers?

3. Synthesis of biodegradable polymers from renewable resources

4. 5-Hydroxymethylfurfural (HMF) as a building block platform: Biological properties, synthesis and synthetic applications

5. Hydroxymethylfurfural, A Versatile Platform Chemical Made from Renewable Resources

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2. Enzymatic bulk synthesis, characterization, rheology, and biodegradability of biobased 2,5-bis(hydroxymethyl)furan polyesters;Green Chemistry;2024

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5. Polymers from Polycondensation (Step) Reactions;Furan Polymers and their Reactions;2023-11-18

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