Synthesis of degradable porous polymers by ring-opening addition of a tri-aziridine and thiol-carboxylic acids
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s10965-024-04056-7.pdf
Reference27 articles.
1. Gleede T, Reisman L, Rieger E, Mbarushimana PC, Rupar PA, Wurm FR (2019) Aziridines and azetidines: building blocks for polyamines by anionic and cationic ring-opening polymerization. Polym Chem 10:3257–3283. https://doi.org/10.1039/C9PY00278B
2. Dermer OC, Ham GE (1969) ETHYLENEIMINE AND OTHER AZIRIDIES – Chemistry and Applications. Academic Press
3. Kobayashi M, Uchino K, Ishizone T (2005) Synthesis of well-defined polymers end-functionalized with crosslinkable aziridine groups by living anionic polymerization. J Polym Sci, Part A, Polym Chem 43:4126–4135. https://doi.org/10.1002/pola.20777
4. Jung S, Kang S, Kuwabara J, Yoon HJ (2019) Aziridine-based polyaddition, post-modification, and crosslinking: can aziridine rival epoxide in polymer chemistry? Polym Chem 10:4506–4512. https://doi.org/10.1039/C9PY00979E
5. Gleede T, Rieger E, Müller TH, Wurm FR (2017) 4-Styrenesulfonyl-(2-methyl)aziridine: The First Bivalent Aziridine-Monomer for Anionic and Radical Polymerization. Macromol Chem Phys 219:1700145. https://doi.org/10.1002/macp.201700145
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