OAK

Synthesis of Alternating Polyisocyanate Copolymers by Anionic Polymerization for Mimicking Amphiphilic Helical Peptides

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Abstract
The amphiphilic conformation of alpha-helical peptides has important biological functions, such as ion transport, antifreeze, and innate immunity, which can be mimicked by alternating polyisocyanate copolymers. We synthesized poly(allyl isocyanate-alt-(S)-(-)-alpha-methylbenzyl is ocyanate (P(AIC-alt-SMBIC)) and ammonium-containing P(AIC-alt-SMBIC) (N-P(AIC-alt-SMBIC)), ensuring the amphiphilic helical conformation. The benzyl group of SMBIC plays an important role in alternating copolymerization with its steric and electron-withdrawing effects, while AIC provides an alkene group capable of introducing a customized functional group. The P(AIC-alt-SMBIC) with predominantly alternating sequence was acquired at f(SMBIC)/f(AIC) = 8 with a controlled molecular weight and narrow dispersity. N-P(AIC-alt-SMBIC)s were synthesized from thiol-ene radical addition with P(AIC-alt-SMBIC).
Author(s)
Bak, In GyuChae, Chang-GuenChoi, JieunSong, Woo-YoungSeo, JiwonLee, EunjiLee, Jae-Suk
Issued Date
2022-12
Type
Article
DOI
10.1002/anie.202212398
URI
https://scholar.gist.ac.kr/handle/local/10498
Publisher
WILEY-V C H VERLAG GMBH
Citation
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.61, no.51
ISSN
1433-7851
Appears in Collections:
Department of Chemistry > 1. Journal Articles
Department of Materials Science and Engineering > 1. Journal Articles
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