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Addressing the mid-point of polymer chains for multiple functionalization purposes through sequential thiol-epoxy 'click' and esterification reactions

Authors
Gadwal, IkhlasEom, TaejunHwang, JiHyeonChoe, YoungsonBang, JoonaKhan, Anzar
Issue Date
2017
Publisher
ROYAL SOC CHEMISTRY
Citation
RSC ADVANCES, v.7, no.32, pp.19439 - 19447
Indexed
SCIE
SCOPUS
Journal Title
RSC ADVANCES
Volume
7
Number
32
Start Page
19439
End Page
19447
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/86404
DOI
10.1039/c7ra02702h
ISSN
2046-2069
Abstract
A synthetic strategy is devised for the preparation of mid-chain multifunctional polymers. In this strategy, small molecules carrying one or two epoxide units along with two polymerization-initiating sites were prepared in two to three synthetic steps. Atom transfer radical polymerization (ATRP) of methylmethacrylate (MMA) monomer using the newly designed initiators gave rise to epoxide-mid-reactive polymers. A careful chain cleavage study confirmed the midpoint location of the reactive site(s) on the polymer chain. Dual-modification of these reactive epoxide unit(s) through sequential thiol-epoxy and esterification reactions then afforded the midpoint multiply functionalized polymeric structures. Due to compatibility of the ATRP process with the reactive epoxide unit(s) and the cascade nature of the functionalization processes, the present strategy is free from the protective-group requirement of organic synthesis. Moreover, it allows for varying the number and nature of functionalities at the midpoint of a polymer chain.
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