Addressing the mid-point of polymer chains for multiple functionalization purposes through sequential thiol–epoxy ‘click’ and esterification reactions
Author:
Affiliation:
1. Department of Chemical and Biological Engineering
2. Korea University
3. Seoul 02841
4. Korea
5. Department of Chemical Engineering
6. Pusan National University
7. Pusan
Abstract
A synthetic strategy is devised for the preparation of mid-chain multifunctional polymers.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/RA/C7RA02702H
Reference116 articles.
1. P. Theato and H.-A.Klok, Functional Polymers by Post- Polymerization Modification, Wiley, Weinheim, Germany, 2013
2. The Convergence of Synthetic Organic and Polymer Chemistries
3. 1,3-Dipolar Cycloadditions of Azides and Alkynes: A Universal Ligation Tool in Polymer and Materials Science
4. Applications of Orthogonal “Click” Chemistries in the Synthesis of Functional Soft Materials
5. Has Click Chemistry Lead to a Paradigm Shift in Polymer Material Design?
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1. Pendant isocyanate and epoxide-containing copolymers: synthesis, sequential dual-functionalization with amines, and surface modifications;Journal of Macromolecular Science, Part A;2023-06-02
2. Thiol-epoxy ‘click’ chemistry: a focus on molecular attributes in the context of polymer chemistry;Chemical Communications;2023
3. Poly(ß-hydroxy thioether)s: synthesis through thiol-epoxy ‘click’ reaction and post-polymerization modification to main-chain polysulfonium salts;Journal of Macromolecular Science, Part A;2021-10-05
4. One‐Step Modification of Diacid‐Functional Polythioethers via Simultaneous Passerini and Esterification Reactions;Macromolecular Chemistry and Physics;2021-03-30
5. Nucleophilic Thiol-yne reaction in Macromolecular Engineering: From synthesis to applications;European Polymer Journal;2020-08
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