Synthesis of Clickable Isotactic Poly(vinyl ether)s through Organocatalytic Stereoselective Cationic Copolymerization
By virtue of the high reliability of click chemistry, polymers with clickable groups provide a useful platform for the rapid synthesis of polymer materials with diverse functionalities and architectures. However, the polymerization of clickable vinyl monomers with a concurrent regulation on tacticity remains underdeveloped. Herein, we report the successful development of a stereoselective cationic copolymerization of C-C triple bond-containing vinyl ethers with simple alkyl vinyl ethers by employing confined Brønsted acid as catalyst, which allows for the synthesis of alkyne-functionalized vinyl ether copolymers with high isotacticity (up to 90 % m), controlled molecular weight, and variable content of C-C triple bonds. Further transformation of the pendant clickable alkyne groups via thiol-yne click reactions and copper(I)-catalyzed alkyne-azide cycloaddition reaction enables a modular access to isotactic polymers with various functional groups.
Authors
- Hui Zhu
- Saihu Liao (ORCID: https://orcid.org/0000-0002-0251-8757)
- Xi Yan (ORCID: https://orcid.org/0000-0001-8439-9087)
- Shuai Zhou (ORCID: https://orcid.org/0000-0002-9490-091X)
- Yun Liao
Institutions
- Xiamen University (CN)
- Fuzhou University (CN)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2024-11-11
- DOI
- https://doi.org/10.1002/chem.202403170
- Primary Topic
- Advanced Polymer Synthesis and Characterization
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Xiamen University
- Recruitment Program of Global Experts