Revisiting Thiol-yne Chemistry: Selective and Efficient Monoaddition for Block and Graft Copolymer Formation
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
The untapped potential of radical thiol-yne mono-addition chemistry is exploited to overcome the known limitations of thiol-ene chemistry in polymer coupling and block copolymer formation. By careful choice of alkyne, the reaction can selectively lead to the mono-addition product with efficiencies surpassing those achieved by traditional thiol-ene chemistry. This improvement is illustrated by the nearly quantitative synthesis of a variety of diblock and graft copolymers. (c) 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 319-326
Details
Original language | English |
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Pages (from-to) | 319-326 |
Number of pages | 8 |
Journal | Journal of Polymer Science, Part A: Polymer Chemistry |
Volume | 53 |
Issue number | 2 |
Publication status | Published - 15 Jan 2015 |
Peer-reviewed | Yes |
Externally published | Yes |
External IDs
Scopus | 84915804264 |
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ORCID | /0000-0002-4531-691X/work/148607947 |
Keywords
Keywords
- Block copolymers, Click chemistry, Functionalization of polymers, Synthesis, Thiol-yne