Abstract
The paper reports the generation of a carbon-center radical (R•) from an alkyl iodide (R-I) via a halogen bonding catalysis using pyridine N-oxide (PO) catalysts. The use of this catalysis in organocatalyzed living radical polymerization was systematically studied over a series of substituted POs. A more electron-donating substitute led to a higher catalytic activity, as experimentally observed and theoretically supported by DFT (density functional theory) calculation. Notably, the polymerization was induced and controlled not only by thermal heating but also by photoirradiation. The polymerization was compatible with several functional monomers and afforded block copolymers.
Original language | English |
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Pages (from-to) | 2156-2163 |
Number of pages | 8 |
Journal | Macromolecules |
Volume | 52 |
Issue number | 5 |
DOIs | |
Publication status | Published - Mar 12 2019 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2019 American Chemical Society.
ASJC Scopus Subject Areas
- Organic Chemistry
- Polymers and Plastics
- Inorganic Chemistry
- Materials Chemistry