Novel Thione-Thiol Rearrangement of Dithiocarbonic Acid O-(2,2,6,6-Tetramethylpiperidin-1-yl) Ester in the Context of Controlled Radical Polymerization
DOI:
https://doi.org/10.2533/chimia.2010.56Keywords:
Acyloxyamines, Alkoxyamines, Controlled/living radical polymerization, Newman-kwart rearrangement, Nitroxides, Thione-thiol rearrangement, ThionitroxidesAbstract
Addition of the lithium salt of N-hydroxy-2,2,6,6-tetramethylpiperidine 10 to carbon disulfide and subsequent methylation affords the rearranged dithiocarbonic acid S-methyl-S'-(2,2,6,6-tetramethylpiperidin-1-yl)-ester 9 rather than the expected xanthate ester S-methyl-O'-(2,2,6,6-tetramethylpiperidin-1-yl)-ester 8. n-Butylacrylate could be polymerized with the novel compound 9 even though the polymerization was not controlled.Downloads
Published
2010-02-26
Issue
Section
Scientific Articles
License
Copyright (c) 2010 Swiss Chemical Society
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
[1]
Chimia 2010, 64, 56, DOI: 10.2533/chimia.2010.56.