|
Authors
|
Sprafke, J. ; Spruell, J. ; Mattson, K. M. ; Montarnal, D. ; McGrath, A. J. ; Pötzsch, R. ; Miyajima, D. ; Hu, J. ; Latimer, A. A. ; Voit, B. ; Aida, T. ; Hawker, C.J.
|
|
Title
|
Revisiting thiol-yne chemistry: Selective and efficient monoaddition for block and graft copolymer formation
|
|
Date
|
15.10.2014
|
|
Number
|
43342
|
|
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. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014
|
|
Publisher
|
Journal of Polymer Science: Part A: Polymer Chemistry
|
|
Wikidata
|
|
|
Citation
|
Journal of Polymer Science: Part A: Polymer Chemistry 53 (2014) 319-326
|
|
DOI
|
https://doi.org/10.1002/pola.27345
|
|
Tags
|
|
