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Polymer end group modifications and polymer conjugations via “click” chemistry employing microreactor technology
Author(s) -
Vandenbergh Joke,
Tura Tiago,
Baeten Evelien,
Junkers Tanja
Publication year - 2014
Publication title -
journal of polymer science part a: polymer chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.768
H-Index - 152
eISSN - 1099-0518
pISSN - 0887-624X
DOI - 10.1002/pola.27112
Subject(s) - microreactor , azide , click chemistry , end group , acrylate , polymer chemistry , alkyne , polymer , chemistry , atom transfer radical polymerization , polystyrene , flow chemistry , copolymer , polymerization , radical polymerization , methyl acrylate , chemical engineering , materials science , catalysis , organic chemistry , engineering
This study presents the development of microreactor protocols for the successful continuous flow end group modification of atom transfer radical polymerization precursor polymers into azide end‐capped materials and the subsequent copper‐catalyzed azide alkyne click reactions with alkyne polymers, in flow. By using a microreactor, the reaction speed of the azidation of poly(butyl acrylate), poly(methyl acrylate), and polystyrene can be accelerated from hours to seconds and full end group conversion is obtained. Subsequently, copper‐catalyzed click reactions are executed in a flow reactor at 80 °C. Good coupling efficiencies are observed and various block copolymer combinations are prepared. Furthermore, the flow reaction can be carried out in only 40 min, while a batch procedure takes several hours to reach completion. The results indicate that the use of a continuous flow reactor for end group modifications as well as click reactions has clear benefits towards the development and improvement of well‐defined polymer materials. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52 , 1263–1274

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