1. Synthesis of anionic amphiphilic diblock copolymers of poly(styrene) and poly(acrylic acid) by reverse iodine transfer polymerization (RITP) in solution and emulsion.
- Author
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Rayeroux, David, N. Patra, Braja, and Lacroix ‐ Desmazes, Patrick
- Subjects
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ADDITION polymerization , *AMPHIPHILES , *DIBLOCK copolymers , *STYRENE , *ACRYLIC acid - Abstract
ABSTRACT Reverse iodine transfer polymerization (RITP), offering the appealing potential of the in situ generation of transfer agents out of molecular iodine I2, is employed in the synthesis of anionic amphiphilic diblock copolymers of poly(styrene) and poly(acrylic acid). Starting with well-characterized poly(styrene) as macro-transfer agents synthesized by RITP, diblock copolymers poly(styrene)- b-poly( tert-butyl acrylate) of various lengths are successfully yielded in solution with a good architectural control. These blocks are then subjected to acid deprotection and subsequent pH control to give rise to anionic amphiphilic poly(styrene)- b-poly(acrylic acid). Besides, homopolymers of tert-butyl acrylate are produced by RITP both in solution and in emulsion. Furthermore, a fruitful trial of the synthesis of diblock copolymers poly( tert-butyl acrylate)- b-poly(styrene) is carried out through chain extension of the poly( tert-butyl acrylate) latex as a macro-transfer agent in seeded emulsion polymerization of styrene. Finally, the prepared block copolymer is deprotected to bring about its amphiphilic nature and a pH control caters for its anionic character. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 4389-4398 [ABSTRACT FROM AUTHOR]
- Published
- 2013
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