The ambient temperature (20 C) reversible addition fragmentation chain transfer (RAFT) polymerization of several water-soluble monomers conducted directly in aqueous media under g-initiation (at dose rates of 30 Gy h À1 ) proceeds in a controlled fashion. Using functional trithiocarbonates, i.e., S,
RAFT Polymerization of N-Isopropylacrylamide and Acrylic Acid under γ-Irradiation in Aqueous Media
✍ Scribed by Pierre-Eric Millard; Leonie Barner; Martina H. Stenzel; Thomas P. Davis; Christopher Barner-Kowollik; Axel H. E. Müller
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 174 KB
- Volume
- 27
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
Summary: The ambient temperature (20 °C) reversible addition fragmentation chain transfer (RAFT) polymerization of N‐isopropylacrylamide (NIPAAm) and acrylic acid (AA) conducted directly in aqueous media under γ‐initiation (at dose rates of 30 Gy · h^−1^) proceeds in a controlled fashion (typically, $\overline M _{\rm w} /\overline M _{\rm n}$ < 1.2) to near quantitative conversions and up to number‐average molecular weights of 2.5 × 10^5^ g · mol^−1^ for PNIPAAm and 1.1 × 10^5^ g · mol^−1^ for PAA via two water‐soluble trithiocarbonate chain transfer agents, i.e., S,S‐bis(α,α′‐dimethyl‐α″‐acetic acid)trithiocarbonate (TRITT) and 3‐benzylsulfanylthiocarbonylsulfanyl propionic acid (BPATT). The generated polymers are successfully chain extended, which suggests that the RAFT agents are stable throughout the polymerization process so that complex and well‐defined architectures can be obtained.
An increase of the monomer/CTA ratio leads to an increase of the molecular weight for the RAFT polymerization of NIPAAm under γ‐radiation in water using TRITT at ambient temperature.
imageAn increase of the monomer/CTA ratio leads to an increase of the molecular weight for the RAFT polymerization of NIPAAm under γ‐radiation in water using TRITT at ambient temperature.
📜 SIMILAR VOLUMES
## Abstract Photopolymerizations of __N__‐isopropylacrylamide (NIPAAm) were carried out in water, initiated by 2‐(__N,N__‐diethyldithiocarbamyl)isobutyric acid sodium salt (DTCA‐Na) as water‐soluble initiator under UV irradiation. The first‐order time‐conversion plots showed slowly decreasing slope