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[5] RAFT polymerization today is mainly carried out by thiocarbonylthio chain transfer agents. It was first reported by Rizzardo et al. in 1998. [6] RAFT is one of the most versatile methods of controlled radical polymerization because it is tolerant of a very wide range of functionality in the monomer and solvent, including aqueous solutions. [7]
Control in RAFT polymerization (scheme 1) is achieved in a far more complicated manner than the homolytic bond formation-bond cleavage of SFRP and ATRP. The CTA for RAFT polymerization must be chosen cautiously because it has an effect on polymer length, chemical composition, rate of the reaction and the number of side reactions that may occur.
ATRP reactions are very robust in that they are tolerant of many functional groups like allyl, amino, epoxy, hydroxy, and vinyl groups present in either the monomer or the initiator. [5] ATRP methods are also advantageous due to the ease of preparation, commercially available and inexpensive catalysts (copper complexes), pyridine-based ligands ...
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The steady-state concentration of the growing polymer chains is 10 −7 M by order of magnitude, and the average life time of an individual polymer radical before termination is about 5–10 s. A drawback of the conventional radical polymerization is the limited control of chain architecture, molecular weight distribution, and composition.
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