Reversible Addition Fragmentation Chain Transfer ( RAFT ) Polymerization: Mechanism, Process and Applications
Christopher Barner‐Kowollik, James P. Blinco, Mathias Destarac, Kristofer J. Thurecht, Sébastien Perrier
Abstract
Christopher Barner‐Kowollik, James P. Blinco, Mathias Destarac, Kristofer J. Thurecht, Sébastien Perrier
Abstract
Abstract The present article gives an overview of the reversible addition fragmentation chain transfer (RAFT) process. RAFT is one of the most versatile living radical polymerization systems and yields polymers of predictable chain length and narrow molecular weight distribution. RAFT relies on the rapid exchange of thiocarbonyl thio groups between growing polymeric chains. The key strengths of the RAFT process for polymer design are its high tolerance of monomer functionality and reaction conditions, the wide range of well‐controlled polymeric architectures achievable, and its (in‐principle) non‐rate‐retarding nature. This article introduces the mechanism of polymerization, the range of polymer molecular weights achievable, the range of monomers in which polymerization is controlled by RAFT, the various polymeric architectures that can be obtained, the type of end‐group functionalities available to RAFT‐made polymers, and the process of RAFT polymerization.
OpenAlex reports 6 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Abstract The present article gives an overview of the reversible addition fragmentation chain transfer (RAFT) process. RAFT is one of the most versatile living radical polymerization systems and yields polymers of predictable chain length and narrow molecular weight distribution. RAFT relies on the rapid exchange of thiocarbonyl thio groups between growing polymeric chains. The key strengths of the RAFT process for polymer design are its high tolerance of monomer functionality and reaction conditions, the wide range of well‐controlled polymeric architectures achievable, and its (in‐principle) non‐rate‐retarding nature. This article introduces the mechanism of polymerization, the range of polymer molecular weights achievable, the range of monomers in which polymerization is controlled by RAFT, the various polymeric architectures that can be obtained, the type of end‐group functionalities available to RAFT‐made polymers, and the process of RAFT polymerization.
Key concepts: Raft, Chain transfer, Reversible addition−fragmentation chain-transfer polymerization, Polymerization, Polymer, Living polymerization, Monomer, Radical polymerization