Controlled radical polymerization of a trialkylsilyl methacrylate by reversible addition-fragmentation chain transfer polymerization

2005 ◽  
Vol 43 (22) ◽  
pp. 5680-5689 ◽  
Author(s):  
M. N. Nguyen ◽  
C. Bressy ◽  
A. Margaillan
2004 ◽  
Vol 58 (11) ◽  
pp. 514-520
Author(s):  
Milena Avramovic ◽  
Lynne Katsikas ◽  
Branko Dunjic ◽  
Ivanka Popovic

The fundamentals of controlled radical polymerization are presented in this review. The paper focuses on reversible addition fragmentation chain transfer (RAFT) polymerization. The mechanism and specifics of this type of polymerization are discussed, as are the possibilities of synthesizing complex macro-molecular structures. The synthesis and properties of RAFT agents, of the general structure Z-C(=S)-S-R, are presented.


Synlett ◽  
2018 ◽  
Vol 29 (12) ◽  
pp. 1543-1551 ◽  
Author(s):  
Mao Chen ◽  
Honghong Gong ◽  
Yu Gu

Fluorinated polymers are important materials for applications in many areas. This article summarizes the development of controlled/living radical polymerization (CRP) of semifluorinated (meth)acrylates, and briefly introduces their reaction mechanisms. While the classical CRP such as atom transfer radical polymerization (ATRP), reversible addition-fragmentation chain transfer (RAFT) polymerization and nitroxide-mediated radical polymerization (NMP) have promoted the preparation of semifluorinated polymers with tailor-designed architectures, recent development of photo-CRP has led to unprecedented accuracy and monomer scope. We expect that synthetic advances will facilitate the engineering of advanced fluorinated materials with unique properties.1 Introduction2 Atom Transfer Radical Polymerization3 Reversible Addition-Fragmentation Chain Transfer Polymerization4 Nitroxide-Mediated Radical Polymerization5 Photo-CRP Mediated with Metal Complexes6 Metal-free Photo-CRP7 Conclusion


2016 ◽  
Vol 12 ◽  
pp. 2378-2389 ◽  
Author(s):  
Judita Britner ◽  
Helmut Ritter

The first detailed study on free-radical polymerization, copolymerization and controlled radical polymerization of the cyclic push–pull-type monomer methylenelactide in comparison to the non-cyclic monomer α-acetoxyacrylate is described. The experimental results revealed that methylenelactide undergoes a self-initiated polymerization. The copolymerization parameters of methylenelactide and styrene as well as methyl methacrylate were determined. To predict the copolymerization behavior with other classes of monomers, Q and e values were calculated. Further, reversible addition fragmentation chain transfer (RAFT)-controlled homopolymerization of methylenelactide and copolymerization with N,N-dimethylacrylamide was performed at 70 °C in 1,4-dioxane using AIBN as initiator and 2-(((ethylthio)carbonothioyl)thio)-2-methylpropanoic acid as a transfer agent.


RSC Advances ◽  
2016 ◽  
Vol 6 (108) ◽  
pp. 106648-106655 ◽  
Author(s):  
Haiying Tan ◽  
Guangchun Zhang ◽  
Yichao Lin ◽  
Li Ma ◽  
Tao Tang

A2A′-type asymmetric stars and A2B-type miktoarm star polymers were prepared by the combination of atom transfer radical polymerization (ATRP) and reversible addition-fragmentation chain transfer polymerization (RAFT) using the designed initiator.


2017 ◽  
Vol 8 (21) ◽  
pp. 3351-3356 ◽  
Author(s):  
In-Hwan Lee ◽  
Emre H. Discekici ◽  
Athina Anastasaki ◽  
Javier Read de Alaniz ◽  
Craig J. Hawker

Herein we report the photoinduced electron transfer–reversible addition–fragmentation chain transfer (PET-RAFT) polymerization of a range of vinyl ketone monomers including methyl, ethyl and phenyl derivatives, using Eosin Y as an organic photoredox catalyst and visible light.


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