scholarly journals Precise Synthesis of Functional Polymers by RAFT Polymerization

2007 ◽  
Vol 64 (10) ◽  
pp. 655-664
Author(s):  
Hideharu MORI ◽  
Takeshi ENDO
2011 ◽  
Vol 2 (3) ◽  
pp. 492-519 ◽  
Author(s):  
Graeme Moad ◽  
Ming Chen ◽  
Matthias Häussler ◽  
Almar Postma ◽  
Ezio Rizzardo ◽  
...  

2014 ◽  
Vol 5 (18) ◽  
pp. 5236-5246 ◽  
Author(s):  
Joris J. Haven ◽  
Carlos Guerrero-Sanchez ◽  
Daniel J. Keddie ◽  
Graeme Moad ◽  
San H. Thang ◽  
...  

The utility of automated high-throughput methods for the one pot synthesis of functional polymers of increased complexity is reported.


2009 ◽  
Vol 62 (8) ◽  
pp. 806 ◽  
Author(s):  
Till Gruendling ◽  
Mathias Dietrich ◽  
Christopher Barner-Kowollik

We report on the successful quantitative transformation of methacrylate and acrylate-type polymers prepared by reversible addition–fragmentation chain transfer (RAFT) polymerization carrying a dithioester-end-group into hydroxy-functional polymers. The simple reaction procedure involves stirring a solution of the dithioester-capped polymer and an azo-initiator in tetrahydrofuran at elevated temperatures (T = 60°C) in the presence of air. This reaction quantitatively yields hydroperoxide functionalities that can be efficiently reduced to hydroxy groups in a one-pot procedure using triphenylphosphine. Size exclusion chromatography–electrospray mass spectrometry was employed to monitor the progress of the reaction. The new backbone-linked hydroxy group provides a versatile anchor for chemical end-group conversions and conjugation reactions with prepared RAFT polymers, which alleviates problems with the rather limited ability of the dithioester-end-group to undergo non-radical transformations.


2016 ◽  
Vol 7 (45) ◽  
pp. 7011-7018 ◽  
Author(s):  
Suzan Aksakal ◽  
C. Remzi Becer

A facile method for synthesizing thioacrylate monomers and their RAFT polymerization have been demonstrated for the first time.


2011 ◽  
Vol 1 (1) ◽  
pp. 222-226 ◽  
Author(s):  
Mathew P. Robin ◽  
Mathew W. Jones ◽  
David M. Haddleton ◽  
Rachel K. O’Reilly

2019 ◽  
Author(s):  
Suhua Li ◽  
Gencheng Li ◽  
Bing Gao ◽  
Sidharam P. Pujari ◽  
Xiaoyan Chen ◽  
...  

The first SuFEx click chemistry synthesis of SOF<sub>4</sub>-derived copolymers based upon the polymerization of bis(iminosulfur oxydifluorides) and bis(aryl silyl ethers) is described. This novel class of SuFEx polymer presents two key characteristics: First, the newly created [-N=S(=O)F-O-] polymer backbone linkages are themselves SuFExable and primed to undergo further high-yielding and precise SuFEx-based post-modification with phenols or amines to yield branched functional polymers. Second, studies of individual polymer chains of several of these new materials indicate the presence of helical polymer structures, which itself suggests a preferential approach of new monomers onto the growing polymer chain upon the formation of the stereogenic linking moiety.


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