An Immobilized/Soluble Hybrid Catalyst System for Atom Transfer Radical Polymerization

2001 ◽  
Vol 34 (15) ◽  
pp. 5099-5102 ◽  
Author(s):  
Sung Chul Hong ◽  
Hyun-jong Paik ◽  
Krzysztof Matyjaszewski
2013 ◽  
Vol 364 ◽  
pp. 679-683
Author(s):  
Chang Hao Yan ◽  
Zhi Jiao Zhang ◽  
Hai Yan Chen ◽  
Zhong Yi Xie ◽  
Ting Zhu ◽  
...  

The polystyrene with end group of Br was synthesized by using MBrP as the initiator, CuBr/ PMDETA as the catalyst system according to atom transfer radical polymerization (ATRP). The effect of reaction temperature was studied and the system was confirmed as the active polymerization. Then PS-Br and CuBr/ PMDETA were respectively used as macroinitiator and catalyst to polymerize tBMA according to atom transfer radical polymerization (ATRP). The structure of the product was characterized by GPCFTIR1H-NMR. The amphiphilic block copolymer was obtained after hydrolysis. And the honeycomb porous film was prepared by PS-b-PMAA through using breath figure method.


2006 ◽  
Vol 11-12 ◽  
pp. 461-464 ◽  
Author(s):  
Shu Xian Shi ◽  
Jian Liu ◽  
Yu Zheng Xia ◽  
Shu Ke Jiao ◽  
Xiao Yu Li

In order to improve the hydrophilicity of poly (D,L-latide) (PDLLA), a novel amphiphilic ABA-type triblock copolymers of poly-N-vinylpyrrolidone (A) and poly (D, L-lactide) (B), were successfully synthesized by atom transfer radical polymerization (ATRP) using N-vinylpyrrolidone (VP) as monomer, bromide-terminated poly (D,L-latide) oligomer (Br-PDLLA-Br) as functional macromolecular initiator which was prepared when hydroxy-terminated poly(D,L-latide) oligomer (HO-PDLLA-OH) reacted with 2-bromopropanoyl bromide, CuBr/2,2’-bipyridine complex as the catalyst system. The resulting copolymers were characterized by various analytical techniques. The results showed that the introduction of poly (N-vinylpyrrolidone) (PVP) segments into polylactide enhanced the surface hydrophilicity of the copolymers remarkably and amphiphilic polymer can self-assemble into core-shell structure (polymer micelle) in water by the balance of the hydrophilic and hydrophobic interaction.


e-Polymers ◽  
2005 ◽  
Vol 5 (1) ◽  
Author(s):  
Gang Wang ◽  
Xiulin Zhu ◽  
Cheng Zhengping ◽  
Jian Zhu

AbstractHeterogeneous atom transfer radical polymerization (ATRP) of styrene initiated by 2-bromo-2-nitropropane in bulk was carried out with CuCl/2,2′-bipyridine as the catalyst. The kinetics was first order in monomer and the numberaverage molecular weight of the polymer increased linearly with monomer conversion, indicating the ‘living’/controlled nature of the polymerization. However, the number-average molecular weight was usually higher than the theoretical one. The nitro group might react with the Cu complex, resulting in insufficient initiation. The amount of catalyst has no effect on the controllability of this catalyst system for the ATRP of styrene. The presence of a halide end group in the obtained polymer was confirmed by both 1H NMR and chain-extension reaction.


2018 ◽  
Vol 9 (44) ◽  
pp. 5348-5358 ◽  
Author(s):  
João R. C. Costa ◽  
Joana R. Góis ◽  
Francesco De Bon ◽  
Arménio C. Serra ◽  
Tamaz Guliashvili ◽  
...  

A new Atom Transfer Radical Polymerization (ATRP) process with triphenylphosphine (PPh3) and [CuIIMe6TREN]2+ as the catalyst system is reported.


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