Moderated copolymerization. Part 5.—Penultimate unit effect in chain-transfer. Systems styrene/methyl acrylate/carbon tetrabromide and styrene/methyl acrylate/1-butane thiol and some general considerations

Author(s):  
Clement H. Bamford ◽  
Sulaiman N. Basahel
Author(s):  
T. T. Vasil'eva ◽  
V. A. Kochetkova ◽  
B. V. Nelyubin ◽  
B. I. Dostovalova ◽  
R. Kh. Freidlina

2002 ◽  
Vol 51 (10) ◽  
pp. 1117-1122 ◽  
Author(s):  
Romain Severac ◽  
Patrick Lacroix-Desmazes ◽  
Bernard Boutevin

2014 ◽  
Vol 87 (5) ◽  
pp. 640-645 ◽  
Author(s):  
B. N. Ionychev ◽  
Yu. D. Semchikov ◽  
N. A. Kopylova ◽  
E. S. Andreeva ◽  
S. D. Zaitsev

1996 ◽  
Vol 29 (21) ◽  
pp. 6717-6723 ◽  
Author(s):  
Harold A. S. Schoonbrood ◽  
Sebastiaan C. J. Pierik ◽  
Bram van den Reijen ◽  
Johan P. A. Heuts ◽  
Anton L. German

2009 ◽  
Vol 62 (11) ◽  
pp. 1473 ◽  
Author(s):  
Robert Rotzoll ◽  
Philipp Vana

The present study introduces the silica-anchored azo-initiator 4,4′-azobis(4-cyano-N-(3″-triethoxysilylpropyl)-valeric amide) (ACTA) for the surface-initiated polymerization of methyl acrylate (MA) with and without additional grafted reversible addition–fragmentation chain transfer (RAFT) agents 1,4-bis(3′-trimethoxysilylpropyltrithiocarbonylmethyl)benzene and 1,6-bis(o,p-2′-trimethoxysilylethylbenzyltrithiocarbonyl)hexane. While the sole use of silica-linked ACTA produced grafted poly(methyl acrylate) (pMA) of high molecular weight, due to a 2D Trommsdorff effect, the polymerization in combination with the fixed RAFT agents exhibited living behaviour with increasing molecular weights during polymerization. Silica-pMA hybrids were further analyzed via thermogravimetric analysis and scanning electron microscopy, which revealed significant differences between the three approaches.


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