Physically Controlled Radical Polymerization of Vaporized Vinyl Monomers on Surfaces. Synthesis of Block Copolymers of Methyl Methacrylate and Styrene with a Conventional Free Radical Initiator

2003 ◽  
Vol 36 (16) ◽  
pp. 5974-5981 ◽  
Author(s):  
Mikio Yasutake ◽  
Shigehiro Hiki ◽  
Yoshito Andou ◽  
Haruo Nishida ◽  
Takeshi Endo

Methyl methacrylate has been polymerized in the presence of poly(methyl methacrylate) by using a free-radical initiator. The efficiency of the initiator is shown to be independent of the viscosity. At high viscosities, chain termination was influenced by the rate of translational diffusion of the polymer radicals. The dependence of the polymerization rate on viscosity is less than that predicted by a simple kinetic scheme. It appears that only those radicals which are above a certain size have their chain termination reactions controlled by the solution viscosity. This limiting size decreases as the viscosity increases.


e-Polymers ◽  
2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Zhengji Song ◽  
Carole Pelletier ◽  
Yinghua Qi ◽  
Jasim Ahmed ◽  
Sunil K. Varshney ◽  
...  

AbstractABA and/or ABC type triblock copolymers were synthesized by living anionic and controlled radical polymerization in which poly(methyl methacrylate) was used as central block. The structural composition of these block copolymers were determined by 1H NMR. The block length/molecular weight and microstructure of these polymers were measured by SEC. The microstructure of resultant central alkyl methacrylate block can be tailored from highly syndiotactic to highly isotactic structure by varying the solvent and/or initiator. The thermal and rheological properties of center poly(methyl methacrylate) block and poly(styreneb- methyl methacrylate-b- styrene) tri block copolymers were studied in detail.


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 ◽  
2021 ◽  
Vol 11 (55) ◽  
pp. 34631-34635
Author(s):  
Talena Rambarran ◽  
Heather D. Sheardown

A versatile method of making block copolymers using conventional radical polymerization of acrylic monomers from a functional radical initiator followed by ‘click’ ligation is described.


2001 ◽  
Vol 79 (5-6) ◽  
pp. 529-535 ◽  
Author(s):  
François Simal ◽  
Dominique Jan ◽  
Lionel Delaude ◽  
Albert Demonceau ◽  
Marie-Rose Spirlet ◽  
...  

New complexes of the type RuCl2(p-cymene)L where the ligand L is either a phosphine or a stable triazolinylidene carbene have been tested and compared to the Grubbs' benzylidene complex RuCl2(=CHPh)(PCy3)2 as catalyst precursors for the controlled atom transfer radical polymerization (ATRP) of methyl methacrylate and of various para-substituted styrenes. Kinetic data and Hammett ρ constants are reported, as well as the X-ray structure of the ortho-metallated triazolinylidene-ruthenium(II) complex RuCl(p-cymene)[1,2-phenylene[3,4-diphenyl-1H-1,2,4-triazol-1-yl-5(4H)-ylidene]].Key words: ruthenium, carbene, chelate complex, homogeneous catalysis, atom transfer radical polymerization.


2016 ◽  
Vol 5 (2) ◽  
pp. 199-202 ◽  
Author(s):  
Dmitry Voylov ◽  
Tomonori Saito ◽  
Bradley Lokitz ◽  
David Uhrig ◽  
Yangyang Wang ◽  
...  

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