Random Poly(methyl methacrylate-co -styrene) Brushes by ATRP to Create Neutral Surfaces for Block Copolymer Self-Assembly

2011 ◽  
Vol 213 (1) ◽  
pp. 108-115 ◽  
Author(s):  
Hui Liu ◽  
Colm T. O'Mahony ◽  
Fabrice Audouin ◽  
Claudia Ventura ◽  
Michael Morris ◽  
...  
Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 2922
Author(s):  
Maria Simonova ◽  
Ivan Ivanov ◽  
Tamara Meleshko ◽  
Alexey Kopyshev ◽  
Svetlana Santer ◽  
...  

Three-component molecular brushes with a polyimide backbone and amphiphilic block copolymer side chains with different contents of the “inner” hydrophilic (poly(methacrylic acid)) and “outer” hydrophobic (poly(methyl methacrylate)) blocks were synthesized and characterized by molecular hydrodynamics and optics methods in solutions of chloroform, dimethylformamide, tetrahydrofuran and ethanol. The peculiarity of the studied polymers is the amphiphilic structure of the grafted chains. The molar masses of the molecular brushes were determined by static and dynamic light scattering in chloroform in which polymers form molecularly disperse solutions. Spontaneous self-assembly of macromolecules was detected in dimethylformamide, tetrahydrofuran and ethanol. The aggregates size depended on the thermodynamic quality of the solvent as well as on the macromolecular architectural parameters. In dimethylformamide and tetrahydrofuran, the distribution of hydrodynamic radii of aggregates was bimodal, while in ethanol, it was unimodal. Moreover, in ethanol, an increase in the poly(methyl methacrylate) content caused a decrease in the hydrodynamic radius of aggregates. A significant difference in the nature of the blocks included in the brushes determines the selectivity of the used solvents, since their thermodynamic quality with respect to the blocks is different. The macromolecules of the studied graft copolymers tend to self-organization in selective solvents with formation of a core–shell structure with an insoluble solvophobic core surrounded by the solvophilic shell of side chains.


2014 ◽  
Author(s):  
Robert Seidel ◽  
Paulina Rincon Delgadillo ◽  
Abelardo Ramirez-Hernandez ◽  
Hengpeng Wu ◽  
Youngjun Her ◽  
...  

e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Dong Chen ◽  
Ruixue Liu ◽  
Zhifeng Fu ◽  
Yan Shi

AbstractAmphiphilic diblock copolymer poly(methyl methacrylate)-b-poly(acrylic acid) (PMMA-b-PAA) was prepared by 1,1-diphenylethene (DPE) method. Firstly, free radical polymerization of methyl methacrylate was carried out with AIBN as initiator in the presence of DPE, giving a DPE-containing PMMA precursor with controlled molecular weight. tert-Butyl acrylate (tBA) was then polymerized in the presence of the PMMA precursor, and PMMA-b-PtBA diblock copolymer with controlled molecular weight was prepared. Finally, amphiphilic diblock copolymer PMMA-b-PAA was obtained by hydrolysis of PMMA-b-PtBA. The formation of PMMA-b-PAA was confirmed by 1H NMR spectrum and gel permeation chromatography. Transmission electron microscopy and dynamic light scattering were used to detect the self-assembly behavior of the amphiphilic diblock polymers in methanol.


2013 ◽  
Vol 46 (4) ◽  
pp. 1261-1267 ◽  
Author(s):  
Qi Zhang ◽  
Guoqiang Yu ◽  
Wen-Jun Wang ◽  
Haomiao Yuan ◽  
Bo-Geng Li ◽  
...  

2019 ◽  
Vol 553 ◽  
pp. 512-523 ◽  
Author(s):  
Hen Moshe Halamish ◽  
Jiří Trousil ◽  
Dmytro Rak ◽  
Kenneth D. Knudsen ◽  
Ewa Pavlova ◽  
...  

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