Creation of dense polymer brush layers by the controlled deposition of an amphiphilic responsive comb polymer

被引:12
|
作者
Tomlinson, Michael R. [1 ]
Cousin, Fabrice [2 ]
Geoghegan, Mark [1 ]
机构
[1] Univ Sheffield, Dept Phys & Astron, Sheffield S3 7RH, S Yorkshire, England
[2] CE Saclay, CEA CNRS, Lab Leon Brillouin, UMR12, F-91191 Gif Sur Yvette, France
关键词
Combs; Brushes; Stars; TRANSFER RADICAL POLYMERIZATION; AIR-WATER-INTERFACE; MOLECULAR-WEIGHT DISTRIBUTION; DIBLOCK COPOLYMER MONOLAYERS; ATOMIC-FORCE MICROSCOPY; AIR/WATER INTERFACE; BLOCK-COPOLYMERS; STAR POLYMER; SURFACE; CHAIN;
D O I
10.1016/j.polymer.2009.05.021
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We introduce a copolymer with a comb topology that has been engineered to assemble in a brush configuration at an air-water interface. The molecule comprises a 6.1 kDa poly(methyl methacrylate) backbone with a statistical amount of poly[2-(dimethyl amino)ethyl methacrylate] polybase side chains averaging 2.43 per backbone.. Brush layers deposited with the hydrophobic PMMA backbone adsorbed to hydrophobized silicon are stable in water even when stored at pH values less than 2.0 for over 24 h. The use of a Langmuir trough allows a simple controlled deposition of the layers at a variety of grafting densities. Depth profiling of brush layers was performed using neutron reflectometry and reveals a significant shifting of the responsiveness of the layer upon changing the grafting density. The degree of swelling of the layers at a pH value of 4 (below the pK(b)) decreases as grafting density increases. Lowering the pH of the subphase during deposition causes the side chains to become charged and more hydrophilic extending to a brush-like configuration while at neutral pH the side chains lie in a "pancake" conformation at the interface. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4829 / 4836
页数:8
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