Stimuli-Responsive Aggregation of High Molar Mass Poly(N,N-Diethylacrylamide)-b-Poly(4-Acryloylmorpholine) in Tetrahydrofuran

被引:5
作者
Plucinski, Alexander [1 ]
Pavlovic, Marko [2 ,3 ]
Clarke, Mairi [4 ]
Bhella, David [4 ]
Schmidt, Bernhard V. K. J. [1 ]
机构
[1] Univ Glasgow, Sch Chem, Glasgow G12 8QQ, Lanark, Scotland
[2] Max Planck Inst Colloids & Interfaces, Dept Colloid Chem, Muhlenberg 1, D-14476 Potsdam, Germany
[3] Univ Glasgow, Scottish Ctr Macromol Imaging, Glasgow G61 1QH, Lanark, Scotland
[4] Univ Novi Sad, BioSense Inst, Dr Zorana Djindjica 1,3-8, Novi Sad 21000, Serbia
基金
瑞士国家科学基金会; 英国医学研究理事会;
关键词
block copolymers; high molecular weight; reversible deactivation radical polymerization; self-assembly; stimuli responsive polymers; BLOCK; MICELLES; POLYMERIZATION; NANOPARTICLES; TEMPERATURE; COPOLYMERS; POLYMERS;
D O I
10.1002/marc.202100656
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The self-assembly of block copolymers constitutes a timely research area in polymer science with implications for applications like sensing or drug-delivery. Here, the unprecedented aggregation behavior of high molar mass block copolymer poly(N,N-diethylacrylamide)-b-poly(4-acryloylmorpholine) (PDEA-b-PAM) (M-n>400 kg mol(-1)) in organic solvent tetrahydrofuran (THF) is investigated. To elucidate the aggregation, dynamic light scattering, cryo-transmission electron microscopy, and turbidimetry are employed. The aggregate formation is assigned to the unprecedented upper critical solution temperature behavior of PAM in THF at elevated concentrations (> 6 wt.%) and high molar masses. Various future directions for this new thermo-responsive block copolymer are envisioned, for example, in the areas of photonics or templating of inorganic structures.
引用
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页数:5
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