Understanding the Temperature-Responsive Self-Assemblies of Amphiphilic Random Copolymers by SANS in D2O Solution

被引:8
|
作者
Domenici, Fabio [1 ,2 ]
Guazzelli, Elisa [3 ]
Masotti, Elena [3 ]
Mahmoudi, Najet [4 ]
Gabrielli, Sara [1 ,2 ]
Telling, Mark T. F. [4 ]
Martinelli, Elisa [3 ]
Galli, Giancarlo [3 ]
Paradossi, Gaio [1 ,2 ]
机构
[1] Univ Roma Tor Vergata, Dept Chem Sci & Technol, Viale Ric Sci, I-00133 Rome, Italy
[2] Ist Nazl Fis Nucl, Viale Ric Sci, I-00133 Rome, Italy
[3] Univ Pisa, Dept Chem & Ind Chem, Via G Moruzzi 13, I-56124 Pisa, Italy
[4] Rutherford Appleton Lab, STFC, ISIS Neutron & Muon Spallat Source, Chilton OX11 0QX, England
基金
英国科学技术设施理事会;
关键词
amphiphilic copolymers; nanoparticles; PEGMA‐ FA; small‐ angle neutron scattering;
D O I
10.1002/macp.202000447
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 behavior, in aqueous solution, of amphiphilic methacrylic random copolymers with perfluoroalkyl and polyoxyethylene side chains and the morphology of the resulting nanostructures are investigated by small-angle neutron scattering (SANS). The results allow to clarify the effect of temperature on the self-assembly features of copolymers and the structural morphology of both unimer single-chain entities and larger multi-chain aggregates of unimers. Shape, flexibility, and size of the aggregates are proved to be modulated by temperature and copolymer composition. The existence of three distinct phases of self-assembled structures is pointed out as a function of increasing temperature: 1) globular unimers; 2) coexistence of extended unimers and aggregates; and 3) aggregates, which overall show full reversibility in a wide range of copolymer concentrations.
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页数:7
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