Polymerisation-Induced Self-Assembly of Graft Copolymers

被引:16
作者
Hakkinen, Satu [1 ]
Tanaka, Joji [1 ,2 ]
Maset, Ramon Garcia [2 ]
Hall, Stephen C. L. [1 ,3 ]
Huband, Steven [2 ]
Rho, Julia Y. [2 ]
Song, Qiao [2 ]
Perrier, Sebastien [1 ,4 ]
机构
[1] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
[2] Univ North Carolina Chapel Hill, Dept Chem, Chapel Hill, NC 27599 USA
[3] Rutherford Appleton Lab, ISIS Neutron & Muon Source, Didcot OX11 0QX, Oxon, England
[4] Univ Warwick, Warwick Med Sch, Coventry CV4 7AL, W Midlands, England
关键词
Graft Copolymer; PISA; Polymerization; RAFT; Self-Assembly; RAFT DISPERSION POLYMERIZATION; BLOCK-COPOLYMERS; NANO-OBJECTS; SOLVENTS; NANOPARTICLES; ARCHITECTURES; FORMULATION; VESICLES; GELS;
D O I
10.1002/anie.202210518
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the polymerisation-induced self-assembly of poly(lauryl methacrylate)-graft-poly(benzyl methacrylate) copolymers during reversible addition-fragmentation chain transfer (RAFT) grafting from polymerisation in a backbone-selective solvent. Electron microscopy images suggest the phase separation of grafts to result in a network of spherical particles, due to the ability of the branched architecture to freeze chain entanglements and to bridge core domains. Small-angle X-ray scattering data suggest the architecture promotes the formation of multicore micelles, the core morphology of which transitions from spheres to worms, vesicles, and inverted micelles with increasing volume fraction of the grafts. A time-resolved SAXS study is presented to illustrate the formation of the inverted phase during a polymerisation. The grafted architecture gives access to unusual morphologies and provides exciting new handles for controlling the polymer structure and material properties.
引用
收藏
页数:9
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