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Molecular Dynamics of Amphiphilic Random Copolymers in the Bulk: A 1 H and 19 F NMR Relaxometry Study
Author(s) -
Martini Francesca,
Guazzelli Elisa,
Martinelli Elisa,
Borsacchi Silvia,
Geppi Marco,
Galli Giancarlo
Publication year - 2019
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201900177
Subject(s) - copolymer , polymer chemistry , side chain , atom transfer radical polymerization , ethylene glycol , amphiphile , methacrylate , acrylate , relaxometry , materials science , polymerization , chemistry , polymer , organic chemistry , medicine , spin echo , magnetic resonance imaging , radiology
A set of amphiphilic random copolymers of poly(ethylene glycol) methacrylate (PEGMA) and perfluorohexylethyl acrylate (FA) with different compositions synthesized by atom transfer radical polymerization (ATRP) is investigated by 1 H and 19 F NMR relaxometry. In particular, a thorough investigation of T 1 and T 2 relaxation times at variable temperature and copolymer composition provides the first complete and detailed characterization of the dynamics of both the main chain backbone and the side chains of the PEGMA‐ co ‐FA copolymers. The results highlight an intramolecular segregation of rigid main chain and mobile side chains, and an additional self‐assembling of the PEGMA and FA side chains into distinct nanodomains, driven by the hydrophobic interactions between FA side chains. The obtainment and observation of nanoscale phase separation in random copolymers is a promising achievement to the aim of controlling self‐assembly in the bulk by suitably modulating copolymers composition, which can open novel avenues to easier fabrications and applications in nanotechnologies.