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.
Domenici, F., Guazzelli, E., Masotti, E., Mahmoudi, N., Gabrielli, S., Telling, M., et al. (2021). Understanding the temperature-responsive self-assemblies of amphiphilic random copolymers by SANS in D2O Solution. MACROMOLECULAR CHEMISTRY AND PHYSICS, 222(5) [10.1002/macp.202000447].
Understanding the temperature-responsive self-assemblies of amphiphilic random copolymers by SANS in D2O Solution
Domenici F.
Investigation
;Paradossi G.
2021-01-01
Abstract
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.File | Dimensione | Formato | |
---|---|---|---|
macp.202000447.pdf
non disponibili
Tipologia:
Versione Editoriale (PDF)
Licenza:
Copyright dell'editore
Dimensione
1.14 MB
Formato
Adobe PDF
|
1.14 MB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.