Solvent-induced transformations of assemblies of structured ionizable block co-polymers
Abstract
Micelles formed by ionizable co-polymers are governed by both van der Waals and electrostatic forces. Slight tweaking of the solvent characteristics often drives large structural transformations. Here, the effects of modulating the electrostatic characteristics of solvents on polymeric assemblies formed by a co-polymer with ABCBA topology and an ionizable polystyrene sulfonate center (C) tethered to polyethylene propylene (B) end-capped by t-butyl styrene (A) are probed by small angle neutron scattering in cyclohexane/propanol solutions. With increasing propanol fraction, the spherical core–shell micelles, with the ionic block in their core, elongate and transition into large “swarms.” Surprisingly, as propanol becomes the major component of the solvent, reentrant spherical assemblies with a smaller polystyrene sulfonate core are formed. The propanol partitions across the interface between the core and the corona, affecting the polymer distribution in the corona and the core-corona boundary’s curvature, resulting in morphing of the shape of assemblies.
Article Details
Journal Info
The Journal of Chemical Physics
American Institute of Physics
Authors (7)
Manjula Senanayake
Department of Chemistry, Clemson University 1 , Clemson, South Carolina 29634,
Sidath Wijesinghe
Department of Chemistry, Clemson University 1 , Clemson, South Carolina 29634,
Supun S. Mohottalalage
Department of Chemistry, Clemson University 1 , Clemson, South Carolina 29634,
Chathurika Kosgallana
Department of Chemistry, Clemson University 1 , Clemson, South Carolina 29634,
Lilin He
Oak Ridge National Laboratory , , , ,
Carl L. Willis
Kraton Polymers US LLC 3 , 16400 Park Row, Houston, Texas 77084,
Dvora Perahia
Department of Chemistry, Clemson University 1 , Clemson, South Carolina 29634,