A novel linear cationic ABCBA pentablock terpolymer composed of a positively charged poly (3-acrylamidopropyl)
trimethyl ammonium chloride)) (PAMPTMA (+)) block at both ends and two thermoresponsive poly (Nisopropylacrylamide)
(PNIPAAM) blocks separated by a hydrophilic poly(ethylene glycol) (PEG) block was
synthesized via a “one-pot” atom transfer radical polymerization procedure (ATRP). The chemical composition
of the pentablock terpolymer was confirmed by nuclear magnetic resonance (NMR) and asymmetric flow fieldflow
fractionation (AFFFF). Depending on the polymer concentration in aqueous solution, this terpolymer forms
unimers and self-assembled structures at elevated temperatures. The effect of concentration and temperatureinduced
self-assembling behavior of the pentablock terpolymer in aqueous solution was examined by using
turbidimetry, shear viscosity, rheo-small angle light scattering (rheo-SALS), dynamic light scattering (DLS), and
small angle neutron scattering (SANS). The turbidity measurements demonstrated that the formation of intermicellar
structures and compaction of the complexes are function of both polymer concentration and temperature.
The viscosity and rheo-SALS experiments elucidated the intricate interplay between building-up and
breaking-up of interchain complexes under the influence of shear flow. The DLS experiments show the coexistence
of small entities and interchain complexes at low temperatures and the evolution of large intermicellar
structures at higher temperatures. At the highest temperatures, compaction of the complexes occurred. The
results from SANS revealed significant temperature-induced changes of the copolymer structure on a semi-local
dimensional scale.