ABSTRACT
The behavior in aqueous solution of the doubly-grafted anionic polyelectrolyte poly(sodium 2-acrylamido-2-methylpropanesulfonate-co-sodium acrylate-)-g-poly(N-isopropylacry-lamide)-g-poly(N,N-dimethylacrylamide), P(AMPSNa-co-ANa)-g-PNIPAM-g-PDMAM, was compared to that of the single-grafted anionic polyelectrolyte poly(sodium 2-acrylamido-2-methylpropanesulfonate-co-sodium acrylate)-g-poly(N-isopropylacrylamide), P(AMPSNa-co-ANa)-g-PNIPAM. The investigation through turbidimetry, pyrene fluorescence probing, viscometry and dynamic light scattering revealed that the existence of the hydrophilic poly(N,N-dimethylacrylamide), PDMAM, side chains in the doubly-grafted copolymer P(AMPSNa-co-ANa)-g-PNIPAM-g-PDMAM did not perturb the thermoresponsiveness of the poly(N-isopropylacrylamide), PNIPAM, side chains, but favoured the stabilization in water of the core-corona nanoparticles, formed upon heating the aqueous solution above the Lower Critical Solution Temperature (LCST) of PNIPAM chains. In a similar manner, the complexes formed between the cationic surfactant N,N,N,N-dodecyltrimethylammonium chloride, DTAC, and the oppositely charged backbone of the doubly-grafted copolymer P(AMPSNa-co-ANa)-g-PNIPAM-g-PDMAM were stabilized in water by the PDMAM side chains. Thus, phase separation was prevented upon heating the aqueous solution above LCST. Moreover, the (1)H NMR study revealed that the fraction of PNIPAM chains forming solid-like aggregates at high temperature increased substantially in the presence of DTAC, as a consequence of the net charge decrease of the backbone due to the polymer/DTAC complexation.
