Abstract
Poly(N-isopropylacrylamide) (PNIPAM)-based tetrafunctional atom transfer radical polymerization (ATRP) macroinitiator (1b) was synthesized via addition reaction of mono-amino-terminated PNIPAM (1a) with glycidol, followed by esterification with excess 2-bromoisobutyryl bromide. Well-defined double hydrophilic miktoarm AB4 star copolymer, PNIPAM-b-(PDEA)4, was then synthesized by polymerizing 2-(diethylamino)ethyl methacrylate (DEA) via ATRP in 2-propanol at 45 degrees C using 1b, where PDEA was poly(2-(diethylamino)ethyl methacrylate). For comparison, PNIPAM-b-PDEA linear diblock copolymer with comparable molecular weight and composition to that of PNIPAM-b-(PDEA)4 was prepared via reversible addition-fragmentation chain transfer (RAFT) polymerization. The pH- and thermoresponsive "schizophrenic" micellization behavior of the obtained PNIPAM65-b-(PDEA63)4 miktoarm star and PNIPAM70-b-PDEA260 linear diblock copolymers were investigated by 1H NMR and laser light scattering (LLS). In acidic solution and elevated temperatures, PNIPAM-core micelles were formed; whereas at slightly alkaline conditions and room temperature, structurally inverted PDEA-core micelles were formed. The size of the PDEA-core micelles of PNIPAM65-b-(PDEA63)4 is much smaller than that of PNIPAM70-b-PDEA260. Furthermore, the pH-induced micellization kinetics of the AB4 miktoarm star and AB block copolymers were investigated by the stopped-flow light scattering technique upon a pH jump from 4 to 10. Typical kinetic traces for the micellization of both types of copolymers can be well fitted with double-exponential functions, yielding a fast (tau1) and a slow (tau2) relaxation processes. tau1 for both copolymers decreased with increasing polymer concentration. tau2 was independent of polymer concentration for PNIPAM65-b-(PDEA63)4, whereas it decreased with increasing polymer concentration for PNIPAM70-b-PDEA260. The chain architectural effects on the micellization properties and the underlying mechanisms were discussed in detail.
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