Characterization of pH-dependent micellization of polystyrene-based cationic block copolymers prepared by reversible addition-fragmentation chain transfer (RAFT) radical polymerization

Abstract

A series of block copolymers composed of a fixed length of an ( ar-vinylbenzyl)trimethylammonium chloride ( Q) block (the number average degree of polymerization of the Q block, DP n,Q=57) and varying lengths of an N, N-dimethylvinylbenzylamine ( A) block (the number average degrees of polymerization of the A blocks, DP n,A, ranging 11–50) were prepared by reversible addition-fragmentation chain transfer (RAFT) radical polymerization, and their pH-dependent micellization was characterized by potentiometric titration, 1H NMR spectroscopy, dynamic and static light scattering, and fluorescence techniques as a function of the A block length. At pH<5.5, the A block is fully protonated, and hence the block copolymers act as a simple polyelectrolyte, dissolving molecularly in acidic water. At pH>7, the A block becomes deprotonated, and thereby the block copolymers aggregate into a micelle composed of hydrophobic microdomains formed from the deprotonated A blocks. Results of light scattering and fluorescence measurements indicated that the micellization behavior depended strongly on the length of the A block. The number of polymer chains comprising one micelle (i.e. mean aggregation number, N agg) increased from 3 to 12 as DP n,A increased from 11 to 50 at pH 10.0. In the case of a random copolymer of Q and A with an A/ Q molar ratio similar to that of a block copolymer with DP n,A=50, N agg∼1 (i.e. unimolecular micelle) was confirmed by static light scattering at pH 10.0.