| Abstract |
Phenanthrene alpha-end-labeled poly(N-decylacrylamide-b-N,N-diethylacrylamide) (PDcA(n)-b-PDEA(m)) block copolymers consisting in a highly hydrophobic block (n = 11) and a thermo responsive block with variable length (79 <= m <= 468) were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization. A new phenanthrene-labeled chain transfer agent (CTA) was synthesized and used to control the RAFT polymerization of a hydrophobic acrylamide derivative, N-decylacrylamide (DcA). This first block was further used as macroCTA to polymerize N,N-diethylacrylamide (DEA) in order to prepare diblock copolymers with the same hydrophobic block of PDcA (number average molecular weight: M-n = 2720 g mol(-1), polydispersity index: M-w/M-n = 1.13) and various PDEA blocks of several lengths M-n = 10,000-60,000 g mol(-1)) with a very high blocking efficiency. The resulting copolymers self-assemble in water forming thermoresponsive micelles. The critical micelle concentration (CMC) was determined using Forster resonance energy transfer (FRET) between phenanthrene linked at the end of the PDcA block and anthracene added to the solution at a low concentration (10(-5) M), based on the fact that energy transfer only occurs when phenanthrene and anthracene are located in the core of the micelle. The CMC (similar to 2 mu M) was obtained at the polymer concentration where the anthracene fluorescence intensity starts to increase. The size of the polymer micelles decreases with temperature increase around the lower critical solution temperature of PDEA in water (LCST similar to 32 degrees C) owing to the thermoresponsiveness of the PDEA shell. (C) 2009 Elsevier Ltd. All rights reserved. |
