4.3 Article

Temperature and anion responsive self-assembly of ionic liquid block copolymers coating gold nanoparticles

Journal

FRONTIERS OF MATERIALS SCIENCE
Volume 10, Issue 2, Pages 178-186

Publisher

HIGHER EDUCATION PRESS
DOI: 10.1007/s11706-016-0334-z

Keywords

block copolymer; dual stimuli-responsive; gold nanoparticles (Au NPs); self-assembly

Funding

  1. National Natural Science Foundation of China [51103035, 51403055]

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In this paper, double hydrophilic ionic liquid block copolymers (ILBCs), poly poly[1-methyl-3-(2-methacryloyloxy propylimidazolium bromine)]-block-(N-isopropylacrylamide) (PMMPImB-b-PNIPAAm) was first synthesized by reversible addition-fragmentation chain transfer (RAFT) and then attached on the surface of gold nanoparticles (Au NPs) via a strong gold-sulfur bonding for preparing hybrid nanoparticles (PMMPImB-b-PNIPAAm-@-Au NPs). The hybrid NPs had a three layers micelle-like structure, including a gold core, thermo-responsive inner shell and anion responsive outer corona. The self-assembling behavior of thermal-and anion-response from shell and corona were respectively investigated by change of temperature and addition of (CF3SO2)(2)N-. The results showed the hybrid NPs retained a stable dispersion beyond the lower critical solution temperature (LCST) because of the space or electrostatic protecting by outer PMMPImB. However, with increasing concentration of (CF3SO2)(2)N-, the micellization of self-assembling PMMPImB-b-PNIPAAm-@-Au NPs was induced to form micellar structure containing the core with hydrophobic PMMPImB(CF3SO2)(2)N- surrounded by composite shell of Au NPs-PNIPAAm via the anion-responsive properties of ILBCs. These results indicated that the block copolymers protected plasmonic nanoparticles remain self-assembling properties of block copolymers when phase transition from outer corona polymer.

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