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

In this paper, double hydrophilic ionic liquid block copolymers (ILBCs), poly poly[1-methyl-3-(2-methacryloyloxy propylimidazolium bromine)]-block-(N.isopro. pylacrylamide) (PMMPImB-b-PNIPAAm) was first synthesized by reversible addition- fragmentation chain transfer (RAFT) and then attached on the...

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Bibliographic Details
Published inFrontiers of materials science Vol. 10; no. 2; pp. 178 - 186
Main Authors LI, Junbo, ZHAO, Jianlong, WU, Wenlan, LIANG, Ju, GUO, Jinwu, ZHOU, Huiyun, LIANG, Lijuan
Format Journal Article
LanguageEnglish
Published Beijing Higher Education Press 01.06.2016
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Summary:In this paper, double hydrophilic ionic liquid block copolymers (ILBCs), poly poly[1-methyl-3-(2-methacryloyloxy propylimidazolium bromine)]-block-(N.isopro. pylacrylamide) (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)2N-. 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 PMMPImBo However, with increasing concentration of (CF3SO2)2N-, the micellization of self-assembling PMMPImB-b-PNIPAAm-@-Au NPs was induced to form micellar structure containing the core with hydrophobic PMMPImB- (CF3SO2)2N- 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 copoly- mers when phase transition from outer corona polymer.
Bibliography:block copolymer; dual stimuli-responsive; gold nanoparticles (Au NPs);self-assembly
11-5985/TB
In this paper, double hydrophilic ionic liquid block copolymers (ILBCs), poly poly[1-methyl-3-(2-methacryloyloxy propylimidazolium bromine)]-block-(N.isopro. pylacrylamide) (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)2N-. 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 PMMPImBo However, with increasing concentration of (CF3SO2)2N-, the micellization of self-assembling PMMPImB-b-PNIPAAm-@-Au NPs was induced to form micellar structure containing the core with hydrophobic PMMPImB- (CF3SO2)2N- 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 copoly- mers when phase transition from outer corona polymer.
Document received on :2015-12-21
self-assembly
Document accepted on :2016-02-29
dual stimuli-responsive
block copolymer
gold nanoparticles (Au NPs)
ISSN:2095-025X
2095-0268
DOI:10.1007/s11706-016-0334-z