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Miktoarm star polymers with poly(N-isopropylacrylamide) or poly(oligo(ethylene glycol) methacrylate) as building blocks: synthesis and comparison of thermally-responsive behaviors
writer:Cheng-guang Mu, Xiao-dong Fan,* Wei Tian,* Yang Bai and Xiang Zhou
keywords:Miktoarm star polymers,poly(N-isopropylacrylamide),poly(oligo(ethylene glycol) methacrylate)
source:期刊
specific source:Polym. Chem., 2012, 3, 1137
Issue time:2012年

We synthesized two thermally-responsive miktoarm star polymers in which poly(Nisopropylacrylamide) (PNIPAM) or poly(oligo(ethylene glycol) methacrylate) (POEGMA) served as the thermosensitive building blocks. Firstly, linear methoxypolyethylene glycol (PEG) with β-cyclodextrin (β-CD) bearing about six chlorines as a terminal (PEG-CD-Clx, x z 6) was synthesized. Then, the thermally-responsive miktoarm star polymer, PEG-CD-PNIPAMx or PEGCD-POEGMAx, was achieved by atom transfer radical polymerization using N-isopropylacrylamide
or oligo(ethylene glycol) methacrylate as the monomer and PEG-CD-Clx as the macroinitiator. The obtained miktoarm star polymers were comprised of a β-CD core, a PEG arm and about six PNIPAM or POEGMA arms. Furthermore, the thermally-responsive behaviors of the miktoarm star polymers were investigated by a combination of UV-vis spectroscopy, DLS, TEM, 1H NMR, fluorescence spectroscopy and DCS. Above the LCST of the polymers in aqueous solution, PEGCD-PNIPAMx can self-assemble into nano-structures with PNIPAM as the core and PEG as the corona, whereas PEG-CD-POEGMAx self-assembled into nano-architectures possessing hydrophilic surfaces which were constructed by the hydrated oligo(ethylene glycol) side chains of the POEGMA arms. The hydrophobic moiety of the nano-architectures was formed by the methacrylate backbone and the dehydrated oligo(ethylene glycol) side chains of POEGMA. Furthermore, it was
found that the thermally-induced dehydration of PEG-CD-PNIPAMx is completely different from that of PEG-CD-POEGMAx. For the former, the dehydration occurs abruptly and intensively near the LCST of PEG-CD-PNIPAMx, whereas the dehydration for the latter is gradual and continuous throughout the whole temperature rise. The architecture of the nano-assemblies formed by PEGCD-
PNIPAMx or PEG-CD-POEGMAx was affected by the thermally-induced dehydration of the polymers.