期刊
POLYMER CHEMISTRY
卷 8, 期 22, 页码 3485-3496出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7py00508c
关键词
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资金
- National Science Foundation [21525419]
- National Science Foundation of China [21474054]
- Ministry of Science and Technology of the People's Republic of China [2016YFA0202503]
- PCSIRT [IRT1257]
Well-defined 4-arm star block copolymer nanospheres of [poly(N-isopropylacrylamide)-block-polystyrene](4) [(PNIPAM-b-PS)(4)] containing a hydrophobic core of the polystyrene (PS) block and a thermo-responsive corona of the 4-arm star poly(N-isopropylacrylamide) (PNIPAM) were prepared by dispersion RAFT polymerization employing a tetrafunctional macro-RAFT agent of tetra(trithiocarbonate)-terminated poly(N-isopropylacrylamide) [(PNIPAM-TTC)(4)]. The size of the 4-arm star (PNIPAM-b-PS)(4) nanospheres increases with the increasing degree of polymerization (DP) of the PS block, whereas it decreases with the DP of the star PNIPAM increasing. A comparison between the 4-arm star (PNIPAM-b-PS)(4) nanospheres and the linear poly(N-isopropylacrylamide)-block-polystyrene (PNIPAM-b-PS) nanospheres is made. It is found that the 4-arm star (PNIPAM-b-PS)(4) nanospheres and the linear PNIPAM-b-PS nanospheres have a similar particle size when the DPs of the PS and PNIPAM blocks in the star and linear block copolymers are close to each other. Interestingly, the topology of PNIPAM is found to exert influence on its thermo-responsive phase transition, and the (PNIPAM(122)-b-PS110)(4) 4-arm star block copolymer nanospheres have a lower critical solution temperature (LCST) lower than the PNIPAM(118)-b-PS125 linear block copolymer nanospheres. At temperatures above LCST of the (PNIPAM(122)-b-PS110)(4) nanospheres, the 4-arm star PNIPAM chains deposit on the PS core to form raspberry-like nanospheres, in which the dehydrated 4-arm star PNIPAM chains form dispersed microdomains on the PS core. This synthesis of (AB)(4) 4-arm star block copolymer nano-assemblies is believed to be efficient and is helpful to study how the topology of PNIPAM affects the thermo-responsive phase transition.
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