2009
DOI: 10.1016/j.reactfunctpolym.2008.12.016
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Structural effect of a series of block copolymers consisting of poly(N-isopropylacrylamide) and poly(N-hydroxyethylacrylamide) on thermoresponsive behavior

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Cited by 25 publications
(12 citation statements)
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“…For example, the cloud point-increasing effect of the more hydrophilic PEG on the block and graft copolymers of PiPA has been well demonstrated[114][115][116][117][118][119], although the demixing temperature and kinetics have been reported to strongly depend on the polymer architecture and concentration, as T dem decreases significantly at high concentrations[120]. The effect of the relative block lengths on the LCSTs has also been demonstrated for other thermo-responsive block copolymers with a single LCST[121][122][123].Laschewsky and coworkers showed a shift in the CPs of dually thermo-responsive PnPA-b-PEA diblock copolymers according to the relative block lengths[124].When the relative length of the more hydrophilic PEA block increased upon changing the nPA:EA ratio from 2:1 to 1:1 and further to 1:3, the CP of the more hydrophobic PnPA block increased from 17 to 23 and then to 27 °C, respectively.The less pronounced CPs of the PEA block were in the range of 60−70 °C. The hydrophobic end group from CTA participated the aggregation process and its immobilization upon aggregation depended on whether it was attached to PnPA or PEA block.…”
mentioning
confidence: 91%
“…For example, the cloud point-increasing effect of the more hydrophilic PEG on the block and graft copolymers of PiPA has been well demonstrated[114][115][116][117][118][119], although the demixing temperature and kinetics have been reported to strongly depend on the polymer architecture and concentration, as T dem decreases significantly at high concentrations[120]. The effect of the relative block lengths on the LCSTs has also been demonstrated for other thermo-responsive block copolymers with a single LCST[121][122][123].Laschewsky and coworkers showed a shift in the CPs of dually thermo-responsive PnPA-b-PEA diblock copolymers according to the relative block lengths[124].When the relative length of the more hydrophilic PEA block increased upon changing the nPA:EA ratio from 2:1 to 1:1 and further to 1:3, the CP of the more hydrophobic PnPA block increased from 17 to 23 and then to 27 °C, respectively.The less pronounced CPs of the PEA block were in the range of 60−70 °C. The hydrophobic end group from CTA participated the aggregation process and its immobilization upon aggregation depended on whether it was attached to PnPA or PEA block.…”
mentioning
confidence: 91%
“…Poly(N-isopropylacrylamide) (PNIPA) is one of the most popular thermosensitive polymers, and undergoes a sharp conformational transition from a water-soluble random coil into water-insoluble globule forms at 32-34°C in aqueous solution [19][20][21][22]. To obtain MtPc catalysts that have a low aggregation tendency and can be recycled, our group has explored a general approach to the synthesis of polymeric MtPc catalysts by introducing a polymerizable N-acrylic carbonyl group into the side chains of cobalt tetraaminophthalocyanine (Co-APc) and then copolymerizing with N-isopropylacrylamide (NIPA) [23].…”
Section: Introductionmentioning
confidence: 99%
“…123 The structural basis of the thermoresponsive property of a series of block copolymers consisting of PNIPAM and poly(N-hydroxyethylacrylamide) (PHEAA) was elucidated by 1 H NMR measurements. 124 Thermosensitive and pegylated polyion complex micelles were formed by co-assembly of the oppositely and permanently charged block copolymers poly(sodium 2-acrylamido-2-methylpropanesulfonate)-bpoly(N-isopropylacrylamide), PAMPS-b-PNIPAM, and poly((3-acrylamidopropyl)-trimethylammonium chloride) (PAMPTMA)-b-PEO. These micelles were characterized by 1 H NMR, SLS, DLS, and TEM.…”
Section: Micelles In Amphiphile-solvent Systemsmentioning
confidence: 99%