2001
DOI: 10.1021/ma0108057
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New Synthetic Methodologies for Amphiphilic Multiblock Copolymers of Ethylene Glycol and Propylene Sulfide

Abstract: A new one pot synthetic method has been developed for preparing amphiphilic block copolymers. The method makes use of episulfide anionic polymerization for generating symmetric or asymmetric tri- or multiblock copolymers with living mechanism. Important features of the method are (a) the use of in situ generated thiolates, which ensures reproducibility in the initiator concentration; (b) the mild character of the reactive species; therefore, also sensitive bioactive groups could be easily incorporated into the… Show more

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Cited by 141 publications
(140 citation statements)
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“…The 'one pot' character of the synthesis [34] allows the use of the method by operators with limited skill in organic synthesis. No traces of toxic reagents or solvents are left after the purification.…”
Section: Peg-pps Vesicles Filaments and Micellesmentioning
confidence: 99%
“…The 'one pot' character of the synthesis [34] allows the use of the method by operators with limited skill in organic synthesis. No traces of toxic reagents or solvents are left after the purification.…”
Section: Peg-pps Vesicles Filaments and Micellesmentioning
confidence: 99%
“…These include the shell crosslinked, disulfide based cystamine-containing triblock copolymer micelles, the polymer micelles with shells crosslinked via thiol-reducible disulfide bonds and also the block copolymers with hydrophilic PEG tethered to hydrophobic poly(propylene sulfide) via a disulfide bridge [2,[20][21][22][23][24].…”
Section: Redox/thiol Responsive Polymersmentioning
confidence: 99%
“…Disulfide can be converted to thiols by exposure to various reducing agents and/or undergo disulfide exchange in the presence of other thiols (Reproduced with kind permission from Reference [2]). [2,[20][21][22][23][24] Disulfide based cystamine-containing triblock copolymer micelles that were shell crosslinked Block copolymers with hydrophilic PEG tethered to hydrophobic poly(propylene sulfide) via a disulfide bridge…”
Section: Redox/thiol-responsivementioning
confidence: 99%
“…1,2 Among these copolymers, stimuliresponsive copolymers are of particular importance, because of their promising potential applications in biomedicine. Recently, considerable efforts were devoted to the development of new polymers which were responsive to various internal and external stimuli, such as pH, [3][4][5][6] temperature, [7][8][9] light, [10][11][12] as well as voltage.…”
mentioning
confidence: 99%
“…After a welldefined characterization for the diblock copolymer structures via FTIR, 1 H NMR and SEC/MALLS, the self-assemble behaviors and the pH-triggered phase transition processes were investigated using UV-vis spectroscopy, DLS, SLS, TEM and fluorescence spectrophotometer.…”
mentioning
confidence: 99%