2003
DOI: 10.1016/s0014-3057(02)00334-8
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New architectures of poly(ethylene glycol) and poly(methylthiirane) in block copolymers

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Cited by 6 publications
(5 citation statements)
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“…The block copolymers were prepared as previously described , and fluorescently labeled as reported recently …”
Section: Methodsmentioning
confidence: 99%
“…The block copolymers were prepared as previously described , and fluorescently labeled as reported recently …”
Section: Methodsmentioning
confidence: 99%
“…The “living” nature of the episulfide ring‐opening anionic polymerisation makes it amenable to the preparation of complex macromolecular architectures, such as star114–116 or block117, 118 copolymers. This feature, together with its tolerance to a number of functional groups and environmental conditions, had made this polymerisation mechanism the most popular technique for producing well‐defined polysulfide‐based structures.…”
Section: Preparative Strategies For Polysulfidesmentioning
confidence: 99%
“…Since the main SEC peak of the crude product exhibits no shoulder at the relevant region where the PS arm elutes, the coupling was quantitatively. The coupling reaction was effected for 2 d at RT in the presence of 1 vol.-% DMEU (in pure THF, the coupling efficiency of thianions is low [37] ), which remarkably enhances the reactivity of lithium thiolates, and a catalytic amount of Bu 4 NBr, which accelerates the reaction by halogen exchange. [38] On the other hand, PtBMA-Li is unreactive against PSSiMe 2 CH 2 Cl precursor 3 (see Figure S2 in Supporting Information) at À20 8C.…”
Section: Synthesis Of Block Copolymersmentioning
confidence: 99%