2015
DOI: 10.1016/j.eurpolymj.2015.05.013
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Mn2(CO)10-photomediated synthesis of poly(vinylidene fluoride)-b-poly(styrene sulfonate)

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Cited by 30 publications
(39 citation statements)
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References 77 publications
(100 reference statements)
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“…[273] The visible light-induced ITP using bifunctional alkyl and perfluoroalkyl iodides afforded telechelic poly(vinylidene fluoride)s with very high (> 95 %) iodide chain-end fidelity, which were further utilized for preparation of a series of ABA triblock copolymers containing vinyl acetate, tert-butyl acrylate, methyl methacrylate, isoprene, styrene, and acrylonitrile segments. [274][275][276] The influence of UV light on photomediated ITP was also investigated under various experimental conditions. [277] ITPs of butyl methacrylate with cyanopropyl iodide as chain transfer agent and a conventional initiator, AIBN, were conducted at 60 °C under dark conditions and in the presence of UV light.…”
Section: Insert Figure 32mentioning
confidence: 99%
“…[273] The visible light-induced ITP using bifunctional alkyl and perfluoroalkyl iodides afforded telechelic poly(vinylidene fluoride)s with very high (> 95 %) iodide chain-end fidelity, which were further utilized for preparation of a series of ABA triblock copolymers containing vinyl acetate, tert-butyl acrylate, methyl methacrylate, isoprene, styrene, and acrylonitrile segments. [274][275][276] The influence of UV light on photomediated ITP was also investigated under various experimental conditions. [277] ITPs of butyl methacrylate with cyanopropyl iodide as chain transfer agent and a conventional initiator, AIBN, were conducted at 60 °C under dark conditions and in the presence of UV light.…”
Section: Insert Figure 32mentioning
confidence: 99%
“…As expected, M n remained independent of conversion (M n ∼ 4−5000) with rather narrow PDI values of ∼1.3−1.5, partially attributable to MeOH precipitation of oligomers. 1,[39][40][41][42][43][44][45][46]53 Interestingly, both M n and the reaction rates…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…The melting points of the hard blocks containing either poly(ethylene-alt-CTFE) or poly(ethylene-alt-TFE) copolymers were 247 or 252 °C, respectively (Scheme 6.3). [46] They later employed this Mn 2 (CO) 10 -system to prepare well-defined sulfonated and fluorinated block copolymers for potential application in fuel cell membranes 222 Functional Polymers by Reversible Deactivation Radical Polymerisation: Synthesis and Applications by sequential copolymerisation of neopentyl styrene sulfonate and VDF [47]. Subsequently, they employed hypervalent iodide carboxylate, (CX 3 CO 2 ) 2 I III Ph, to develop a metal-free protocol in conjunction with external [I(CF 2 ) 6 I] and in situ generated (CF 3 I) iodinated CTA to achieve the RDRP of VDF and to produce poly(VDF)-b-poly(M) block copolymers [48] [where 'M' stands for styrene (S), butadiene, 2,2,2-trifluoroethyl methacrylate (TFEMA), and surprisingly methyl-2-(trifluoromethyl) acrylate], known not to homopolymerise under radical conditions [49].…”
Section: History and Production Of Copolymers Produced By Iodine Tranmentioning
confidence: 99%