Abstract
The first copper(0) mediated controlled radical polymerization (CRP) of methyl methacrylate (MMA) toward CF bonds onto poly(vinylidene fluoride) (PVDF) is reported with rather high activity. By avoiding the halogen exchange, Cu0 instead of CuI complexes utilized as catalyst is responsible for the significantly improved polymerization activity. Using FH decoupled nuclear magnetic resonance technique, the grafting sites onto PVDF are finely located. From this, detailed topologic information including the grafting density, average length of each side chain, along with the overall grafted content of PMMA, is detected by tracking the polymerization as a function of time. This work offers not only a facile CRP strategy based on inactive CF bonds but also a deep insight into the cleavage of F-bearing compounds in organic chemistry.
The first copper(0) mediated controlled radical polymerization of methyl methacrylate toward CF bonds onto poly(vinylidene fluoride) (PVDF) with rather high activity is reported. This method may provide a facile strategy to prepare PVDF-based graft copolymers.
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