Abstract
In this paper, we present facile synthetic strategies enabling production of well-defined poly(ionic liquids) PILs based on 1-vinyl-4-benzyl-3-methylimidazolium- (VBIm) and 1-vinyl-4-benzyl-3-methylpyrrolidium (VBPy) ionic liquids (IL) possessing different counterions (chloride Cl−vs. bis(trifluoromethanesulfonyl)imide NTf2-) (VBIm/NTf2,VBIm/Cl, VBPy/NTf2,VBPy/Cl). The reaction routes have been selected to design two types of polyelectrolytes i) linear homopolymers showing solid-like behavior and ii) grafted copolymers composing of poly(siloxane) segments extended with analogous ionic domains that shows gel-like behavior. The former one has been produced via controlled radical polymerization methods (CRP) such as atom transfer radical polymerization (ATRP) or reversible addition fragmentation chain-transfer polymerization (RAFT), whereas the second one using thiol-ene coupling photo-polymerization. It was found that the glass transition temperature, Tg, of the synthesized herein linear homopolymer-based systems (both VBIm/NTf2 and VBPy/NTf2- -based) increases with their molecular weight, Mn, similarly as reported for its N-conjugated analogs described in our previous study [Maksym et al.,Polym. Chem., 2017, 8, 5433]. However, they are characterized by markedly lower conductivity, σdc (σdc~10−15 S/cm vs.σdc~10−16S/cm for PVBIm/NTf2vs. PVBPy/NTf2- at Tg determined from calorimetric experiments) when compared to N-conjugated one (σdc~10−9 S/cm for poly(N-vinyl-imidazole)/NTf2). Interestingly, the ionic conductivity value at Tg of grafted is similar to its corresponding linear analogs. Nevertheless, at T = 293K both anhydrous linear and grafted imidazolium-based PILs are characterized by high σdc, reaching values σdc~10−4S/cm and σdc~10−7S/cm, respectively.
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