Facile Synthesis of Tetra-Branched Tetraimidazolium and Tetrapyrrolidinium Ionic Liquids

[Image: see text] A facile synthetic route for tetra-branched tetraimidazolium and tetrapyrrolidinium ionic liquids was developed. In contrast to the previous synthetic scheme, the new synthetic route requires only three reaction steps instead of seven. The total yield of tetracation was also improved from 17–21 to 39–41%. Using the new synthetic scheme, four kinds of tetracations were synthesized from the combination of two cationic units (imidazolium and pyrrolidinium) and two counteranions [bis(fluorosulfonyl)imide (FSI) and bis(trifluoromethanesulfonyl)imide (TFSI)]. Basic physical properties including glass transition temperature, thermal decomposition temperature, density, viscosity, and ionic conductivity were determined. The counterion exchange from TFSI to FSI resulted in lower glass transition temperature and higher ionic conductivity. Tetrapyrrolidinium exhibited higher viscosity and lower ionic conductivity than tetraimidazolium. The counterion exchange from TFSI to FSI resulted in lower viscosity in the case of tetraimidazolium, while the opposite result was obtained in the case of tetrapyrrolidinium. Tetracations composed of ethyl imidazolium units, diethylene glycol spacers, and FSI counterions exhibited the highest ionic conductivity of 3.5 × 10(–4) S cm(–1) at 25 °C under anhydrous conditions. This is the best ionic conductivity in the tetracations ever reported.