In this review, the roles of room temperature ionic liquids (RTILs) and RTIL based solvent systems as proposed alternatives for conventional organic electrolyte solutions are described. Ionic liquids are introduced as well as the relevant properties for their use in electrochemistry (reduction of ohmic losses), such as diffusive molecular motion and ionic conductivity. We have restricted ourselves to provide a survey on the latest, most representative developments and progress made in the use of ionic liquids as electrolytes, in particular achieved by the cyclic voltammetry technique. Thus, the present review comprises literature from 2015 onward covering the different aspects of RTILs, from the knowledge of these media to the use of their properties for electrochemical processes. Out of the scope of this review are heat transfer applications, medical or biological applications, and multiphasic reactions.

The transformation of biomass and the utilization of all the by products derived from chemical conversion of biomass resources is one of the most important challenges nowadays. The impact in society and the level of awareness that already exists inside and outside the scientific community, makes the challenge of improving conversion of biomass to commodities a hot topic. Glycerol, a by-product obtained from the biodiesel production, is a key player compound due to its chemical versatility. The possibility of being used as solvent, reagent, reducing agent (in the polyol method), and so forth, makes glycerol an extremely appealing commodity. When used within nanotechnology, namely combined with nanomaterials, its potential becomes even higher. This review summarizes the work developed by the scientific community, during the last five years, in the use of glycerol with nano oxides. The analysis goes from the simple role of solvent to the oxidation of glycerol by nano oxides.

The catalytic activity of the iron(II) C-scorpionate complexes [FeCl₂{HC(pz)₃}] 1 (pz = pyrazol-1-yl) and [FeCl₂{HOCH₂C(pz)₃}] 2, and of their precursor FeCl₂·2H₂O 3, towards cyclohexane oxidation with tert-butyl hydroperoxide was evaluated and compared in different media: acetonitrile, ionic liquids (1-butyl-3-methylimidazolium hexafluorophosphate, [bmim][PF₆], and 1-butyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate, [bmim][FAP]), supercritical carbon dioxide (scCO₂), and scCO₂/[bmim][X] (X = PF₆ or FAP) mixtures. The use of such alternative solvents led to efficient and selective protocols for the oxidation of cyclohexane. Moreover, tuning the alcohol/ketone selectivity was possible by choosing the suitable solvent.

For the first time, a magnetic C-scorpionate catalyst was prepared from the iron(II) complex [FeCl₂{κ³-HC(pz)₃}] (pz = pyrazol-1-yl) and ferrite, using the sustainable mechanochemical synthetic procedure. Its catalytic activity for the cyclohexane oxidation with tert-butyl hydroperoxide (TBHP) was evaluated in different conditions, namely under microwave irradiation and under the effect of an external magnetic field. The use of such magnetic conditions significantly shifted the catalyst alcohol/ketone selectivity, thus revealing a promising, easy new protocol for tuning selectivity in important catalytic processes.