A general strategy for the synthesis of arylthio cyclopropyl carbaldehydes and ketones via acid catalysed arylthiol addition/ring contraction reaction sequence has been exploited. The procedure led to a wide panel of cyclopropyl carbonyl compounds in high yields and broad substrate scope.

It is not the first time in human history, nor will it be the last for that matter, that a collective problem calls for a collective response. Climate change fueled by greenhouse emissions affects humankind alike. Despite the disagreement among policymakers and scientists on the severity of the issue, the truth is that the problem remains. A broad look at different technologies being used today in different fields has led to the idea of bringing them together in an attempt to offer a viable solution to reducing anthropogenic CO 2 . The following paper describes how the nanotechnologies, available or soon to be available, would make CO 2 capture, cache, and conversion (coined the three Cs) a valid way for achieving a more sustainable energy society. Authors also set out to highlight with this work how knowledge transfer is instrumental in the development of technology and how methodical assessment of crossovers can expedite research when time plays against us.

The acid-promoted syntheses of 2-(benzyloxy)cyclobutanones and bis(benzyloxy)dioxatricyclo decanes were achieved starting from 2-hydroxycyclobutanone and variously functionalized benzyl alcohols. The reaction sequences afforded the desired products in good to high yields and in a solvent-dependent chemoselective fashion.

Membranes with high CO2 solubility are essential for developing a separation technology with low carbon footprint. To this end, physical blend membranes of [BMIM][Ac] and [BMIM][Succ] as Ionic Liquids (ILs) and PIM-1 as the polymer were prepared trying to combine the high permeability properties of PIM-1 with the high CO2 solubility of the chosen ILs. Membranes with a PIM-1/[BMIM][Ac] 4/1 ratio nearly double their CO2 solubility at 0.8 bar (0.86 cm3 (STP)/cm3 cmHg), while other ratios still maintain similar solubilities to PIM-1 (0.47 cm3 (STP)/cm3 cmHg). Moreover, CO2 permeability of PIM-1 /[BMIM][Ac] blended membranes were between 1050 and 2090 Barrer for 2/1 and 10/1 ratio, lower than PIM-1 membrane, but still highly permeable. The here presented self-standing and mechanically resistant blend membranes have yet a lower permeability compared to PIM-1 yet an improved CO2 solubility, which eventually will translate in higher CO2/N2 selectivity. These promising preliminary results will allow us to select and optimize the best performing PIM-1 /ILs blends to develop outstanding membranes for an improved gas separation technology.

Graphene is a 2D carbon material with peculiar features such as high electrical conductivity, high thermal conductivity, mechanical stability, and a high ratio between surface and thickness. Applications are continuously growing, and the possibility of dispersing graphene in low-boiling green solvents could reduce its global environmental impact. Pristine graphene can be dispersed in high concentration only in polar aprotic solvents that usually have high boiling points and high toxicity. For this reason, the oxidized form of graphene is always used, as it is easier to disperse and to subsequently reduce to reduced graphene oxide. However, compared to pristine graphene, reduced graphene oxide has more defects and has inferior properties respect to graphene. In this work, the polymerization of (diethyl maleate derivate) on graphene obtained by sonication was performed in a microwave reactor. The obtained material has good stability in ethanol even after a long period of time, therefore, it can be used to deposit graphene by mass production of inks or by casting and easy removal of the solvent. The thermal annealing by heating at 300–400 °C in inert atmosphere allows the removal of the polymer to obtain pristine graphene with a low number of defects.