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BACKGROUND Due to environmental concerns, there is a need to eliminate or drastically reduce the use of conventional organic solvents, as these are environmentally harmful. This paper reports on a novel one-pot synthesis of tetrabromoethylcyclohexane ( TBECH) in aqueous medium, using amino-functionalized ionic liquids, which catalyze the reaction and make it more environmentally friendly. RESULTS Compared with the traditional synthesis, tetrabromoethylcyclohexane is obtained with equivalent yield (90%), at room temperature, in a short reaction time (∼2 h compared with the previous 17 h) and with a strong reduction of the use of organic solvents; finally two isomers are obtained instead of four. Furthermore, a novel procedure to prepare the ionic liquids has been designed and two new ones have also been synthesised. The calculated environmental factors ( EFs), which measure the environmental sustainability, showed a strong reduction of the use of organic solvents for all syntheses of ionic liquids and TBECHs. CONCLUSIONS The excellent properties of amino-functionalized ionic liquids as solvents and catalysts for chemo- and diastereo-selective bromination of C  C bonds in water were confirmed with the synthesis of tetrabromoethylcyclohexane. Given the wide use of brominated compounds in the chemical industry, this procedure could be of wide interest. © 2015 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

New surface active ionic liquids (SAILs), based on cholinium cations and dodecylbenzenesulfonate as anion, have been synthesized and their potential application as antimicrobial colonization agents on cultural heritage (CH)stone materials investigated. The biocidal activity and antifouling capabilities were, preliminarily, evaluated by a screening on pure Gram (+) and Gram (−) bacteria strain cultures, yeasts, hyphomycetes and single-celled algae. Tests on stone materials (marble and tufa) vs. a stabilized community, constituted by a mixture of microbial strains, revealed that some SAILs display both antimicrobial and preventive antibiofilm action against new colonization. Analogous tests have been performed on the cholinium@halide precursors. [ABSTRACT FROM AUTHOR]

Abstract: Electron-rich and electron-poor alkenes have been dibrominated using a rapid and sustainable procedure. The reactions were conducted in aqueous medium and basic ionic liquids which catalyzed the direct addition of bromine. The protocol leads to remarkable results, high yields under mild conditions, complete chemo- and stereo-selectivity and allows the recycling of ionic liquids, reducing costs, and environmental impact. [Copyright &y& Elsevier]

Various alkenes such as (I), (III) and (V) are chemo- and diastereoselectively dibrominated in a mixture of water and basic ionic liquids, which catalyze the direct addition of bromine. [ABSTRACT FROM AUTHOR]