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Acidic ionic liquid, [(Py) 2 SO][HSO 4 ] 2 has been used as an efficient catalyst for the reaction of ketone with thiosemicarbazide in ethanol at room temperature for the eco-friendly synthesis of spiro-1,2,4-triazolidine-3-thiones. Smooth reactions, ambient temperature, use of alcohol as a solvent, high yields, easy workup procedure and excellent recyclability of ionic liquid and high atom economy are the auxiliary advantages of the present protocol, which makes it ecofriendly. All the synthesized 1,2,4-trioazoles were screened for antimicrobial activity. Most of compounds displayed moderate to good biological activity.

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In situ coalescence of copper on polymer supported ascorbate functionalized task specific ionic liquid, acts as an efficient catalyst for Huisgen 1,3 dipolar cycloaddition.

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A new task specific ionic liquid with hydroxyl and prolinate functionalities acts as a reducing agent and serves as a ligand and stabilizer for in situ formed palladium nanoparticles. This system displays high catalytic activity for Suzuki–Miyaura cross-coupling in water.

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