Related Experiment Video
Updated: Sep 19, 2025

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction
Published on: August 23, 2018
Selective Chemo-Divergent Hydrogenation of Ethylene Carbonate Enabled by Multi-Functional Poly(Ionic
Joan Vignolle1,2, Wenjuan Wang2, Thierry Tassaing1
1University of Bordeaux, CNRS, Bordeaux INP, Laboratoire de Chimie des Polymères Organiques (LCPO), UMR 5629, 16 Av. Pey Berland, Pessac cedex, 33607, France.
None:
Cyclic carbonates, in particular ethylene carbonate (EC), are pivotal compounds across chemical sciences because of their unique properties. Although, their transformation into valuable products has attracted great attention, efficient and selective transformations remain challenging. In this work, we report a catalytic system composed of Ru nanoparticles (RuNPs) stabilized by poly(ionic liquids) (Ru@PIL), that enables the selective chemo-divergent hydrogenation of EC into either EtOH and CO2 or EG and CH4, under solvent-free conditions. Those transformations relied on the multi-task ability of poly(ionic liquids) (PILs), which provides efficient electro-steric protection of the NPs, good solubility in neat carbonates, and organocatalytic activity depending on the nature of the PIL counter-anions. Hence, PIL incorporating nucleophilic anions, such as I-, triggers the cascade transformation of EC into EtOH via a sequential decarboxylation-hydrogenation process. Conversely, in the presence of non-nucleophilic anions, the PIL is catalytically a spectator, yielding to the "direct hydrogenation" of EC by the RuNPs.
More Related Videos
06:46Facile Preparation of 2Z,4E-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
12:08Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Regioselectivity of Electrophilic Additions-Peroxide Effect
Regioselectivity of Electrophilic Additions to Alkenes: Markovnikov's Rule
The hydrohalogenation of an unsymmetrical alkene can yield two haloalkane products, depending on which vinylic carbon takes up the halogen. However, one product usually predominates, where hydrogen adds to the vinylic carbon bearing the...
Radical Anti-Markovnikov Addition to Alkenes: Overview