Publication

Biphasic Hydrogenation over PVP Stabilized Rh Nanoparticles in Hydroxyl Functionalized Ionic Liquids

Paul Joseph Dyson, Lioubov Kiwi, Gabor Laurenczy, Zhaofu Fei, Ning Yan, Rocio Micaela Crespo Quesada, Yuehui Li, Xuemei Yang
2008
Journal Articles

Abstract

Polyvinylpyrrolidone stabilized rhodium nanoparticles are highly sol. in hydroxyl-functionalized ionic liqs., providing an effective and highly stable catalytic system. In hydrogenation reactions, excellent results were obtained, and transmission electron microscopy, soly. detns., and leaching expts. were employed to quantify the advantages of this catalytic system.

Official source

https://infoscience.epfl.ch/entities/publication/559e6335-0331-42f0-b2cc-7e213d973bd8

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Paul Joseph Dyson, Lioubov Kiwi, Gabor Laurenczy, Zhaofu Fei, Ning Yan, Rocio Micaela Crespo Quesada, Yuehui Li, Xuemei Yang
2008
Journal Articles

Abstract

Official source

https://infoscience.epfl.ch/entities/publication/559e6335-0331-42f0-b2cc-7e213d973bd8

About this result

Related concepts (21)

Asymmetric hydrogenation

Asymmetric hydrogenation is a chemical reaction that adds two atoms of hydrogen to a target (substrate) molecule with three-dimensional spatial selectivity. Critically, this selectivity does not come from the target molecule itself, but from other reagents or catalysts present in the reaction. This allows spatial information (what chemists refer to as chirality) to transfer from one molecule to the target, forming the product as a single enantiomer.

Hydrogenation

Hydrogenation is a chemical reaction between molecular hydrogen (H2) and another compound or element, usually in the presence of a catalyst such as nickel, palladium or platinum. The process is commonly employed to reduce or saturate organic compounds. Hydrogenation typically constitutes the addition of pairs of hydrogen atoms to a molecule, often an alkene. Catalysts are required for the reaction to be usable; non-catalytic hydrogenation takes place only at very high temperatures.

Transfer hydrogenation

In chemistry, transfer hydrogenation is a chemical reaction involving the addition of hydrogen to a compound from a source other than molecular . It is applied in laboratory and industrial organic synthesis to saturate organic compounds and reduce ketones to alcohols, and imines to amines. It avoids the need for high-pressure molecular used in conventional hydrogenation. Transfer hydrogenation usually occurs at mild temperature and pressure conditions using organic or organometallic catalysts, many of which are chiral, allowing efficient asymmetric synthesis.

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