Koen Binnemans
Katholieke Universiteit Leuven
684 Papers
4.8K Citations
Koen Binnemans is an academic researcher from Katholieke Universiteit Leuven. The author has contributed to research in topics: Ionic liquid & Chemistry. The author has an hindex of 85, co-authored 636 publications. Previous affiliations of Koen Binnemans include Kazan State Technological University & University of Arizona.
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Papers
Oxidation of cyclic acetals by ozone in ionic liquid media.
Charlie Van Doorslaer,Annelies Peeters,Pascal Mertens,Christiaan Vinckier,Koen Binnemans,Dirk De Vos +5 more
TL;DR: The application of ozone-stable pyrrolidinium based ionic liquids as safe reaction media resulted in selective hydroxy ester formation upon ozonation of cyclic acetals without using low temperatures or acetylating reagents.
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Lanthanide(III) nitrobenzenesulfonates and p-toluenesulfonate complexes of lanthanide(III), iron(III), and copper(II) as novel catalysts for the formation of calix(4)resorcinarene
TL;DR: In this article, the reaction of resorcinol with benzaldehyde yields two isomers, the all-cis isomer (rccc) and the cis-trans-trans isomer(rctt) with the relative isomer ratios depending on the reaction conditions.
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Spectroscopic properties of neodymium(III)-containing polyoxometalates in aqueous solution
Sławomir But,Stefan Lis,Rik Van Deun,Tatjana N. Parac-Vogt,Christiane Görller-Walrand,Koen Binnemans +5 more
TL;DR: Marked differences were found between the luminescence lifetimes of the complexes of the types Nd(POM) and those of the type Nd (POM)(2), due to a better shielding of the neodymium(III) ions from the bulk water molecules in the latter type of complexes.
14
Electrodeposition of indium from non-aqueous electrolytes
TL;DR: Deposits obtained at room temperature from 1,2-dimethoxyethane were rough, while spherical structures were formed in PEG400 at 160 °C, SEM analysis showed.
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Highly active gauze-supported skeletal nickel catalysts
TL;DR: The activity and selectivity of the structured RANEY® nickel surpass those of commercial RANey® nickel in the hydrogenation of acetophenone.
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