Palladium complex in a room temperature ionic liquid: A convenient recyclable reagent for catalytic oxidation

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dc.contributor.authorDileep, R.
dc.contributor.authorBadekai Ramachandra, B.
dc.contributor.authorSuresha Kumara, T.H.S.
dc.date.accessioned2026-02-05T09:34:31Z
dc.date.issued2014
dc.description.abstractPalladium (Pd)-catalyzed carbonylation of alcohols proceeds in ionic liquid (IL) media (1-ethyl-3-methylimidazolium hexafluorophosphate). Carbonylation of primary/secondary alcohols to aldehydes/ketones was greatly accelerated by the use of a Pd-based catalyst in the presence of NaOCl as an oxidant. The catalyst was more easier to recycle in the IL [Emim]PF<inf>6</inf> with an equal-proportioned CH<inf>2</inf>Cl<inf>2</inf> than in the single CH<inf>2</inf>Cl<inf>2</inf> or IL. © 2014 The Author(s). Published by Taylor & Francis.
dc.identifier.citationGreen Chemistry Letters and Reviews, 2014, 7, 1, pp. 32-36
dc.identifier.issn17518253
dc.identifier.urihttps://doi.org/10.1080/17518253.2014.891660
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/26646
dc.publisherTaylor and Francis Ltd.
dc.subjectalcohol
dc.subjectaldehyde
dc.subjectcatalysis
dc.subjectcatalyst
dc.subjectketone
dc.subjectoxidation
dc.subjectpalladium
dc.subjectreaction kinetics
dc.subjecttemperature effect
dc.titlePalladium complex in a room temperature ionic liquid: A convenient recyclable reagent for catalytic oxidation

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