Nickel(BiPhePhos)-catalyzed hydrocyanation of styrene - highly increased catalytic activity by optimized operational procedures

dc.contributor.authorKöhler, Till
dc.contributor.authorRienhoff, Bernd
dc.contributor.authorVogt, Dieter
dc.date.accessioned2024-05-22T12:22:42Z
dc.date.available2024-05-22T12:22:42Z
dc.date.issued2024-03-21
dc.description.abstractNitriles are versatile and highly desired chemical intermediates for a range of products. Their economic large-scale production requires highly efficient and selective synthesis. The nickel- catalyzed hydrocyanation of C=C double bonds provides such selective and 100% atom-economical access to nitriles, but the catalysts hitherto lack activity and longevity. Yet, the literature focusing on increased catalytic activity or optimized operational procedures is scarce, at the least. Here, we present a thorough investigation and optimization of operational procedures using a commercially available diphosphite ligand and styrene as a model substrate. This led us to achieve a TOF20 of more than 300,000 h−1.de
dc.identifier.urihttp://hdl.handle.net/2003/42514
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-24350
dc.language.isoende
dc.relation.ispartofseriesCatalysts;14(3)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/de
dc.subjecthydrocyanationde
dc.subjectactivity enhancementde
dc.subjectBiPhePhosde
dc.subjecthomogeneous catalysisde
dc.subjectnickelde
dc.subjecthydrogen cyanidede
dc.subject.ddc660
dc.titleNickel(BiPhePhos)-catalyzed hydrocyanation of styrene - highly increased catalytic activity by optimized operational proceduresde
dc.typeTextde
dc.type.publicationtypeArticlede
dcterms.accessRightsopen access
eldorado.secondarypublicationtruede
eldorado.secondarypublication.primarycitationKöhler, T., Rienhoff, B. and Vogt, D. (2024) ‘Nickel(BiPhePhos)-catalyzed hydrocyanation of styrene - highly increased catalytic activity by optimized operational procedures’, Catalysts, 14(3). Available at: https://doi.org/10.3390/catal14030210de
eldorado.secondarypublication.primaryidentifierhttps://doi.org/10.3390/catal14030210de

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