Please use this identifier to cite or link to this item: https://doi.org/10.1039/c8sc00742j
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dc.titleEfficient cleavage of aryl ether C-O linkages by Rh-Ni and Ru-Ni nanoscale catalysts operating in water
dc.contributor.authorBulut, S.
dc.contributor.authorSiankevich, S.
dc.contributor.authorVan Muyden, A.P.
dc.contributor.authorAlexander, D.T.L.
dc.contributor.authorSavoglidis, G.
dc.contributor.authorZhang, J.
dc.contributor.authorHatzimanikatis, V.
dc.contributor.authorYan, N.
dc.contributor.authorDyson, P.J.
dc.date.accessioned2021-11-16T09:30:37Z
dc.date.available2021-11-16T09:30:37Z
dc.date.issued2018
dc.identifier.citationBulut, S., Siankevich, S., Van Muyden, A.P., Alexander, D.T.L., Savoglidis, G., Zhang, J., Hatzimanikatis, V., Yan, N., Dyson, P.J. (2018). Efficient cleavage of aryl ether C-O linkages by Rh-Ni and Ru-Ni nanoscale catalysts operating in water. Chemical Science 9 (25) : 5530-5535. ScholarBank@NUS Repository. https://doi.org/10.1039/c8sc00742j
dc.identifier.issn2041-6520
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/206487
dc.description.abstractBimetallic Ru-Ni and Rh-Ni nanocatalysts coated with a phase transfer agent efficiently cleave aryl ether C-O linkages in water in the presence of hydrogen. For dimeric substrates with weaker C-O linkages, i.e. ?-O-4 and ?-O-4 bonds, low loadings of the precious metal (Rh or Ru) in the nanocatalysts quantitatively afford monomers, whereas for the stronger 4-O-5 linkage higher amounts of the precious metal are required to achieve complete conversion. Under the optimized, relatively mild operating conditions, the C-O bonds in a range of substituted ether compounds are efficiently cleaved, and mechanistic insights into the reaction pathways are provided. This work paves the way to sustainable approaches for the hydrogenolysis of C-O bonds. © 2018 The Royal Society of Chemistry.
dc.publisherRoyal Society of Chemistry
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScopus OA2018
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1039/c8sc00742j
dc.description.sourcetitleChemical Science
dc.description.volume9
dc.description.issue25
dc.description.page5530-5535
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