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dc.contributor.authorHoughton, Adrian Y.
dc.contributor.authorKarttunen, Virve
dc.contributor.authorPiers, Warren E.
dc.contributor.authorTuononen, Heikki
dc.date.accessioned2015-12-01T07:38:46Z
dc.date.available2015-12-01T07:38:46Z
dc.date.issued2014
dc.identifier.citationHoughton, A. Y., Karttunen, V., Piers, W. E., & Tuononen, H. (2014). Hydrogen activation with perfluorinated organoboranes: 1,2,3- tris(pentafluorophenyl)-4,5,6,7-tetrafluoro-1-boraindene. <i>Chemical Communications</i>, <i>50</i>(11), 1295-1298. <a href="https://doi.org/10.1039/C3CC48796B" target="_blank">https://doi.org/10.1039/C3CC48796B</a>
dc.identifier.otherCONVID_23652382
dc.identifier.otherTUTKAID_61722
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/47898
dc.description.abstractThe perfluorinated boraindene 3 was synthesized and fully characterized. Both computational and crystallographic data show that 3 is antiaromatic. Compound 3 was shown to react reversibly with H2 and to catalyse the hydrogenation of cyclohexene. The mechanism of catalysis was probed experimentally and computationally.
dc.language.isoeng
dc.publisherRSC Publications
dc.relation.ispartofseriesChemical Communications
dc.subject.otherorganoboraanit
dc.subject.othervedyn aktivointi
dc.subject.otherfluorattu boraindeeni
dc.subject.otherorganoboron compounds
dc.subject.otherhydrogen activation
dc.subject.otherperfluorinated boraindene
dc.titleHydrogen activation with perfluorinated organoboranes: 1,2,3- tris(pentafluorophenyl)-4,5,6,7-tetrafluoro-1-boraindene
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201511263836
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2015-11-26T07:15:08Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange1295-1298
dc.relation.issn1359-7345
dc.relation.numberinseries11
dc.relation.volume50
dc.type.versionacceptedVersion
dc.rights.copyright© The Royal Society of Chemistry 2014. This is a final draft version of an article whose final and definitive form has been published by RSC. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevelopenAccessfi
dc.relation.doi10.1039/C3CC48796B
dc.type.okmA1


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