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dc.contributor.authorCaputo, Christine
dc.contributor.authorBrazeau, Allison
dc.contributor.authorHynes, Zachery
dc.contributor.authorPrice, Jacquelyn
dc.contributor.authorTuononen, Heikki
dc.contributor.authorJones, Nathan
dc.date.accessioned2015-11-24T12:10:17Z
dc.date.available2015-11-24T12:10:17Z
dc.date.issued2009
dc.identifier.citationCaputo, C., Brazeau, A., Hynes, Z., Price, J., Tuononen, H., & Jones, N. (2009). A Cation-Captured Palladium(0) Anion: Synthesis, Structure, and Bonding of [PdBr(PPh3)2]− Ligated by an N-Heterocyclic Phosphenium Cation. <i>Organometallics</i>, <i>28</i>(17), 5261-5265. <a href="https://doi.org/10.1021/om9006278" target="_blank">https://doi.org/10.1021/om9006278</a>
dc.identifier.otherCONVID_19245578
dc.identifier.otherTUTKAID_38388
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/47803
dc.description.abstractUnsaturated N-heterocyclic phosphenium cations (uNHP) stabilize the [Pd0(PR3)2X]− anion proposed over the past decade to be the crucial but elusive intermediate in palladium-catalyzed cross-coupling reactions (X = halide). Insertion of metal into the P−Br bond of the precursor mesityl-substituted bromophosphine gives the structurally characterized Pd(0)-phosphenium complex (uNHPMes)Pd(PPh3)2Br, which features a long Pd−Br bond (2.7240(9) Å) and the shortest known Pd−P bond (2.1166(17) Å). The reaction is proposed to proceed by an associative pathway involving a Pd-bromophosphine complex that undergoes P-to-Pd bromide transfer.
dc.language.isoeng
dc.publisherACS
dc.relation.ispartofseriesOrganometallics
dc.subject.otherpalladium-fosfiini -kompleksit
dc.subject.otherpalladium-phosphine complexes
dc.titleA Cation-Captured Palladium(0) Anion: Synthesis, Structure, and Bonding of [PdBr(PPh3)2]− Ligated by an N-Heterocyclic Phosphenium Cation
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201511203749
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.updated2015-11-20T13:15:07Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange5261-5265
dc.relation.issn0276-7333
dc.relation.numberinseries17
dc.relation.volume28
dc.type.versionacceptedVersion
dc.rights.copyright© 2009 American Chemical Society. This is a final draft version of an article whose final and definitive form has been published by ACS. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevelopenAccessfi
dc.relation.doi10.1021/om9006278
dc.type.okmA1


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