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dc.contributor.authorForster, Taryn
dc.contributor.authorKrahulic, Kelly
dc.contributor.authorTuononen, Heikki
dc.contributor.authorMcDonald, Robert
dc.contributor.authorParvez, Masood
dc.contributor.authorRoesler, Roland
dc.date.accessioned2015-11-30T07:34:29Z
dc.date.available2015-11-30T07:34:29Z
dc.date.issued2006
dc.identifier.citationForster, T., Krahulic, K., Tuononen, H., McDonald, R., Parvez, M., & Roesler, R. (2006). A σ-Donor with a Planar Six-π-Electron B2N2C2 Framework: Anionic N-Heterocyclic Carbene or Heterocyclic Terphenyl Anion?. <i>Angewandte Chemie, International Edition</i>, <i>45</i>(38), 6356-6359. <a href="https://doi.org/10.1002/anie.200601229" target="_blank">https://doi.org/10.1002/anie.200601229</a>
dc.identifier.otherCONVID_16479167
dc.identifier.otherTUTKAID_23549
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/47851
dc.description.abstractNB! The anionic ligand 2 was synthesized through deprotonation of a planar, formally zwitterionic diazadiborine precursor, isolated as a lithium salt, and structurally characterized. According to experimental evidence and theoretical calculations, 2 can be considered as an intermediate between two classical classes of ligands: N-heterocyclic carbenes 1 and terphenyls 3.
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesAngewandte Chemie, International Edition
dc.subject.otherN-heterosykliset karbeenit
dc.subject.otherterfenyylit
dc.subject.otherN-heterocyclic carbenes
dc.subject.otherterphenyls
dc.titleA σ-Donor with a Planar Six-π-Electron B2N2C2 Framework: Anionic N-Heterocyclic Carbene or Heterocyclic Terphenyl Anion?
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201511253813
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.updated2015-11-25T13:15:18Z
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.format.pagerange6356-6359
dc.relation.issn1433-7851
dc.relation.numberinseries38
dc.relation.volume45
dc.type.versionacceptedVersion
dc.rights.copyright© 2006 Wiley-VCH Verlag GmbH & Co. This is a final draft version of an article whose final and definitive form has been published by Wiley. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevelopenAccessfi
dc.relation.doi10.1002/anie.200601229


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