| dc.contributor.author | Forster, Taryn | |
| dc.contributor.author | Krahulic, Kelly | |
| dc.contributor.author | Tuononen, Heikki | |
| dc.contributor.author | McDonald, Robert | |
| dc.contributor.author | Parvez, Masood | |
| dc.contributor.author | Roesler, Roland | |
| dc.date.accessioned | 2015-11-30T07:34:29Z | |
| dc.date.available | 2015-11-30T07:34:29Z | |
| dc.date.issued | 2006 | |
| dc.identifier.citation | Forster, 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.other | CONVID_16479167 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/47851 | |
| dc.description.abstract | NB! 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.iso | eng | |
| dc.publisher | Wiley | |
| dc.relation.ispartofseries | Angewandte Chemie, International Edition | |
| dc.subject.other | N-heterosykliset karbeenit | |
| dc.subject.other | terfenyylit | |
| dc.subject.other | N-heterocyclic carbenes | |
| dc.subject.other | terphenyls | |
| dc.title | A σ-Donor with a Planar Six-π-Electron B2N2C2 Framework: Anionic N-Heterocyclic Carbene or Heterocyclic Terphenyl Anion? | |
| dc.type | research article | |
| dc.identifier.urn | URN:NBN:fi:jyu-201511253813 | |
| dc.contributor.laitos | Kemian laitos | fi |
| dc.contributor.laitos | Department of Chemistry | en |
| dc.contributor.oppiaine | Epäorgaaninen ja analyyttinen kemia | fi |
| dc.contributor.oppiaine | Inorganic and Analytical Chemistry | en |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| dc.date.updated | 2015-11-25T13:15:18Z | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | 6356-6359 | |
| dc.relation.issn | 1433-7851 | |
| dc.relation.numberinseries | 38 | |
| dc.relation.volume | 45 | |
| dc.type.version | acceptedVersion | |
| 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.accesslevel | openAccess | fi |
| dc.type.publication | article | |
| dc.relation.doi | 10.1002/anie.200601229 | |
| dc.type.okm | A1 | |
