| dc.contributor.author | Ly, Hanh | |
| dc.contributor.author | Moilanen, Jani | |
| dc.contributor.author | Tuononen, Heikki | |
| dc.contributor.author | Parvez, Masood | |
| dc.contributor.author | Roesler, Roland | |
| dc.date.accessioned | 2015-11-25T07:26:38Z | |
| dc.date.available | 2015-11-25T07:26:38Z | |
| dc.date.issued | 2011 | |
| dc.identifier.citation | Ly, H., Moilanen, J., Tuononen, H., Parvez, M., & Roesler, R. (2011). More electron rich than cyclopentadienyl: 1,2-diaza-3,5-diborolyl as a ligand in ferrocene and ruthenocene analogs. <i>Chemical Communications</i>, <i>47</i>(29), 8391-8393. <a href="https://doi.org/10.1039/C1CC12281A" target="_blank">https://doi.org/10.1039/C1CC12281A</a> | |
| dc.identifier.other | CONVID_20703438 | |
| dc.identifier.other | TUTKAID_46669 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/47811 | |
| dc.description.abstract | Ruthenium and iron sandwich complexes incorporating cyclopentadienyl analogs with CB2N2− skeletons were characterized. Electrochemical measurements supported by computational studies revealed that in combination with larger metal ions such as Ru the CB2N2− ligand can be more electron-rich than its organic counterpart. | |
| dc.language.iso | eng | |
| dc.publisher | RSC | |
| dc.relation.ispartofseries | Chemical Communications | |
| dc.subject.other | syklopentadienyylianalogit | |
| dc.subject.other | cyclopentadienyl analogues | |
| dc.title | More electron rich than cyclopentadienyl: 1,2-diaza-3,5-diborolyl as a ligand in ferrocene and ruthenocene analogs | |
| dc.type | article | |
| dc.identifier.urn | URN:NBN:fi:jyu-201511243778 | |
| 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 | 2015-11-24T07:15:21Z | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | 8391-8393 | |
| dc.relation.issn | 1359-7345 | |
| dc.relation.numberinseries | 29 | |
| dc.relation.volume | 47 | |
| dc.type.version | acceptedVersion | |
| dc.rights.copyright | © The Royal Society of Chemistry 2011. 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.accesslevel | openAccess | fi |
| dc.relation.doi | 10.1039/C1CC12281A | |
| dc.type.okm | A1 | |
