<link rel="stylesheet" href="styles.f3b1fba60ec7970c.css">

Metal Complexes with di(N-heterocyclic carbene) Ligands Bearing a Rigid Ortho-, Meta or Para-phenylene Bridge

avondale-bepress.context-key9759004
avondale-bepress.submission-pathsci_math_papers/84
avondale.facultyScience
avondale.reporting.isPeerReviewedPeer Reviewed
avondale.reporting.versionPublished Version
dc.contributor.authorBarnard, Peter J.
dc.contributor.authorWilson, David J.
dc.contributor.authorPell, Thomas P.
dc.contributor.authorAccorsi, Gianluca
dc.contributor.authorGraiff, Claudia
dc.contributor.authorSgarbossa, Paolo
dc.contributor.authorBasato, Marino
dc.contributor.authorBaron, Marco
dc.contributor.authorTubaro, Cristina
dc.contributor.authorMonticelli, Marco
dc.date.accessioned2023-11-01T00:24:42Z
dc.date.available2023-11-01T00:24:42Z
dc.date.issued2016-06-21
dc.date.submitted2017-02-27T19:48:00Z
dc.description.abstract<p>Three novel dinuclear bis-dicarbene silver(I) complexes of general formula [Ag2(MeIm-phenylene-MeIm)2] (PF6)2 (Im = imidazol-2-ylidene) were synthesized. The corresponding copper(I) and gold(I) complexes were obtained by transmetalation of the di(N-heterocyclic carbene) ligand from the silver(I) species, and both coordination geometry and stoichiometry are maintained for all three group 11 metals as expected. The photophysical properties of the Ag(I) and Au(I) complexes were also investigated and discussed; in particular the most strongly emitting complex was also studied via DFT calculations. In addition, the ruthenium(II) and iridium(III) complexes [RuCl(MeIm-(o-phenylene)-MeIm)(p-cym)](PF6) and [IrClCp*- (MeIm-(o-phenylene)-MeIm)](PF6) were prepared and shown to present in these cases a chelating coordination of the di(N-heterocyclic carbene) ligand.</p>
dc.identifier.citation<p>Monticelli, M., Tubaro, C., Baron, M., Basato, M., Sgarbossa, P... Barnard, P. J. (2016). Metal complexes with di(N-heterocyclic carbene) ligands bearing a rigid ortho-, meta or para-phenylene bridge. <em>Dalton Transactions, 45</em>(23), 9540-9552. doi: 10.1039/C6DT01129B</p>
dc.identifier.doihttps://doi.org/10.1039/C6DT01129B
dc.identifier.issn1477-9226
dc.identifier.urihttps://research.avondale.edu.au/handle/1897/09759004
dc.language.isoen_us
dc.provenance<p>This article was originally published as:</p> <p>Monticelli, M., Tubaro, C., Baron, M., Basato, M., Sgarbossa, P... Barnard, P. J. (2016). Metal complexes with di(N-heterocyclic carbene) ligands bearing a rigid ortho-, meta or para-phenylene bridge. <em>Dalton Transactions, 45</em>(23), 9540-9552. doi: 10.1039/C6DT01129B</p> <p>ISSN: 1477-9226</p>
dc.relation.ispartofDalton Transactions
dc.rights<p>Due to copyright restrictions this article is unavailable for download.</p> <p>Copyright © 2016 Royal Society of Chemistry</p>
dc.titleMetal Complexes with di(N-heterocyclic carbene) Ligands Bearing a Rigid Ortho-, Meta or Para-phenylene Bridge
dc.typeJournal Article

Files

Avondale University acknowledges our Sovereign God as Creator and Provider of all things. We respectfully acknowledge the Awabakal and Darramuragal people as the traditional custodians of the lands on which we live, work, study and worship across our Lake Macquarie and Sydney campuses. We pay our respects to Elders past, present and emerging, and extend that respect to all First Nations People.

Aboriginal Peoples are advised the Library Collection contains images, voices and names of deceased people in physical and online resources. The Library recognises the significance of the traditional cultural knowledges contained within its Collection. The Library acknowledge some materials contain language that may not reflect current attitudes, was published without consent or recognition, or, is offensive. These materials reflect the views of the authors and/or the period in which they were produced and do not represent the views of the Library.

Avondale University is a member of the worldwide Seventh-day Adventist system of universities and colleges.

CRICOS Provider No.: 02731D. RTO: 91191. TEQSA: PRV12015. ABN: 53 108 186 401.

© Avondale University Ltd 2026