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dc.contributor.authorMejuto, Carmen
dc.contributor.authorRoyo, Beatriz
dc.contributor.authorGuisado-Barrios, Gregorio
dc.contributor.authorPeris, Eduardo
dc.date.accessioned2016-02-10T08:08:35Z
dc.date.available2016-02-10T08:08:35Z
dc.date.issued2015-12-14
dc.identifier.citationMEJUTO, Carmen, et al. Rhodium, iridium and nickel complexes with a 1, 3, 5-triphenylbenzene tris-MIC ligand. Study of the electronic properties and catalytic activities. Beilstein journal of organic chemistry, 2015, vol. 11, no 1, p. 2584-2590.ca_CA
dc.identifier.issn1860-5397
dc.identifier.urihttp://hdl.handle.net/10234/149365
dc.description.abstractThe coordination versatility of a 1,3,5-triphenylbenzene-tris-mesoionic carbene ligand is illustrated by the preparation of complexes with three different metals: rhodium, iridium and nickel. The rhodium and iridium complexes contained the [MCl(COD)] fragments, while the nickel compound contained [NiCpCl]. The preparation of the tris-MIC (MIC = mesoionic carbene) complex with three [IrCl(CO)2] fragments, allowed the estimation of the Tolman electronic parameter (TEP) for the ligand, which was compared with the TEP value for a related 1,3,5-triphenylbenzene-tris-NHC ligand. The electronic properties of the tris-MIC ligand were studied by cyclic voltammetry measurements. In all cases, the tris-MIC ligand showed a stronger electron-donating character than the corresponding NHC-based ligands. The catalytic activity of the tri-rhodium complex was tested in the addition reaction of arylboronic acids to α,β-unsaturated ketones.ca_CA
dc.description.sponsorShipWe gratefully acknowledge financial support from MINECO of Spain (CTQ2014-51999-P), UJI (P11B2014-02), Generalitat Valenciana (GV/2015/097) and FCT-Fundação para a Ciência e a Tecnologia (UID/Multi/04551/2013 and PTDC/QEQ- QIN/ 0565/2012). C. M. is thankful to the FPI program for a fellowship, B. R. thanks FCT for IF/00346/2013 and G. G.-B. thanks the MINECO for a postdoctoral grant (FPDI-2013-16525). The authors are grateful to the Serveis Centrals d’Instrumentació Científica (SCIC) of the Universitat Jaume I for providing with spectroscopic and X-ray facilities, and to FCT (RECI/BBBBQB/ 0230/2012).ca_CA
dc.format.extent7 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherBeilstein-Institutca_CA
dc.relation.isPartOfBeilstein journal of organic chemistry, 2015, vol. 11, no 1ca_CA
dc.rights© 2015 Mejuto et al; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc)ca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectarylation of unsaturated ketonesca_CA
dc.subjectmesoionic carbenesca_CA
dc.subjectnickelca_CA
dc.subjectiridiumca_CA
dc.subjectrhodiumca_CA
dc.titleRhodium, iridium and nickel complexes with a 1,3,5-triphenylbenzene tris-MIC ligand. Study of the electronic properties and catalytic activitiesca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.3762/bjoc.11.278
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_CA
dc.relation.publisherVersionhttp://www.beilstein-journals.org/bjoc/single/articleFullText.htm?publicId=1860-5397-11-278ca_CA


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