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dc.contributor.authorIzquierdo, F.
dc.contributor.authorManzini, S.
dc.contributor.authorNolan, S.P.
dc.date.accessioned2015-02-04T09:31:08Z
dc.date.available2015-02-04T09:31:08Z
dc.date.issued2014-12-11
dc.identifier158004006
dc.identifierc89e1c09-24c3-49d6-ae40-b01d1d58bab7
dc.identifier84908638636
dc.identifier000344596700002
dc.identifier.citationIzquierdo , F , Manzini , S & Nolan , S P 2014 , ' The use of the sterically demanding IPr ∗ and related ligands in catalysis ' , Chemical Communications , vol. 50 , no. 95 , pp. 14926-14937 . https://doi.org/10.1039/c4cc05289gen
dc.identifier.issn1359-7345
dc.identifier.urihttps://hdl.handle.net/10023/6064
dc.descriptionThe authors acknowledge the EC for funding through the seventh framework program SYNFLOW, the ERC (Advanced Investigator Award ‘FUNCAT’ to SPN) and the EPSRC. SPN is a Royal Society Wolfson Research Merit Award holder.en
dc.description.abstractThis account highlights the synthesis and applications of one of the very bulky NHC ligands, IPr∗ (1,3-bis(2,6-bis(diphenylmethyl)-4-methylphenyl)imidazo-2-ylidene). This ligand and some of its derivatives have been found very effective in several catalytic applications and have enabled the isolation of highly reactive organometallic complexes. More specifically, applications of this ligand in Pd and Ni chemistry have permitted challenging transformations under mild reaction conditions and low catalyst loadings. We report the successes as well as the limitations encountered using transition-metal systems bearing this ligand-type. This report will hopefully serve as a guide to synthetic chemists, providing insights as to when the very sterically demanding IPr∗ ligand (and its congeners) and in a broader context, very bulky NHC ligands, should be used.
dc.format.extent12
dc.format.extent1838037
dc.language.isoeng
dc.relation.ispartofChemical Communicationsen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleThe use of the sterically demanding IPr∗ and related ligands in catalysisen
dc.typeJournal articleen
dc.contributor.sponsorEuropean Research Councilen
dc.contributor.sponsorEuropean Commissionen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1039/c4cc05289g
dc.description.statusPeer revieweden
dc.identifier.grantnumberFP7-227817 FUNCATen
dc.identifier.grantnumber246461en


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