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pubmed-article:21562648rdf:typepubmed:Citationlld:pubmed
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pubmed-article:21562648pubmed:issue24lld:pubmed
pubmed-article:21562648pubmed:dateCreated2011-6-17lld:pubmed
pubmed-article:21562648pubmed:abstractTextThe N-heterocyclic olefin, IPr=CH(2) (IPr = [(HCNDipp)(2)C], Dipp = 2,6-(i)Pr(2)C(6)H(3)) has been demonstrated to be of sufficient Lewis basicity to stabilize main group hydrides in unusually low oxidation states.lld:pubmed
pubmed-article:21562648pubmed:languageenglld:pubmed
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pubmed-article:21562648pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:21562648pubmed:monthJunlld:pubmed
pubmed-article:21562648pubmed:issn1364-548Xlld:pubmed
pubmed-article:21562648pubmed:authorpubmed-author:FergusonMicha...lld:pubmed
pubmed-article:21562648pubmed:authorpubmed-author:McDonaldRober...lld:pubmed
pubmed-article:21562648pubmed:authorpubmed-author:RivardEricElld:pubmed
pubmed-article:21562648pubmed:authorpubmed-author:Al-RafiaS M...lld:pubmed
pubmed-article:21562648pubmed:authorpubmed-author:MalcolmAdam...lld:pubmed
pubmed-article:21562648pubmed:authorpubmed-author:LiewSean KSKlld:pubmed
pubmed-article:21562648pubmed:copyrightInfoThis journal is © The Royal Society of Chemistry 2011lld:pubmed
pubmed-article:21562648pubmed:issnTypeElectroniclld:pubmed
pubmed-article:21562648pubmed:day28lld:pubmed
pubmed-article:21562648pubmed:volume47lld:pubmed
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pubmed-article:21562648pubmed:pagination6987-9lld:pubmed
pubmed-article:21562648pubmed:year2011lld:pubmed
pubmed-article:21562648pubmed:articleTitleIntercepting low oxidation state main group hydrides with a nucleophilic N-heterocyclic olefin.lld:pubmed
pubmed-article:21562648pubmed:affiliationDepartment of Chemistry, University of Alberta, Edmonton, AB, Canada.lld:pubmed
pubmed-article:21562648pubmed:publicationTypeJournal Articlelld:pubmed