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Diphosphane 2,2′-binaphtho[1,8-de][1,3,2]dithiaphosphinine and the easy formation of a stable phosphorus radical cation

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dc.contributor.authorKirst, Christin
dc.contributor.authorBode, Bela Ernest
dc.contributor.authorCordes, David Bradford
dc.contributor.authorNejman, Phillip
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.contributor.authorKaraghiosoff , Konstantin
dc.contributor.authorWoollins, J Derek
dc.date.accessioned2017-03-12T00:32:57Z
dc.date.available2017-03-12T00:32:57Z
dc.date.issued2016-04-21
dc.identifier241560663
dc.identifierf1078002-7f38-4363-8004-cf6f6eb313f2
dc.identifier84964680223
dc.identifier000373994800007
dc.identifier.citationKirst , C , Bode , B E , Cordes , D B , Nejman , P , Slawin , A M Z , Karaghiosoff , K & Woollins , J D 2016 , ' Diphosphane 2,2′-binaphtho[1,8-de][1,3,2]dithiaphosphinine and the easy formation of a stable phosphorus radical cation ' , Dalton Transactions , vol. 45 , no. 15 , pp. 6348-6351 . https://doi.org/10.1039/C6DT00304Den
dc.identifier.issn1477-9226
dc.identifier.otherORCID: /0000-0002-5366-9168/work/28023982
dc.identifier.otherORCID: /0000-0002-3384-271X/work/27582722
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861394
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779164
dc.identifier.urihttps://hdl.handle.net/10023/10455
dc.description.abstractA convenient synthesis route to 2,2’-binaphtho[1,8-de][1,3,2]di-thiaphosphinine (3) was found. Its stable radical cation 3•+ was accessed easily through one-electron oxidation with NOBF4.
dc.format.extent524368
dc.format.extent1150841
dc.language.isoeng
dc.relation.ispartofDalton Transactionsen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleDiphosphane 2,2′-binaphtho[1,8-de][1,3,2]dithiaphosphinine and the easy formation of a stable phosphorus radical cationen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Centre of Magnetic Resonanceen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. Office of the Principalen
dc.identifier.doi10.1039/C6DT00304D
dc.description.statusPeer revieweden
dc.date.embargoedUntil2017-03-11


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