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dc.contributor.authorBergsch, Jan U.
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.contributor.authorKilian, Petr
dc.contributor.authorChalmers, Brian Alexander
dc.date.accessioned2023-05-30T16:30:08Z
dc.date.available2023-05-30T16:30:08Z
dc.date.issued2023-05-30
dc.identifier286590202
dc.identifierbf300209-4ec4-4fd3-81ab-5da78fd47dcd
dc.identifier85163723107
dc.identifier.citationBergsch , J U , Slawin , A M Z , Kilian , P & Chalmers , B A 2023 , ' Phosphine-stibine and phosphine-stiborane peri -substituted donor-acceptor complexes ' , Molbank , vol. 2023 , no. 2 , M1653 . https://doi.org/10.3390/M1653en
dc.identifier.issn1422-8599
dc.identifier.otherORCID: /0000-0002-2999-2272/work/136288351
dc.identifier.otherORCID: /0000-0001-6379-3026/work/136288468
dc.identifier.otherORCID: /0000-0002-9527-6418/work/136288706
dc.identifier.urihttps://hdl.handle.net/10023/27700
dc.description.abstractTwo novel Sb(III) and Sb(V) peri-substituted acenaphthene phosphorus−antimony compounds were prepared. The Sb(III) compound, 1, was prepared via reacting the organolithium precursor with dichloro(p-tolyl)Stibine, and 2 was prepared by the chlorination of 1. Both 1 and 2 were characterized by multinuclear (1H, 13C and 31P) NMR spectroscopy, and their molecular structures resolved by single-crystal X-ray diffraction. Both compounds show a dative P−Sb interaction with the antimony being the acceptor group in both cases owing to its Lewis acidity.
dc.format.extent9
dc.format.extent1570885
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.subjectX-ray crystallographyen
dc.subjectDonor-acceptoren
dc.subjectp-block chemistryen
dc.subjectNMR spectroscopyen
dc.subjectInert atmosphere synthesisen
dc.subjectPhosphorousen
dc.subjectAntimonyen
dc.subjectQD Chemistryen
dc.subjectQH301 Biologyen
dc.subjectDASen
dc.subjectMCCen
dc.subject.lccQDen
dc.subject.lccQH301en
dc.titlePhosphine-stibine and phosphine-stiborane peri-substituted donor-acceptor complexesen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doi10.3390/M1653
dc.description.statusPeer revieweden
dc.identifier.urlhttps://www.mdpi.com/1422-8599/2023/2/M1653en


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