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Organo phosphorus-sulfur-nitrogen heterocycles from thionation of Schiff bases

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dc.contributor.authorHua, Guoxiong
dc.contributor.authorCordes, David Bradford
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.contributor.authorWoollins, J Derek
dc.date.accessioned2020-07-16T09:30:01Z
dc.date.available2020-07-16T09:30:01Z
dc.date.issued2021-02-24
dc.identifier.citationHua , G , Cordes , D B , Slawin , A M Z & Woollins , J D 2021 , ' Organo phosphorus-sulfur-nitrogen heterocycles from thionation of Schiff bases ' , Zeitschrift für Anorganische und Allgemeine Chemie , vol. 647 , no. 4 , pp. 239-244 . https://doi.org/10.1002/zaac.202000226en
dc.identifier.issn1521-3749
dc.identifier.otherPURE: 268906969
dc.identifier.otherPURE UUID: 48c6bad5-14b1-4f4d-8b1f-a2842a4e8b6e
dc.identifier.otherORCID: /0000-0002-9527-6418/work/77524551
dc.identifier.otherORCID: /0000-0002-1498-9652/work/77524562
dc.identifier.otherORCID: /0000-0002-5366-9168/work/77524572
dc.identifier.otherWOS: 000550855200001
dc.identifier.otherScopus: 85088100362
dc.identifier.urihttp://hdl.handle.net/10023/20264
dc.descriptionFunding: University of St Andrews.en
dc.description.abstractA series of heteroatom derivatives were prepared from the reactions of amido-Schiff bases as well as simpler imine with 2,4-diferrocenyl-1,3,2,4-diathiadiphosphetane 2,4-disulfide ( FcLR ). Six related structures have been characterized by single crystal X-ray diffraction.
dc.format.extent7
dc.language.isoeng
dc.relation.ispartofZeitschrift für Anorganische und Allgemeine Chemieen
dc.rightsCopyright © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleOrgano phosphorus-sulfur-nitrogen heterocycles from thionation of Schiff basesen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1002/zaac.202000226
dc.description.statusPeer revieweden


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