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2,2'-Trisulfanediyldibenzoyl chloride

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dc.contributor.authorAitken, R Alan
dc.contributor.authorCampbell, Alexandra H.
dc.contributor.authorFletcher, Chloé E.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.date.accessioned2023-09-25T10:30:10Z
dc.date.available2023-09-25T10:30:10Z
dc.date.issued2023-09-21
dc.identifier293953301
dc.identifier092981ba-23bd-453c-b84f-fab1e19044ac
dc.identifier85172795393
dc.identifier.citationAitken , R A , Campbell , A H , Fletcher , C E & Slawin , A M Z 2023 , ' 2,2'-Trisulfanediyldibenzoyl chloride ' , Molbank , vol. 2023 , no. 3 , M1731 . https://doi.org/10.3390/M1731en
dc.identifier.issn1422-8599
dc.identifier.otherORCID: /0000-0001-6959-5311/work/142904654
dc.identifier.otherORCID: /0000-0002-9527-6418/work/142904668
dc.identifier.urihttps://hdl.handle.net/10023/28442
dc.description.abstractThe X-ray structure of the title compound, formed in low conversion in the reaction of thiosalicylic acid with thionyl chloride, has been determined. The acid chloride groups are oriented to permit an attractive non-bonding O…S interaction. Mechanisms are suggested for formation of this unexpected product. 1H and 13C NMR data are also reported for the first time for the major reaction product, 2-mercaptobenzoyl chloride.
dc.format.extent6
dc.format.extent1660194
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.subjectX-ray structureen
dc.subjectTrisulfaneen
dc.subjectChalcogen-chalcogen interactionen
dc.subjectAcid chlorideen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.title2,2'-Trisulfanediyldibenzoyl chlorideen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doi10.3390/M1731
dc.description.statusPeer revieweden


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