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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/111058
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dc.contributor.authorBruce, M.-
dc.contributor.authorHead, N.-
dc.contributor.authorSkelton, B.-
dc.contributor.authorSpackman, M.-
dc.contributor.authorWhite, A.-
dc.date.issued2018-
dc.identifier.citationAustralian Journal of Chemistry: an international journal for chemical science, 2018; 71(1):70-73-
dc.identifier.issn0004-9425-
dc.identifier.issn1445-0038-
dc.identifier.urihttp://hdl.handle.net/2440/111058-
dc.description.abstractThe X-ray structure of tetraiodoallene is reported. On standing, atmospheric hydrolysis converts this compound into 2,2-diiodoacrylic acid, for which a structure has also been determined. Energy framework diagrams have been constructed for the two compounds.-
dc.description.statementofresponsibilityMichael I. Bruce, Nicholas J. Head, Brian W. Skelton, Mark A. Spackman and Allan H. White-
dc.language.isoen-
dc.publisherCSIRO Publishing-
dc.rightsJournal compilation © CSIRO 2018-
dc.source.urihttp://dx.doi.org/10.1071/ch17348-
dc.titleTetraiodoallene, I₂C=C=CI₂ - the missing link between I₂C=CI₂ and I₂C=C=C=CI₂ - and the oxidation product, 2,2-diiodoacrylicacid, I₂C=CH(CO₂H)-
dc.title.alternativeTetraiodoallene, I(2)C=C=CI(2) - the missing link between I(2)C=CI(2) and I(2)C=C=C=CI(2) - and the oxidation product, 2,2-diiodoacrylicacid, I(2)C=CH(CO(2)H)-
dc.typeJournal article-
dc.identifier.doi10.1071/CH17348-
dc.relation.grantARC-
pubs.publication-statusPublished-
dc.identifier.orcidBruce, M. [0000-0002-8377-7186]-
Appears in Collections:Aurora harvest 8
Chemistry publications

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