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dc.contributor.authorCanfield, Peter John
dc.date.accessioned2022-11-03T21:17:48Z
dc.date.available2022-11-03T21:17:48Z
dc.date.issued2018en
dc.identifier.urihttps://hdl.handle.net/2123/29686
dc.description.abstractArchive file containing three different formats of the same animation. Animation of the four transoid B2OF2pqx stereoisomers rotating in space to illustrate the structural differences. See Thesis chapter 4 for details.en
dc.format.extent00:00:11en
dc.format.medium.avi, .gif, .moven
dc.language.isoenen
dc.publisherNature Chemistryen
dc.relation.ispartofA New Fundamental Type of Conformational Isomerismen
dc.rightsOtheren
dc.subjectAkamptisomersen
dc.subjectPolytope Formalismen
dc.subjectBond Angle Invertomeren
dc.subjectBond Angle Reflectomeren
dc.titleE_File_2 four transoid B2OF2pqx isomers.zipen
dc.typeAudiovisualen
dc.subject.asrc03 Chemical Sciencesen
dc.subject.asrc0306 Physical Chemistry (incl. Structural)en
dc.subject.asrc0307 Theoretical and Computational Chemistryen
dc.identifier.doi10.1038/s41557-018-0043-6
dc.relation.arcDP0666378
dc.relation.arcDP0773847
dc.relation.arcDP150103137
dc.rights.otherCite: Canfield, P.J., Blake, I.M., Cai, ZL. et al. A new fundamental type of conformational isomerism. Nature Chem 10, 615–624 (2018). https://doi.org/10.1038/s41557-018-0043-6en
dc.relation.otherGritton Scholarship
dc.relation.otherResearch Training Program Stipend (SC1999)
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen
usyd.citation.volume10en
workflow.metadata.onlyNoen


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