Show simple item record

FieldValueLanguage
dc.contributor.authorCanfield, Peter John
dc.date.accessioned2022-11-03T21:23:40Z
dc.date.available2022-11-03T21:23:40Z
dc.date.issued2018en_AU
dc.identifier.urihttps://hdl.handle.net/2123/29688
dc.description.abstractArchive file containing three different formats of the same animation. Animation of the akamptisomerisation reaction interconverting two diastereomeric transoid B2OF2pqx stereoisomers. See Thesis chapter 4 for details.en_AU
dc.format.extent00:00:06en_AU
dc.format.medium.avi, .gif, .moven_AU
dc.language.isoenen_AU
dc.publisherNature Chemistryen_AU
dc.relation.ispartofA new fundamental type of conformational isomerismen_AU
dc.subjectAkamptisomerism. Akamptismerisationen_AU
dc.subjectBond Angle Inversionen_AU
dc.subjectBond Angle Reflectionen_AU
dc.titleE_File_4 diastereomeric akamptisomerisation.zipen_AU
dc.typeAudiovisualen_AU
dc.subject.asrc03 Chemical Sciencesen_AU
dc.subject.asrc0306 Physical Chemistry (incl. Structural)en_AU
dc.subject.asrc0307 Theoretical and Computational Chemistryen_AU
dc.identifier.doi10.1038/s41557-018-0043-6
dc.relation.arcDP0666378
dc.relation.arcDP0773847
dc.relation.arcDP150103137
dc.relation.arcResearch Training Program Stipend (SC1999)
dc.rights.otherCite as: 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_AU
dc.relation.otherGritton Scholarship
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.citation.volume10en_AU
workflow.metadata.onlyNoen_AU


Show simple item record

Associated file/s

Associated collections

Show simple item record

There are no previous versions of the item available.