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dc.contributor.authorLynch, DE
dc.contributor.authorCooper, CJ
dc.contributor.authorChauhan, V
dc.contributor.authorSmith, G
dc.contributor.authorHealy, P
dc.contributor.authorParsons, S
dc.date.accessioned2017-05-03T13:43:32Z
dc.date.available2017-05-03T13:43:32Z
dc.date.issued1999
dc.identifier.issn0004-9425
dc.identifier.doi10.1071/CH99020
dc.identifier.urihttp://hdl.handle.net/10072/15554
dc.description.abstractSix molecular complexes containing the herbicidally active (2,4-dichlorophenoxy)acetic acid (2,4-d) and (2,4,5-trichlorophenoxy)acetic acid (2,4,5-t) have been prepared and studied by using single-crystal X-ray diffraction techniques. These adduct structures are 2,4-d with 4,4'-dipyridine (2 : 1 complex), and 2,4,5-t with respectively 5-nitroquinoline (1 : 1), 4,4'-dipyridine (2 : 1), 2-amino-2-thiazoline (1 : 1), 2-aminobenzothiazole (1 : 1) and 2-amino-5-ethyl-1,3,4-thiadiazole (1 : 1). The conformations of the phenoxyacetic acid molecules were found to be either synclinal (in three cases) or antiperiplanar (in the other three cases). A general review is also made about the conformational aspects of previously reported adducts of phenoxyacetic acid derivatives and how they compare to their free acid structures.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.languageEnglish
dc.language.isoeng
dc.publisherCSIRO Publishing
dc.publisher.placeAustralia
dc.relation.ispartofpagefrom695
dc.relation.ispartofpageto703
dc.relation.ispartofjournalAustralian Journal of Chemistry
dc.relation.ispartofvolume52
dc.subject.fieldofresearchChemical sciences
dc.subject.fieldofresearchcode34
dc.titleConformational Comparisons Between Phenoxyacetic Acid Derivatives in Adducts and in the Free Form
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.date.issued2015-05-22T00:05:25Z
gro.hasfulltextNo Full Text
gro.griffith.authorHealy, Peter C.


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