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Co-ordination compounds of nickel quinoline and isoquinoline thiocyanates

dc.contributor.authorCode word 238
dc.date.accessioned2011-03-16T22:36:49Z
dc.date.accessioned2022-10-25T06:05:36Z
dc.date.available2011-03-16T22:36:49Z
dc.date.available2022-10-25T06:05:36Z
dc.date.copyright[19--]
dc.date.issued[19--]
dc.description.abstractThe existence of a red nickel diquinoline thiocyanate had previously been reported from this laboratory. As this colour is unusual among nickel compounds, the further investigation of the substance was undertaken as the object of the first half of this thesis. With this in view, a comparison was made of the series comprising nickal tetraquinoline thiocyanate (green), nickel diquinoline thiocyanate (red), and anhydrous nickel thiocyanate (yellow). It was hoped that some serial relationship might be found between the cause of colour and the molecular structure. A comparison was likewise made of nickel tetra-and di-quinoline thiocyanates with the corresponding nickel isoquinoline thiocyanates. It was hoped that some explanation might be brought forward for the marked differences in physical properties of the isomeric tetrammines.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/23375
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.titleCo-ordination compounds of nickel quinoline and isoquinoline thiocyanatesen_NZ
dc.typeTexten_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

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