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"Some cyclic tetramine nickel complexes"

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dc.contributor.author Gordon, Gerard James
dc.date.accessioned 2011-03-10T22:58:07Z
dc.date.accessioned 2022-10-25T05:02:01Z
dc.date.available 2011-03-10T22:58:07Z
dc.date.available 2022-10-25T05:02:01Z
dc.date.copyright 1964
dc.date.issued 1964
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/23233
dc.description.abstract Five aliphatic Schiff base nickel complexes have been prepared using previously reported methods but increasing the percentage yields wherever possible. Three of these five Schiff bases were reduced by hydrogenation with platinum catalysts producing three previously unreported cyclic tetramine nickel complexes. One of the remaining two Schiff base complexes was reduced electrolytically for the first time. From reports on previous work with this fourth cyclic tetramine nickel complex it was expected that cyanide treatment of the three previously unreported cyclic tetramine nickel complexes would readily cause the precipitation of the cyclic tetramines. This was not found to be the case and an explanation for the non-precipitation is presented. en_NZ
dc.format pdf en_NZ
dc.language en_NZ
dc.language.iso en_NZ
dc.publisher Te Herenga Waka—Victoria University of Wellington en_NZ
dc.title "Some cyclic tetramine nickel complexes" en_NZ
dc.type Text en_NZ
vuwschema.type.vuw Awarded Research Masters Thesis en_NZ
thesis.degree.discipline Chemistry en_NZ
thesis.degree.grantor Te Herenga Waka—Victoria University of Wellington en_NZ
thesis.degree.level Masters en_NZ
thesis.degree.name Master of Science en_NZ


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