Structural studies of some copper(II) coordination compounds

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dc.contributor.advisor Associate Professor T. N. Waters en
dc.contributor.advisor Professor D. Hall en
dc.contributor.author Baker, Edward Neill en
dc.date.accessioned 2008-07-09T03:19:51Z en
dc.date.available 2008-07-09T03:19:51Z en
dc.date.issued 1967 en
dc.identifier.citation Thesis (PhD--Chemistry)--University of Auckland, 1967. en
dc.identifier.uri http://hdl.handle.net/2292/2594 en
dc.description.abstract The crystal structures of four coordination compounds of copper(II) have been investigated by three-dimensional X-ray methods. The structure of one crystalline form of bis-(N-ethyl-salicylaldiminato) copper(II) has revealed that the copper atom in such a compound may adopt a tetrahedrally-distorted coordination geometry under less severe steric conditions than had previously been supposed. The structures of a methylamine perchlorate adduct of NN’-ethylenebis-(acetylacetoneiminato) copper(II) and p-nitrophenol and chloroform adducts of NN’-ethylenebis-(salicylaldiminato) copper(II) have indicated that the bonding requirements of the copper atom can be modified by hydrogen bonding involving a ligand atom. en
dc.format Scanned from print thesis en
dc.language.iso en en
dc.publisher ResearchSpace@Auckland en
dc.relation.ispartof PhD Thesis - University of Auckland en
dc.relation.isreferencedby UoA216109 en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.title Structural studies of some copper(II) coordination compounds en
dc.type Thesis en
thesis.degree.discipline Chemistry en
thesis.degree.grantor The University of Auckland en
thesis.degree.level Doctoral en
thesis.degree.name PhD en
dc.subject.marsden Fields of Research::250000 Chemical Sciences en
dc.rights.holder Copyright: The author en
pubs.local.anzsrc 03 - Chemical Sciences en
pubs.org-id Faculty of Science en
dc.identifier.wikidata Q112029983


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