{"id":{"repo_id":"cape-town","oai_identifier":"oai:open.uct.ac.za:11427/18381"},"canonical_url":"https://search.dev.ndltd.org/etd/cape-town/oai:open.uct.ac.za:11427/18381","repository":{"repo_id":"cape-town","name":"University of Cape Town","base_url":"https://open.uct.ac.za/oai/request"},"display":{"title":"Isotopic labelling applied to the infrared spectra of metal complexes","abstract":"An ir investigation of a series of 2-aminomethylpyridine complexes of first transition metal(II) perchlorates, tetrafluoroborates, halides and thiocyanates is reported. Comparisons with the spectra of related complexes of 2,2'-bipyridine and ethylenediamine together with metal-ion substitution, deuteration and ¹⁵N isotopic labelling of the amino group in 2-aminomethylpyridine enable reliable band assignments to be made. The study shows that in complexes of the type M(amp)nX₂, metal-to-amino-nitrogen stretches occur at frequencies greater than 350 cm⁻¹ , while the metal-to-pyridine-nitrogen stretches are generally below 300 cm⁻¹, the assignment of the latter being generally complicated by the presence of metal-to-halogen vibrations. In addition to an x-ray crystallographic investigation of the complex [Ni(amp)₃](BF₃ ₄)₂, considerable structural information about these complexes is obtained from correlations between the number of M-L vibrations observed in the far ir and those predicted for localized molecular point symmetries on a group theoretical basis.","abstract_html":"An ir investigation of a series of 2-aminomethylpyridine complexes of first transition metal(II) perchlorates, tetrafluoroborates, halides and thiocyanates is reported. Comparisons with the spectra of related complexes of 2,2'-bipyridine and ethylenediamine together with metal-ion substitution, deuteration and ¹⁵N isotopic labelling of the amino group in 2-aminomethylpyridine enable reliable band assignments to be made. The study shows that in complexes of the type M(amp)nX₂, metal-to-amino-nitrogen stretches occur at frequencies greater than 350 cm⁻¹ , while the metal-to-pyridine-nitrogen stretches are generally below 300 cm⁻¹, the assignment of the latter being generally complicated by the presence of metal-to-halogen vibrations. In addition to an x-ray crystallographic investigation of the complex [Ni(amp)₃](BF₃ ₄)₂, considerable structural information about these complexes is obtained from correlations between the number of M-L vibrations observed in the far ir and those predicted for localized molecular point symmetries on a group theoretical basis.","abstract_has_math":false,"creators":["Niven, Margaret Lilian"],"institution":"Department of Chemistry","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Percy, G C","Thornton, David A"],"committee_chairs":[],"committee_members":[],"year":1980,"date_issued":"1980","date_published":"1980","updated_at":"2026-07-22T22:23:07Z","subjects":[],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/11427/18381","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Percy, G C","Thornton, David A"]},{"key":"dc:creator","label":"Author","values":["Niven, Margaret Lilian"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2016-03-30T07:11:43Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2016-03-30T07:11:43Z"]},{"key":"dc:date.issued","label":"Date","values":["1980"]},{"key":"dc:publisher.department","label":"Dc Publisher Department","values":["Department of Chemistry"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["University of Cape Town"]},{"key":"dc:type","label":"Dc Type","values":["Doctoral Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["Doctoral"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["PhD"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/11427/18381"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["An ir investigation of a series of 2-aminomethylpyridine complexes of first transition metal(II) perchlorates, tetrafluoroborates, halides and thiocyanates is reported. Comparisons with the spectra of related complexes of 2,2'-bipyridine and ethylenediamine together with metal-ion substitution, deuteration and ¹⁵N isotopic labelling of the amino group in 2-aminomethylpyridine enable reliable band assignments to be made. The study shows that in complexes of the type M(amp)nX₂, metal-to-amino-nitrogen stretches occur at frequencies greater than 350 cm⁻¹ , while the metal-to-pyridine-nitrogen stretches are generally below 300 cm⁻¹, the assignment of the latter being generally complicated by the presence of metal-to-halogen vibrations. In addition to an x-ray crystallographic investigation of the complex [Ni(amp)₃](BF₃ ₄)₂, considerable structural information about these complexes is obtained from correlations between the number of M-L vibrations observed in the far ir and those predicted for localized molecular point symmetries on a group theoretical basis."]},{"key":"dc:title","label":"Title","values":["Isotopic labelling applied to the infrared spectra of metal complexes"]}]}],"canonical_facts":{"dc:contributor.advisor":["Percy, G C","Thornton, David A"],"dc:creator":["Niven, Margaret Lilian"],"dc:date.accessioned":["2016-03-30T07:11:43Z"],"dc:date.available":["2016-03-30T07:11:43Z"],"dc:date.issued":["1980"],"dc:description.abstract":["An ir investigation of a series of 2-aminomethylpyridine complexes of first transition metal(II) perchlorates, tetrafluoroborates, halides and thiocyanates is reported. Comparisons with the spectra of related complexes of 2,2'-bipyridine and ethylenediamine together with metal-ion substitution, deuteration and ¹⁵N isotopic labelling of the amino group in 2-aminomethylpyridine enable reliable band assignments to be made. The study shows that in complexes of the type M(amp)nX₂, metal-to-amino-nitrogen stretches occur at frequencies greater than 350 cm⁻¹ , while the metal-to-pyridine-nitrogen stretches are generally below 300 cm⁻¹, the assignment of the latter being generally complicated by the presence of metal-to-halogen vibrations. In addition to an x-ray crystallographic investigation of the complex [Ni(amp)₃](BF₃ ₄)₂, considerable structural information about these complexes is obtained from correlations between the number of M-L vibrations observed in the far ir and those predicted for localized molecular point symmetries on a group theoretical basis."],"dc:identifier.uri":["http://hdl.handle.net/11427/18381"],"dc:language.iso":["eng"],"dc:publisher.department":["Department of Chemistry"],"dc:publisher.institution":["University of Cape Town"],"dc:title":["Isotopic labelling applied to the infrared spectra of metal complexes"],"dc:type":["Doctoral Thesis"],"dc:type.qualificationlevel":["Doctoral"],"dc:type.qualificationname":["PhD"]},"updated_at":"2026-07-22T22:23:07Z"}