{"id":{"repo_id":"cape-town","oai_identifier":"oai:open.uct.ac.za:11427/6337"},"canonical_url":"https://search.dev.ndltd.org/etd/cape-town/oai:open.uct.ac.za:11427/6337","repository":{"repo_id":"cape-town","name":"University of Cape Town","base_url":"https://open.uct.ac.za/oai/request"},"display":{"title":"Synthesis and characterization of nickel, palladium and chromium complexes as olefin oligomerization catalysts","abstract":"New N-functionalized 2-phosphinobenzaldimino (P^N) ligands (L) bearing 3-picolyl (41), furfuryl (42), thiophene-2-methyl (43), thiophene-2-ethyl (44), and benzyl (45) groups have been prepared in good yield. In addition, 2-iminopyridyl (N^N) (46), 2-bromobenzaldimino (47), and 2-phenoxyimino (O^N) (48) ligands and precursors, bearing furfuryl groups, were prepared in good yield. The amino analogues of 47 and 48 were obtained by reduction of the imine bonds using sodium borohydride. All compounds were fully characterized using spectroscopic and analytical techniques, including melting point, ¹H, ¹³C, and ³¹P NMR, IR spectroscopy, MS, and elemental analysis. These ligands (L) were reacted with appropriate metal precursors to give the corresponding metal complexes of the type PdLMeCl (51 – 55), PdLCl₂ (56 – 63), NiLBr₂ (75 – 82), and CrL(THF)Cl₃ (83 – 88).","abstract_html":"New N-functionalized 2-phosphinobenzaldimino (P^N) ligands (L) bearing 3-picolyl (41), furfuryl (42), thiophene-2-methyl (43), thiophene-2-ethyl (44), and benzyl (45) groups have been prepared in good yield. In addition, 2-iminopyridyl (N^N) (46), 2-bromobenzaldimino (47), and 2-phenoxyimino (O^N) (48) ligands and precursors, bearing furfuryl groups, were prepared in good yield. The amino analogues of 47 and 48 were obtained by reduction of the imine bonds using sodium borohydride. All compounds were fully characterized using spectroscopic and analytical techniques, including melting point, ¹H, ¹³C, and ³¹P NMR, IR spectroscopy, MS, and elemental analysis. These ligands (L) were reacted with appropriate metal precursors to give the corresponding metal complexes of the type PdLMeCl (51 – 55), PdLCl₂ (56 – 63), NiLBr₂ (75 – 82), and CrL(THF)Cl₃ (83 – 88).","abstract_has_math":false,"creators":["Mogorosi, Moses Mokgolela"],"institution":"Department of Chemistry","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Moss, John R","Smith, Gregory S"],"committee_chairs":[],"committee_members":[],"year":2009,"date_issued":"2009","date_published":"2009","updated_at":"2026-07-22T22:23:24Z","subjects":[],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/11427/6337","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Moss, John R","Smith, Gregory S"]},{"key":"dc:creator","label":"Author","values":["Mogorosi, Moses Mokgolela"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2014-08-13T14:27:16Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2014-08-13T14:27:16Z"]},{"key":"dc:date.issued","label":"Date","values":["2009"]},{"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/11427/6337"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Includes abstract.","Includes bibliographical references.","Has accompanying material on CD."]},{"key":"dc:description.abstract","label":"Abstract","values":["New N-functionalized 2-phosphinobenzaldimino (P^N) ligands (L) bearing 3-picolyl (41), furfuryl (42), thiophene-2-methyl (43), thiophene-2-ethyl (44), and benzyl (45) groups have been prepared in good yield. In addition, 2-iminopyridyl (N^N) (46), 2-bromobenzaldimino (47), and 2-phenoxyimino (O^N) (48) ligands and precursors, bearing furfuryl groups, were prepared in good yield. The amino analogues of 47 and 48 were obtained by reduction of the imine bonds using sodium borohydride. All compounds were fully characterized using spectroscopic and analytical techniques, including melting point, ¹H, ¹³C, and ³¹P NMR, IR spectroscopy, MS, and elemental analysis. These ligands (L) were reacted with appropriate metal precursors to give the corresponding metal complexes of the type PdLMeCl (51 – 55), PdLCl₂ (56 – 63), NiLBr₂ (75 – 82), and CrL(THF)Cl₃ (83 – 88)."]},{"key":"dc:title","label":"Title","values":["Synthesis and characterization of nickel, palladium and chromium complexes as olefin oligomerization catalysts"]}]}],"canonical_facts":{"dc:contributor.advisor":["Moss, John R","Smith, Gregory S"],"dc:creator":["Mogorosi, Moses Mokgolela"],"dc:date.accessioned":["2014-08-13T14:27:16Z"],"dc:date.available":["2014-08-13T14:27:16Z"],"dc:date.issued":["2009"],"dc:description":["Includes abstract.","Includes bibliographical references.","Has accompanying material on CD."],"dc:description.abstract":["New N-functionalized 2-phosphinobenzaldimino (P^N) ligands (L) bearing 3-picolyl (41), furfuryl (42), thiophene-2-methyl (43), thiophene-2-ethyl (44), and benzyl (45) groups have been prepared in good yield. In addition, 2-iminopyridyl (N^N) (46), 2-bromobenzaldimino (47), and 2-phenoxyimino (O^N) (48) ligands and precursors, bearing furfuryl groups, were prepared in good yield. The amino analogues of 47 and 48 were obtained by reduction of the imine bonds using sodium borohydride. All compounds were fully characterized using spectroscopic and analytical techniques, including melting point, ¹H, ¹³C, and ³¹P NMR, IR spectroscopy, MS, and elemental analysis. These ligands (L) were reacted with appropriate metal precursors to give the corresponding metal complexes of the type PdLMeCl (51 – 55), PdLCl₂ (56 – 63), NiLBr₂ (75 – 82), and CrL(THF)Cl₃ (83 – 88)."],"dc:identifier.uri":["http://hdl.handle.net/11427/6337"],"dc:language.iso":["eng"],"dc:publisher.department":["Department of Chemistry"],"dc:publisher.institution":["University of Cape Town"],"dc:title":["Synthesis and characterization of nickel, palladium and chromium complexes as olefin oligomerization catalysts"],"dc:type":["Doctoral Thesis"],"dc:type.qualificationlevel":["Doctoral"],"dc:type.qualificationname":["PhD"]},"updated_at":"2026-07-22T22:23:24Z"}