{"id":{"repo_id":"vt","oai_identifier":"oai:vtechworks.lib.vt.edu:10919/44467"},"canonical_url":"https://search.dev.ndltd.org/etd/vt/oai:vtechworks.lib.vt.edu:10919/44467","repository":{"repo_id":"vt","name":"Virginia Tech","base_url":"https://vtechworks.lib.vt.edu/oai/request"},"display":{"title":"An investigation of the nickel (II) and cobalt (II) complexes employing pentadentate ligands derived from salicylaldehyde and bis (3,3'- aminopropyl) ether or sulfide","abstract":"Complexes of the general formula M(X-SALDAPE) and M(X-SALDAPS) formed by the reaction of substituted salicylaldehydes and bis(3,3'-aminopropyl)ether or bis(3,3'-aminopropyl)sulfide with nickel(II) and cobalt(II) have been isolated. The complexes have been characterized by elemental analysis, mass spectra, infrared spectra, magnetic susceptibility measurements, and ultraviolet-visible-near infrared spectra. In the solid state the nickel(II) complexes, Ni(X-SALDAPE) and Ni(X-SALDAPS), where X = H, 5-Br, 3-(CH₃)₂CH, or 3-CH₃O, are speculated as pseudo-square planar or weak low-spin five-coordinate structures. The complexes exhibit anomalous magnetic behavior explained in terms of a spin state isomerism between singlet and triplet spin states. In a non-coordinating solvent, the nickel complexes are pseudo-square planar losing all five-coordinate structural features due to salvation. When dissolved in a coordinating solvent, the complexes are high-spin pseudo-octahedral. The cobalt(II) complexes, Co(H-SALDAPE) and Co(X-SALDAPS) where X = H, or 3-(CH₃)₂CH, were found to be high-spin pseudo-tetrahedral in the solid state with magnetic moments of approximately 3.4 B.M. The olive green nickel complexes are stable to air and moisture. The brownish cobalt complexes are stable as dry solids, but very easily oxidized when wet.","abstract_html":"Complexes of the general formula M(X-SALDAPE) and M(X-SALDAPS) formed by the reaction of substituted salicylaldehydes and bis(3,3&#x27;-aminopropyl)ether or bis(3,3&#x27;-aminopropyl)sulfide with nickel(II) and cobalt(II) have been isolated. The complexes have been characterized by elemental analysis, mass spectra, infrared spectra, magnetic susceptibility measurements, and ultraviolet-visible-near infrared spectra. In the solid state the nickel(II) complexes, Ni(X-SALDAPE) and Ni(X-SALDAPS), where X = H, 5-Br, 3-(CH₃)₂CH, or 3-CH₃O, are speculated as pseudo-square planar or weak low-spin five-coordinate structures. The complexes exhibit anomalous magnetic behavior explained in terms of a spin state isomerism between singlet and triplet spin states. In a non-coordinating solvent, the nickel complexes are pseudo-square planar losing all five-coordinate structural features due to salvation. When dissolved in a coordinating solvent, the complexes are high-spin pseudo-octahedral. The cobalt(II) complexes, Co(H-SALDAPE) and Co(X-SALDAPS) where X = H, or 3-(CH₃)₂CH, were found to be high-spin pseudo-tetrahedral in the solid state with magnetic moments of approximately 3.4 B.M. The olive green nickel complexes are stable to air and moisture. The brownish cobalt complexes are stable as dry solids, but very easily oxidized when wet.","abstract_has_math":false,"creators":["St. Clair, Anne K."],"institution":"Virginia Tech","degree_name":"Master of Science","degree_level":"masters","degree_discipline":"Chemistry","degree_department":"Chemistry","school":null,"contributors":[],"advisors":[],"committee_chairs":["Taylor, Larry T."],"committee_members":["Wightman, James P.","Ogliaruso, Michael A."],"year":1972,"date_issued":"1972","date_published":"1972","updated_at":"2026-07-22T22:20:41Z","subjects":[],"languages":[],"rights":["In Copyright"],"rights_urls":["http://rightsstatements.org/vocab/InC/1.0/"],"identifier_entries":[{"key":"dc:identifier.other","label":"Dc Identifier Other","values":["etd-08282003-155335"],"render_values":[{"text":"etd-08282003-155335","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/10919/44467","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.committeechair","label":"Committee Chair","values":["Taylor, Larry T."]},{"key":"dc:contributor.committeemember","label":"Committee Member","values":["Wightman, James P.","Ogliaruso, Michael A."]},{"key":"dc:contributor.department","label":"Department","values":["Chemistry"]},{"key":"dc:creator","label":"Author","values":["St. Clair, Anne K."]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2014-03-14T21:43:56Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2014-03-14T21:43:56Z","2003-08-28"]},{"key":"dc:date.issued","label":"Date","values":["1972"]},{"key":"dc:publisher","label":"Institution","values":["Virginia Tech"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.dcmitype","label":"Dc Type Dcmitype","values":["Text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Virginia Polytechnic Institute and State University"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:rights","label":"Dc Rights","values":["In Copyright"]},{"key":"dc:rights.uri","label":"Rights URI","values":["http://rightsstatements.org/vocab/InC/1.0/"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.other","label":"Dc Identifier Other","values":["etd-08282003-155335"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10919/44467"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Complexes of the general formula M(X-SALDAPE) and M(X-SALDAPS) formed by the reaction of substituted salicylaldehydes and bis(3,3'-aminopropyl)ether or bis(3,3'-aminopropyl)sulfide with nickel(II) and cobalt(II) have been isolated. The complexes have been characterized by elemental analysis, mass spectra, infrared spectra, magnetic susceptibility measurements, and ultraviolet-visible-near infrared spectra. In the solid state the nickel(II) complexes, Ni(X-SALDAPE) and Ni(X-SALDAPS), where X = H, 5-Br, 3-(CH₃)₂CH, or 3-CH₃O, are speculated as pseudo-square planar or weak low-spin five-coordinate structures. The complexes exhibit anomalous magnetic behavior explained in terms of a spin state isomerism between singlet and triplet spin states. In a non-coordinating solvent, the nickel complexes are pseudo-square planar losing all five-coordinate structural features due to salvation. When dissolved in a coordinating solvent, the complexes are high-spin pseudo-octahedral. The cobalt(II) complexes, Co(H-SALDAPE) and Co(X-SALDAPS) where X = H, or 3-(CH₃)₂CH, were found to be high-spin pseudo-tetrahedral in the solid state with magnetic moments of approximately 3.4 B.M. The olive green nickel complexes are stable to air and moisture. The brownish cobalt complexes are stable as dry solids, but very easily oxidized when wet."]},{"key":"dc:description.degree","label":"Dc Description Degree","values":["Master of Science"]},{"key":"dc:format.medium","label":"Dc Format Medium","values":["BTD"]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["An investigation of the nickel (II) and cobalt (II) complexes employing pentadentate ligands derived from salicylaldehyde and bis (3,3'- aminopropyl) ether or sulfide"]}]}],"canonical_facts":{"dc:contributor.committeechair":["Taylor, Larry T."],"dc:contributor.committeemember":["Wightman, James P.","Ogliaruso, Michael A."],"dc:contributor.department":["Chemistry"],"dc:creator":["St. Clair, Anne K."],"dc:date.accessioned":["2014-03-14T21:43:56Z"],"dc:date.available":["2014-03-14T21:43:56Z","2003-08-28"],"dc:date.issued":["1972"],"dc:description.abstract":["Complexes of the general formula M(X-SALDAPE) and M(X-SALDAPS) formed by the reaction of substituted salicylaldehydes and bis(3,3'-aminopropyl)ether or bis(3,3'-aminopropyl)sulfide with nickel(II) and cobalt(II) have been isolated. The complexes have been characterized by elemental analysis, mass spectra, infrared spectra, magnetic susceptibility measurements, and ultraviolet-visible-near infrared spectra. In the solid state the nickel(II) complexes, Ni(X-SALDAPE) and Ni(X-SALDAPS), where X = H, 5-Br, 3-(CH₃)₂CH, or 3-CH₃O, are speculated as pseudo-square planar or weak low-spin five-coordinate structures. The complexes exhibit anomalous magnetic behavior explained in terms of a spin state isomerism between singlet and triplet spin states. In a non-coordinating solvent, the nickel complexes are pseudo-square planar losing all five-coordinate structural features due to salvation. When dissolved in a coordinating solvent, the complexes are high-spin pseudo-octahedral. The cobalt(II) complexes, Co(H-SALDAPE) and Co(X-SALDAPS) where X = H, or 3-(CH₃)₂CH, were found to be high-spin pseudo-tetrahedral in the solid state with magnetic moments of approximately 3.4 B.M. The olive green nickel complexes are stable to air and moisture. The brownish cobalt complexes are stable as dry solids, but very easily oxidized when wet."],"dc:description.degree":["Master of Science"],"dc:format.medium":["BTD"],"dc:format.mimetype":["application/pdf"],"dc:identifier.other":["etd-08282003-155335"],"dc:identifier.uri":["http://hdl.handle.net/10919/44467"],"dc:publisher":["Virginia Tech"],"dc:rights":["In Copyright"],"dc:rights.uri":["http://rightsstatements.org/vocab/InC/1.0/"],"dc:title":["An investigation of the nickel (II) and cobalt (II) complexes employing pentadentate ligands derived from salicylaldehyde and bis (3,3'- aminopropyl) ether or sulfide"],"dc:type":["Thesis"],"dc:type.dcmitype":["Text"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["masters"],"thesis:degree_name":["Master of Science"],"thesis:institution_name":["Virginia Polytechnic Institute and State University"]},"updated_at":"2026-07-22T22:20:41Z"}