{"id":{"repo_id":"vt","oai_identifier":"oai:vtechworks.lib.vt.edu:10919/41963"},"canonical_url":"https://search.dev.ndltd.org/etd/vt/oai:vtechworks.lib.vt.edu:10919/41963","repository":{"repo_id":"vt","name":"Virginia Tech","base_url":"https://vtechworks.lib.vt.edu/oai/request"},"display":{"title":"A polarographic investigation of the reduction mechanism of certain cobalt (III) complex ions","abstract":"A series of eight compounds with bis-diamine cores were prepared and their electrochemical behavior was explored polarographically. The behavior of the compounds was studied at the dropping mercury electrode and the rotating platinum electrode. Trans-dinitro-bis-(ethylenediamine) cobalt (III) nitrate shows reversible behavior in well-buffered solutions at the dropping mercury electrode, The mechanism for the reduction is proposed as; rapid, reversible election transfer; decomposition of the reduced species; and, in solutions sufficiently alkaline, the formation of tris-(ethylenediamine) cobalt (II), thereby accounting for the observed second wave. The reduction of cis dithiocyanato-bis-(ethylenediamine) cobalt (III) thiocyanate and oxalato-bis-(ethylenediamine) cobalt (III) chloride both give irreversible waves, thereby complicating any proposal of a mechanism. The observed second reduction wave, though, appears to be caused by the formation of tris-(ethylenediamine) cobalt (II), as in the case of the dinitro compound. A proposal of the mechanism for the other five compounds was not possible as they either reduced at too positive a potential, aquated too rapidly, or both.","abstract_html":"A series of eight compounds with bis-diamine cores were prepared and their electrochemical behavior was explored polarographically. The behavior of the compounds was studied at the dropping mercury electrode and the rotating platinum electrode. Trans-dinitro-bis-(ethylenediamine) cobalt (III) nitrate shows reversible behavior in well-buffered solutions at the dropping mercury electrode, The mechanism for the reduction is proposed as; rapid, reversible election transfer; decomposition of the reduced species; and, in solutions sufficiently alkaline, the formation of tris-(ethylenediamine) cobalt (II), thereby accounting for the observed second wave. The reduction of cis dithiocyanato-bis-(ethylenediamine) cobalt (III) thiocyanate and oxalato-bis-(ethylenediamine) cobalt (III) chloride both give irreversible waves, thereby complicating any proposal of a mechanism. The observed second reduction wave, though, appears to be caused by the formation of tris-(ethylenediamine) cobalt (II), as in the case of the dinitro compound. A proposal of the mechanism for the other five compounds was not possible as they either reduced at too positive a potential, aquated too rapidly, or both.","abstract_has_math":false,"creators":["White, Richard Lee"],"institution":"Virginia Tech","degree_name":"Master of Science","degree_level":"masters","degree_discipline":"Chemistry","degree_department":"Chemistry","school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1962,"date_issued":"1962","date_published":"1962","updated_at":"2026-07-22T22:19:18Z","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-04072010-020112"],"render_values":[{"text":"etd-04072010-020112","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/10919/41963","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.department","label":"Department","values":["Chemistry"]},{"key":"dc:creator","label":"Author","values":["White, Richard Lee"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2014-03-14T21:33:10Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2014-03-14T21:33:10Z","2010-04-07"]},{"key":"dc:date.issued","label":"Date","values":["1962"]},{"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"]}]},{"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-04072010-020112"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10919/41963"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["A series of eight compounds with bis-diamine cores were prepared and their electrochemical behavior was explored polarographically. The behavior of the compounds was studied at the dropping mercury electrode and the rotating platinum electrode. Trans-dinitro-bis-(ethylenediamine) cobalt (III) nitrate shows reversible behavior in well-buffered solutions at the dropping mercury electrode, The mechanism for the reduction is proposed as; rapid, reversible election transfer; decomposition of the reduced species; and, in solutions sufficiently alkaline, the formation of tris-(ethylenediamine) cobalt (II), thereby accounting for the observed second wave. The reduction of cis dithiocyanato-bis-(ethylenediamine) cobalt (III) thiocyanate and oxalato-bis-(ethylenediamine) cobalt (III) chloride both give irreversible waves, thereby complicating any proposal of a mechanism. The observed second reduction wave, though, appears to be caused by the formation of tris-(ethylenediamine) cobalt (II), as in the case of the dinitro compound. A proposal of the mechanism for the other five compounds was not possible as they either reduced at too positive a potential, aquated too rapidly, or both."]},{"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":["A polarographic investigation of the reduction mechanism of certain cobalt (III) complex ions"]}]}],"canonical_facts":{"dc:contributor.department":["Chemistry"],"dc:creator":["White, Richard Lee"],"dc:date.accessioned":["2014-03-14T21:33:10Z"],"dc:date.available":["2014-03-14T21:33:10Z","2010-04-07"],"dc:date.issued":["1962"],"dc:description.abstract":["A series of eight compounds with bis-diamine cores were prepared and their electrochemical behavior was explored polarographically. The behavior of the compounds was studied at the dropping mercury electrode and the rotating platinum electrode. Trans-dinitro-bis-(ethylenediamine) cobalt (III) nitrate shows reversible behavior in well-buffered solutions at the dropping mercury electrode, The mechanism for the reduction is proposed as; rapid, reversible election transfer; decomposition of the reduced species; and, in solutions sufficiently alkaline, the formation of tris-(ethylenediamine) cobalt (II), thereby accounting for the observed second wave. The reduction of cis dithiocyanato-bis-(ethylenediamine) cobalt (III) thiocyanate and oxalato-bis-(ethylenediamine) cobalt (III) chloride both give irreversible waves, thereby complicating any proposal of a mechanism. The observed second reduction wave, though, appears to be caused by the formation of tris-(ethylenediamine) cobalt (II), as in the case of the dinitro compound. A proposal of the mechanism for the other five compounds was not possible as they either reduced at too positive a potential, aquated too rapidly, or both."],"dc:description.degree":["Master of Science"],"dc:format.medium":["BTD"],"dc:format.mimetype":["application/pdf"],"dc:identifier.other":["etd-04072010-020112"],"dc:identifier.uri":["http://hdl.handle.net/10919/41963"],"dc:publisher":["Virginia Tech"],"dc:rights":["In Copyright"],"dc:rights.uri":["http://rightsstatements.org/vocab/InC/1.0/"],"dc:title":["A polarographic investigation of the reduction mechanism of certain cobalt (III) complex ions"],"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"]},"updated_at":"2026-07-22T22:19:18Z"}