{"title":"Labile Ligand‐Substitution Reactions of Intermediate‐Spin Six‐Coordinate Cobalt(III) Complexes","authors":"C. Becker","doi":"10.1081/SIM-200026582","DOIUrl":null,"url":null,"abstract":"Abstract Three intermediate‐spin, six‐coordinate Co(III) complexes, [Co(CNCH2Ph)4{OAs(C6H4Me‐p)3}2](BF4)3, [Co(CNC6H11)4(OSbPh3)2](ClO4)3, and [Co(CNCH2Ph)4(OSbPh3)2](BF4)3, are shown to undergo labile ligand‐substitution reactions with selected trialkylphosphine ligands. Percent yields in reactions of [Co(CNCH2Ph)4{OAs(C6H4Me‐p)3}2](BF4)3 increase significantly when reactions are performed at lowered temperatures. [Co(CNC6H11)4(OSbPh3)2](ClO4)3 and [Co(CNCH2Ph)4(OSbPh3)2](BF4)3 react with P(C3H7‐n)3 and P(C4H9‐n)3 immediately at 0 °C to produce the known complexes, trans‐[Co(CNR)4(PR′3)2]X3, in good yields.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"17 1","pages":"1543 - 1549"},"PeriodicalIF":0.0000,"publicationDate":"2004-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1081/SIM-200026582","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Abstract Three intermediate‐spin, six‐coordinate Co(III) complexes, [Co(CNCH2Ph)4{OAs(C6H4Me‐p)3}2](BF4)3, [Co(CNC6H11)4(OSbPh3)2](ClO4)3, and [Co(CNCH2Ph)4(OSbPh3)2](BF4)3, are shown to undergo labile ligand‐substitution reactions with selected trialkylphosphine ligands. Percent yields in reactions of [Co(CNCH2Ph)4{OAs(C6H4Me‐p)3}2](BF4)3 increase significantly when reactions are performed at lowered temperatures. [Co(CNC6H11)4(OSbPh3)2](ClO4)3 and [Co(CNCH2Ph)4(OSbPh3)2](BF4)3 react with P(C3H7‐n)3 and P(C4H9‐n)3 immediately at 0 °C to produce the known complexes, trans‐[Co(CNR)4(PR′3)2]X3, in good yields.