The Supramolecular and Coordination Chemistry of Cobalt(II) Extraction by Phosphinic Acids. Issue 13 (3rd April 2018)

• Record Type: Journal Article
• Authors: Carson, Innis; Tasker, Peter A.; Love, Jason B.; Moser, Michael; Fischmann, Adam J.; Jakovljevic, Boban; Soderstrom, Matthew D.; Morrison, Carole A.
• Is Part Of: European journal of inorganic chemistry. Issue 13(2018)
• Page Start: 1511
• Page End: 1521
• Publication Date: 2018-04-03
• Subjects: Structure elucidation -- Coordination polymers -- Industrial chemistry -- Self‐assembly; Chemistry, Inorganic -- Periodicals; Organometallic chemistry -- Periodicals; Bioinorganic chemistry -- Periodicals; Solid state chemistry -- Periodicals; 546
• DOI: 10.1002/ejic.201701473
• Languages: English
• ISSNs: 1434-1948

Abstract

Abstract : A combination of mass spectrometry, DFT calculations and 31 P{ 1 H} NMR spectroscopy has been used to define the mode of action of the commercial cobalt extractant, bis(2, 4, 4‐trimethylpentyl)phosphinic acid (CYANEX®272, L 1 H) in Co recovery. The nature of the Co II complexes formed in the water‐immiscible phase is determined largely by the propensity of phosphinates to form strong interligand H‐bonds in the outer coordination sphere and also to form stable µ2 ‐Co–O–P–O–Co bridges. At low Co loading levels, the predominant species is the 4:1 complex, [Co(L 1 ·L 1 H)2 ], in which coordinated neutral phosphinic acid ligands form strong H‐bonds to adjacent anionic phosphinates. At higher Co loading, oligomers such as [(L 1 ·L 1 H)Co(L 1 2 Co) n (L 1 ·L 1 H)] are formed with µ2 ‐phosphinate bridging, resulting in a substantial increase in the viscosity of the water‐immiscible phase. The presence of tris(2, 4, 4‐trimethylpentyl)phosphine oxide (L 2 ) in the commercial formulation reduces the viscosity because its incorporation into oligomeric complexes such as [(L 2 )Co{L 1 3 CoL 1 CoL 1 3 Co}m L 1 ] can terminate chains, resulting in a lower average molecular weight. The uptake of Zn byL 1 H shows a very similar dependence of viscosity on loading, and DOSY spectra and mass spectrometry demonstrate that higher molecular weight species are present at high Zn loading. Abstract : 31 P{ 1 H} NMR spectroscopy, ESI‐mass spectrometry, and DFT calculations elucidate solution structures of Co II phosphinate complexes, which account for increased viscosity at high Co‐loading in solvent extraction by CYANEX® 272.