270
Views
31
CrossRef citations to date
0
Altmetric
Original Articles

Crystallographic Determination of Three Ni-α-Hydroxyoxime-Carboxylic Acid Synergist Complexes

, , &
Pages 778-792 | Published online: 06 Nov 2010
 

Abstract

X-ray crystal structures of three dicarboxylato-bis-α-hydroxyoximenickel(II) complexes have been obtained. These contain a short chained (C8) analogue of LIX®63 hydroxyoxime, along with either benzoate, isobutyrate or propionate. All have pseudo-octahedral structures with monodentate carboxylate anions located cis to one another and neutral, chelating α-hydroxyoxime ligands. Intra-molecular hydrogen bonding between each anionic acid's carboxylate group and an adjacent oxime hydroxyl group is evident. Inter-molecular hydrogen bonding is also observed. These provide the first definitive structural elucidation of the types of nickel complexes that could be formed during synergistic extraction by LIX®63 and carboxylic acids.

ACKNOWLEDGMENTS

The support of the Minerals Down Under National Research Flagship and Parker CRC for Integrated Hydrometallurgy Solutions (established and supported under the Australian Government's Cooperative Research Centres Program) is gratefully acknowledged. Mr. D. Shiers and Dr. M. Tsuntsaeva obtained the UV spectra of the commercial reagent nickel complexes.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 876.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.