Tbe quantitative extraction of iron(II1) and gallium(II1) was investigated with the recently synthesized macrocyclic Schiff base containing bisphenol A subunits. The phenol groups in the Schiff base moiety led to a large increase in the percent extraction of trivalent metal ions. The substitution of
Liquid-liquid extraction of manganese(II), copper(II) and zinc(II) with acyclic and macrocyclic Schiff bases containing bisphenol A subunits
✍ Scribed by Shigeki Abe; Kazuhito Fujii; Tyo Sono
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 566 KB
- Volume
- 293
- Category
- Article
- ISSN
- 0003-2670
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✦ Synopsis
Acyclic and macrocyclic Schiff bases containing bisphenol A subunits were synthesized and the effect of ligand atoms on the liquid-liquid extraction of manganese(II), copper(U) and zinc011 was studied. The phenol groups in the Schiff base moiety led to a large increase in the percent extraction of transition metal ions. The substitution of methoxy groups for phenolic OH ligands resulted in a marked decrease in the extractability of metal ions. Compared with a macrocyclic Schiff base, the corresponding acyclic counterpart was found to have a reasonable reactivity toward metal ions and a better solubility in organic solvents. The copper(H) complexes with acyclic Schiff bases were quantitatively extracted into nitrobenz.ene without the presence of bulky counter anions. Mutual separation of &&I), copper(H) and manganese(I1) can be achieved by a proper selection of pH and extractant.
📜 SIMILAR VOLUMES
## Abstract Three ferrocenyl Schiff bases containing a phenol moiety have been formed by 1:1 molar condensation of acetylferrocene with 2‐aminophenol, 2‐amino‐5‐picoline or 2‐amino‐5‐chlorophenol. These ligands form 2:1 complexs with cobalt(II), copper(II), nickel(II), and zinc(II) ions. From the d