Journal
TALANTA
Volume 84, Issue 4, Pages 1047-1056Publisher
ELSEVIER
DOI: 10.1016/j.talanta.2011.03.008
Keywords
Adduct formation; ICP-MS; Lanthanoids; MM2 calculation; Polyether; Substituent effect; Synergistic extraction
Categories
Funding
- Ministry of Education, Culture, Sports, Science and Technology of the Government of Japan [18550068]
- Grants-in-Aid for Scientific Research [18550068] Funding Source: KAKEN
Ask authors/readers for more resources
The synergistic extraction of 14 trivalent lanthanoids (Ln(3+)) into 1,2-dichloroethane with a linear polyether (DEO6), HO(C2H4O)(6)C12H25, and beta-diketones (HA) having different substituents was investigated at 25.0 degrees C. The HAs used were trifluoroacetylacetone (Htfa), thenoyltrifluoroacetone (Htta), benzoyltrifluoroacetone (Hbta), naphthoyltrifluoroacetone (Hnta), and pivaloyltrifluoroacetone (Hpta). By the extraction of Ln(3+) with beta-diketone alone, the extraction constants of the neutral LnA(3) complex, K-ex = [LnA(3)](org)[H+](aq)(3)/[Ln(3+)](aq) [HA](org)(3), were determined. The intrinsic extraction constants, K-ex(center dot) = [LnA(3)](org)/[Ln(3+)](aq)[A(-)](aq)(3), were evaluated by employing the regular solution theory. Results indicate that the extractability of LnA(3) is dependent on the lipophilicity of the ligand, and the planar aromatic rings do not cause steric hindrance in the formation of the binary complex. Addition of DEO6 significantly enhanced the extraction of Ln(3+) by the formation of LnA(3)(DEO6). The ternary complex formation constants, beta(add), were determined for all the Ln(3+) and HA. The beta(add) of bta(-) and nta(-) complexes is similar with those of tfa(-) complexes, indicating that planar aromatic rings do not sterically hinder even the formation of the ternary complex. The higher values of beta(add) for the complexes of tta(-), which has a slightly dipolar thenoyl moiety, can be accounted for the presence of ligand-ligand interaction. The formation constants of the ternary complexes of pta(-) were lower compared to complexes of other beta-diketones because of steric hindrance due to the bulky t-butyl moiety. The detailed structures of the ternary complexes in solution were elucidated by NMR spectroscopy. Estimated structures sufficiently explain the variation in stability constants of LnA(3)(DEO6) among HAs and across the series of Ln(3+). The structures thus obtained were ascertained by the molecular models created by MM2 calculation. (C) 2011 Elsevier B.V. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available