Tuning the solubilities of bis-triazinylphenanthroline ligands (BTPhens) and their complexes

[thumbnail of HeterocyclesPaper.pdf]
Preview
Text - Accepted Version
· Please see our End User Agreement before downloading.
| Preview

Please see our End User Agreement.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email

Laventine, D. M., Afsar, A., Hudson, M. J. and Harwood, L. M. orcid id iconORCID: https://orcid.org/0000-0002-8442-7380 (2012) Tuning the solubilities of bis-triazinylphenanthroline ligands (BTPhens) and their complexes. Heterocycles. ISSN 1881-0942 doi: 10.3987/COM-12-S(N)102

Abstract/Summary

A series of bis-triazinylphenanthroline ligands (BTPhens) was synthesized by modifying the triazine substituents. It was found that varying these substituents altered the solubilities of the ligands in a number of non-polar solvents. Thus C5-BTPhen showed significantly higher solubility in octanol than C1-BTPhen. The high solubility of C5-BTPhen and its complexes was exploited to facilitate the NMR titration experiments. These experiments shown that the dominant species in solution were the 1:2 complexes [Ln(III)(BTPhen)2], even at high Ln concentrations, and that the relative stability of the 2:1 to 1:1 BTPhen-Ln complexes varied with different lanthanides. C5-BTPhen therefore shows considerable promise for a once-through selective actinide separation process.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/29466
Identification Number/DOI 10.3987/COM-12-S(N)102
Refereed Yes
Divisions Interdisciplinary centres and themes > Chemical Analysis Facility (CAF)
Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
Publisher The Japan Institute of Heterocyclic Chemistry
Download/View statistics View download statistics for this item

Downloads

Downloads per month over past year

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar