Molecular Design of a Calix[6]arene-Based Super-Uranophile with C3 Symmetry. High UO22+ Selectivity in Solvent Extraction
- 1 May 1993
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 22 (5), 829-832
- https://doi.org/10.1246/cl.1993.829
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Stereognostic coordination chemistry. 1. The design and synthesis of chelators for the uranyl ionJournal of the American Chemical Society, 1992
- A New Calix[6]arene-Based Uranophile with Phosphonate Groups as LigandsBulletin of the Chemical Society of Japan, 1991
- Molecular design of calixarene-based uranophiles which exhibit remarkably high stability and selectivityJournal of the American Chemical Society, 1987
- Macrocyclic tridithiocarbamate as a specific uranophileJournal of the American Chemical Society, 1984
- Templated syntheses of cyclic acetylacetone hosts, their affinities for divalent ions, and an example of a slow proton transfer from enol to hydroxide ionJournal of the American Chemical Society, 1977