Structure Activity Relationship Approach toward the Improved Separation of Rare-Earth Elements Using Diglycolamides
Author(s) -
Diāna Stamberga,
Mary R. Healy,
Vyacheslav S. Bryantsev,
Camille Albisser,
Yana Karslyan,
Benjamin Reinhart,
Alena Paulenová,
Mac Foster,
Ilja Popovs,
Kevin L. Lyon,
Bruce A. Moyer,
Santa JansonePopova
Publication year - 2020
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.0c02861
Subject(s) - lanthanide , chemistry , steric effects , alkyl , hydrochloric acid , rare earth , selectivity , extraction (chemistry) , inorganic chemistry , crystallography , stereochemistry , ion , organic chemistry , catalysis , mineralogy
The separation of adjacent lanthanides continues to be a challenge worldwide because of the similar physical and chemical properties of these elements and a necessity to advance the use of clean-energy applications. Herein, a systematic structure-performance relationship approach toward understanding the effect of N -alkyl group characteristics in diglycolamides (DGAs) on the separation of lanthanides(III) from a hydrochloric acid medium is presented. In addition to the three most extensively studied DGA complexants [ N , N , N ', N '-tetra( n -octyl)diglycolamide, TODGA; N , N , N ', N '-tetra(2-ethylhexyl)diglycolamide, TEHDGA; N , N '-dimethyl- N , N '-di( n -octyl)diglycolamide, DMDODGA], 12 new extracting agents with varying substitution patterns were designed to study the interplay of steric and electronic effects that control rare-earth element extraction. Subtle changes in the structure around diglycolamide carbonyl oxygen atoms result in dramatic shifts in the lanthanide extraction strength and selectivity. The effects of the chain length and branching position of N -alkyl substituents in DGAs are elaborated on with the use of experimental, computational, and solution-structure characterization techniques.
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