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The impact of alicyclic substituents on the extraction ability of new family of 1,10-phenanthroline-2,9-diamides
Development of efficient extractants for the separation of actinides and lanthanides in the technologies of nuclear fuel cycle is one of the most urgent and complex tasks in modern nuclear energetics. New family of 4,7-dichloro-1,10-phenanthroline-2,9-dicarboxylic acid diamides based on cyclic amine...
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Published in: | RSC advances 2020-07, Vol.1 (44), p.2622-2633 |
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Main Authors: | , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Development of efficient extractants for the separation of actinides and lanthanides in the technologies of nuclear fuel cycle is one of the most urgent and complex tasks in modern nuclear energetics. New family of 4,7-dichloro-1,10-phenanthroline-2,9-dicarboxylic acid diamides based on cyclic amines was synthesized and shown to exhibit high selectivity in the La/Am pair separation (SF (Am/La 10)) and in the Am/Eu pair separation (SF (Am/Eu 12)). It was shown that pyrrolidine derived diamide is more efficient extractant for americium, curium and lanthanides from highly acidic HNO
3
solution than its non-cyclic
N
,
N
,
N
′,
N
′-tetraalkyl analogues. The structures of synthesized compounds were studied in details by IR, NMR spectroscopy, and single crystal X-ray diffraction. According to spectroscopy data, incorporation of aromatic rings to the amide fragment of ligand leads to complex dynamic behavior in solutions what is believed to strongly affect the extraction ability of synthesized ligands.
Some unexpected "structure-extraction properties" patterns were found for new family of 1,10-phenanthroline-2,9-diamide derived ligands. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/d0ra05182a |