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Activation of the Aromatic Core of 3,3′-(Pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol)—Effects on Extraction Performance, Stability Constants, and Basicity
[Image: see text] The “CHON” compatible water-soluble ligand 3,3′-(pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol) (PTD) has shown promise for selectively stripping actinide ions from an organic phase containing both actinide and lanthanide ions, by preferential complexation of the...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6863594/ https://www.ncbi.nlm.nih.gov/pubmed/31609595 http://dx.doi.org/10.1021/acs.inorgchem.9b02325 |
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author | Weßling, Patrik Trumm, Michael Macerata, Elena Ossola, Annalisa Mossini, Eros Gullo, Maria Chiara Arduini, Arturo Casnati, Alessandro Mariani, Mario Adam, Christian Geist, Andreas Panak, Petra J. |
author_facet | Weßling, Patrik Trumm, Michael Macerata, Elena Ossola, Annalisa Mossini, Eros Gullo, Maria Chiara Arduini, Arturo Casnati, Alessandro Mariani, Mario Adam, Christian Geist, Andreas Panak, Petra J. |
author_sort | Weßling, Patrik |
collection | PubMed |
description | [Image: see text] The “CHON” compatible water-soluble ligand 3,3′-(pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol) (PTD) has shown promise for selectively stripping actinide ions from an organic phase containing both actinide and lanthanide ions, by preferential complexation of the former. Aiming at improving its complexation properties, PTD-OMe was synthesized, bearing a methoxy group on the central pyridine ring, thus increasing its basicity and hence complexation strength. Unfortunately, solvent extraction experiments in the range of 0.1–1 mol/L nitric acid proved PTD-OMe to be less efficient than PTD. This behavior is explained by its greater pK(a) value (pK(a) = 2.54) compared to PTD (pK(a) = 2.1). This counteracts its improved complexation properties for Cm(III) (log β(3)(PTD-OMe) = 10.8 ± 0.4 versus log β(3)(PTD) = 9.9 ± 0.5). |
format | Online Article Text |
id | pubmed-6863594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-68635942019-11-20 Activation of the Aromatic Core of 3,3′-(Pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol)—Effects on Extraction Performance, Stability Constants, and Basicity Weßling, Patrik Trumm, Michael Macerata, Elena Ossola, Annalisa Mossini, Eros Gullo, Maria Chiara Arduini, Arturo Casnati, Alessandro Mariani, Mario Adam, Christian Geist, Andreas Panak, Petra J. Inorg Chem [Image: see text] The “CHON” compatible water-soluble ligand 3,3′-(pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol) (PTD) has shown promise for selectively stripping actinide ions from an organic phase containing both actinide and lanthanide ions, by preferential complexation of the former. Aiming at improving its complexation properties, PTD-OMe was synthesized, bearing a methoxy group on the central pyridine ring, thus increasing its basicity and hence complexation strength. Unfortunately, solvent extraction experiments in the range of 0.1–1 mol/L nitric acid proved PTD-OMe to be less efficient than PTD. This behavior is explained by its greater pK(a) value (pK(a) = 2.54) compared to PTD (pK(a) = 2.1). This counteracts its improved complexation properties for Cm(III) (log β(3)(PTD-OMe) = 10.8 ± 0.4 versus log β(3)(PTD) = 9.9 ± 0.5). American Chemical Society 2019-10-14 2019-11-04 /pmc/articles/PMC6863594/ /pubmed/31609595 http://dx.doi.org/10.1021/acs.inorgchem.9b02325 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Weßling, Patrik Trumm, Michael Macerata, Elena Ossola, Annalisa Mossini, Eros Gullo, Maria Chiara Arduini, Arturo Casnati, Alessandro Mariani, Mario Adam, Christian Geist, Andreas Panak, Petra J. Activation of the Aromatic Core of 3,3′-(Pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol)—Effects on Extraction Performance, Stability Constants, and Basicity |
title | Activation of the Aromatic Core of 3,3′-(Pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol)—Effects
on Extraction Performance, Stability Constants, and Basicity |
title_full | Activation of the Aromatic Core of 3,3′-(Pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol)—Effects
on Extraction Performance, Stability Constants, and Basicity |
title_fullStr | Activation of the Aromatic Core of 3,3′-(Pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol)—Effects
on Extraction Performance, Stability Constants, and Basicity |
title_full_unstemmed | Activation of the Aromatic Core of 3,3′-(Pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol)—Effects
on Extraction Performance, Stability Constants, and Basicity |
title_short | Activation of the Aromatic Core of 3,3′-(Pyridine-2,6-diylbis(1H-1,2,3-triazole-4,1-diyl))bis(propan-1-ol)—Effects
on Extraction Performance, Stability Constants, and Basicity |
title_sort | activation of the aromatic core of 3,3′-(pyridine-2,6-diylbis(1h-1,2,3-triazole-4,1-diyl))bis(propan-1-ol)—effects
on extraction performance, stability constants, and basicity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6863594/ https://www.ncbi.nlm.nih.gov/pubmed/31609595 http://dx.doi.org/10.1021/acs.inorgchem.9b02325 |
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