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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
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).
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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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