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Tailoring the pore size of expanded porphyrinoids for lanthanide selectivity

Despite increase in demand, capacity for the recycling of rare earth elements remains limited, partly due to the inefficiencies with processes currently utilised in the separation of lanthanides. This study highlights the potential use of expanded porphyrinoids in lanthanide separation through selec...

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Detalles Bibliográficos
Autores principales: Malcomson, Thomas, Edwards-Yates, Lewis, Kerridge, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523133/
https://www.ncbi.nlm.nih.gov/pubmed/37771918
http://dx.doi.org/10.1039/d3ra05710k
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author Malcomson, Thomas
Edwards-Yates, Lewis
Kerridge, Andrew
author_facet Malcomson, Thomas
Edwards-Yates, Lewis
Kerridge, Andrew
author_sort Malcomson, Thomas
collection PubMed
description Despite increase in demand, capacity for the recycling of rare earth elements remains limited, partly due to the inefficiencies with processes currently utilised in the separation of lanthanides. This study highlights the potential use of expanded porphyrinoids in lanthanide separation through selective binding, dependent on the tailored pore size of the macrocycle. Each emerging trend is subjected to multi-factored analysis to decompose the underlying source. Results promote the viability of size-based separation with preferential binding of larger lanthanum(iii) ions to amethyrin and isoamethyrin macrocycles, while smaller macrocycles such as pentaphyrin(0.0.0.0.0) present a preferential binding of lutetium(iii) ions. Additionally, the porphyrin(2.2.2.2) macrocycle shows a selectivity for gadolinium(iii) ions over both larger and smaller ions. An upper limit of applicable pore size is shown to be ≈2.8 Å, beyond which the formed complexes are predicted to be less stable than the corresponding nitrate complexes.
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spelling pubmed-105231332023-09-28 Tailoring the pore size of expanded porphyrinoids for lanthanide selectivity Malcomson, Thomas Edwards-Yates, Lewis Kerridge, Andrew RSC Adv Chemistry Despite increase in demand, capacity for the recycling of rare earth elements remains limited, partly due to the inefficiencies with processes currently utilised in the separation of lanthanides. This study highlights the potential use of expanded porphyrinoids in lanthanide separation through selective binding, dependent on the tailored pore size of the macrocycle. Each emerging trend is subjected to multi-factored analysis to decompose the underlying source. Results promote the viability of size-based separation with preferential binding of larger lanthanum(iii) ions to amethyrin and isoamethyrin macrocycles, while smaller macrocycles such as pentaphyrin(0.0.0.0.0) present a preferential binding of lutetium(iii) ions. Additionally, the porphyrin(2.2.2.2) macrocycle shows a selectivity for gadolinium(iii) ions over both larger and smaller ions. An upper limit of applicable pore size is shown to be ≈2.8 Å, beyond which the formed complexes are predicted to be less stable than the corresponding nitrate complexes. The Royal Society of Chemistry 2023-09-27 /pmc/articles/PMC10523133/ /pubmed/37771918 http://dx.doi.org/10.1039/d3ra05710k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Malcomson, Thomas
Edwards-Yates, Lewis
Kerridge, Andrew
Tailoring the pore size of expanded porphyrinoids for lanthanide selectivity
title Tailoring the pore size of expanded porphyrinoids for lanthanide selectivity
title_full Tailoring the pore size of expanded porphyrinoids for lanthanide selectivity
title_fullStr Tailoring the pore size of expanded porphyrinoids for lanthanide selectivity
title_full_unstemmed Tailoring the pore size of expanded porphyrinoids for lanthanide selectivity
title_short Tailoring the pore size of expanded porphyrinoids for lanthanide selectivity
title_sort tailoring the pore size of expanded porphyrinoids for lanthanide selectivity
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523133/
https://www.ncbi.nlm.nih.gov/pubmed/37771918
http://dx.doi.org/10.1039/d3ra05710k
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