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Lanthanide Luminescence in Visible-Light-Promoted Photochemical Reactions

The excitation of lanthanides with visible light to promote photochemical reactions has garnered interest in recent years. Lanthanides serve as initiators for photochemical reactions because they exhibit visible-light-promoted 4f→5d transitions that lead to emissive states with electrochemical poten...

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Autores principales: Barraza, Ramiro, Allen, Matthew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503482/
https://www.ncbi.nlm.nih.gov/pubmed/32858962
http://dx.doi.org/10.3390/molecules25173892
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author Barraza, Ramiro
Allen, Matthew J.
author_facet Barraza, Ramiro
Allen, Matthew J.
author_sort Barraza, Ramiro
collection PubMed
description The excitation of lanthanides with visible light to promote photochemical reactions has garnered interest in recent years. Lanthanides serve as initiators for photochemical reactions because they exhibit visible-light-promoted 4f→5d transitions that lead to emissive states with electrochemical potentials that are more negative than the corresponding ground states. The lanthanides that have shown the most promising characteristics for visible-light promoted photoredox are Sm(II), Eu(II), and Ce(III). By understanding the effects that ligands have on the 5d orbitals of Sm(II), Eu(II), and Ce(III), luminescence and reactivity can be rationally modulated using coordination chemistry. This review briefly overviews the photochemical reactivity of Sm(II), Eu(II), and Ce(III) with visible light; the properties that influence the reactivity of these ions; and the research that has been reported towards modulating their photochemical-relevant properties using visible light and coordination chemistry.
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spelling pubmed-75034822020-09-23 Lanthanide Luminescence in Visible-Light-Promoted Photochemical Reactions Barraza, Ramiro Allen, Matthew J. Molecules Review The excitation of lanthanides with visible light to promote photochemical reactions has garnered interest in recent years. Lanthanides serve as initiators for photochemical reactions because they exhibit visible-light-promoted 4f→5d transitions that lead to emissive states with electrochemical potentials that are more negative than the corresponding ground states. The lanthanides that have shown the most promising characteristics for visible-light promoted photoredox are Sm(II), Eu(II), and Ce(III). By understanding the effects that ligands have on the 5d orbitals of Sm(II), Eu(II), and Ce(III), luminescence and reactivity can be rationally modulated using coordination chemistry. This review briefly overviews the photochemical reactivity of Sm(II), Eu(II), and Ce(III) with visible light; the properties that influence the reactivity of these ions; and the research that has been reported towards modulating their photochemical-relevant properties using visible light and coordination chemistry. MDPI 2020-08-26 /pmc/articles/PMC7503482/ /pubmed/32858962 http://dx.doi.org/10.3390/molecules25173892 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Barraza, Ramiro
Allen, Matthew J.
Lanthanide Luminescence in Visible-Light-Promoted Photochemical Reactions
title Lanthanide Luminescence in Visible-Light-Promoted Photochemical Reactions
title_full Lanthanide Luminescence in Visible-Light-Promoted Photochemical Reactions
title_fullStr Lanthanide Luminescence in Visible-Light-Promoted Photochemical Reactions
title_full_unstemmed Lanthanide Luminescence in Visible-Light-Promoted Photochemical Reactions
title_short Lanthanide Luminescence in Visible-Light-Promoted Photochemical Reactions
title_sort lanthanide luminescence in visible-light-promoted photochemical reactions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503482/
https://www.ncbi.nlm.nih.gov/pubmed/32858962
http://dx.doi.org/10.3390/molecules25173892
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