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Sensitization-initiated electron transfer via upconversion: mechanism and photocatalytic applications
Sensitization-initiated electron transfer (SenI-ET) describes a recently discovered photoredox strategy that relies on two consecutive light absorption events, triggering a sequence of energy and electron transfer steps. The cumulative energy input from two visible photons gives access to thermodyna...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317647/ https://www.ncbi.nlm.nih.gov/pubmed/34349964 http://dx.doi.org/10.1039/d1sc02085d |
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author | Glaser, Felix Kerzig, Christoph Wenger, Oliver S. |
author_facet | Glaser, Felix Kerzig, Christoph Wenger, Oliver S. |
author_sort | Glaser, Felix |
collection | PubMed |
description | Sensitization-initiated electron transfer (SenI-ET) describes a recently discovered photoredox strategy that relies on two consecutive light absorption events, triggering a sequence of energy and electron transfer steps. The cumulative energy input from two visible photons gives access to thermodynamically demanding reactions, which would be unattainable by single excitation with visible light. For this reason, SenI-ET has become a very useful strategy in synthetic photochemistry, but the mechanism has been difficult to clarify due to its complexity. We demonstrate that SenI-ET can operate via sensitized triplet–triplet annihilation upconversion, and we provide the first direct spectroscopic evidence for the catalytically active species. In our system comprised of fac-[Ir(ppy)(3)] as a light absorber, 2,7-di-tert-butylpyrene as an annihilator, and N,N-dimethylaniline as a sacrificial reductant, all photochemical reaction steps proceed with remarkable rates and efficiencies, and this system is furthermore suitable for photocatalytic aryl dehalogenations, pinacol couplings and detosylation reactions. The insights presented here are relevant for the further rational development of photoredox processes based on multi-photon excitation, and they could have important implications in the greater contexts of synthetic photochemistry and solar energy conversion. |
format | Online Article Text |
id | pubmed-8317647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-83176472021-08-03 Sensitization-initiated electron transfer via upconversion: mechanism and photocatalytic applications Glaser, Felix Kerzig, Christoph Wenger, Oliver S. Chem Sci Chemistry Sensitization-initiated electron transfer (SenI-ET) describes a recently discovered photoredox strategy that relies on two consecutive light absorption events, triggering a sequence of energy and electron transfer steps. The cumulative energy input from two visible photons gives access to thermodynamically demanding reactions, which would be unattainable by single excitation with visible light. For this reason, SenI-ET has become a very useful strategy in synthetic photochemistry, but the mechanism has been difficult to clarify due to its complexity. We demonstrate that SenI-ET can operate via sensitized triplet–triplet annihilation upconversion, and we provide the first direct spectroscopic evidence for the catalytically active species. In our system comprised of fac-[Ir(ppy)(3)] as a light absorber, 2,7-di-tert-butylpyrene as an annihilator, and N,N-dimethylaniline as a sacrificial reductant, all photochemical reaction steps proceed with remarkable rates and efficiencies, and this system is furthermore suitable for photocatalytic aryl dehalogenations, pinacol couplings and detosylation reactions. The insights presented here are relevant for the further rational development of photoredox processes based on multi-photon excitation, and they could have important implications in the greater contexts of synthetic photochemistry and solar energy conversion. The Royal Society of Chemistry 2021-07-01 /pmc/articles/PMC8317647/ /pubmed/34349964 http://dx.doi.org/10.1039/d1sc02085d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Glaser, Felix Kerzig, Christoph Wenger, Oliver S. Sensitization-initiated electron transfer via upconversion: mechanism and photocatalytic applications |
title | Sensitization-initiated electron transfer via upconversion: mechanism and photocatalytic applications |
title_full | Sensitization-initiated electron transfer via upconversion: mechanism and photocatalytic applications |
title_fullStr | Sensitization-initiated electron transfer via upconversion: mechanism and photocatalytic applications |
title_full_unstemmed | Sensitization-initiated electron transfer via upconversion: mechanism and photocatalytic applications |
title_short | Sensitization-initiated electron transfer via upconversion: mechanism and photocatalytic applications |
title_sort | sensitization-initiated electron transfer via upconversion: mechanism and photocatalytic applications |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317647/ https://www.ncbi.nlm.nih.gov/pubmed/34349964 http://dx.doi.org/10.1039/d1sc02085d |
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