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A flavin-inspired covalent organic framework for photocatalytic alcohol oxidation

Covalent organic frameworks (COFs) offer a number of key properties that predestine them to be used as heterogeneous photocatalysts, including intrinsic porosity, long-range order, and light absorption. Since COFs can be constructed from a practically unlimited library of organic building blocks, th...

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Autores principales: Trenker, Stefan, Grunenberg, Lars, Banerjee, Tanmay, Savasci, Gökcen, Poller, Laura M., Muggli, Katharina I. M., Haase, Frederik, Ochsenfeld, Christian, Lotsch, Bettina V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612393/
https://www.ncbi.nlm.nih.gov/pubmed/34909156
http://dx.doi.org/10.1039/d1sc04143f
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author Trenker, Stefan
Grunenberg, Lars
Banerjee, Tanmay
Savasci, Gökcen
Poller, Laura M.
Muggli, Katharina I. M.
Haase, Frederik
Ochsenfeld, Christian
Lotsch, Bettina V.
author_facet Trenker, Stefan
Grunenberg, Lars
Banerjee, Tanmay
Savasci, Gökcen
Poller, Laura M.
Muggli, Katharina I. M.
Haase, Frederik
Ochsenfeld, Christian
Lotsch, Bettina V.
author_sort Trenker, Stefan
collection PubMed
description Covalent organic frameworks (COFs) offer a number of key properties that predestine them to be used as heterogeneous photocatalysts, including intrinsic porosity, long-range order, and light absorption. Since COFs can be constructed from a practically unlimited library of organic building blocks, these properties can be precisely tuned by choosing suitable linkers. Herein, we report the construction and use of a novel COF (FEAx-COF) photocatalyst, inspired by natural flavin cofactors. We show that the functionality of the alloxazine chromophore incorporated into the COF backbone is retained and study the effects of this heterogenization approach by comparison with similar molecular photocatalysts. We find that the integration of alloxazine chromophores into the framework significantly extends the absorption spectrum into the visible range, allowing for photocatalytic oxidation of benzylic alcohols to aldehydes even with low-energy visible light. In addition, the activity of the heterogeneous COF photocatalyst is less dependent on the chosen solvent, making it more versatile compared to molecular alloxazines. Finally, the use of oxygen as the terminal oxidant renders FEAx-COF a promising and “green” heterogeneous photocatalyst.
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spelling pubmed-86123932021-12-13 A flavin-inspired covalent organic framework for photocatalytic alcohol oxidation Trenker, Stefan Grunenberg, Lars Banerjee, Tanmay Savasci, Gökcen Poller, Laura M. Muggli, Katharina I. M. Haase, Frederik Ochsenfeld, Christian Lotsch, Bettina V. Chem Sci Chemistry Covalent organic frameworks (COFs) offer a number of key properties that predestine them to be used as heterogeneous photocatalysts, including intrinsic porosity, long-range order, and light absorption. Since COFs can be constructed from a practically unlimited library of organic building blocks, these properties can be precisely tuned by choosing suitable linkers. Herein, we report the construction and use of a novel COF (FEAx-COF) photocatalyst, inspired by natural flavin cofactors. We show that the functionality of the alloxazine chromophore incorporated into the COF backbone is retained and study the effects of this heterogenization approach by comparison with similar molecular photocatalysts. We find that the integration of alloxazine chromophores into the framework significantly extends the absorption spectrum into the visible range, allowing for photocatalytic oxidation of benzylic alcohols to aldehydes even with low-energy visible light. In addition, the activity of the heterogeneous COF photocatalyst is less dependent on the chosen solvent, making it more versatile compared to molecular alloxazines. Finally, the use of oxygen as the terminal oxidant renders FEAx-COF a promising and “green” heterogeneous photocatalyst. The Royal Society of Chemistry 2021-11-15 /pmc/articles/PMC8612393/ /pubmed/34909156 http://dx.doi.org/10.1039/d1sc04143f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Trenker, Stefan
Grunenberg, Lars
Banerjee, Tanmay
Savasci, Gökcen
Poller, Laura M.
Muggli, Katharina I. M.
Haase, Frederik
Ochsenfeld, Christian
Lotsch, Bettina V.
A flavin-inspired covalent organic framework for photocatalytic alcohol oxidation
title A flavin-inspired covalent organic framework for photocatalytic alcohol oxidation
title_full A flavin-inspired covalent organic framework for photocatalytic alcohol oxidation
title_fullStr A flavin-inspired covalent organic framework for photocatalytic alcohol oxidation
title_full_unstemmed A flavin-inspired covalent organic framework for photocatalytic alcohol oxidation
title_short A flavin-inspired covalent organic framework for photocatalytic alcohol oxidation
title_sort flavin-inspired covalent organic framework for photocatalytic alcohol oxidation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612393/
https://www.ncbi.nlm.nih.gov/pubmed/34909156
http://dx.doi.org/10.1039/d1sc04143f
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