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Silver-Exchanged Zeolite Y Catalyzes a Selective Insertion of Carbenes into C–H and O–H Bonds

[Image: see text] Commercially available zeolite Y modulates the catalytic activity and selectivity of ultrasmall silver species during the Buchner reaction and the carbene addition to methylene and hydroxyl bonds, by simply exchanging the counter cations of the zeolite framework. The zeolite acts a...

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Autores principales: Zheng, Yongkun, Vidal-Moya, Alejandro, Hernández-Garrido, Juan Carlos, Mon, Marta, Leyva-Pérez, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655197/
https://www.ncbi.nlm.nih.gov/pubmed/37922487
http://dx.doi.org/10.1021/jacs.3c08317
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author Zheng, Yongkun
Vidal-Moya, Alejandro
Hernández-Garrido, Juan Carlos
Mon, Marta
Leyva-Pérez, Antonio
author_facet Zheng, Yongkun
Vidal-Moya, Alejandro
Hernández-Garrido, Juan Carlos
Mon, Marta
Leyva-Pérez, Antonio
author_sort Zheng, Yongkun
collection PubMed
description [Image: see text] Commercially available zeolite Y modulates the catalytic activity and selectivity of ultrasmall silver species during the Buchner reaction and the carbene addition to methylene and hydroxyl bonds, by simply exchanging the counter cations of the zeolite framework. The zeolite acts as a macroligand to tune the silver catalytic site, enabling the use of this cheap and recyclable solid catalyst for the in situ formation of carbenes from diazoacetate and selective insertion in different C–H (i.e., cyclohexane) and C–O (i.e., water) bonds. The amount of catalyst in the reaction can be as low as ≤0.1 mol % silver. Besides, this reactivity allows deeply drying the HY zeolite framework by making the strongly adsorbed water molecules react with the in situ formed carbenes.
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spelling pubmed-106551972023-11-17 Silver-Exchanged Zeolite Y Catalyzes a Selective Insertion of Carbenes into C–H and O–H Bonds Zheng, Yongkun Vidal-Moya, Alejandro Hernández-Garrido, Juan Carlos Mon, Marta Leyva-Pérez, Antonio J Am Chem Soc [Image: see text] Commercially available zeolite Y modulates the catalytic activity and selectivity of ultrasmall silver species during the Buchner reaction and the carbene addition to methylene and hydroxyl bonds, by simply exchanging the counter cations of the zeolite framework. The zeolite acts as a macroligand to tune the silver catalytic site, enabling the use of this cheap and recyclable solid catalyst for the in situ formation of carbenes from diazoacetate and selective insertion in different C–H (i.e., cyclohexane) and C–O (i.e., water) bonds. The amount of catalyst in the reaction can be as low as ≤0.1 mol % silver. Besides, this reactivity allows deeply drying the HY zeolite framework by making the strongly adsorbed water molecules react with the in situ formed carbenes. American Chemical Society 2023-11-03 /pmc/articles/PMC10655197/ /pubmed/37922487 http://dx.doi.org/10.1021/jacs.3c08317 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Zheng, Yongkun
Vidal-Moya, Alejandro
Hernández-Garrido, Juan Carlos
Mon, Marta
Leyva-Pérez, Antonio
Silver-Exchanged Zeolite Y Catalyzes a Selective Insertion of Carbenes into C–H and O–H Bonds
title Silver-Exchanged Zeolite Y Catalyzes a Selective Insertion of Carbenes into C–H and O–H Bonds
title_full Silver-Exchanged Zeolite Y Catalyzes a Selective Insertion of Carbenes into C–H and O–H Bonds
title_fullStr Silver-Exchanged Zeolite Y Catalyzes a Selective Insertion of Carbenes into C–H and O–H Bonds
title_full_unstemmed Silver-Exchanged Zeolite Y Catalyzes a Selective Insertion of Carbenes into C–H and O–H Bonds
title_short Silver-Exchanged Zeolite Y Catalyzes a Selective Insertion of Carbenes into C–H and O–H Bonds
title_sort silver-exchanged zeolite y catalyzes a selective insertion of carbenes into c–h and o–h bonds
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655197/
https://www.ncbi.nlm.nih.gov/pubmed/37922487
http://dx.doi.org/10.1021/jacs.3c08317
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