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  5. Low-temperature hydroformylation of ethylene by phosphorous stabilized Rh sites in a one-pot synthesized Rh-(O)-P-MFI zeolite

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Article
English
2023

Low-temperature hydroformylation of ethylene by phosphorous stabilized Rh sites in a one-pot synthesized Rh-(O)-P-MFI zeolite

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English
2023
Nature Communications
Vol 14 (1)
DOI: 10.1038/s41467-023-42938-4

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Avelino Avelino
Avelino Avelino

Instituto de Tecnología Química

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Minjie Zhao
Chengeng Li
Daviel Gómez
+8 more

Abstract

Zeolites containing Rh single sites stabilized by phosphorous were prepared through a one-pot synthesis method and are shown to have superior activity and selectivity for ethylene hydroformylation at low temperature (50 °C). Catalytic activity is ascribed to confined Rh2O3 clusters in the zeolite which evolve under reaction conditions into single Rh3+ sites. These Rh3+ sites are effectively stabilized in a Rh-(O)-P structure by using tetraethylphosphonium hydroxide as a template, which generates in situ phosphate species after H2 activation. In contrast to Rh2O3, confined Rh0 clusters appear less active in propanal production and ultimately transform into Rh(I)(CO)2 under similar reaction conditions. As a result, we show that it is possible to reduce the temperature of ethylene hydroformylation with a solid catalyst down to 50 °C, with good activity and high selectivity, by controlling the electronic and morphological properties of Rh species and the reaction conditions.

How to cite this publication

Minjie Zhao, Chengeng Li, Daviel Gómez, Francisco Gonell, Vlad Martin‐Diaconescu, Laura Simonelli, Miguel López‐Haro, José J. Calvino, Débora Motta Meira, Patricia Concepción, Avelino Avelino (2023). Low-temperature hydroformylation of ethylene by phosphorous stabilized Rh sites in a one-pot synthesized Rh-(O)-P-MFI zeolite. Nature Communications, 14(1), DOI: 10.1038/s41467-023-42938-4.

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Publication Details

Type

Article

Year

2023

Authors

11

Datasets

0

Total Files

0

Language

English

Journal

Nature Communications

DOI

10.1038/s41467-023-42938-4

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