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Palladium supported on an acidic metal–organic framework as an efficient catalyst in selective aerobic oxidation of alcohols

Chen, Gongzhou, Wu, Shijian, Liu, Hongli, Jiang, Huanfeng, Li, Yingwei·2013·Green Chem.

Abstract

Highly dispersed palladium nanoparticles were deposited on an acidic MOF (MIL-101) by using a simple colloidal method. The resulting Pd/MIL-101 catalyst was highly active in the liquid-phase aerobic oxidation of a wide range of alcohols including benzyl, allylic, aliphatic and heterocyclic alcohols as well as diols, affording the desired oxidation products in high yields under base-free and mild conditions. The catalyst was shown to be able to efficiently catalyze aerobic oxidation even at ambient temperature using air instead of pure O2. The solvent-free oxidation of benzyl alcohol gave a remarkably high turnover frequency (TOF) of approximately 16 900 h−1. However, the catalytic activity was significantly suppressed when ethylenediamine was grafted on the uncoordinated Cr sites of the MIL-101 support, which suggests that the open Cr sites might play an important role in promoting the oxidation of alcohols in the present catalytic system.

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Metadata

Authors
Chen, G., Wu, S., Liu, H., Jiang, H., & Li, Y.
Venue
Green Chem.
Published
2013
Volume
15
Issue
1
Pages
230-235
ISSN
  • 1463-9262 (ISSN-L)
  • 1463-9270
OpenAlex
W2070745862
Cited by
163
References
1
FWCI
7.00
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Palladium supported on an acidic metal–organic framework as an efficient catalyst in selective aerobic oxidation of alcohols. https://app.cochat.ai/papers/10.1039/c2gc36618e
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Chen, G., Wu, S., Liu, H., Jiang, H., & Li, Y. (2013). Palladium supported on an acidic metal–organic framework as an efficient catalyst in selective aerobic oxidation of alcohols. Green Chem. https://doi.org/10.1039/c2gc36618e

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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