4.5 Article

Comparative study of size-selected gold clusters (Au38) and gold nanoparticles over porous cerium-based metal-organic frameworks with UiO-66 architecture for aerobic oxidation of cinnamyl alcohol

Journal

RESEARCH ON CHEMICAL INTERMEDIATES
Volume 47, Issue 6, Pages 2589-2604

Publisher

SPRINGER
DOI: 10.1007/s11164-021-04427-5

Keywords

Au-38(SCH2CH2Ph)(24) clusters; Oxidation of cinnamyl alcohol; Ce-metal-organic frameworks; Oxygen thermal pretreatment; 2-phenylethane thiol

Funding

  1. Assiut University, Egypt

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The catalytic activity of size-selected gold clusters Au-38 in Ce-UiO-66 framework was studied, showing excellent performance in aerobic oxidation of cinnamyl alcohol. The catalyst achieved higher conversion rates in aqueous solvents compared to organic solvents, demonstrating the influence of the support material on catalytic activity.
The catalytic activity of the size-selected gold clusters Au-38(SCH2CH2Ph)(24) (abbreviated with Au-38) in 3-D nanoporous Ce-metal-organic framework (Ce-UiO-66) was studied. The Au-38 nanoclusters were in situ immersed in Ce-UiO-66 with a loading percentage of 1 wt%. The Au-38@Ce-UiO-66 catalyst demonstrated excellent catalytic activity for aerobic oxidation of cinnamyl alcohol. The oxidation reaction was tested from 40 to 100 degrees C utilizing O-2 gas (30 ml min(-1)) as an oxidizing agent in atmospheric pressure. 0.1 mol% of the Au-38@Ce-UiO-66 catalyst achieved 65% cinnamyl alcohol conversion at 100 degrees C within an hour with 100% selectivity toward cinnamaldehyde in toluene. In the case of using an aqueous solvent instead of an organic solvent (toluene), the conversion was increased to 75% under the same reaction condition. The cinnamyl alcohol conversion was increased gradually by increasing the reaction time over Au-38@Ce-UiO-66 catalyst, where the conversion was enhanced to 93% after 5 h of heating at 100 degrees C in water. The catalytic activity of the Au-38@Ce-UiO-66 catalyst was largely enhanced after oxygen thermal pretreatment at 100-200 degrees C, where the catalyst achieved 990 h(-1) turnover frequency (TOF) after O-2-pretreatment at 175 degrees C with 92% cinnamaldehyde and 8% cinnamic acid selectivity. The unique atomic packing structure and electronic properties of the size-selected gold nanoclusters (Au-38) are responsible for their extraordinary catalytic activity. Moreover, the support (Ce-UiO-66) has a big role in the catalyst activity, since it has a high ability to absorb large quantities from oxygen on the Ce(III)/Ce(IV) centers and generate active oxygen species such as superoxo and peroxo species on the catalyst surface, which help in oxidation of cinnamyl alcohol. For comparison, gold nanoparticles were loaded over the same support, where the Au(III) ions were reduced by two different reduction methods utilizing NaBH4 in the absence of the ligand and hydrogen reduction at 200 degrees C, 4 h. The particle size of the Au-38 clusters and gold nanoparticles over Ce-UiO-66 was investigated by a high-resolution transmission electron microscope (HR-TEM). The charge of the gold clusters and nanoparticles was zero as confirmed by X-ray photoelectron spectroscopy (XPS). The crystallinity and surface texture properties of the prepared catalysts and the pure support were measured by powder X-ray diffraction analysis and N-2 gas sorption isotherm at - 196 degrees C, respectively.

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