Related Experiment Video
Updated: Jan 9, 2026

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Novel Ni/Zn MOFs for Sorbitol Production via Catalytic Transfer Hydrogenation
Vuyolwethu Tokoyi1, Nirmala Deenadayalu1
1Department of Chemistry, Faculty of Applied Sciences, Durban University of Technology, Durban P.O. Box 1334, South Africa.
Abstract:
Researchers continue to explore alternative catalysts that are more abundant and effective for hydrogenation reactions to produce sorbitol, such as those using nickel, ruthenium, or zirconium metal centers. This study examined the catalytic transfer hydrogenation of glucose to sorbitol using different alcohol hydrogen donors, specifically ethanol, isopropanol, 1,4-butanediol, and 1,4-cyclohexanediol, with the prepared Ni/Zn MOF catalysts. It also assessed how sacrificial alcohols affected the transformation and selectivity toward sorbitol. The results confirmed the successful catalytic activity and feasibility of this process using MOFs, especially the Ni-based one, which produced up to 51.8% sorbitol, while the Zn-based catalyst yielded 42.3% sorbitol in 1,4-cyclohexanediol. Sacrificial diols exhibited enhanced efficacy as hydrogen donors relative to short-chain alcohols, specifically terminal diols such as 1,4-butanediol and 1,4-cyclohexanediol, which provided substantial hydrogen donation potential and improved selectivity in the conversion of glucose to sorbitol, achieving maximum yields of 45.12% with 1,4-butanediol and 51.8% with 1,4-cyclohexanediol. Regarding the catalysts, both Ni and Zn MOFs improved the transfer hydrogenation process in sugar alcohol mixtures compared to aqueous solutions, and particularly the Ni MOF, with its high surface area and multiple active sites, enhanced the catalytic transformation process. The results clearly indicate that the structural and chemical properties of these alcohols affect the quantity of hydrogen generated and transferred, which is crucial for the efficient overall yield of sorbitol. This insight enhances the understanding of this engineered system and its potential future applications in sustainable biomass utilization.
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Hydroboration-Oxidation of Alkenes
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Catalysis

