Issue 9, 2024

Molybdenum oxide with a varied valency ratio to enable selective d-galactose epimerization to d-talose

Abstract

D-Talose, classified as a rare and expensive sugar molecule, is gaining attraction due to its antimicrobial and anti-inflammatory properties. Its production is widely investigated by adopting biological enzymes, which is costly. However, alternative chemical methodologies have reported its formation as a side product and in minor amounts. We report for the first time its significant synthesis using D-galactose (which comprises whey and hemicellulose) by employing a finely tuned molybdenum oxide (MoO3) solid acid catalyst. The nitric acid treatment of MoO3 modulated the valency ratio in Mo species (Mo5+/6+), resulting in an improved Lewis acidity with up to 199 μmol g−1 acidic sites and porosity of up to 48% relative to the pristine MoO3, attributed to the generated oxygen vacancies. Combined together these have assisted in an augmented D-talose synthesis with as high as 25% yield, 70% selectivity and 98% carbon balance in a water medium under modest reaction conditions (120 °C and 30 min). As proposed, Mo's interaction with D-galactose to form a Mo–sugar complex has influenced the C1–C2 carbon shift to yield D-talose. Furthermore, the typical isotopic labelling NMR characterization has confirmed the Bílik mechanism of C2-galactose epimerization. Overall, the heterogeneous catalytic setup represents a sustainable and feasible method for producing rare sugar for food additive and pharma applications.

Graphical abstract: Molybdenum oxide with a varied valency ratio to enable selective d-galactose epimerization to d-talose

Supplementary files

Article information

Article type
Paper
Submitted
09 Feb 2024
Accepted
28 May 2024
First published
28 May 2024

React. Chem. Eng., 2024,9, 2293-2305

Molybdenum oxide with a varied valency ratio to enable selective D-galactose epimerization to D-talose

B. Devi, S. M. Arumugam, R. K. Kunchala, P. Kaur, S. Mahala and S. Elumalai, React. Chem. Eng., 2024, 9, 2293 DOI: 10.1039/D4RE00076E

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