Active Sites in Sn-Beta for Glucose Isomerization to Fructose and Epimerization to Mannose

• Published in: ACS catalysis 2014-07, Vol.4 (7), p.2288-2297
• Main Authors: Bermejo-Deval, Ricardo, Orazov, Marat, Gounder, Rajamani, Hwang, Son-Jong, Davis, Mark E
• Format: Article
• Language: English
• ISSN: 2155-5435; 2155-5435
• DOI: 10.1021/cs500466j

Framework Lewis acidic tin sites in hydrophobic, pure-silica molecular sieves with the zeolite beta topology (Sn-Beta) have been reported previously to predominantly catalyze glucose−fructose isomerization via 1,2 intramolecular hydride shift in water and glucose–mannose epimerization via 1,2 intramolecular carbon shift in methanol. Here, we show that alkali-free Sn-Beta predominantly isomerizes glucose to fructose via 1,2 intramolecular hydride shift in both water and methanol. Increasing extents of postsynthetic Na+ exchange onto Sn-Beta, however, progressively shifts the reaction pathway toward glucose–mannose epimerization via 1,2 intramolecular carbon shift. Na+ remains exchanged onto silanol groups proximal to Sn centers during reaction in methanol solvent, leading to nearly exclusive selectivity toward epimerization. In contrast, decationation occurs with increasing reaction time in aqueous solvent and gradually shifts the reaction selectivity to isomerization at the expense of epimerization. Decationation and the concomitant selectivity changes are mitigated by the addition of NaCl to the aqueous reaction solution. Preadsorption of ammonia onto Sn-Beta leads to near complete suppression of infrared and 119Sn nuclear magnetic resonance spectroscopic signatures attributed to open Sn sites and of glucose−fructose isomerization pathways in water and methanol. These data provide evidence that Lewis acidic open Sn sites with either proximal silanol groups or Na-exchanged silanol groups are respectively the active sites for glucose–fructose isomerization and glucose–mannose epimerization.