Acid–Base Bifunctional Zirconium N-Alkyltriphosphate Nanohybrid for Hydrogen Transfer of Biomass-Derived Carboxides

Catalytic transfer hydrogenation (CTH) reactions are efficient transformation routes to upgrade biobased chemicals. Herein, we report a facile and template-free route to synthesize a series of heterogeneous nitrogen-containing alkyltriphosphonate–metal hybrids with enhancive Lewis acid and base sites, and their catalytic activity in converting biomass-derived carbonyl compounds to corresponding alcohols in 2-propanol. Particularly, a quantitative yield of furfuryl alcohol (FFA) was obtained from furfural (FUR) over organotriphosphate–zirconium hybrid (ZrPN) under mild conditions. The presence of Lewis basic sites adjacent to acid sites with an appropriate base/acid site ratio (1:0.7) in ZrPN significantly improved the yield of FFA. Mechanistic studies for the transformation of FUR to FFA with ZrPN in 2-propanol-d 8 evidently indicate CTH reaction proceeding via a direct intermolecular hydrogen transfer route. It was also found that ZrPN could catalyze isomerization of C 3 –C 6 aldoses to ketoses involving intramolecular hydrogen transfer in water.