Abstract
A novel bifunctional ordered phenolic resin with Brønsted acid and Lewis acid sites (Yb(OTf)2/PhSO3H-MPR) was prepared for the first time by a two-step sulfonation and postgrafting protocol. The Brønsted acids (benzenesulfonic acids) were transformed from the phenyl groups that existed in the skeleton of ordered mesoporous phenolic resin. Meanwhile, the benzenesulfonic acids can coordinate with Yb(OTf)3 compound, resulting in the generation of Lewis acids in the pore channels of ordered phenolic resin. Yb(OTf)2/PhSO3H-MPR sample retained large specific surface and well-ordered hexagonal mesopores. As expected, it can promote one-pot cascade reaction by using glucose as the reactant to produce 5-hydroxymethylfurfural with good conversion and moderate selectivity. This synergistic catalytic performance could be attributed to its uniformly distributed Brønsted-Lewis acids. Meanwhile, the intrinsic hydrophobic pore surface can decrease the interference of water solvent, leading to enhanced catalytic efficiency. Besides, it was reused more than five times, showing good stability in water.