异构化
选择性
山梨糖
果糖
化学
路易斯酸
介孔材料
钛
催化作用
微型多孔材料
沸石
核化学
有机化学
作者
Michael J. Cordon,Juan Carlos Vega‐Vila,Alyssa Casper,Zige Huang,Rajamani Gounder
标识
DOI:10.1002/anie.202005207
摘要
Abstract Aqueous‐phase isomerization of d ‐glucose to d ‐fructose and l ‐sorbose is catalyzed in parallel by Lewis acidic Ti sites in siliceous frameworks. Glucose isomerization rates (per Ti, 373 K) are undetectable when Ti sites are confined within mesoporous voids (Ti‐MCM‐41, TiO 2 ‐SiO 2 ) and increase to detectable values when Ti sites are confined within the smaller 12‐membered ring (12‐MR) micropores of Ti‐Beta. Isomerization rates decrease to lower values (by ≈20×) with further decreases in micropore size as Ti sites are confined within 10‐MR pores (Ti‐MFI, Ti‐CON), likely because of intrapore reactant diffusion restrictions, and reach undetectable values within the 8‐MR pores of Ti‐CHA as size exclusion prevents glucose from accessing active sites. Remarkably, the selectivity toward l ‐sorbose over d ‐fructose increases systematically as spatial constraints around Ti sites become tighter, and is >10 on Ti‐MFI. These findings demonstrate the marked influence of confinement around Ti active sites on the selectivity between parallel stereoselective sugar isomerization pathways.
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