解聚
可再生能源
机制(生物学)
纤维素
反应机理
化学
糖苷键
势能
纳米技术
生化工程
材料科学
催化作用
有机化学
工程类
物理
酶
电气工程
量子力学
作者
Saeed Amirjalayer,Harald Fuchs,Dominik Marx
标识
DOI:10.1002/anie.201811091
摘要
Abstract On the way to establishing biomass as a renewable and environmentally friendly source to cover the ever‐increasing global demand on energy and chemicals, one great challenge is the efficient depolymerization of cellulose. Enhanced conversion rates have been discovered in ball‐milling experiments, thus opening a mechanocatalytic approach. However, an understanding of the impact of mechanical forces on the acid‐catalyzed cleavage of glycosidic bonds at the molecular level is still missing. Herein, we contribute such fundamental insight based on atomistic modeling. Mechanically stressing the macromolecular backbone radically changes the depolymerization pathway from a complex high‐barrier reaction upon thermal activation to a low‐energy single‐step mechanocatalytic process. In addition to revealing a regioselective increase in basicity under a mechanical force, our results provide molecular‐level explanations of the experimental findings and might therefore guide rational ways to improve such mechanocatalytic processes.
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