A combined solid-state NMR and quantum chemical calculation study of hydrogen bonding in two forms of α-D-glucose

Hydrogen bonding plays an important role in the structure and function of a wide range of materials. Solid-state 1H nuclear magnetic resonance (NMR) spectroscopy provides a very sensitive tool to investigate the local structure of hydrogen atoms involved in hydrogen bonding. While there is extensive 1H solid-state NMR data on O-H - -O hydrogen bonding in solid carboxylic acids, there has been no systematic 1H solid-state NMR studies of hydroxyl groups in carbohydrates (and hydroxyl groups in general). With a view to studying the hydrogen bonding in more complex materials such as cellulose polymorphs, we carried out a detailed solid-state 1H NMR investigation of the model compounds alpha-D-glucose and alpha-D-glucose monohydrate. Through a combination of fast magic-angle spinning (MAS), combined rotation and multiple pulse spectroscopy (CRAMPS), and two-dimensional (2D) correlation experiments carried out at ultrahigh magnetic fields, it was possible to assign all of the aliphatic (CH), hydroxyl (OH), and water (H2O) 1H chemical shifts in both forms of alpha-D-glucose. Plane -wave DFT calculations were employed to improve the hydrogen atom positions for alpha-D-glucose monohydrate and to calculate 1H chemical shifts, providing additional support for the experimentally determined peak as-signments. Finally, the relationship between the hydroxyl 1H chemical shifts and their hydrogen bonding ge-ometry was investigated and compared to the well-established relationship for carboxylic acid protons.