Advanced characterization of regioselectively substituted methylcellulose model compounds by DNP enhanced solid-state NMR spectroscopy

Published: June 11, 2021

Berruyer, Pierrick, Martin Gericke, Pinelopi Moutzouri, Dörthe Jakobi, Michel Bardet, Leif Karlson, Staffan Schantz, Thomas Heinze, and Lyndon Emsley. “Advanced Characterization of Regioselectively Substituted Methylcellulose Model Compounds by DNP Enhanced Solid-State NMR Spectroscopy.” Carbohydrate Polymers 262 (June 2021): 117944.

https://doi.org/10.1016/j.carbpol.2021.117944.

Dynamic Nuclear Polarization MAS NMR is introduced to characterize model methylcellulose ether compounds at natural isotopic abundance. In particular an approach is provided to determine the position of the methyl ether group within the repeating unit. Specifically, natural abundance 13C-13C correlation experiments are used to characterize model 3-O-methylcellulose and 2,3-O-dimethylcellulose, and identify changes in chemical shifts with respect to native cellulose. We also probe the use of through space connectivity to the closest carbons to the CH3 to identify the substitution site on the cellulose ether. To this end, a series of methylcellulose ethers was prepared by a multistep synthesis approach. Key intermediates in these reactions were 2,6-O-diprotected thex­ yldimethylsilyl (TDMS) cellulose and 6-O-monoprotected TDMS cellulose methylated under homogeneous con­ ditions. The products had degrees of substitution of 0.99 (3-O-methylcellulose) and 2.03 (2,3-Odimethylcellulose) with exclusively regioselective substitution. The approaches developed here will allow characterization of the substitution patterns in cellulose ethers.